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Friday, May 1
 

8:30am EDT

A Guide to Becoming A Sports Medicine Pharmacist in the Ambulatory Care Setting
Friday May 1, 2026 8:30am - 8:50am EDT
Authors: Deena Alsabbah, Alexis Shook, Brian Atkinson, and Graham Grush

Background: Pharmacists have proven valuable across various clinical areas and interprofessional teams, especially in ambulatory care settings, improving health outcomes and quality of care. Within the past few decades, sports medicine pharmacy has emerged as a unique specialty, ranging from counseling individuals in local club sports and fitness to advising elite Olympic athletes. Despite this, sports or sports medicine pharmacy remains underrepresented in pharmacy education and practice. The aim of this project was to design a guide for becoming a sports medicine pharmacist in the ambulatory care setting that addresses roles and responsibilities, areas for interprofessional collaboration, and resources to expand knowledge and networking opportunities.

Methods:
A literature review was conducted to gather information on sports pharmacy organizations and resources, education and training opportunities, and roles and responsibilities. A 13-question qualitative survey was also distributed to practicing sports pharmacists within 3 sports pharmacy organizations (Sports Pharmacy Network, International Sports Pharmacist Network, and/or U.S. Sports Pharmacy Group) to obtain perspectives on current practice. Responses were summarized to highlight most common themes. 

Results: This abstract describes results from the qualitative survey and how it translates to ambulatory care practice.
Survey respondents (n = 14) reported diverse practice backgrounds across multiple settings, including ambulatory care, independent community pharmacy, student health, athletics, acute care, and scientific writing. The majority of respondents had been practicing for 2-5 years (42.9%), followed by 10-20+ years (35.7%), and 0-1 years (21.4%). 78.6% of respondents reported working with nutritionists, as well as physicians, nurse practitioners, nurses, athletic trainers, physical therapists, sports psychologists, and sports dentists. The most common roles and responsibilities included medication and therapeutic management (50%), clinical assessment and screening (28.6%), personalized care and performance planning (28.6%), consultation and education (71.4%), and scientific and educational content development (21.4%). Respondents frequently managed conditions such as pain and injury, Relative Energy Deficiency in Sport (RED-S), mental health disorders, infectious diseases, and many more.
Primary barriers to sports pharmacy practice included lack of buy-in and awareness from other parties and sustainable reimbursement. Funding sources varied considerably, with 42.8% of respondents receiving private or cash payments, while others relied on educational sites and programs or additional employment.

Conclusions: There are a variety of ways pharmacists can make an impact in sports medicine, particularly in ambulatory care settings. Resources and organizations, like the International Sports Pharmacists Network, Global DRO, WADA, and Sports Pharmacy Network, are just a few of many that provide the necessary education, skills, and networking opportunities for pharmacists and student pharmacists to enter a career path caring for a unique patient population.
Moderators
avatar for Devin Lavender

Devin Lavender

Clinical Assistant Professor, UGAA1University of Georgia College of Pharmacy (Ambulatory Care)PGY2
Ambulatory Care, Scholarship of Teaching and Learning, Resident and Student Development.
Presenters
avatar for Deena Alsabbah

Deena Alsabbah

PGY1 Ambulatory Care Resident, Mountain Area Health Education Center (MAHEC)
Deena is originally from Kenosha, WI and completed her Doctor of Pharmacy degree at Drake University College of Pharmacy and Health Sciences in Des Moines, IA. Following graduation, she moved to Asheville, NC to complete an ambulatory care-focused PGY1 residency. Her clinical interests... Read More →
Evaluators
Friday May 1, 2026 8:30am - 8:50am EDT
Parthenon 1

8:30am EDT

Adherence to Recommended Vaccinations in a Veteran Rheumatology Population: A Quality Improvement Initiative
Friday May 1, 2026 8:30am - 8:50am EDT
ADHERENCE TO RECOMMENDED VACCINATIONS IN A VETERAN RHEUMATOLOGY POPULATION: A QUALITY IMPROVEMENT INITIATIVE  
Avery Zapp, Lilian Culp, Whitney White

Birmingham VA Healthcare System – Birmingham, AL


Background/Purpose: This project aimed to systematically evaluate the vaccination status of patients managed by the rheumatology clinic at a Veterans Affairs Medical Center, with a focus on adherence to current immunization guidelines. The interventions also aimed to promote provider engagement and patient awareness. The effectiveness of a multifaceted pharmacist–provider intervention on vaccination rates among veterans was evaluated.
Methodology: Eligible participants include those who are followed in the Birmingham VA rheumatology clinic, currently taking a JAK inhibitor and due for the herpes zoster vaccination. Intervention included pharmacist dashboard monitoring to evaluate patients due for vaccination, with those patients subsequently sent to providers as reminder for their upcoming appointment. Reminder notifications were also sent to eligible patients. Intervention with nursing staff was also performed to address triage and patient education. Vaccination rates in the rheumatology clinic were assessed before and after the interventions were implemented.  
Results: Twenty-nine patients with upcoming appointments were reviewed, all prescribed tofacitinib or upadacitinib. At baseline, 46 percent had at least one documented dose of recombinant zoster vaccine, while 54 percent had no documentation. Most patients (25 of 29) were established in primary care. Overall clinic vaccination rates increased by approximately 1 percent during the study period, with completion of the two‑dose series rising from 41 percent to 42 percent. The primary barriers were patient preference and hesitancy, often related to safety concerns or misperceptions about risk. Documentation gaps, particularly for vaccines administered outside the VA, likely contributed to underestimation of true vaccination status.
Conclusions: Pharmacist‑driven provider reminders and patient outreach efforts improved awareness of vaccination needs but did not produce a substantial increase in herpes zoster vaccination rates during the short study interval. Persistent patient hesitancy and documentation inconsistencies remained barriers to adherence. These findings highlight the need for ongoing, multifaceted strategies - particularly targeted patient education, streamlined documentation processes, and incorporation of additional staff support - to enhance vaccine acceptance in Veterans receiving JAK inhibitors. Future expansion of this initiative will address additional immunization gaps in the rheumatology population.
Presentation Objective: By the end of this presentation, participants will be able to identify key factors affecting herpes zoster vaccination adherence in Veteran rheumatology patients on JAK inhibitors and develop strategies to improve these rates. Self-Assessment: What intervention is most likely to improve recombinant herpes zoster vaccination rates in veterans receiving JAK inhibitors?



Moderators
avatar for Brian Leith

Brian Leith

Clinical Pharmacist, VA Medical Center
I am currently the emergency medicine and antimicrobial stewardship pharmacist at the VA Medical Center in Fayetteville, NC.
Presenters
AZ

Avery Zapp

PGY1 Resident, Birmingham VA Health Care System
Evaluators
BK

Brian Knott

Clinical Pharmacy Manager, AdventHealth Winter Park
Friday May 1, 2026 8:30am - 8:50am EDT
Olympia 2

8:30am EDT

VOICES OF WOMEN’S HEALTH: A SURVEY TO SHAPE ACCESSIBLE, PHARMACIST-LED CARE
Friday May 1, 2026 8:30am - 8:50am EDT
Title: VOICES OF WOMEN’S HEALTH: A SURVEY TO SHAPE ACCESSIBLE, PHARMACIST-LED CARE 

Authors: MK Schwaemmle, Fallon Hartsell, Courtney E. Gamston, Kimberly B. Lloyd 

Background/Purpose
: Women’s health has been a topic that has been historically neglected by the medical community at large, and limited research regarding specific conditions that primarily affect women, make it difficult for practitioners and patients to navigate and manage disease states such as endometriosis, menopause, migraines, pelvic floor disorders, and others. According to the Center for Disease Control and Prevention (CDC) in 2023, 15.6% of women 18 years old and older in the United States reported to be in fair or poor health. In addition, 3 out of 4 people diagnosed with an autoimmune disease are women. Many women lack consistent support for their health needs, providing pharmacists an opportunity for addressing health care needs in this underserved patient population. This survey seeks to identify which women's health services are needed and desired within a self-insured adult female population and the acceptability of having pharmacists provide these services. 

Methodology: An incentivized, anonymous online survey was distributed via email, social media, and flyers. Eligible participants were females covered by the employee insurance plan at a large, self-insured employer and were 18 years old and older. Survey domains included demographics, assessment of general health, gynecologic history, sexual health, current health concerns, facilitators and barriers to care, brief health history, and desire for pharmacist-led services.  The survey took participants between 20 and 30 minutes to complete. Data was reported as descriptive statistics. The results of this study will identify the status of women’s health needs in the community, characterize this patient population, and inform the development of pharmacy-provided services.  

Results: In progress 

Conclusions
: In progress 

Moderators Presenters Evaluators
CT

Christina Thurber

PGY-1 Residency Program Coordinator
Friday May 1, 2026 8:30am - 8:50am EDT
Parthenon 2

8:30am EDT

Effects of Ketamine Infusion Rate and Dosing on Delirium in Medical ICU Patients
Friday May 1, 2026 8:30am - 8:50am EDT
Introduction:
Ketamine, an N-methyl-D-aspartate (NMDA) receptor antagonist, is increasingly utilized for analgosedation in mechanically ventilated intensive care unit (ICU) patients due to its analgesic and sedative properties. Its effects are dose dependent, with lower infusion rates (0.1–0.4 mg/kg/hr) providing analgesia and higher rates (0.4–1.0 mg/kg/hr) producing sedation. At higher doses, ketamine may cause dissociative or psychiatric effects that can resemble ICU delirium. However, existing data on the relationship between ketamine and delirium are limited and conflicting, often without adequate adjustment for confounders or consideration of dosing variability. This study aimed to evaluate the association between maximum daily ketamine infusion rate and ICU delirium. A secondary objective assessed the relationship between cumulative ketamine dose and delirium.
Methods:
This multicenter retrospective cohort study included adult medical ICU patients requiring mechanical ventilation and received ketamine infusions for sedation between January 1, 2013 and June 30, 2025 at two tertiary care hospitals. Patients were excluded if ketamine was used for non-sedation indications, administered for less than 24 hours, or if continuous neuromuscular blockade was used. Demographic and clinical data were collected, including age, race, sex, Sequential Organ Failure Assessment (SOFA) score, comorbidities, history of substance use or psychiatric illness, and sedation-related variables. Additional data included ketamine infusion rates, cumulative ketamine dose, duration of ketamine therapy, timing of ketamine initiation, concomitant sedative or analgesic use, Richmond Agitation-Sedation Scale (RASS) scores, and Confusion Assessment Method for the ICU (CAM-ICU) scores.  
The primary outcome was ICU delirium, defined by a positive CAM-ICU at any point during ICU stay. A modified Poisson regression evaluated linear associations of delirium with the primary exposure variable, highest daily ketamine rate, and secondary exposure variable, cumulative ketamine dose. Covariates included SOFA score, cumulative morphine milligram equivalents (MME), cumulative benzodiazepines, and ICU length of stay (LOS). Logistic spline models and multivariate logistic regression were also conducted for both exposure variables. Other secondary outcomes, including mortality and LOS were analyzed using descriptive statistics, Mann Whitney U, or Chi Square as appropriate. 
Results:
Of 837 screened patients, 114 met inclusion criteria and 42 (36.8%) developed delirium. Baseline characteristics were similar between groups, with a median age of 57–58 years. There was no difference between those who developed delirium and those who did not with regard to the maximum daily ketamine infusion rate (0.6 vs 0.43 mg/kg/hr, p=0.08) and cumulative doses (3440.6 vs 2461.4 mg, p=0.10). Patients with delirium had longer mechanical ventilation duration (210.7 vs 140.9 hours, p<0.01), longer ICU length of stay (364.7 vs 268.6 hours, p=0.04), and higher opioid exposure (5126.8 vs 2911.8 morphine milligram equivalents, p=0.85). Benzodiazepine use and mortality were not significantly different.
In the modified Poisson regression, there was no association between maximum daily ketamine infusion rate and delirium (Relative risk ratio (RR) 1.15, p=0.21) or cumulative ketamine dose and delirium (RR 1.0, p=0.97). Duration of mechanical ventilation was independently associated with delirium in both regression models (RR 1.0, p<0.01). No association between maximum daily ketamine infusion rate or cumulative ketamine dose with delirium was seen in logistic spline or multivariate regression models.   
Conclusion:
Neither maximum daily ketamine infusion rate nor cumulative dose was associated with ICU delirium after adjustment for confounders. As seen in previous literature, duration of mechanical ventilation was associated with delirium. These findings suggest ketamine infusion rate and dosing may not significantly influence delirium risk, though prospective studies are needed to confirm these results.


Moderators
avatar for Brittany NeSmith

Brittany NeSmith

PGY1 Residency Program Director, BSSFBon Secours St. Francis DowntownPGY1
Presenters Evaluators
BB

Brooke Bibb

Ascension Saint Thomas Hospital West
Friday May 1, 2026 8:30am - 8:50am EDT
Athena J

8:30am EDT

Evaluation of Guideline-Recommended Duration of Levetiracetam Prophylaxis Prescribed in Patients After Traumatic Brain Injury
Friday May 1, 2026 8:30am - 8:50am EDT
Title: Evaluation of Guideline-Recommended Duration of Levetiracetam Prophylaxis Prescribed in Patients After Traumatic Brain Injury
Authors: Michael Kim, Kameron Hicks, Rachel Friend, Donley Galloway
Background: Traumatic brain injuries (TBI) may lead to early post-traumatic seizures (PTS), especially in instances of severe TBI and to a lesser extent in mild to moderate TBI. Early PTS are mechanistically distinct from late PTS and most often occur within seven to fourteen days of the inciting TBI. They are associated with poor morbidity and mortality outcomes. Recent guidelines by the Neurocritical Care Society suggest that there is no statistical difference in the reduction of early seizures with or without the use of antiseizure medications. However, levetiracetam is commonly used as seizure prophylaxis due to its favorable adverse drug effect profile. The use of antiseizure medications for a shorter duration of time of ≤ 7 days is recommended because the studies have identified no statistical difference with longer duration of antiseizure medication therapy and worse adverse effect incidence. As the use of prophylactic levetiracetam provides limited benefits in preventing early seizures, the purpose of this study is to evaluate its current prescribing practices to potentially provide evidence to support standardized as lengthy duration and high dose is not well supported by current evidence.
Methods: This was an IRB approved single-centered, retrospective evaluation of adult patients diagnosed with traumatic brain injury and given levetiracetam as seizure prophylaxis who were admitted to one of four inpatient neurologic or trauma units between June 1, 2025, to May 31, 2025. Patients were excluded if they had any prior history of seizures, on any maintenance antiepileptic medications, used any other antiepileptic medications for seizure prophylaxis, or were prisoners. The primary outcome of this study was the rate of guideline recommended duration of levetiracetam prophylaxis. Secondary outcomes included documented seizure activity within the encounter, dose and frequency of levetiracetam used as prophylaxis, number of patients discharged home with levetiracetam, and any documented CNS or hypersensitivity reactions from levetiracetam. The collected data was analyzed using descriptive statistics and chi-square test.
Results: A total of 111 patients were included. The rate of guideline recommended duration of levetiracetam for seizure prophylaxis after TBI was 43.2% (n=48/111. The rate of guideline directed duration of therapy in just the inpatient days of prophylactic therapy yielded 82% (n=91/111). Within the subgroups, the rate of guideline directed duration of therapy was 47.4% (n=27/57) in the STICU, 48.6% (n=17/35) in the NICU, 18.2% (n=2/11) in E5, and 25% (n=2/8) in E4. The frequency of the maintenance prophylaxis was twice daily dosing. The doses administered inpatient were varied, but was most commonly 500 mg twice daily (63.1%, n=71/111). The number of those discharged on levetiracetam was 51.4% (n=57/111) with durations ranging from 1-90 days and doses ranging from 500mg-1000mg. Possible CNS effects from levetiracetam was seen in 21 patients (18.9%). One patient (0.9%) had evidence of seizure activity.
Conclusions: Guideline recommended duration of levetiracetam as early post-traumatic seizure prophylaxis was seen in less than half of the patients within this institution’s main trauma and neurologic units when accounting for both initial inpatient and outpatient continuation of prophylactic therapy. Most patients in the inpatient setting received the recommended duration of therapy of seven days or fewer, but prescription orders at discharge for prophylaxis up to 90 days were observed. With the only seizure having been seen in the severe TBI patient, potential adverse drug effects seen, and long duration of prophylaxis that the majority of these patients received, more conservative management with seizure prophylaxis may be warranted. Future studies that evaluate the seizure incidence between evidence supported shorter duration of therapy and extended duration of therapy may contribute to the potential de-prescribing efforts of pharmacists.

Contact Information: [email protected]
Moderators
avatar for Christele Robinson

Christele Robinson

Emergency Medicine Clinical Pharmacy Specialist, Emory University Hospital
Christele Robinson, PharmD, is board certified in pharmacotherapy. She is a member of the Department of Pharmacy at Emory University Hospital and currently practicing as an Emergency Medicine Clinical Pharmacy Specialist. Dr. Robinson obtained a Bachelor of Science degree at the... Read More →
Presenters
avatar for Michael Kim

Michael Kim

PGY1 Pharmacy Resident, Atrium Health Navicent - The Medical Center
Michael Kim is a PGY1 Resident at Atrium Health Navicent in Macon, GA. He graduated from the University of Georgia College of Pharmacy in 2025. After residency, Michael will continue his career as a clinical pharmacist at his current institution. He is a current member of ASHP and... Read More →
Evaluators
avatar for Cody Parker

Cody Parker

Clinical Pharmacy Specialist, St. Joseph's/Candler
Dr. Cody Parker is the PGY1 Pharmacy Residency Program Director at St. Joseph's/Candler in Savannah, GA. He received his Doctor of Pharmacy from the University of Georgia and completed a Postgraduate Year One (PGY1) Pharmacy Practice Residency at St. Joseph’s/Candler. Dr. Parker is a Clinical Pharmacy Sp... Read More →
Friday May 1, 2026 8:30am - 8:50am EDT
Athena D

8:30am EDT

Evaluation of Post-Intubation Sedation Practices Following Rapid Sequence Intubation in a Community Hospital Emergency Department
Friday May 1, 2026 8:30am - 8:50am EDT
Background: Rapid-sequence intubation (RSI) involves administration of an induction agent and neuromuscular blocking agent to facilitate patient comfort and endotracheal intubation. Following RSI, initiation of post-intubation sedation is essential to maintain patient comfort, reduce agitation, and prevent awareness with paralysis (AWP), which has been associated with psychological distress and other adverse outcomes. Several factors may contribute to AWP, including the use of long-acting neuromuscular blocking agents such as rocuronium, underdosing of induction agents, and delays in initiation of post-intubation sedation. In many emergency department (ED) settings, post-intubation sedation may be delayed, inconsistently initiated, or omitted, potentially increasing the risk of “awake paralysis.” At our community hospital, pharmacists are not routinely involved in the RSI process, as medication orders are auto-verified and pharmacy staff are not alerted when intubations occur. Additionally, the existing RSI order set does not include guidance for post-intubation sedation. Pharmacists may play an important role in supporting medication selection, preparation, and timely initiation of sedation following RSI. The purpose of this study was to evaluate to evaluate post-intubation sedation practices following RSI in the ED at a community hospital.

Methodology: This single-center, IRB-reviewed, determined exempt retrospective evaluation assessed adult patients undergoing RSI in the ED between January 2025 and March 2025. Adult patients aged ≥ 18 years who underwent RSI with an induction agent and neuromuscular blocking agent in the ED were included. Patients were excluded if intubation or post-intubation management was performed by a non-ED provider, RSI occurred outside the ED, the patient died in the ED, or ED length of care was less than one hour. Outcomes evaluated included receipt of a sedative within one hour following RSI and time to first sedative administration. Continuous variables were summarized using descriptive statistics, and categorical variables were reported as frequencies and percentages.

Results: A total of 186 patients were screened, of which 52 patients met inclusion criteria for evaluation. The mean age was 65 years (SD 13.3), and 54% were female. The most common indication for RSI was respiratory distress (58%), followed by altered mental status (21%) and unresponsiveness (13%). Etomidate was the most commonly used induction agent (79%), and rocuronium was the most frequently used neuromuscular blocking agent (77%). Overall, 81% of patients received at least one sedative agent within one hour following RSI. Fentanyl was the most commonly used agent (88%), while propofol was the second most frequently used sedative (63%), followed by midazolam (21%). The mean time to first sedative dose was 29.4 minutes.

Conclusion: In this evaluation of post-intubation sedation practices following RSI in the ED, most patients received a sedative within one hour; however, variability in the timing and initiation of therapy was observed. Delays or absence of sedation following RSI may increase the risk of complications such as inadequate sedation and awareness with paralysis. These findings highlight an opportunity to improve the consistency and timeliness of post-intubation sedation practices. Greater pharmacist involvement during RSI events may help optimize medication selection and promote more timely initiation of sedation. Future efforts should focus on establishing a consistent pharmacy presence in the ED and developing a standardized workflow to facilitate pharmacist involvement during RSI events.
Moderators
AQ

April Quidley

PGY1 Residency Program Director, ECU Health Medical Center
Presenters Evaluators
AJ

Audrey Johnson

Surgical/Trauma Critical Care Pharmacist, Memorial Health University Medical Center
Friday May 1, 2026 8:30am - 8:50am EDT
Olympia 1

8:30am EDT

Standardized Calcium Replacement During Massive Transfusion Protocol in Trauma
Friday May 1, 2026 8:30am - 8:50am EDT
Purpose: Historically, trauma resuscitation has focused on three main complicating factors known as the “lethal triad”: hypothermia, acidosis, and coagulopathy. However, recent literature has begun to recognize hypocalcemia as a fourth pillar in mortality rates. Data has shown up to 97% of patients can experience an exacerbation of hypocalcemia during massive transfusion protocol (MTP), of which 71% may experience severe hypocalcemia (ionized calcium < 0.9 mmol/L). The purpose of this study is to evaluate the effect of a standardized protocol for calcium repletion in trauma patients requiring MTP. 
Methods: This was a single center, retrospective, descriptive, observational study among trauma patients who presented to Wellstar Kennestone Regional Medical Center Emergency Department (WKRMCED). Data was collected prior to implementation of a calcium repletion protocol from July 1, 2023 to May 31, 2024, and post-protocol implementation from August 1, 2024 to June 30, 2025. Patients were included if they presented to WKRMCED during the specified treatment dates as a tier 1 trauma requiring activation of MTP for administration of blood products. Patients were excluded if they were pregnant, ≤ 15 years old, had activation of MTP for a non-trauma related reason, did not have documentation of calcium levels after transfusion, or if the calcium replacement protocol was not followed after transfusion of blood products. The primary outcome was calcium levels up to 24h following the last documented blood product given post-transfusion. Secondary outcomes included total amount of blood products transfused within 24h of MTP initiation, hospital length of stay, intensive care unit length of stay, and in-hospital mortality.  
Results: Of the 6217 patients screened for inclusion in this study, 122 met inclusion criteria. Patients were screened further based on the predefined exclusion criteria and a total of 98 patients were included in the study (pre-protocol n=62; post protocol n=36).  Although this study was observational, and descriptive statistics were used, there did not appear to be any vast differences, numerically in demographic information. The primary outcome increased nearly 25% from pre-protocol (51.5%) to post-protocol (75%). Regarding the secondary outcomes, more elemental calcium was given in the post-protocol group, and there was a decrease from pre- to post-protocol in the time difference between the first unit of blood being given and the first dose of calcium being administered (pre-protocol: median 1.17 hours, IQR 3.21 hours; post-protocol: median 0.45 hours, IQR 0.65 hours). In the pre-protocol group, the baseline to follow up iCAL was 1.07 to 1.1. Comparatively, the difference in baseline to follow up iCAL in the post-protocol group was 0.195 mmol/L, which is a 6.5 times greater increase than the pre-protocol of 0.03 mmol/L. 
Conclusions: The implementation of a calcium repletion protocol during MTP in trauma suggests maintenance of higher serum calcium levels and thus may decrease the risk of complications during trauma resuscitation. Future studies should focus on the inclusion of larger populations for better generalizability and defining a dose of calcium (gluconate, chloride, or both) that is most efficacious among any trauma patient requiring massive transfusion protocol. 

Moderators
CW

Cassandra Wade

Pharmacy Procurement Coordinator, John D Archbold Memorial Hospital
Presenters Evaluators
avatar for Madison Yates

Madison Yates

Clinical Pharmacist Practitioner, PGY1 Ambulatory Residency Program Coordinator, Cone Health
Friday May 1, 2026 8:30am - 8:50am EDT
Athena G

8:30am EDT

Streamlining Phenobarbital Usage in Alcohol Withdrawal Patients at a Large Community Hospital
Friday May 1, 2026 8:30am - 8:50am EDT
Authors: Leah Franks, Jeremy Ray, and Mickala Thompson
 
Background: Alcohol withdrawal syndrome (AWS) is a serious condition that progresses in severity. The most severe symptoms include withdrawal seizures and delirium tremens. Phenobarbital is a barbiturate currently classified as an alternative agent for severe AWS in the 2020 American Society of Addiction Medicine’s “Clinical Practice Guideline on Alcohol Withdrawal Management.” A 2023 meta-analysis conducted by Umar, et al. concluded that phenobarbital can be used safely and effectively for AWS within the ICU setting. Phenobarbital prescribing practices have not been analyzed thus far at our institution. Therefore, the purpose of this research is to assess the current utilization and dosing schemes of phenobarbital for AWS at our large community hospital.
 
Methods: A single-center, institutional review committee-approved pre-post analysis was conducted at Huntsville Hospital to assess the safety, efficacy, and outcomes of patients receiving phenobarbital after the implementation of a streamlined-dosing order set. Information from an initial chart review was utilized to develop an order set based on current guideline recommendations/literature while also aligning with current prescribing practices at our institution. After implementation of streamlined dosing, a post-hoc analysis will be conducted. Adult patients, greater than 18 years of age, who received phenobarbital for management of AWS were included in the study. Exclusion criteria included vulnerable patients and those who received phenobarbital for underlying seizure disorders. The primary endpoints are the utilization of a pre-determined, guideline-directed dosing scheme and benzodiazepine usage post-phenobarbital loading dose administration. Secondary endpoints include ICU admission, need for intubation, withdrawal seizure or delirium tremens occurrence, and adverse events.
 
Results: A total of 54 patients in the pre-implementation group and 29 patients in the post-implementation group were included in this study. Baseline characteristics were similar between pre-post data regarding age (mean ~ 50 years), sex (majority male), baseline liver dysfunction (~50% for both groups), and receipt of CNS depressants (26% vs 21%) prior to phenobarbital. In terms of the primary endpoints, 38% of the providers utilized the phenobarbital order set. Benzodiazepine usage (in lorazepam equivalents - mg, median [IQR]) post-phenobarbital was comparable (4 [7.8] vs 4 [7.25]). Lastly, variability amongst secondary outcomes occurred with the need for ICU admission and the need for intubation post-phenobarbital between the pre-implementation group (56% and 13%) and the post-implementation group (31% and 21%).
 
Conclusion: Overall, order set utilization was minimal, which hindered appropriate comparison between pre-post implementation data. Limitations included the variety of ordering providers, a single center study, as well as the order set not initially being in all alcohol withdrawal order sets. Future directions include implementing further education across all provider types and improving visibility of the order set to providers by adding it to the overall alcohol withdrawal admission and add-on order sets. 
Moderators
avatar for Aayush Patel

Aayush Patel

Clinical Pharmacy Specialist, Emergency Medicine, Piedmont Columbus Regional Midtown
Presenters
avatar for Leah Franks

Leah Franks

PGY-2 Pharmacy Resident, Huntsville Hospital
Leah Franks is a PGY-1 Pharmacy Resident at Huntsville Hospital in Huntsville, Alabama and is originally from Meridian, Mississippi. She earned her Doctor of Pharmacy degree in 2024 from the University of Mississippi. Leah will continue her post-graduate training at Huntsville Hospital... Read More →
Evaluators
Friday May 1, 2026 8:30am - 8:50am EDT
Athena A

8:30am EDT

Tirofiban use following mechanical thrombectomy with emergent stent placement in acute ischemic stroke
Friday May 1, 2026 8:30am - 8:50am EDT
Title: Tirofiban use following mechanical thrombectomy with emergent stent placement in acute ischemic stroke
Author Names: Taylor Dodd, Mallory Stringer, Eric Shaw
Resident E-mail: [email protected]

Background
Tandem lesions are present in 15-25% of all acute ischemic strokes (AIS) presenting with a large vessel occlusion (LVO) and are associated with increased morbidity and mortality. Treatment of tandem lesions is not standardized, but may include intra-arterial thrombolysis, balloon angioplasty, and/or emergent stent placement during mechanical thrombectomy. Emergent stent placement requires antiplatelet therapy which may include glycoprotein (GP) IIb/IIIa inhibitors (e.g. tirofiban), aspirin, and/or P2Y12 inhibitors. Currently, there is inconsistent data regarding the dosing and duration of tirofiban infusion following mechanical thrombectomy with emergent stent placement in AIS. Retrospective data suggests similar rates of symptomatic intracranial hemorrhage (ICH), mortality, and reperfusion rates with tirofiban use compared to without tirofiban. The study objective is to evaluate the safety and efficacy of tirofiban followed by dual antiplatelet therapy (DAPT) compared to antiplatelet therapy alone in AIS patients post mechanical thrombectomy with emergent stent placement.

Methods
This was a single-center retrospective study conducted at a 711-bed DNV certified comprehensive stroke academic medical center. Adults admitted to the neurovascular intensive care unit (ICU) for AIS following mechanical thrombectomy and emergent stent placement that received tirofiban and/or antiplatelet therapy were included. Protected populations were excluded. The primary outcome was symptomatic ICH, defined as ICH on imaging with any of the following: need for neurosurgical intervention, intubation, decrease in Glasgow Coma Scale score ≥ 2 within 24 hours of tirofiban or DAPT. Secondary outcomes included any ICH, hospital and ICU length of stay (LOS), successful reperfusion (defined as a thrombolysis in cerebral infarction (TICI) score ≥ 2b), neurologic improvement (change in modified Rankin scale (mRS) from admission to discharge), and all-cause mortality.

Results
In this study, 56 patients were included with 27 patients in the tirofiban group and 29 patients in the group without tirofiban. Four patients (14.8%) in the tirofiban group compared to none in the without tirofiban group experienced symptomatic ICH within 24 hours of receiving tirofiban or DAPT (p<0.001). Any ICH was more prevalent in the tirofiban group compared to without tirofiban (51.9% vs. 6.9%, p<0.001). Hospital LOS (6.9 days vs. 6.1 days, p=0.386) and ICU LOS (3.8 vs. 3.7 p=0.444) were similar between groups. Successful reperfusion was achieved in 92% of patients in the tirofiban group compared to 84.6% in the without tirofiban group (p=0.668). Changes in mRS were not statistically different between groups (p=0.733). All-cause mortality was similar between groups (22.2% vs. 20.7%, p=0.837).

Conclusions
In our study population, the use of tirofiban had more ICH compared to patients not receiving tirofiban in AIS patients following mechanical thrombectomy and emergent stent placement.
Moderators
JK

Joseph Kohn

PRIS2Prisma Health Richland-University of South CarolinaPGY1
Presenters
avatar for Taylor Dodd

Taylor Dodd

PGY2 Critical Care Pharmacy Resident, Memorial Health University Medical Center
My name is Taylor Dodd and I am a PGY2 critical care pharmacy resident at Memorial Health University Medical Center in Savannah, Georgia. I graduated from University of South Carolina College of Pharmacy in 2024 and completed a PGY1 pharmacy residency at Memorial Health University... Read More →
Evaluators
avatar for Jolie Gallagher

Jolie Gallagher

Clinical Pharmacy Specialist, Critical Care, Emory University Hospital
I am the clinical pharmacy manager at Emory University Hospital.  My background training is in critical care.  My current areas of interest are optimization of transitions of care and pharmacist burnout and resilience.
Friday May 1, 2026 8:30am - 8:50am EDT
Athena I

8:30am EDT

Hospital acquired anemia in non-surgical patients receiving therapeutic anticoagulation versus venous thromboembolism prophylactic anticoagulation
Friday May 1, 2026 8:30am - 8:50am EDT
Purpose:
    Hospital-acquired anemia (HAA) is a common complication of hospitalization and is associated with increased length of stay, healthcare costs, readmissions, and mortality. Although anticoagulation therapy carries a known bleeding risk, its role as an independent contributor to HAA has not been well defined. This study evaluated compared the incidence of HAA in non-surgical hospitalized patients receiving prophylactic versus therapeutic anticoagulation.
Methods:
    This retrospective cohort study included adults (≥18 years) hospitalized for more than 4 days who received prophylactic or therapeutic anticoagulation for over 75% of their admission. Prophylactic regimens included subcutaneous heparin, prophylactic-dose enoxaparin, or fondaparinux 2.5 mg daily. Therapeutic anticoagulation included direct oral anticoagulants, intravenous heparin, therapeutic-dose enoxaparin, argatroban, or fondaparinux ≥ 5 mg daily. Patients were required to have hemoglobin measured on admission and within 72 hours of discharge. Exclusion criteria included anemia on admission, surgical procedures (excluding minor/low-risk procedures), therapies affecting hemoglobin, or documented physiologic bleeding.
Results:
    Hospital-acquired anemia occurred in 44.8% of patients receiving prophylactic anticoagulation and 51.3% receiving therapeutic anticoagulation, with no significant difference between groups (p = 0.28). No differences were observed in anemia severity, absolute hemoglobin change (p = 0.93), or rate of hemoglobin decline (p = 0.74).
Conclusion:
    Hospital-acquired anemia was common in non-surgical hospitalized patients, with no significant differences between prophylactic and therapeutic anticoagulation. Anticoagulation intensity alone may not be a primary contributor to HAA.
Moderators Presenters
avatar for Kaitlyn Kuntz

Kaitlyn Kuntz

PGY-1 Resident, University of Tennessee Medical Center
Evaluators
avatar for Anh Nguyen

Anh Nguyen

Clinical Pharmacy Specialist, Emory Decatur Hospital
I’m a Board‑Certified Critical Care Pharmacy Specialist with a passion for taking care of some of the sickest patients in the hospital. I’ve worked in both intermediate and intensive care settings, where every day brings a new challenge and a new opportunity to make a meaningful... Read More →
Friday May 1, 2026 8:30am - 8:50am EDT
Athena H

8:30am EDT

Hydrocortisone vs. Methylprednisolone for the Treatment of Refractory Septic Shock
Friday May 1, 2026 8:30am - 8:50am EDT
Title: Hydrocortisone vs. Methylprednisolone for the Treatment of Refractory Septic Shock 
Authors: Erin Weippert, Sydney Kisala, Van Bui, Sarah Jung, Marina Rabinovich  
Background: The 2024 Society of Critical Care Medicine Guidelines on the Use of Corticosteroids in Sepsis recommend the use of corticosteroids in patients with septic shock. The recommended regimen is hydrocortisone 200 – 300 mg intravenously (IV) per day in divided doses or as a continuous infusion. Due to an ongoing IV hydrocortisone shortage, IV methylprednisolone is increasingly used as an alternative, though evidence for its safety and efficacy in septic shock is limited. The purpose of this study was to compare the effectiveness and safety of methylprednisolone to hydrocortisone in the management of refractory septic shock. 
Methods: This was a single-center, retrospective, cohort study conducted at a safety net hospital in Atlanta, GA. Patients with septic shock who received methylprednisolone during the primary and secondary IV hydrocortisone shortage periods (February 2023 - February 2024 and May - August 2025) were compared with patients who received hydrocortisone (February 2024 - February 2025). Eligible patients were at least 18 years old, admitted to an intensive care unit (ICU), diagnosed with septic shock requiring at least two vasopressors, and received at least 48 hours of either IV methylprednisolone or IV hydrocortisone. Patients were excluded if they were pregnant, received corticosteroids for an alternative indication, or received both hydrocortisone and methylprednisolone. Variables collected include patient demographics, highest serum lactate level, initial Sequential Organ Failure Assessment (SOFA) score, type and number of vasopressors received, source of infection, steroid duration, and time from shock onset to steroid initiation. The primary outcome was time to shock resolution, defined as the attainment of a goal mean arterial pressure (MAP) ≥ 65 mmHg without vasopressor support for at least 24 hours. Secondary outcomes included the incidence of shock recurrence, time to achieving lactate of < 2 mmol/L, receipt of vasopressors and corticosteroids beyond 7 days, hospital mortality at 28 days, ICU length of stay, and duration of corticosteroid therapy. Safety outcomes included the incidence of hyperglycemia, hypernatremia, and gastrointestinal bleeding. Descriptive statistics were used for analysis and categorical variables were compared using a chi-square or Fisher’s exact test while continuous variables were compared using the Mann-Whitney U test. A p-value of 0.05 was considered statistically significant. 
Results: A total of 191 patients were included for analysis with 116 included in the hydrocortisone group and 75 in the methylprednisolone group. Baseline characteristics were similar between groups with the majority of patients being male, of Black or African American race, median age of 60 years, and admitted to the medical ICU. However, patients in the methylprednisolone group had a greater need for renal replacement therapy (50.6% vs. 35.3%, p=0.036). 85 patients (73.3%) in the hydrocortisone group and 50 patients (67%) in the methylprednisolone group achieved shock resolution (p=0.327). The primary outcome of time to shock resolution was similar in the two groups (4 days vs. 3.9 days, p=0.479). For secondary outcomes, there were no significant differences between the groups for recurrence of shock, time to achieving lactate of < 2 mmol/L, or ICU length of stay. More patients in the hydrocortisone group received vasopressors and corticosteroids beyond seven days (25.9% vs. 9.3%, p=0.005), while the methylprednisolone group exhibited a higher 28-day hospital mortality (56% vs. 38.8%, p=0.02). There were no significant differences in safety outcomes between the groups. 
Conclusions: The results of this study demonstrated no difference in time to shock resolution between hydrocortisone and methylprednisolone in critically ill patients with septic shock. These results suggest that methylprednisolone may be a reasonable alternative to hydrocortisone in this patient population, although larger prospective studies are needed to confirm these findings and evaluate long-term outcomes.  

Moderators
avatar for Abigayle Campbell

Abigayle Campbell

Clinical Specialist, Psychiatry; PGY1 Acute Care RPC, Self Regional Healthcare
For the past 6 years, I have served as the Clinical Pharmacy Specialist within the Inpatient Behavior Health Center at Self Regional Healthcare in Greenwood, SC. Recently, I have transitioned into a new role as the Medication Utilization and Quality Coordinator. I completed my bachelor's... Read More →
Presenters
avatar for Erin Weippert

Erin Weippert

PGY-1 Pharmacy Resident, Grady Memorial Hospital
Evaluators
Friday May 1, 2026 8:30am - 8:50am EDT
Athena B

8:30am EDT

Incidence of Ribociclib-Induced Serum Creatinine Elevation in Hormone Receptor-Positive Breast Cancer
Friday May 1, 2026 8:30am - 8:50am EDT
Background: Ribociclib is a cyclin-dependent kinase 4 and 6 inhibitor approved for treatment of   advanced or metastatic hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) negative breast cancer at a dose of 600 mg and adjuvantly for high-risk, early-stage HR+, HER2- breast cancer at a dose of 400 mg . While ribociclib has resulted in improved cancer-related outcomes, the incidence of ribociclib-induced serum creatinine (SCr) elevations has been reported in 8-65% of patients in phase 3 trials although up to 73% of those cases are attributed to a phenomenon known as pseudo-acute kidney injury (AKI). The proposed mechanism is thought to be due to ribociclib’s competitive inhibition of renal tubular secretion transporters, OCT2, MATE1, MATE2-K, blocking creatinine secretion into urine without affecting actual glomerular filtration rate. Cystatin C is an alternative surrogate marker of renal function that is not affected by ribociclib’s inhibition of renal tubular transporters and thus may be utilized to distinguish pseudo-AKI from true kidney injury. This study aimed to further describe the nature and clinical significance of ribociclib-induced SCr elevation in patients with HR+, HER2- breast cancer in a real-world setting.  

Methods: This IRB approved, single-center, retrospective chart review included all adult patients prescribed ribociclib for HR+, HER2- breast cancer at Emory Winship Cancer Institute between October 2022 and August 2025. Patients were excluded if ribociclib was prescribed by an external provider, used for investigational purposes, or if baseline SCr documentation at least 6 months prior to ribociclib initiation was missing. The primary outcome was incidence of ribociclib-induced SCr elevation, defined as ≥ grade 1 per CTCAE v5.0. Cystatin C, defined as > 0.95 mg/dL, was utilized to assess reduced renal function. Use of concomitant nephrotoxic medications including CT contrast, zoledronic acid, diuretics, NSAIDs, metformin, antihypertensives, and antibiotics was assessed.  

Results: 168 females and 2 males were reviewed, median age 58 years old. The majority (139 patients, 81.7%), were prescribed ribociclib for metastatic disease; 31 (18.2%) adjuvantly. Ribociclib-induced SCr elevation occurred in 49 patients (28.8%). Of those patients, 40 (81.6%) had metastatic disease, the initial dose was 600 mg for 36 (73.5%), and 47 (95.9%) were prescribed concomitant nephrotoxic medications though not statistically significant (p-value, 0.515). Median absolute change in SCr from baseline was 0.45 mg/dL (range, 0.34-0.54 mg/dL); median time to SCr elevation was 33 days (range, 15-83 days). Most events were grade 2 (35, 71.4%); 14 (28.6%) were grade 1. Of those with elevated SCr, 5 patients (10.2%) had true kidney injury as indicated by an elevated cystatin C warranting consideration of dose interruption or reduction. Median time to SCr recovery was 155 days (range, 27-316 days).

Conclusion: Ribociclib-induced SCr elevation often occurred within the first or second cycle and remained elevated yet stable through the first six cycles. The majority were grade 1 or 2 events and did not require dose reductions or interruptions.
Moderators Presenters
avatar for Madeline Adams

Madeline Adams

PGY1 Acute Care Pharmacy Resident, Emory University Hospital Midtown
Evaluators
avatar for Allie Hale

Allie Hale

Clinical Pharmacist and Residency Program Director, Parkridge Health System
Friday May 1, 2026 8:30am - 8:50am EDT
Athena C

8:50am EDT

EVALUATION OF A PHARMACY RESIDENT-LED VIRTUAL POPULATION HEALTH CLINIC
Friday May 1, 2026 8:50am - 9:10am EDT
EVALUATION OF A PHARMACY RESIDENT-LED VIRTUAL POPULATION HEALTH CLINIC 
Katrina Bitcon, Katie Sfirlea, Catie Harper, Madison Yates 

Background/Purpose: A value-based care delivery model aims to enhance patient care by reimbursing providers based on patient outcomes and the quality of care instead of the quantity of services delivered. In 2024, our health system established a new objective to expand value-based care throughout all areas of our system. Pharmacists in the health system's primary care clinics deliver chronic disease management services using a value-based care model; however, access to pharmacists working within these clinics has historically been limited to traditional business hours. To expand access to pharmacy services for patients experiencing barriers to this model, staffing for ambulatory care interested PGY1 pharmacy residents was structured to include virtual care outside of traditional business hours. During these visits, chronic disease states were assessed and documented, as well as any recommendations that the resident made for therapeutic management. The purpose of this study was to characterize this pharmacy resident-led virtual population health clinic and assess its impact on patient care. 


Methodology: Fifty patients were included in this single health system, retrospective, cohort study. Patients were eligible for inclusion if they completed at least one pharmacy resident-led virtual visit between October 1, 2024, and May 31, 2025.  The primary objective of this study was to determine the percentage of pharmacy resident recommendations approved by the primary care provider (PCP), which was defined as corresponding orders in the electronic medical record within 10 days of the visit. Secondary objectives included the percentage of patients achieving an A1C <8%, blood pressure (BP) <140/90 mm Hg, and LDL-C <70 mg/dL pre- and post-intervention, as well as the types of recommendations made by the pharmacy resident. 


Results: A total of 204 resident visits among 50 patients were conducted with the pharmacy residents. Of the 77 recommendations provided by the pharmacy residents, 97.3% were accepted by the referring PCP, with the most common recommendations being an increase in dose or addition of medication. There was an increase in patients achieving the goal A1C by 22% (P < 0.01), blood pressure by 24.2% (P < 0.05), and LDL-C by 20.6% (P > 0.05). The most common disease state managed by the pharmacy residents was diabetes. After the intervention, 32% were helped with medication access, 16% gained access to CGM, and 4% of patients gained access to home blood pressure monitors. 


Conclusions: The results of this study show that the majority of pharmacy resident recommendations were approved and implemented by the PCP. Additionally, there was a significant reduction in A1C and blood pressure after pharmacy resident intervention. Alongside improvements in disease state management, patients were able to gain access to home monitoring devices and assisted with medication access. Based on the findings of this study, providing after-hours virtual visits with a pharmacy resident is an effective method for reaching patients who face barriers to traditional healthcare hours.
Moderators
avatar for Aayush Patel

Aayush Patel

Clinical Pharmacy Specialist, Emergency Medicine, Piedmont Columbus Regional Midtown
Presenters Evaluators
Friday May 1, 2026 8:50am - 9:10am EDT
Athena A

8:50am EDT

Remote Continuous Glucose Monitoring Service Pilot in an Ambulatory Care Setting
Friday May 1, 2026 8:50am - 9:10am EDT
Background: Traditional markers of glycemic control – such as quarterly A1C measurements and patient-reported self-monitored blood glucose – offer only brief, intermittent views of glucose trends. These limited snapshots can delay necessary therapy adjustment and often contribute to inadequate glycemic control. Continuous glucose monitoring (CGM), by contrast, provides real-time, detailed glucose information that supports more timely clinical decisions and a more proactive approach to diabetes management. Current guidelines now recommend CGM not only for individuals using insulin but also for those on any form of glucose-lowering therapy. Despite the expansion, pharmacist-led remote monitoring of CGM data remains limited. At the Piedmont Columbus Family Medicine Center, patients referred for diabetes management share CGM data with clinical pharmacists for ongoing remote assessment and intervention. Pharmacists conduct weekly remote monitoring outside of standard clinic appointments, including scheduled phone visit with patients to meet study criteria. This study will assess changes in A1C,hypoglycemia events utilizing time below range (TBR) <70 mg/dL from CGM initiation through study completion, and will characterize the pharmacist-driven interventions employed to optimize glycemic control. 

Methods: This single-center, retrospective, and IRB-approved study included adult patients with Type 1 or Type 2 diabetes, a baseline A1c >7%, and active use of a continuous glucose monitor capable of remote data sharing. Patients with available CGM data between July 1, 2025, and December 31, 2025, were included. Baseline demographics, A1C, and CGM summary metrics were extracted from the electronic medical record. Primary outcomes were changes in A1C and time below range (TBR) from baseline to study completion. Pharmacist interventions were recorded and categorized. Only CGM reports with adequate sensor wear time were included. Pre-post comparisons will be analyzed using paired statistical methods.

Results: A total of 19 patients were included in this study. Mean baseline A1c was 9.4%, which was decreased to 8% following pharmacy intervention, reflecting a mean reduction of 1.4% (p=0001). Nearly all participants (94.7%) experienced an A1c reduction, and 21.1% achieved glycemic control with A1c <7%. Hypoglycemia events (TBR <70 mg/dL) occurred in 42% of patients at baseline and 37% at follow-up. Pharmacists delivered a total of 473 interventions with the most being diabetes education (n=211).

Conclusions: Implementation of a pharmacist-CGM collaboration was associated with clinically meaningful improvements in glycemic control among adults with uncontrolled diabetes. These findings suggest that pharmacy-CGM collaboration can enhance diabetes management in ambulatory care settings. Future work should explore barriers to completing phone visits and evaluate scalability in larger populations.

Contact: [email protected]







Moderators
avatar for Abigayle Campbell

Abigayle Campbell

Clinical Specialist, Psychiatry; PGY1 Acute Care RPC, Self Regional Healthcare
For the past 6 years, I have served as the Clinical Pharmacy Specialist within the Inpatient Behavior Health Center at Self Regional Healthcare in Greenwood, SC. Recently, I have transitioned into a new role as the Medication Utilization and Quality Coordinator. I completed my bachelor's... Read More →
Presenters Evaluators
Friday May 1, 2026 8:50am - 9:10am EDT
Athena B

8:50am EDT

Efficacy of Intravenous Lidocaine Infusion vs. Liposomal Bupivacaine for Analgesia following MIDCAB
Friday May 1, 2026 8:50am - 9:10am EDT

Graham Anglin, Adam L. Wiss 
Ascension Saint Thomas Hospital West - Nashville, TN 

Introduction: Multimodal analgesia has become a cornerstone of perioperative pain management, reducing opioid exposure and associated adverse effects. At Ascension Saint Thomas Hospital West (ASTHW), continuous intravenous lidocaine infusions have been utilized to improve postoperative pain control in minimally invasive direct coronary artery bypass (MIDCAB) procedures. However, safety concerns and intensive care unit (ICU) monitoring requirements limit their broader use. In June 2022, liposomal bupivacaine, a long-acting local anesthetic, was added to the formulary as an alternative strategy for prolonged analgesia. While studies have shown mixed outcomes depending on surgical type and administration technique, data specific to cardiothoracic surgery remain limited. The objective of this study was to compare intravenous lidocaine and liposomal bupivacaine for postoperative pain management in patients undergoing MIDCAB. 

Methods: This single-center retrospective chart review included adults who underwent MIDCAB at ASTHW between June 2022 and July 2025. Patients received either a single dose of liposomal bupivacaine or a continuous intravenous lidocaine infusion for postoperative analgesia. Exclusion criteria included substance use disorder, concurrent buprenorphine, methadone, or naltrexone therapy; pregnancy, incarceration, surgical re-exploration for bleeding within 24 hours of MIDCAB, or use of mechanical circulatory support. The primary outcome was postoperative opioid use, reported as morphine milligram equivalents (MME) within 72 hours. Secondary outcomes included postoperative pain scores, ICU and total hospital length of stay (LOS), and incidence of adverse effects such as hypotension, bradycardia, arrhythmia, and nausea. 

Results: One-hundred fifty patients were included in the study (intravenous lidocaine = 75; liposomal bupivacaine = 75). Baseline characteristics were comparable, with both groups consisting predominantly of Caucasian males (median age 66 years). All patients received multimodal analgesia; however, the intravenous lidocaine group had higher use of methocarbamol (17% vs 3%, p = 0.007) and erector spinae plane blocks (77% vs 1%, p < 0.001).  There was no statistically significant difference in postoperative MME usage between the intravenous lidocaine group and liposomal bupivacaine group on postoperative day 0/1 (61 vs. 72; p = 0.659), postoperative day 2 (23 vs. 23; p = 0.467) or postoperative day 3 (8 vs. 8 ; p = 0.92). The groups were also similar in postoperative pain scores, hospital and ICU LOS, and incidence of adverse effects.

Conclusion: In this study evaluating postoperative analgesia following MIDCAB surgery, patients who received continuous infusion of intravenous lidocaine had comparable postoperative opioid consumption to those who received a single administration of liposomal bupivacaine with no difference in adverse events between groups. While either of these analgesia strategies may be effective in patients undergoing MIDCAB, further investigation is warranted to determine the role other treatments (i.e., local anesthetic blocks and muscle relaxers) may have had on outcomes in our population.




Moderators Presenters
avatar for Graham Anglin

Graham Anglin

PGY1 Pharmacy Resident, Ascension Saint Thomas
Ascension Saint Thomas Hospital West
PGY1 Pharmacy Resident
Evaluators
avatar for Allie Hale

Allie Hale

Clinical Pharmacist and Residency Program Director, Parkridge Health System

Friday May 1, 2026 8:50am - 9:10am EDT
Athena C

8:50am EDT

Evaluating Different Bromocriptine Doses for Central Fever in the Intensive Care Unit
Friday May 1, 2026 8:50am - 9:10am EDT
Evaluating Different Bromocriptine Doses for Central Fever in the Intensive Care Unit 
Maggie Nobles, Zackery Moreo, Sam Pournezhad, Chelsea Wamsley 
[email protected]  
Grady Health System Department of Pharmacy 

Background: Central fever is a diagnosis of exclusion characterized by persistent, noninfectious hyperthermia that is unresponsive to antipyretics and antimicrobial therapy. It is commonly observed in patients with acute neurologic injury and is thought to result from disruption of hypothalamic thermoregulatory pathways. Central fever has been associated with increased metabolic demand, prolonged ICU length of stay, and worse neurologic outcomes. Bromocriptine, a dopamine-2 receptor agonist, has been used off-label for central fever due to its ability to reduce hypothalamic set point and sympathetic activity. While prior studies support its antipyretic efficacy, there is limited evidence guiding optimal dosing strategies. This study aimed to evaluate the effectiveness of different bromocriptine doses for central fever in critically ill patients with neurologic injury to inform dosing decisions and institutional practice.  
Methods: This single-center, retrospective chart review was conducted at an academic safety-net hospital and included adult patients (≥18 years) admitted to the neurocritical care unit or surgical-trauma ICU between January 2023 and June 2025. Eligible patients received at least one dose of bromocriptine 2.5 mg, 5 mg, or 10 mg for suspected central fever. Patients were excluded if they had evidence of active infection, prior bromocriptine use before admission, death within 48 hours of bromocriptine initiation, or belonged to a protected population. Baseline demographic and clinical characteristics, neurologic diagnoses, and use of potential confounding therapies were collected. The primary outcome was fever resolution, defined as a temperature of ≤ 38.3°C within 2 hours of the initial bromocriptine dose, compared across initial dose groups. Secondary outcomes included sustained fever resolution at 8, 24, and 48 hours, assessed according to total daily bromocriptine dose. 
Results: A total of 274 patients were screened; 47 met inclusion criteria for the primary outcome analysis. Baseline characteristics were largely similar across groups, though differences in neurologic diagnosis and ICU admission location were observed. Fever resolution within 2 hours occurred in 78.6% of patients receiving an initial dose of 2.5 mg, compared with 37.5% in the 5 mg group and 47.1% in the 10 mg group. Fever resolution within 2 hours was significantly more frequent with 2.5 mg compared with 5 mg (p=0.024), while no statistically significant differences were observed between the 2.5 mg and 10 mg groups (p=0.073) or between the 5 mg and 10 mg groups (p=0.579). Secondary outcomes were similar across total daily dose groups, with no significant differences observed in sustained fever resolution at 8, 24, or 48 hours. Duration of therapy tended to increase with higher daily doses, though this did not reach statistical significance. No differences were observed in ICU length of stay or in-hospital mortality. 
Conclusion: More patients achieved fever resolution within 2 hours with the 2.5 mg dose, while no differences were observed between dose groups in sustained fever control. These findings suggest that bromocriptine’s antipyretic effect may not be dose dependent, and that lower initial dosing strategies may be reasonable for the management of central fever. Prospective studies are needed to further define optimal dosing strategies and evaluate safety outcomes. 


Moderators
avatar for Brittany NeSmith

Brittany NeSmith

PGY1 Residency Program Director, BSSFBon Secours St. Francis DowntownPGY1
Presenters
avatar for Maggie Nobles

Maggie Nobles

PGY-1 Pharmacy Resident, Grady Memorial Hospital
Evaluators
BB

Brooke Bibb

Ascension Saint Thomas Hospital West
Friday May 1, 2026 8:50am - 9:10am EDT
Athena J

8:50am EDT

Evaluation of Antibiotic De-escalation from Intravenous to Oral Antimicrobial Therapy in Critically Ill Patients with Gram-Negative Bacteremia
Friday May 1, 2026 8:50am - 9:10am EDT
Background 
Gram-negative bloodstream infections (GN-BSI) are associated with significant morbidity and mortality and traditionally managed with intravenous (IV) antibiotics. However, emerging evidence supports the use of oral (PO) antibiotics as step-down therapy in uncomplicated GN-BSI.1-7 Oral agents such as fluoroquinolones, sulfamethoxazole-trimethoprim, and β-lactams have demonstrated efficacy in this setting.1-2 Transitioning to a PO agent offers several benefits such as reduced cost, easier administration, and less risk of IV-associated complications, which include venous thrombosis, extravasation, and phlebitis.8-9 Despite these potential benefits, data on this practice in critically ill patients remain limited. This study aims to evaluate the safety and efficacy of IV therapy alone versus IV to PO step-down therapy in the treatment of critically ill patients with a GN-BSI. 
 
Methods 
This is a multicenter retrospective cohort analysis that evaluated adult patients with an uncomplicated GN-BSI who were initiated on appropriate empiric IV antibiotic treatment within 24 hours of their initial blood culture collection. The study included patients who were admitted to an intensive care unit (ICU) within Emory Healthcare (EHC) between May 1, 2023 and May 1, 2025. Patients were excluded if the duration of PO therapy was less than 48 hours, there was polymicrobial growth or presence of an organism other than Enterobacterales or Pseudomonas spp., hospice or comfort care was initiated within 72 hours of initial blood culture, or the organism(s) isolated was not susceptible to an available PO agent. The primary outcome was treatment failure, defined as a composite of 90-day mortality or recurrence of the same causative GN-BSI within 30 days of treatment completion. Secondary efficacy outcomes include ICU and inpatient length of stay, recurrence of GN-BSI within 90 days of treatment completion, emergence of resistance to study antibiotics, antibiotic duration, and IV to PO transition time. Secondary safety outcomes include adverse drug events leading to discontinuation or change in antibiotic therapy. Baseline demographics and outcomes were summarized with descriptive statistics while continuous data was summarized with means and standard deviations. 
 
Results 
Patients were separated into two cohorts based on antibiotic regimen: IV only (n=108) versus IV to PO (n=33). Baseline characteristics differed between groups, with patients in the IV only group demonstrating higher illness severity, depicted by higher median APACHE II (18 vs 14) and Pitt bacteremia scores (3 vs 2). The most common pathogens were Escherichia coli, Klebsiella pneumoniae, Serratia marcescens, Enterobacter cloacae, and Pseudomonas aeruginosa. Pulmonary sources were more prevalent in the IV only group, while genitourinary sources were more common in the IV to PO group. Treatment failure occurred more frequently in the IV only group compared to the IV to PO group (41.7% vs 15.1%). Recurrence of the same causative bacteria within 90 days was similar between groups (4.6% vs 6.1%), as was the emergence of resistance to study antibiotics (7.4% vs 9.1%). ICU and hospital length of stay were longer in the IV only group (13 vs 4 days and 21 vs 11 days). However, total antibiotic duration was longer in the IV to PO group (13 vs 9 days). Adverse drug events were uncommon in both groups. 
 
Conclusions 
While IV to PO step-down therapy was associated with lower rates of treatment failure, further research is needed to optimize treatment by determining appropriate drug selection and timing of transition. For critically ill patients with uncomplicated GN-BSI and adequate source control, this approach appears to be appropriate and may reduce length of stay without compromising effectiveness. These findings align with existing literature supporting PO step-down therapy as a method with comparable efficacy to continued IV therapy. 
Moderators
JK

Joseph Kohn

PRIS2Prisma Health Richland-University of South CarolinaPGY1
Presenters
avatar for Nina Casanova

Nina Casanova

PGY-2 Critical Care Pharmacy Resident, Emory University Hospital
Evaluators
avatar for Jolie Gallagher

Jolie Gallagher

Clinical Pharmacy Specialist, Critical Care, Emory University Hospital
I am the clinical pharmacy manager at Emory University Hospital.  My background training is in critical care.  My current areas of interest are optimization of transitions of care and pharmacist burnout and resilience.
Friday May 1, 2026 8:50am - 9:10am EDT
Athena I

8:50am EDT

Evaluation of Antiepileptic Therapy and Outcomes in Status Epilepticus Patients Presenting to the Emergency Department - Michelle Tubolino
Friday May 1, 2026 8:50am - 9:10am EDT
Evaluation of Antiepileptic Therapy and Outcomes in Status Epilepticus Patients Presenting to the Emergency Department
Michelle Tubolino, Megan Heath
DCH Regional Medical Center-Tuscaloosa, Alabama
Background/Purpose: Assess guideline-based selection and dosing of the initial antiepileptic drug (AED) administered in the emergency department (ED) in patients presenting with status epilepticus (SE) at a large community hospital.  

Methodology: Retrospective chart review where patients were screened from July 15, 2023 to July 14, 2025. Eligible patients were those who received greater than or equal to one AED in the emergency department and had a status epilepticus diagnosis documented by a provider during that encounter. AED selection and dose were assessed for appropriateness in accordance with the American Epilepsy Society (AES) 2016 guidelines.

Results: 63 patients were included in this study. Thirty-six patients had a documented history of seizure disorder and thirty were on antiepileptic medications at home. Thirty-nine patients received a benzodiazepine prior to ED arrival, with midazolam being the most frequently used. Average time to first AED administration from seizure onset was nine minutes. 18 (28.6%) patients received an appropriate agent and weight-based dose in the ED. Out of the 13 patients who receive guideline adherent weight-based dosing of a second-line agent, 12 had pharmacists involved in their care.

Conclusions: Majority of patients received lower than recommended weight-based doses of benzodiazepines and second-line AEDs in the ED. Most patients who received the appropriate initial agent and dose for status epilepticus had pharmacist involvement in their care, suggesting the impact of pharmacist intervention on treatment optimization.

Presentation Objective: the application of the American Epilepsy Society (AES) treatment guidelines for pharmacologic management of status epilepticus in the emergency department. Self-Assessment: What is one of the most common reasons for benzodiazepine underdosing in status epilepticus?

Moderators
avatar for Devin Lavender

Devin Lavender

Clinical Assistant Professor, UGAA1University of Georgia College of Pharmacy (Ambulatory Care)PGY2
Ambulatory Care, Scholarship of Teaching and Learning, Resident and Student Development.
Presenters Evaluators
Friday May 1, 2026 8:50am - 9:10am EDT
Parthenon 1

8:50am EDT

Evaluation of Periprocedural Anticoagulant Management in Patients Undergoing Cardiac Catheterization at a Large Community Hospital
Friday May 1, 2026 8:50am - 9:10am EDT
Authors: Madison Farkas and Gregg Knowles

Background: Periprocedural management of chronic anticoagulation is an important consideration for patients undergoing invasive cardiovascular procedures such as cardiac catheterization. Anticoagulant therapy is often temporarily held to reduce procedural bleeding risk; however, delayed or missed resumption after the procedure may increase the risk of thromboembolic complications. Current evidence, including the 2022 CHEST Guideline and Expert Panel Report: Perioperative Management of Antithrombotic Therapy and findings from the PAUSE trial, supports standardized, time-based strategies for interruption and resumption of anticoagulants to balance bleeding and thrombotic risks. Despite these recommendations, variability in real-world practice and inconsistent documentation of post-procedure anticoagulant management may result in unnecessary therapy interruptions and increased patient safety risks. The purpose of this research is to determine the frequency of delayed resumption of anticoagulation in post cardiac catheterization patients and evaluate the impact of a pharmacy-driven intervention on addressing gaps in care

Methods: This single-center, pre-post implementation study evaluated periprocedural anticoagulation management in patients undergoing cardiac catheterization at a large community hospital. An electronic daily report was developed to identify patients who may require resumption of chronic anticoagulation following cardiac catheterization. The report populates based on the following criteria: (1) presence of post–cardiac catheterization orders, (2) documentation of an anticoagulant on the patient’s home medication list, and (3) absence of an active inpatient anticoagulant medication order. The report is reviewed daily by the investigator to identify patients whose chronic anticoagulation may have been held for the procedure but not yet resumed. For patients meeting these criteria, the medical record is reviewed to assess procedural details, bleeding risk, and clinical appropriateness for anticoagulation resumption. If anticoagulation appears appropriate and has not been restarted within 48 hours of the cardiac catheterization, the investigator communicates with the responsible clinical team to recommend therapy resumption when clinically indicated. The primary endpoint of this study is Proportion of patients without appropriate resumption of anticoagulation post cardiac catheterization. The secondary endpoint is the Proportion of patients with anticoagulation resumed following pharmacist intervention.

Results: Delayed resumption of home anticoagulation within 48 hours of cardiac catheterization occurred in 38% (25/66) of patients in the pre-implementation group and 45% (22/49) of patients in the post-implementation group. Among patients in whom anticoagulation was not resumed, inappropriate holds were identified in 9% (6/66) pre-implementation and 12% (6/49) post-implementation. In the post-implementation group, pharmacy intervened in 5 of 6 cases of inappropriately held anticoagulation (1 patient was lost to follow-up). Of these, 4 interventions were accepted, resulting in resumption of therapy. Common reasons for inappropriate holds included omission from the home medication list and delayed recognition prior to pharmacist intervention. Overall, pharmacy intervened to request anticoagulation resumption in 10% (5/49) of patients. The mean number of patients identified on the daily anticoagulation surveillance report was 0.84 (SD 0.87).

Conclusion: Delayed anticoagulation resumption occurred more frequently than originally reported which emphasized the need for process improvement. Pharmacy involvement via the daily surveillance report played a key role in ensuring appropriate and timely resumption when clinically indicated.
Moderators
CW

Cassandra Wade

Pharmacy Procurement Coordinator, John D Archbold Memorial Hospital
Presenters
avatar for Madison Farkas

Madison Farkas

PGY-2 Critical Care Pharmacy Resident, Huntsville Hospital
Madison Pinke graduated from Samford University with both a Bachelor of Science and a Doctor of Pharmacy degree. She completed her PGY-1 pharmacy residency at Huntsville Hospital and early committed for PGY-2 critical care. Outside of pharmacy, Madison enjoys spending time with friends... Read More →
Evaluators
avatar for Madison Yates

Madison Yates

Clinical Pharmacist Practitioner, PGY1 Ambulatory Residency Program Coordinator, Cone Health
Friday May 1, 2026 8:50am - 9:10am EDT
Athena G

8:50am EDT

Impact of Oral Naloxone on Analgesia in Critically Ill Patients with Opioid-Induced Constipation
Friday May 1, 2026 8:50am - 9:10am EDT
Background: Opioid-induced constipation (OIC) is a frequent and challenging side effect of pain management in critically ill patients. While it is standard of care to initiate conventional laxatives concurrently with opioid therapy, they do not directly address the underlying mechanism of OIC. Oral naloxone offers a targeted approach by acting as a mu-opioid receptor antagonist. Due to its low oral absorption, it is thought to primarily exert peripheral effects, helping relieve constipation with minimal impact on central analgesia. Despite its theoretical safety profile, evidence regarding its effects on pain control is not well defined in the available literature. This study aimed to evaluate the effect of oral naloxone on pain scores and opioid requirements in a large, real-world cohort of critically ill patients.

Methods: This multicenter, retrospective pre–post cohort study was conducted across eight community teaching hospitals within AdventHealth Central Florida Division South. Adult patients admitted to an intensive care unit (ICU) who received at least one dose of oral naloxone for OIC and received opioid treatment for at least 24 hours prior to the first dose of oral naloxone were eligible. Patients with chronic opioid use, concurrent peripherally acting mu-opioid receptor antagonists, or chronic naloxone use were excluded. The primary outcome was within-patient change in pain scores 24 hours before and after naloxone initiation, stratified by assessment tool. Secondary outcomes included changes in scheduled and rescue opioid use (morphine milligram equivalents [MME]) and bowel movement occurrence. Continuous outcomes were analyzed using the Wilcoxon signed-rank test and categorical outcomes using the exact McNemar test.

Results: Among 105 patients, fentanyl was the predominant opioid (81%). Pain was most commonly assessed using the Critical Care Pain Observation Tool (CPOT) (77%), followed by the Numeric Rating Scale (NRS) (20%), and Visual Analogue Scale (VAS) (3%). No significant change in pain scores was observed in the CPOT group (median 0.10 vs 0; p = 0.073). NRS scores showed a small but statistically significant decrease (median 2.9 vs 2.5; p = 0.031), while VAS scores did not change significantly (median 2.6 vs 1.8; p = 0.593). Scheduled opioid use decreased significantly (median 555 vs 357.5 MME; p = 0.004), with no change in rescue opioid use (median 5 vs 0 MME; p = 0.831). Bowel movement occurrence increased from 13% to 44% (p <0.001).

Conclusion: In critically ill patients predominantly receiving fentanyl infusions, oral naloxone was not associated with increased pain scores and was associated with increased bowel movement occurrence. These findings suggest that oral naloxone may be a safe adjunct for the management of OIC in ICU patients without compromising analgesia.
Moderators
AQ

April Quidley

PGY1 Residency Program Director, ECU Health Medical Center
Presenters
avatar for Madiha Ali

Madiha Ali

PGY1 Pharmacy Resident, AdventHealth Orlando
Madiha Ali is a PGY1 Pharmacy Resident at AdventHealth Orlando. Dr. Ali received a Bachelor of Science in Psychology and Doctor of Pharmacy at the University of Florida.
Evaluators
AJ

Audrey Johnson

Surgical/Trauma Critical Care Pharmacist, Memorial Health University Medical Center
Friday May 1, 2026 8:50am - 9:10am EDT
Olympia 1

8:50am EDT

Incidence of Mechanical Ventilation in the Emergency Department among Patients with Acute Pulmonary Edema Utilizing High versus Low Dose Intravenous Nitroglycerin
Friday May 1, 2026 8:50am - 9:10am EDT
TITLE: Incidence of Mechanical Ventilation in the Emergency Department among Patients with Acute Pulmonary Edema Utilizing High versus Low Dose Intravenous Nitroglycerin

AUTHORS: Saralyn Hardin, Kira Council, Erica Merritt, Megan Cavagnini

BACKGROUND: Heart failure affects approximately 2% of adults in the United States, with an estimated 33% at risk of developing the condition. It is classified into progressive stages, with Stage C characterized by symptomatic disease and Stage D representing advanced heart failure. Patients with Stage D heart failure frequently experience debilitating symptoms that significantly impact daily life and often result in recurrent hospitalizations. According to the American Heart Association/American College of Cardiology/Heart Failure Society of America guidelines, nitroglycerin may be considered for the management of pulmonary edema in acute heart failure presentations, provided hypotension is not present. Nitroglycerin is a targeted vasodilator that primarily reduces preload; at higher doses, it also induces arterial vasodilation, thereby decreasing afterload. While typically initiated at low infusion rates, higher rates (≥100 mcg/min) have demonstrated improved clinical outcomes in the treatment of pulmonary edema.

METHODS: This retrospective, observational chart review evaluated the incidence of mechanical ventilation in patients in the emergency department at St. Joseph’s or Candler Hospitals diagnosed with acute pulmonary edema based on the nitroglycerin dose in the first hour of treatment.  The health system’s software and a computer-generated list using MedMined services was used to identify patients with acute pulmonary edema then filtered based on the inclusion and exclusion criteria between January l, 2023, and January 1, 2024.
Patients were identified, and data was gathered to include demographic information, nitroglycerin infusion rate within the first hour, blood pressure, baseline serum creatinine and admission location. The primary objective was to determine the rate of mechanical ventilation in patients who received high dose nitroglycerin in comparison to those who received low dose nitroglycerin. The secondary endpoints of the study were the average nitroglycerin dose within the first hour of initiation, admitted level of care, percent of patients that develop acute kidney injury or hypotension after infusion initiation, average length of time in minutes the infusion was active, and all-cause mortality.

RESULTS: Three patients were screened for eligibility with 36 meeting inclusion criteria. Ten (27%) received high dose nitroglycerin (rate ≥100mcg/min) and 26 (72%) received low dose nitroglycerin (rate <100mcg/min). The mean number of patients requiring mechanical intubation was found to be 0.2 in the high dose nitroglycerin compared to 0.04 in the low dose group. Of the thirty-six patients three required mechanical ventilation and one of the three had a prior medical history revealing asthma and chronic obstructive pulmonary disease. Overall, there was found to be no statically significant correlations between the nitroglycerin dosing group and adverse events including admittance into the intensive care unit, incidence of hypotension, incidence of acute kidney injury, and all-cause mortality.

CONCLUSION: The overall nitroglycerin dosage administered to patients during the first hour following a pulmonary edema diagnosis was not comparable to the incidence of mechanical intubation in prior studies. Considering the study’s limitations of small sample size, further research with larger, multicenter data should explore potential relationship between nitroglycerin dosing within the first hour of diagnosis to adverse events.
Moderators Presenters Evaluators
avatar for Anh Nguyen

Anh Nguyen

Clinical Pharmacy Specialist, Emory Decatur Hospital
I’m a Board‑Certified Critical Care Pharmacy Specialist with a passion for taking care of some of the sickest patients in the hospital. I’ve worked in both intermediate and intensive care settings, where every day brings a new challenge and a new opportunity to make a meaningful... Read More →
Friday May 1, 2026 8:50am - 9:10am EDT
Athena H

8:50am EDT

Impact of a Pharmacist-Led COPD Transitions of Care Program on 30-Day Readmission Rates
Friday May 1, 2026 8:50am - 9:10am EDT
Title: Impact of a Pharmacist-Led COPD Transitions of Care Program on 30-Day Readmission Rates

Authors: Allison Edmondson, Quyen Nguyen, Jeremy Walley

Background: Chronic obstructive pulmonary disease (COPD) is a leading cause of mortality in the United States. The total annual medical costs for COPD near 24 billion dollars, with the cost of inpatient care accounting for 6.3 billion of those dollars. Additionally, COPD is a target condition under the Centers for Medicare and Medicaid Services under the Hospital Readmissions Reduction Program. COPD readmissions pose a significant economic burden to the healthcare system and may result from gaps in care during transitions from the hospital back to home. Transitions of care interventions by pharmacists can assist in bridging gaps in care for these patients.

Methods: This study will implement a pharmacist-led transitions of care program for patients admitted to the hospital with a COPD exacerbation. Pharmacists will assist in optimizing COPD regimens, medication and inhaler technique counseling, medication access, education on symptom self-management, and post-discharge follow-up phone calls. The primary objective is to evaluate the impact of the transitions of care service on 30-day readmission rates for COPD exacerbation within the facility. Secondary objectives will include pharmacist interventions performed.

Results: A total of 102 patients were included in the study. Readmission rates among COPD patients prior to the transition of care service in December 2024 to March 2025 were 27%, compared with 17% following the implementation of the service between December 2025 to March 2026. The primary pharmacist interventions performed included recommendations to change inhaler therapy, phone call follow up, and patient education. Among patient home medications, there was a 20.7% increase of patients on guideline-directed COPD therapy from admission to discharge.

Conclusions: The implementation of a pharmacist-led COPD transitions of care service appeared to decrease 30-day readmission rates. Pharmacists can play a role in helping to optimize therapy, medication access, patient education, and enhancing follow-up care.
Moderators
avatar for Brian Leith

Brian Leith

Clinical Pharmacist, VA Medical Center
I am currently the emergency medicine and antimicrobial stewardship pharmacist at the VA Medical Center in Fayetteville, NC.
Presenters Evaluators
BK

Brian Knott

Clinical Pharmacy Manager, AdventHealth Winter Park
Friday May 1, 2026 8:50am - 9:10am EDT
Olympia 2

8:50am EDT

Impact of a Practice Advisory Alert on the Duration of Antibiotics Prescribed at Discharge
Friday May 1, 2026 8:50am - 9:10am EDT
Authors: Savannah Odom, Lauren Freeman, Hannah Harpe
Objective: This study evaluates the effectiveness of a practice advisory alert in improving antibiotic prescribing at hospital discharge.
Background: Antimicrobial resistance is a major and growing global public health threat, driven largely by antimicrobial misuse and overuse. Inappropriate antibiotic prescribing at hospital discharge is a key contributor, with studies demonstrating that durations frequently exceed guideline recommendations. Prior research has shown that antibiotic overuse occurs in up to 75% of patients, primarily due to excessive treatment duration and failure to account for inpatient therapy. This highlights a critical opportunity for antimicrobial stewardship interventions targeting transitions of care to optimize antibiotic use and improve patient outcomes. Building on a prior institutional initiative in which a fluoroquinolone-specific alert significantly reduced treatment duration, this study assesses whether expanding the alert to additional antibiotic agents results in similar improvements in prescribing practices. The alert prompts providers to account for inpatient antibiotic days when determining discharge durations, supporting appropriate therapy length and antimicrobial stewardship efforts.
Self Assessment Question: What was the main finding after implementation of the practice advisory?
Methods: This retrospective, multi-center, quasi-experimental study evaluates adults discharged on oral antibiotics before (January 2025-February 2025) and after (January 2026-February 2026) implementation of a practice advisory. A random sample from the pre-intervention group is matched 1:1 to the post-intervention group by antibiotic and indication. Patients receiving antibiotics for prophylaxis or suppression, those immunocompromised, or those with severe or complicated infections were excluded. Data collected include demographics, antibiotic regimen and indication, infectious diseases consultation, and prescriber credentials. The primary outcome is the proportion of patients discharged with antibiotic durations consistent with guidelines or infectious diseases recommendations, adjusted for inpatient days of therapy. Secondary outcomes include 30-day treatment for Clostridioides difficile and 30-day all-cause readmission. 
Results: A total of 300 patients were included, with 150 patients in both the pre- and post-intervention groups. Baseline characteristics, including age, sex, infection type, and antibiotic selection, were well balanced between groups. Implementation of the practice advisory alert was associated with a significant improvement in guideline-concordant antibiotic prescribing at discharge, increasing from 53.3% in the pre-intervention group to 81.3% in the post-intervention group (p < 0.001). Thirty-day all-cause readmission rates were 13.3% in the pre-intervention group versus 12% in the post-intervention group (p = 0.73). Additionally, no patients in either group required treatment for Clostridioides difficile infection within 30 days of discharge.
Conclusion: Implementation of an electronic practice advisory alert that incorporates inpatient antibiotic days resulted in a clinically meaningful and statistically significant improvement in appropriate antibiotic duration at discharge. Expansion of this alert beyond fluoroquinolones to a broader range of antimicrobial agents successfully optimized prescribing practices. Importantly, these improvements were achieved without negatively impacting patient safety outcomes, as evidenced by unchanged readmission rates and absence of Clostridioides difficile infection events. Overall, this study demonstrates that targeted electronic clinical decision support tools are an effective and scalable antimicrobial stewardship strategy
Moderators Presenters
avatar for Savannah Odom

Savannah Odom

PGY-1 Pharmacy Resident, McLeod Regional Medical Center
Evaluators
CT

Christina Thurber

PGY-1 Residency Program Coordinator
Friday May 1, 2026 8:50am - 9:10am EDT
Parthenon 2

8:50am EDT

Resident Presentation Abstract - Jessica Arnold
Friday May 1, 2026 8:50am - 9:10am EDT
The purpose of this study was to evaluate the effect of a pharmacist-led transitions of care (TOC) consult service, specifically designed to address medication access barriers, on patients undergoing inpatient percutaneous coronary interventions. The study sought to assess the program’s impact on medication adherence and hospital readmission rates at 30- and 90-days post-discharge, while also contextualizing these outcomes within the existing body of literature. This retrospective study evaluated the impact of pharmacist-led interventions during TOC consults on medication adherence and hospital readmission. The study period extended from April 1, 2023, through April 1, 2025, providing a two-year window to ensure adequate patient capture. Data were extracted from the electronic health record and entered into REDCap, with all protected health information excluded to maintain confidentiality and compliance with institutional review standards. The primary outcome was the first-fill rate of antiplatelet medications among patients admitted under the post–coronary artery stent pathway who underwent percutaneous coronary intervention during their inpatient stay at this academic medical center, assessing whether pharmacist engagement improved timely medication initiation in a population at elevated cardiovascular risk. Secondary outcomes included 30-day and 90-day readmission rates, documentation of pharmacist clinical interventions across inpatient and outpatient settings, and the type of medication access support provided to patients who filled their antiplatelet prescriptions at the hospital’s affiliated outpatient pharmacy at discharge, providing additional insight into the broader impact of pharmacist involvement during care transitions. The primary endpoint was analyzed using a chi-square test, and descriptive and inferential statistics were applied to secondary outcomes as appropriate. Collectively, this study aimed to characterize the role of pharmacists in optimizing medication use, reducing readmissions, and improving outcomes for patients undergoing percutaneous coronary intervention.
Moderators
avatar for Christele Robinson

Christele Robinson

Emergency Medicine Clinical Pharmacy Specialist, Emory University Hospital
Christele Robinson, PharmD, is board certified in pharmacotherapy. She is a member of the Department of Pharmacy at Emory University Hospital and currently practicing as an Emergency Medicine Clinical Pharmacy Specialist. Dr. Robinson obtained a Bachelor of Science degree at the... Read More →
Presenters
avatar for Jessica Arnold

Jessica Arnold

PGY1 Pharmacy Resident, University of Tennessee Medical Center
Evaluators
avatar for Cody Parker

Cody Parker

Clinical Pharmacy Specialist, St. Joseph's/Candler
Dr. Cody Parker is the PGY1 Pharmacy Residency Program Director at St. Joseph's/Candler in Savannah, GA. He received his Doctor of Pharmacy from the University of Georgia and completed a Postgraduate Year One (PGY1) Pharmacy Practice Residency at St. Joseph’s/Candler. Dr. Parker is a Clinical Pharmacy Sp... Read More →
Friday May 1, 2026 8:50am - 9:10am EDT
Athena D

9:10am EDT

Evaluating the Impact of Clinical Pharmacist Interventions on the New Anticholinergic Measure in a Private Primary Care Setting
Friday May 1, 2026 9:10am - 9:30am EDT
Title: Evaluating the Impact of Clinical Pharmacist Interventions on the New Anticholinergic Measure in a Private Primary Care Setting

Authors: Sarah Emily Strickland, Leah A. Surbaugh, Whitney Aultman

Background: Ambulatory care clinical pharmacists have historically been involved in interventions to improve quality metrics set forth by the Centers for Medicare and Medicaid Services Star Ratings. The Centers for Medicare and Medicaid Services recently established a new star rating which includes patient’s 65 years or older, prescribed and filling 2 or more anticholinergic medications concurrently for 30 days or more on a Medicare Part D plan. The purpose of this study is to evaluate the impact on metric improvement following clinical pharmacists' interventions on the Polypharmacy: Use of Anticholinergic Medications (POLY-ACH) quality metric.

Methods: Patients evaluated for inclusion in the study were identified from data provided by BlueCross BlueShield and Humana Medicare Advantage Plans. Selection of these Medicare Advantage plans was based on those currently monitoring or tracking the anticholinergic metric as well as insurance plans holding a gain share contract with the private care practice site. Patients were included if they were 65 years or older, followed by a primary care provider within State of Franklin Healthcare Associates, which is a physician-led and employee-owned private medical group with over 30 practices across Northeast Tennessee and Southwest Virginia with the majority being internal medicine or family medicine practices. Patients must be prescribed 1 or more anticholinergic medication and there must have been communication of medication recommendations made to the provider from the clinical pharmacist related to the anticholinergic medication prescribed. All patients included needed an appointment scheduled on or before December 31, 2025. Data collection points included patient demographics, baseline and follow up anticholinergic burden score, anticholinergic medication use and duration, prescribing physician, and intervention response. The primary outcome was a composite endpoint of the impact of interventions made by the clinical pharmacist. This included medication changed based on pharmacist recommendations, patient declined alternative therapy despite provider encouragement, or the provider contacted an outside prescriber with alternative recommendation provided by clinical pharmacist. Data analysis included a one-sample proportion test for the primary outcome and descriptive statistics for the secondary outcomes, along with a paired t-test for anticholinergic burden score comparison.

Results: A total of 459 patients were screened for inclusion, and 99 patients were included in final analysis. The average patient was 76 years of age, and a majority of patients were female. The average number of baseline anticholinergic agents for each patient was 1.1. The result for the primary outcome was 73.7%. Most patients had been prescribed the anticholinergic agent for more than a year. The most common anticholinergic class prescribed was antihistamine followed by antidepressant and skeletal muscle relaxant. The average baseline anticholinergic burden score for patients enrolled was 4.6, with the follow up anticholinergic burden score showing a decrease to 3.1.

Conclusions: The results of this study highlight that clinical pharmacist interventions on anticholinergic medications led to an improvement in the Polypharmacy: Use of Anticholinergic Medications (POLY-ACH) quality metric and potentially increased reimbursement rates from Medicare Advantage Plans. The impact from the clinical pharmacist intervention also led to a reduction in patient’s anticholinergic burden score, showing a positive impact on patient outcomes. Future directions include developing educational materials based on prescribing trends identified to influence future prescribing practices.


Moderators Presenters
avatar for Sarah Emily Strickland

Sarah Emily Strickland

PGY2 Ambulatory Care Resident, East Tennessee State University Bill Gatton College of Pharmacy
Evaluators
CT

Christina Thurber

PGY-1 Residency Program Coordinator
Friday May 1, 2026 9:10am - 9:30am EDT
Parthenon 2

9:10am EDT

Impact of the Implementation of Vitamin D Screening and Supplementation on COPD Exacerbations
Friday May 1, 2026 9:10am - 9:30am EDT
Background: Vitamin D deficiency is common among patients with chronic obstructive pulmonary disorder (COPD) and has been associated with increased frequency of exacerbations and higher mortality. Recent Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines recommend assessing the vitamin D status of all patients hospitalized for COPD exacerbations, specifically to identify those with severe vitamin D deficiency, defined as <10 ng/mL, as this population has been shown to benefit the most from receiving supplementation. As of January 1, 2024, Piedmont Columbus Midtown Medical Clinic (MMC) orders vitamin D levels for COPD patients, if not previously obtained while inpatient, and prescribes supplementation for patients with below normal vitamin D levels, defined as <30 ng/mL. This study assesses the impact of this intervention on COPD exacerbation rates and time to repeat exacerbation.

Methods: A single-center, retrospective, observational, pre-post chart review compared clinical outcomes of COPD patients who completed a post-discharge visit at Piedmont Columbus MMC during January 1 to December 31, 2023, (pre-implementation) and January 1 to December 31, 2024, (post-implementation) following a COPD-related hospitalization at either Piedmont Columbus Regional (PCR) Midtown or PCR Northside. Patients were excluded if they received vitamin D supplementation prior to hospitalization or had a past medical history of lung cancer or parathyroid disorder. The primary objective was mean number of COPD exacerbations per person year. The secondary objective was time to repeat COPD exacerbation. Post-implementation results for each objective were stratified by baseline vitamin D levels into three pre-defined categories: sufficiency (≥30 ng/mL), deficiency (10-29 ng/mL), and severe deficiency (<10 ng/mL). A student t-test was used to evaluate the primary outcome, while the secondary outcome and stratification of post-implementation results were evaluated using descriptive statistics.

Results: A total of 30 patients were included in the study, with 17 being in the pre-implementation cohort and 13 being in the post-implementation cohort. Age was similar between groups, but a large difference was seen with sex and race. The post-implementation cohort had an average baseline vitamin D level of 18.7 ng/mL, which correlated with deficiency. The post-implementation cohort had fewer COPD exacerbations per person year on average (1.46 vs 1.71, p=0.76) but had a shorter time to repeat exacerbation compared to the pre-implementation cohort (98.6 days vs 142 days). Within the post-implementation cohort, patients with deficient baseline vitamin D levels experienced fewer exacerbations per person year and had a longer time to repeat exacerbation compared to those with sufficient or severely deficient baseline vitamin D levels.

Conclusion: Routine screening and supplementation of vitamin D in COPD patients may be associated with fewer exacerbations, though no statistically significant difference was observed in this small sample. Trends toward reduced exacerbation frequency following implementation suggest potential benefit, particularly among patients with baseline vitamin D deficiency. Larger studies are warranted to further evaluate the clinical impact of vitamin D optimization in this population.

Contact: [email protected]
Moderators
avatar for Abigayle Campbell

Abigayle Campbell

Clinical Specialist, Psychiatry; PGY1 Acute Care RPC, Self Regional Healthcare
For the past 6 years, I have served as the Clinical Pharmacy Specialist within the Inpatient Behavior Health Center at Self Regional Healthcare in Greenwood, SC. Recently, I have transitioned into a new role as the Medication Utilization and Quality Coordinator. I completed my bachelor's... Read More →
Presenters
avatar for Shelby Barron

Shelby Barron

PGY1 Pharmacy Resident, Piedmont Columbus Regional Midtown
Shelby Barron, PharmD, is a PGY1 Pharmacy Resident at Piedmont Columbus Regional Midtown in Columbus, Georgia, where she will continue her training as the PGY2 Ambulatory Care Pharmacy Resident upon completion of her PGY1 year. She earned her Doctor of Pharmacy degree from Auburn... Read More →
Evaluators
Friday May 1, 2026 9:10am - 9:30am EDT
Athena B

9:10am EDT

Evaluation of the Safety and Tolerability of Intravenous Push Dose Valproic Acid
Friday May 1, 2026 9:10am - 9:30am EDT
​​​​Title: Evaluation of the Safety and Tolerability of Intravenous Push Dose Valproic Acid   
Authors’ names: Maryam Hashem, Kaitlyn Wallace, Olivia Morgan, Katleen Chester 
Email: [email protected] 

Background: Valproic acid (VPA) is an antiseizure medication that inhibits voltage-gated sodium channels and gamma-aminobutyric acid (GABA) transaminase and enhances GABA synthesis. Multiple VPA formulations are commercially available, but intravenous (IV) administration is preferred when patients lack oral access or require emergent treatment. Grady Memorial Hospital (GMH) transitioned from IV VPA maintenance doses administered via IV piggyback (IVPB) at a rate of 6 mg/kg/minute to slow IV push (IVP) over 2 to 5 minutes, due to the fluid shortages following Hurricane Helene. The transition to IVP VPA was based on limited available evidence evaluating the safety and operational efficiency of this administration strategy. The objective of this study was to investigate the safety, tolerability, and operational efficiency of IVP VPA compared to IVPB VPA.   

Methods: This was a single center, retrospective, observational study evaluating the safety, tolerability, and operational efficiency of IVP VPA maintenance doses (≤1500 mg) compared to IVPB from July 2024 to January 2025. Included patients were aged 18 years or older who received at least one dose of IV VPA. The primary outcome was the incidence of injection site reactions including injection site pain, discomfort, phlebitis, burning, infiltration, extravasation, or erythema. Secondary outcomes included number of doses received prior to a reaction, type of reaction, type of line medication was administered through, dispense location (central pharmacy or floor pyxis), and time from order verification to administration. Baseline characteristics such as age, gender, weight, location at the time of initial administration, and type of line were collected. Descriptive statistics were used to summarize baseline characteristics and outcoming using medians and interquartile ranges, or means and standard deviation, as appropriate. Continuous variables were compared using the Mann-Whitney U test, and categorical variables were compared using chi-square test.  

Results: A total of 200 patients met inclusion criteria and were included in the analysis. Baseline characteristics were similar between groups, with no significant differences in age between the IVPB and IVP groups or weight. In the IVPB VPA cohort, there were a total of 1,338 administrations; only 2 administrations resulted in a reaction. In the IVP VPA cohort, there were a total of 1,068 administrations; 8 administrations resulted in a reaction. Infiltration was the most common reaction, occurring in 2 patients in the IVPB group and 5 patients in the IVP group (p-value=0.07).  Burning occurred in two patients and erythema in one patient in the IVP group; neither finding was statistically significant (p-value=0.14 and 0.30, respectively). All patients continued to receive IV VPA after the initial reaction without a reported reoccurrence. Dispense location differed significantly between groups. All IVPB doses were prepared by the central pharmacy, whereas only 39% of IVP doses came from the pharmacy and 61% were dispensed from automated dispensing cabinets (p-value <0.001). The median time from pharmacist verification to administration of the first maintenance dose was 85 minutes in the IVPB group and 78 minutes in the IVP group; however, this finding was not statistically significant (p-value = 0.168).  

Conclusion: Injection site reactions were low overall. Implementation of IVP VPA did not result in a significant increase in injection site reactions when compared to IVPB VPA for maintenance doses, indicating that the switch to IVP for maintenance dosing is a safe and efficient practice. 
 

Moderators
avatar for Brittany NeSmith

Brittany NeSmith

PGY1 Residency Program Director, BSSFBon Secours St. Francis DowntownPGY1
Presenters Evaluators
BB

Brooke Bibb

Ascension Saint Thomas Hospital West
Friday May 1, 2026 9:10am - 9:30am EDT
Athena J

9:10am EDT

Impact of Docusate De-Implementation on Invasive Laxative Use in Intensive Care Unit Patients with Thoracic Trauma
Friday May 1, 2026 9:10am - 9:30am EDT
  • Title: Impact of docusate de-implementation on invasive laxative use in intensive care unit patients with thoracic trauma
  • Authors: Isaiah Hicks, Blake Henderson, Spencer Roper, Amanda McKinney
  • Objective: Explain the impact of docusate de-implementation and consider benefits to patients and institutions.
  • Self-Assessment Question: Which of the following are reasons that contribute to the use of docusate in many institutions? Select all that apply.
  • Background: The purpose of this study is to establish if the de-implementation of docusate from opioid pathways reduced the use of invasive laxatives in trauma surgical intensive care unit patients with thoracic trauma.
  • Methods: The primary outcome of this retrospective chart review was the use of invasive laxatives such as rectal suppositories (i.e. glycerin, bisacodyl) and enemas (i.e. sodium phosphate; lactulose; admixture of saline, mineral oil, glycerin). Mean number of non-invasive laxatives (e.g. polyethylene glycol, senna, magnesium citrate), intensive care unit length of stay (ICU LOS), hospital length of stay (HLOS), and morphine milligram equivalents (MMEs) were secondary outcomes. Patients were divided into pre-removal and post-removal groups.
  • Results: In this study, 378 patients were screened, and 160 patients were included in statistical analysis. There was no statistically significant difference in invasive laxative use between pre- and post-removal groups (30.9% vs 27.3%, p = 0.62). There was no statistically significant difference in mean number of non-invasive laxatives used (1.45±0.6 vs 1.48±0.5, p = 0.52), mean HLOS (8.1±5.2 days vs 8.2±5.5 days, p = 0.73), or mean MMEs (31.3±54.3 vs 39.4±42.7, p = 0.07). Mean ICU LOS was statistically significant between the pre- and post-removal groups (3.3±2.1 days vs 2.8±2.2 days, p = 0.04).
  • Conclusion: A reduction in invasive laxative use after the removal of docusate from opioid order pathways was not established, likely due to limited sample size. Notably, removal was associated with shorter ICU LOS. Further analysis focusing on financial impact would provide insight into potential cost savings and decreasing pill burden.
  • (Link to Abstract Document)
Moderators
avatar for Christele Robinson

Christele Robinson

Emergency Medicine Clinical Pharmacy Specialist, Emory University Hospital
Christele Robinson, PharmD, is board certified in pharmacotherapy. She is a member of the Department of Pharmacy at Emory University Hospital and currently practicing as an Emergency Medicine Clinical Pharmacy Specialist. Dr. Robinson obtained a Bachelor of Science degree at the... Read More →
Presenters
avatar for Isaiah Hicks

Isaiah Hicks

PGY1 Pharmacy Resident, University of Tennessee Medical Center
Isaiah Hicks, PharmD is a PGY1 Pharmacy Resident at University of Tennessee Medical Center. He completed his Doctor of Pharmacy and Bachelor of Science degrees at Virginia Commonwealth University in the state he calls home. In July of this year, Isaiah will begin his PGY2 in Emergency... Read More →
Evaluators
avatar for Cody Parker

Cody Parker

Clinical Pharmacy Specialist, St. Joseph's/Candler
Dr. Cody Parker is the PGY1 Pharmacy Residency Program Director at St. Joseph's/Candler in Savannah, GA. He received his Doctor of Pharmacy from the University of Georgia and completed a Postgraduate Year One (PGY1) Pharmacy Practice Residency at St. Joseph’s/Candler. Dr. Parker is a Clinical Pharmacy Sp... Read More →
Friday May 1, 2026 9:10am - 9:30am EDT
Athena D

9:10am EDT

Sedation Practices in Patients Undergoing Targeted Temperature Management at 36° C
Friday May 1, 2026 9:10am - 9:30am EDT
Sedation Practices in Patients Undergoing Targeted Temperature Management at 36° C
Grace Clark, Anais Solomon, Joanna Brennan, Bibidh Subedi
AdventHealth Orlando, FL

Background: Targeted temperature management (TTM) is the practice of cooling patients’ core body temperature for comatose patients after cardiac arrest to prevent brain damage. Historically, patients undergoing TTM to a goal of 33° C have been deeply sedated with Richmon Agitation and Sedation Scale (RASS) goals of -4 to -5 to avoid shivering, which increases the cerebral metabolic demand. In 2013, the TTM trial was published, prompting the 2015 ACLS guidelines to include 36° C for TTM. TTM to 36° C reduces shivering and possibly sedation needs. The objective of this study was to characterize sedation practices during TTM at 36° C, focusing on RASS goals and the sedation level achieved.


Methods: This was a multicenter, retrospective cohort study with 75 patients from AdventHealth Central Florida campuses who were enrolled between 4/1/2025 and 9/30/2025. Adult patients 18 years of age or older were included if they received TTM at 36° C after out-of-hospital or in-hospital cardiac arrest. Patients were excluded if they were pregnant, had multiple cardiac arrests, or if they were placed on extracorporeal membrane oxygenation (ECMO). The primary outcome was sedation level achieved measured by the RASS score for five days post cardiac arrest. Secondary outcomes included prescribed RASS goal, if the RASS goal was changed during TTM, sedation medications utilized, cumulative doses of sedative medications, Glascow Coma Scale (GCS) at baseline and on day five, time to extubation, incidence of seizure, incidence of tracheostomy, ICU and in-hospital mortality, and ICU and hospital length of stay.


Results: All 75 patients were included in analysis. The average age of our patients was 62 years old with 68% being male. Witnessed arrests occurred in 77.3% of patients with 25.3% having a shockable rhythm initially. The median time to ROSC in witnessed arrests was 12 minutes. Around 61.3% of patients received vasoactive agents within 1 hour of hospital admission. The median RASS achieved was -2.5 on day 1 and 0 on days 2-5. The most common RASS goals were -1 to -2 (73.3%) and 0 to -1 (14.7%), with 29.3% of patients having their RASS goals changed during TTM. The most common continuous sedation medications were fentanyl (78.67%), propofol (76%), midazolam (58.67%), and dexmedetomidine (30.67%). The cumulative daily dose for dexmedetomidine increased over the first 72 hours, while fentanyl, midazolam, and propofol doses decreased. Patients were on sedative continuous infusions for a median of 36 hours with a TTM median duration of 72 hours. The number of patients on continuous sedation was 67 (89.3%), 48 (64%), 38 (50.7%), 25 (33.3%), and 16 (21.3%) respectively for days 1-5. The number of patients on as needed sedation was 8 (10.7%), 11 (14.7%), 11 (14.7%), 8 (10.7%), and 7 (9.3%) respectively for days 1-5. Around 37% of patients had TTM discontinued early with 5.3% of them due to the patient following commands. Median GCS was 15 at baseline and 10 on day 5. Seizures occurred in 19 people (25.3%) for a median of 2.63 days. Shivering occurred in 11 people (14.7%) and 8 people (10.7%) received tracheostomy. The median time to extubation was 2.7 days. The median lengths of stay were 4 days for the ICU and 7 days for the whole hospitalization. Mortality occurred in 46 cases (61.3%) with all the patients dying during their ICU stay.


Conclusions: Our study found that most patients undergoing TTM at 36° C had lower sedation targets prescribed and achieved than have been historically attained. Most patients were able to complete the full 72 hours of TTM. Further prospective studies are warranted to evaluate optimal sedation target in this demographic.

Presentation Objective: Analyze current targeted temperature management (TTM) sedation practices within AdventHealth Central Florida division.
Moderators
JK

Joseph Kohn

PRIS2Prisma Health Richland-University of South CarolinaPGY1
Presenters
avatar for Grace Clark

Grace Clark

PGY1 Pharmacy Resident, AdventHealth Orlando
Evaluators
avatar for Jolie Gallagher

Jolie Gallagher

Clinical Pharmacy Specialist, Critical Care, Emory University Hospital
I am the clinical pharmacy manager at Emory University Hospital.  My background training is in critical care.  My current areas of interest are optimization of transitions of care and pharmacist burnout and resilience.
Friday May 1, 2026 9:10am - 9:30am EDT
Athena I

9:10am EDT

Appropriate Diagnosis of Sepsis via SIRS Criteria and Opportunities for Reduction in Broad-Spectrum Antibiotic Use in the Emergency Department
Friday May 1, 2026 9:10am - 9:30am EDT
Purpose: Time-sensitive completion of bundled interventions is the focus of the Severe Sepsis and Septic Shock Early Management Bundle (SEP-1) Centers for Medicaid and Medicare Services (CMS) quality measure, which aims to reduce sepsis-related morbidity and mortality. To avoid missed cases of sepsis, clinicians often rely on the Systemic Inflammatory Response Syndrome (SIRS) criteria as the major identifier of sepsis, which has inadvertently raised concerns for potential overdiagnoses. This study evaluated the incidence of patients diagnosed with sepsis in the emergency department (ED) who did not meet SIRS criteria and/or lacked a documented source of infection. Recognizing such cases may highlight opportunities to reduce unnecessary use of broad-spectrum antibiotics and ultimately support more targeted antimicrobial stewardship in sepsis care.
Methods: This study design was submitted to the Ballad Health System Institutional Review Board for approval. This was a retrospective electronic chart review that included adult patients aged 18 years and older who presented to the ED of Bristol Regional Medical Center, Holston Valley Medical Center, or Johnson City Medical Center between December 2025 and March 2026 with a sepsis ICD-10 diagnosis. Using the electronic health record, we identified patients who were reported to have met the SIRS criteria. Among these qualifying candidates, patients were then assessed whether there was a documented source of infection and whether broad-spectrum antibiotics were administered. Data collected included patient age, gender, ethnicity, respiratory rate, heart rate, temperature, white blood cell count, and antibiotics received. Provider documentation was reviewed to verify whether there was a documented source of infection. All data was reviewed and recorded in a manner that ensured complete patient anonymity. Statistical analysis was conducted to compare groups meeting sepsis criteria, antibiotic use, and documented infection source.
Results: Among evaluated patients, 11% of those diagnosed with sepsis in the ED did not meet greater than two SIRS criteria at initial presentation, while 89% met SIRS criteria. Additionally, 3% of the study population lacked a documented or suspected source of infection. Clinician compliance with SIRS-based sepsis diagnosis across facilities ranged from 81% to 97%, exceeding the pre-study hypothesis of 70%. Cefepime and vancomycin were the most commonly utilized antimicrobials, with broad-spectrum antibiotic use occurring in approximately 90% of patients.
Conclusions: Majority of patients diagnosed with sepsis in the ED met SIRS criteria, with compliance rates higher than initially anticipated. However, a subset of patients did not meet diagnostic criteria or lacked an identifiable infectious source, suggesting potential opportunities for improvement with diagnostic accuracy and reducing unnecessary broad-spectrum antibiotic use. Further studies with larger sample sizes and less exclusion criteria are warranted to better assess antimicrobial appropriateness based on patient-specific risk factors and presumed sources of infection.
Moderators
avatar for Brian Leith

Brian Leith

Clinical Pharmacist, VA Medical Center
I am currently the emergency medicine and antimicrobial stewardship pharmacist at the VA Medical Center in Fayetteville, NC.
Presenters
avatar for AnaLeigh Cook

AnaLeigh Cook

PGY1 Pharmacy Resident, Bristol Regional Medical Center


Evaluators
BK

Brian Knott

Clinical Pharmacy Manager, AdventHealth Winter Park
Friday May 1, 2026 9:10am - 9:30am EDT
Olympia 2

9:10am EDT

Comparing Safety and Efficacy of Subcutaneous Unfractionated Heparin Dosing Frequencies for Venous Thromboembolism Prophylaxis in a Community Hospital
Friday May 1, 2026 9:10am - 9:30am EDT
Comparing Safety and Efficacy of Subcutaneous Unfractionated Heparin Dosing Frequencies for Venous Thromboembolism Prophylaxis in a Community Hospital
Authors: Jonathan Johnson, Adam Harnden, Madison Sanders, M. Trey Dailey, Nancy Bailey, Matthew Hadley
Background: Venous thromboembolism (VTE) is a major cause of in-hospital morbidity and mortality with an estimated 375,000 new cases and approximately 100,000 deaths annually in the United States. Patients in the hospital are at a higher risk of developing VTE due to underlying conditions and acute illness. Using unfractionated heparin (UFH) to prevent VTE is an appropriate choice of therapy to decrease the risk of VTE events and death; however, there is not a consensus on administration frequencies. This study aimed to assess the safety and efficacy between dosing strategies in patients that were admitted to a community hospital.
Methods: This retrospective, institutional review board approved study, was conducted at a 344-bed community hospital in Montgomery, Alabama. A clinical decision support tool was utilized to identify patients receiving UFH 5,000 units subcutaneously twice daily (BID) or three times daily (TID) between January 1, 2024 to December 31, 2024. Patients included in the study were at least 19 years old, non-surgical, and received prophylactic UFH 5,000 units for at least 48 hours dosed either BID or TID. Patient populations excluded were pregnant patients, trauma patients, those on continuous renal replacement therapy, those who had a major bleed upon admission, therapeutic anticoagulation doses for more than 12 hours, received low molecular weight heparin or fondaparinux, or if patients received both UFH dosing schedules for at least 48 hours. Patients were separated into two cohorts of UFH dosing: BID or TID. The primary endpoint of this study was the incidence of VTE events. Secondary endpoints included incidence of the individual components of VTE: deep vein thrombosis and pulmonary embolism. Other secondary endpoints included major and minor bleeding, heparin-induced thrombocytopenia, hospital length of stay (LOS), hospital re-admission, and in-hospital mortality. Data for the study were collected from an on-site secure electronic medical record where patient information was reviewed. Power was calculated through an open-access statistical analysis software such that 120 patients were required to reach 90% power. Appropriate statistical tests were applied to analyze data as well as appropriate use of descriptive statistics.
Results: A total of 140 patients were included in this study with 70 patients in each arm, meeting protocol. A total of 156 patients were excluded with the majority due to not receiving doses for at least 48 hours.  The primary outcome, incidence of VTE, occurred in 1/70 (1%) patients in the TID dosing group compared to no incidence of VTE in the BID group (P=1). The incidence of VTE that occurred in the TID group was due to a deep vein thrombosis. Major bleeding occurred in 1/70 (1%) patients in the TID group and minor bleeding occurred in 1/70 patients (1%) of both the BID and TID groups. Re-admission rates occurred in 35 patients in the BID group compared to 23 patients in the TID group (P=0.06). Incidence of in-hospital mortality occurred in 3 patients in the BID group compared to 10 patients in the TID group (P=0.08). Mean number of days for LOS was 7.94 for the BID group and 10.57 for the TID group (P=0.13).
Conclusion: In this study, patients receiving UFH 5,000 units for VTE prophylaxis had similar safety and efficacy endpoints when comparing BID and TID dosing. Limitations of this study include being a single center study that relied on medical record documentation and having difficulty in extrapolating the results due to the prevalence of hospital acquired VTE.
Moderators
avatar for Devin Lavender

Devin Lavender

Clinical Assistant Professor, UGAA1University of Georgia College of Pharmacy (Ambulatory Care)PGY2
Ambulatory Care, Scholarship of Teaching and Learning, Resident and Student Development.
Presenters
avatar for Jonathan Johnson

Jonathan Johnson

PGY1 Pharmacy Resident, Jackson Hospital and Clinic
For my undergraduate, I graduated from The Citadel, the Military College of South Carolina for biology, and I graduated from the Medical University of South Carolina (MUSC) for pharmacy school. I am a current PGY1 Pharmacy Resident with Jackson Hospital and Clinic in Montgomery, Alabama... Read More →
Evaluators
Friday May 1, 2026 9:10am - 9:30am EDT
Parthenon 1

9:10am EDT

Evaluating the implementation of prolonged beta-lactam infusions for sepsis patients in the ICU
Friday May 1, 2026 9:10am - 9:30am EDT
Title: Evaluating the implementation of prolonged beta-lactam infusions for sepsis patients in the ICU
Authors: Nathaniel Park, Jeremy Frens, Alex Chappell, and Dustin Zeigler
Background/Purpose:
Beta-lactams are generally the preferred and most frequently prescribed antibiotics to treat patients with sepsis due to their broad spectrum of activity and favorable safety profile. Their efficacy is dependent on time above minimum inhibitory concentration (MIC) with requirements depending on beta-lactam class. Therefore, patients are at risk of treatment failure if beta-lactam concentrations at the site(s) of infection fall below the MIC for extended periods of time. Recently, data from the BLING-III trial and subsequent meta-analyses have suggested that there may be benefits in terms of clinical cure and reduced 90-day mortality with prolonged beta-lactam infusions in comparison with conventional, intermittent infusions. As a result, Cone Health adopted prolonged or continuous infusion protocols for piperacillin/tazobactam, penicillin G, and nafcillin. More recently, additional prolonged infusion protocols were implemented for cefepime, ceftazidime, and meropenem in critically ill patients with sepsis or septic shock. The aim of this study was to evaluate the efficacy and safety associated with the implementation of a prolonged infusion regimen protocol for cefepime, ceftazidime, and meropenem in ICU patients with sepsis or septic shock.
Methodology:
This Institutional Review Board (IRB) reviewed, determined exempt, retrospective, multicenter, single-health system, pre-post study was conducted from October 2024 to December 2025. Patients were included if they were > 18 years old; ICU admission for sepsis or septic shock; had documented site of infection or strong suspicion for bacterial infection; initiated on meropenem, cefepime, or ceftazidime < 24 hours from sepsis or septic shock diagnosis; and > 1 sign of organ dysfunction [mean arterial pressure (MAP) < 60 mm Hg for > 1 hour, vasopressor required > 4 hours, respiratory support required for > 1 hour, or serum creatinine > 2.49 mg/dL]. Exclusion criteria included renal replacement requirement at the time of antibiotic initiation, received antibiotics < 48 hours, and antibiotics not initiated within 24 hours of sepsis diagnosis. Baseline demographic data, safety data, and data relevant to the primary and secondary endpoints were collected among eligible patients. The primary endpoint was ICU length-of-stay (LOS) defined as days on ICU unit. Secondary endpoints were clinical cure (defined as completion of antibiotics within 14 days without resumption within 48 hours of cessation), vasopressor-free days, and 30-day all-cause mortality. Continuous data was analyzed with Student’s t-test or Mann-Whitney U test, and categorical data was analyzed with chi-square test or Fisher’s exact test. Two-sided alpha was set at 0.05.
Results:
In total, 200 patients were screened for inclusion (100 in pre- and 100 in post-intervention cohort). Ultimately, 38 patients were analyzed – 18 in the pre-intervention cohort, and 20 in the post-intervention cohort. Less than half of the patients were female (n=17, 44.7%) with an average age of 71 years old. Most patients were started on cefepime (n=29, 76.3%), with pulmonary and urinary sources accounting for most of the suspected sepsis sources (n=28, 73.7%). Of the 20 patients in the post-intervention cohort, 14 patients met criteria for prolonged beta-lactam infusion. Among patients meeting criteria (n=14), 1 patient (7.1%) received prolonged beta-lactam infusion. For the primary endpoint, the post-intervention group had a shorter median ICU LOS (2.7 vs 5.0 days, p=0.285). For secondary endpoints, the post-intervention group had less vasopressor-free days (0.7 vs 1.1 days, p=0.055), reduced 30-day mortality (15.0% vs 33.3%), and increased clinical cure (90.0% vs 77.8%). One occurrence of a new C. difficile infection occurred, which was in the pre-intervention cohort, and beta-lactams were appropriately renally adjusted in the 27 patients meeting criteria for renal dosing.
Conclusions:
Although numeric differences were observed in favor of the prolonged beta-lactam infusion protocol cohort with decreased ICU LOS, increased vasopressor-free days, 30-day mortality, and clinical cure, there were no statistical differences among any of the primary or secondary endpoints. Additionally, the observed low implementation rate of prolonged beta-lactam infusion among eligible patients further complicates interpretation. Most likely, the cohort identification methods did not have the sensitivity to identify more patients administered prolonged beta-lactam infusions. The results of this study should not dissuade use of the prolonged beta-lactam infusion protocol.
Moderators Presenters Evaluators
avatar for Anh Nguyen

Anh Nguyen

Clinical Pharmacy Specialist, Emory Decatur Hospital
I’m a Board‑Certified Critical Care Pharmacy Specialist with a passion for taking care of some of the sickest patients in the hospital. I’ve worked in both intermediate and intensive care settings, where every day brings a new challenge and a new opportunity to make a meaningful... Read More →
Friday May 1, 2026 9:10am - 9:30am EDT
Athena H

9:10am EDT

Evaluation of Febrile Neutropenia Prophylaxis Use in Inpatient Oncology
Friday May 1, 2026 9:10am - 9:30am EDT
Evaluation of Febrile Neutropenia Prophylaxis Use in Inpatient Oncology
Olivia Jones, PharmD; Sarah Bowman, PharmD, BCOP; Samantha Lightle, PharmD
Huntsville Hospital – Huntsville, AL


Background: Febrile neutropenia is a common and potentially serious complication among patients with hematologic malignancies. The National Comprehensive Cancer Network (NCCN) provides evidence-based guidance to identify oncology patients who qualify for prophylactic antimicrobial therapy to prevent febrile neutropenia. Consistent application of these recommendations is critical for reducing infection-related morbidity and mortality. Prior evaluation at our institution has highlighted gaps in guideline adherence, particularly among high-risk populations such as patients with acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), myelodysplastic syndromes (MDS), and multiple myeloma (MM). The purpose of this retrospective chart review is to evaluate current antimicrobial prescribing patterns and associated outcomes in these populations.


Methodology: This single-center, IRB-approved, pre–post implementation study was conducted at Huntsville Hospital to evaluate prescribing patterns of prophylactic antimicrobials and associated outcomes in patients at high risk for febrile neutropenia. The pre-intervention group included hospitalized patients with the aforementioned hematologic malignancies between January 1, 2025 and August 31, 2025. Data extracted from the electronic medical record included demographics, chemotherapy regimens, risk factors, use of prophylactic antimicrobial agents, and incidence of febrile neutropenia. Following analysis of baseline data, a disease specific decision support tool and educational initiative were developed and delivered to oncology nurse practitioners and pharmacists in early March 2026. Post-intervention data was collected from the same patient population following March 10, 2026.  The primary outcome was percentage of eligible patients who received appropriate prophylactic antimicrobials.


Results: A total of 87 patients were included in the pre-implementation group and 15 patients in the post-implementation group. Appropriate prophylactic antimicrobial use among eligible patients increased from 42.8% (3/7) to 100% (3/3) for antibacterial prophylaxis and from 50% (10/20) to 100% (3/3) for antifungal prophylaxis. Antiviral prophylaxis increased from 50.9% (26/51) to 57.1% (8/14). Median time to prophylaxis initiation decreased from 80.7 to 4.7 hours for antibacterial agents and from 17.9 to 4.7 hours for antifungal agents. Antiviral prophylaxis showed minimal change in time to initiation (19.6 vs 18.6 hours). Febrile neutropenia incidence did not differ consistently between groups. In the pre-implementation cohort, patients who received prophylaxis had lower absolute neutrophil counts and longer hospital lengths of stay compared to those who did not receive prophylaxis.


Conclusions: A pharmacist-driven educational initiative was associated with improved adherence to guideline-recommended prophylactic antimicrobial use, particularly for antibacterial and antifungal agents, and significantly reduced time to initiation. Variability in antiviral prescribing practices may explain the more modest changes observed in this group. These findings highlight the impact of pharmacist involvement and support further efforts to standardize prophylaxis use earlier in hospitalization.
Moderators
CW

Cassandra Wade

Pharmacy Procurement Coordinator, John D Archbold Memorial Hospital
Presenters
avatar for Olivia Jones

Olivia Jones

PGY-1 Resident, Huntsville Hospital
Evaluators
avatar for Madison Yates

Madison Yates

Clinical Pharmacist Practitioner, PGY1 Ambulatory Residency Program Coordinator, Cone Health
Friday May 1, 2026 9:10am - 9:30am EDT
Athena G

9:10am EDT

Evaluation of Glucagon-like Peptide-1 Receptor Agonist Use and the Risk of Pancreatitis
Friday May 1, 2026 9:10am - 9:30am EDT
Authors: Isaac Sauvageau, Kerri Smith, Brittney Bright, Ryan Imel, Blake Sloan 

Background: Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are a therapeutic class that mimics the naturally occurring incretin hormone GLP-1. Through this mechanism, they enhance glucose-dependent insulin secretion, suppress glucagon release, delay gastric emptying, and promote satiety. These effects make GLP-1 RAs effective agents for the management of type 2 diabetes mellitus (T2DM) and chronic weight management. They have also demonstrated cardiovascular and renal protective benefits, leading to increased use in patients with cardio-renal comorbidities. Despite their broad acceptance in clinical practice, early clinical trials and observational studies suggest a potential increase in the risk of pancreatitis (0.4% versus 0.03% in the general population). Multiple studies identify an increased risk of pancreatitis across the class, though results remain inconsistent, and the underlying mechanisms are not fully established. 

Methods: This was a multi-center, matched case-control design that included adult patients with active GLP-1 RAs on their home medication lists from May 1, 2024 – October 1, 2025. The primary objective was to determine the incidence of pancreatitis in patients using GLP-1 RAs at North Carolina Baptist Hospital, Highpoint Medical Center, and Davie Medical Center. The secondary objective was to identify patient-specific factors associated with pancreatitis risk among GLP-1 RA users. Patients were excluded from the study if they initiated GLP-1 RA therapy within 30 days of data collection. The incidence of pancreatitis was calculated from the unadjusted population prior to case matching. Cases were defined as GLP-1 RA users admitted to the hospital with a primary diagnosis of pancreatitis. Controls consist of GLP-1 RA users without hospitalization for pancreatitis and were matched to cases in a 1:1 ratio by age category, sex, and residential zip code to minimize confounding variables.  

Results: A total of 6,109 GLP-1 RA users were identified, of which 34 were admitted to the hospital with a primary problem of pancreatitis. This corelates with an 0.56% incidence of pancreatitis. After matching, 50 patients were included; 25 pancreatitis cases and 25 matched controls. The median age was 54 years, and 60% of the cohort was male. The median BMI was 35 kg/m2. The majority of patients were obese (82%) and had type 2 diabetes (78%). Semaglutide (56%) and tirzepatide (32%) were the most common GLP‑1 RAs used. Significant differences between cases and controls were observed for GLP‑1 RA agent distribution (p = 0.004), presence of chronic kidney disease (CKD) (36% vs. 8%; p = 0.017), cholelithiasis/cholecystitis (32% vs. 0%; p = 0.004), and serum creatinine levels (0.99 vs. 0.81 mg/dL; p = 0.038). 

Univariable logistic regression indicated increased odds of pancreatitis associated with CKD (OR 6.47; 95% CI 1.43–46.3; p = 0.027) and higher serum creatinine (OR 5.32; 95% CI 1.32–42.7; p = 0.059). Tirzepatide use was associated with significantly lower odds of pancreatitis (OR 0.11; 95% CI 0.02–0.44; p = 0.003) compared with semaglutide. GLP‑1 RA dose category, HbA1c, triglycerides, alcohol use, smoking status, and baseline metabolic parameters were not significantly associated with pancreatitis. In multivariable regression adjusting for CKD and agent, CKD remained an independent predictor (OR 8.95; p = 0.028), while tirzepatide maintained a protective association (OR 0.10; p = 0.005). 

Conclusions: The incidence of pancreatitis in GLP-1 RA users was 0.56%, which correlates with a higher risk of pancreatitis when compared to 0.03% in the general population. CKD and elevated serum creatinine were significantly associated with increased odds of pancreatitis in GLP-1 RA users, whereas tirzepatide was associated with reduced risk compared with semaglutide.

Moderators
avatar for Aayush Patel

Aayush Patel

Clinical Pharmacy Specialist, Emergency Medicine, Piedmont Columbus Regional Midtown
Presenters
Friday May 1, 2026 9:10am - 9:30am EDT
Athena A

9:10am EDT

Evaluation of Thromboprophylaxis Strategies for Orthopedic Surgery Patients
Friday May 1, 2026 9:10am - 9:30am EDT
Title: Evaluation of Thromboprophylaxis Strategies for Orthopedic Surgery Patients

Background: Orthopedic surgery patients are high-risk for post-operative venous thromboembolism (VTE) and often require prolonged prophylaxis. Several studies demonstrated that aspirin (ASA) is non-inferior to traditional prophylactic regimens, such as enoxaparin (LMWH), in orthopedic surgery, however these studies are limited regarding therapeutic durations, transitions of care, and inpatient versus outpatient practices. This has led to significant heterogeneity in practice regarding VTE prophylactic agents. This study aims to compare local rates of post-operative VTE and bleeding for patients receiving ASA vs LMWH prophylaxis.

Methods: This retrospective, observational cohort study included adults with surgical femur fractures or femur fractures with prosthetic replacement at Prisma Health Midlands sites between May 2024 and May 2025 receiving either ASA or LMWH for inpatient post-operative VTE prophylaxis. Therapeutic anticoagulation and those with contraindications to either therapy were excluded. The primary outcome was a composite of VTE events or bleeding during post-operative admission. Secondary outcomes included outpatient VTE or bleeding within 60 days, and evaluation of factors that may affect choice of agent. Tertiary outcomes evaluated therapeutic durations, duplications, and transition opportunities.

Results: Rates of the primary outcome of VTE and bleeding during post-operative admissions were not significantly different between groups (adjusted OR 1.05, 95% CI 0.39-2.28), nor were rates of VTE and bleeding from discharge to 60 days post-op (adjusted OR 0.78, 95% CI 0.26-2.40). Provider factors had the largest influence on choice of agent. Half of patients who received LMWH inpatient were switched to ASA on discharge and only 62% of patients had an appropriate stop date on their prophylactic agent.

Conclusion: No significant differences in VTE and bleeding were found between ASA and LMWH groups, both inpatient and post-discharge. Opportunities for improvement exist for several aspects of prophylactic therapy related to transitions of care.
Moderators Presenters
avatar for Chiara Huber

Chiara Huber

PGY-2 Internal Medicine Resident, Prisma Health Richland - University of South Carolina
I am a PGY-2 Internal Medicine pharmacy resident at Prisma Health Richland - University of South Carolina, with interests in internal medicine, family medicine, and women's health.
Evaluators
avatar for Allie Hale

Allie Hale

Clinical Pharmacist and Residency Program Director, Parkridge Health System
Friday May 1, 2026 9:10am - 9:30am EDT
Athena C

9:10am EDT

EVALUATION OF MEDICATION ACCESS INTERVENTIONS BY TRANSITIONS OF CARE PHARMACIST FOR PATIENTS REQUIRING HIGH-COST CARDIAC MEDICATIONS
Friday May 1, 2026 9:10am - 9:30am EDT
EVALUATION OF MEDICATION ACCESS INTERVENTIONS BY TRANSITIONS OF CARE PHARMACIST FOR PATIENTS REQUIRING HIGH-COST CARDIAC MEDICATIONS  
Esther Cho, Alexandra Cooper, Laura Provost, Nathan Wayne, Maegan Whitworth Wellstar MCG Health – Augusta, GA 
Background/Purpose: Centers for Medicare and Medicaid Services (CMS) monitors 30-day readmission rates per the CMS Hospital Readmission Reduction Program based on relative conditions or procedures including acute myocardial infarction (AMI), heart failure (HF), and coronary artery bypass graft (CABG). These three conditions have a high readmission rate per the CDC 2021 national data, with HF having the highest readmission rate at 22% (AMI 16% and CABG 13%). Current studies show TOC interventions, by a multidisciplinary team, lower 30-day readmission, but there is no literature focusing on an exclusive pharmacist-led intervention, with a specific focus to medication access such as medication affordability. n these studies, since most hospitals do not have a dedicated Transitions of Care (TOC) pharmacists, “standard of care” is considered to be general patient care, whereas TOC interventions are established to ensure continuity and coordinate care to patients. Therefore, further evaluation is required to evaluate the effectiveness and impact of pharmacist-led TOC intervention.

Methodology: This is a retrospective chart review of adult patients who were discharged from a cardiac floor with high-cost cardiac medications (e.g. Eliquis, Entresto, Jardiance) between November 4, 2024 – May 31, 2025. Interventions made by a non-TOC pharmacist, pregnant patients, and prisoners were excluded in this study. The primary outcome is overall 30-day readmission rate. Secondary outcomes include quantification and classification of TOC pharmacy interventions, patient assistance applications initiated and/or approved, percentage of prescriptions filled at discharge, and 30-day readmission cause.

Results: Overall, 186 patients were included in the pharmacist-led TOC intervention group and 79 patients were included in the non-TOC intervention group. No significant difference was observed in rate of readmission within 30 days of discharge between TOC intervention and non-intervention groups (24% vs 20%, p=0.62). However, higher percentage of patients in the intervention group filled new high cost medication prescriptions at discharge (60% vs 47%, p=0.30), more medications were prescribed to meds-to-beds pharmacy (47% vs 32%, p=0.22), and patients in the TOC intervention group were less likely to be readmitted for medication related events (2% vs 12%, p=0.11).

Conclusions: No difference was observed in overall 30-day readmission rate between pharmacy-led TOC intervention group vs non-TOC intervention group. More providers prescribed new high-cost medications to Wellstar MCG Meds-to-Beds pharmacy, and a higher percentage of new prescriptions were dispensed at discharge with TOC pharmacist intervention. Additionally, patients were less likely to be readmitted for medication-related events in the TOC intervention group.
Moderators
AQ

April Quidley

PGY1 Residency Program Director, ECU Health Medical Center
Presenters
avatar for Esther Cho

Esther Cho

PGY1 Pharmacy Resident, Wellstar MCG Health
Evaluators
AJ

Audrey Johnson

Surgical/Trauma Critical Care Pharmacist, Memorial Health University Medical Center
Friday May 1, 2026 9:10am - 9:30am EDT
Olympia 1

9:30am EDT

Burnout Amongst Pharmacy Preceptors Across the United States
Friday May 1, 2026 9:30am - 9:50am EDT
Authors: Rachel Denison; Danielle Lott; Eric K. Shaw; Audrey Johnson
Contact Information: [email protected]
Background
Burnout is a growing epidemic affecting healthcare professionals worldwide. A 2023 study found that 45% of pharmacists reported burnout. As a profession that relies heavily on hands-on learning, the need for assessment of burnout amongst pharmacy preceptors is critical. A 2022 survey-based study of pharmacy preceptors in northern California found that 57% of participants were experiencing burnout. Other studies have examined burnout amongst pharmacists and pharmacy leadership, but there remains limited information regarding burnout amongst pharmacy preceptors across the United States.
Methods
This survey-based study aimed to assess burnout amongst pharmacy preceptors across the United States. Preceptors were contacted by email through health system and professional society registries. Participants were included if they self-identified as a pharmacist preceptor for pharmacy students and/or residents. The primary outcome was the percentage of burnout amongst participating pharmacy preceptors using the Copenhagen Burnout Inventory. Burnout was defined as a Copenhagen Burnout Inventory score ≥ 50. Secondary outcomes included subcategories of burnout: personal, work-related, and learner-related. Secondary outcomes were analyzed by additional contributing factors related to pharmacy preceptors. Statistical analyses utilized were Pearson’s chi-square test and Fischer’s exact test.
Results
From the invitations sent, 638 participants across the United States completed the survey. A total of 311/638 (48.7%) pharmacy preceptors had scores that indicated burnout. Of the participants experiencing burnout, the following also indicated burnout in learner-related, personal, and work-related subcategories: 230/311 (74%) learner-related burnout, 283/311 (91%) personal burnout, and 281/311 (90.4 %) work-related burnout. Factors related to participants who scored above threshold for burnout include: highest level of postgraduate training, precepting at university-affiliated teaching hospitals, greater percentage of students/residents that were difficult to teach and/or unmotivated, greater average number of hours worked per week, preceptors who participate in daily rounding, and greater amount of free time spent on work-related responsibilities. Factors related to participants who scored below threshold for burnout were: precepting at non-teaching hospitals, compensation or rewards for precepting, having adequate time for administrative or precepting duties, and having children/dependents.
Conclusion
This study examined current burnout trends facing pharmacy preceptors across the United States. Our survey recognized that 48.7% of participating preceptors are experiencing burnout. These results provide information about contributing factors to burnout, specifically learner-related, personal, and work-related burnout factors. Due to different cultures amongst employers, this study could be replicated at individual sites to determine levels of burnout and site-specific risk factors. Limitations of this study include possible biases created by a survey-based study, underrepresentation in several regions of the U.S., inability to rule out duplicate responses, and inability to verify survey responses. Our survey illustrates the need to further develop processes and initiatives that could be incorporated to improve reduce preceptor burnout.
Moderators Presenters Evaluators
CT

Christina Thurber

PGY-1 Residency Program Coordinator
Friday May 1, 2026 9:30am - 9:50am EDT
Parthenon 2

9:30am EDT

Agitation and Delirium in the ICU: Management with Valproic Acid
Friday May 1, 2026 9:30am - 9:50am EDT
Agitation and Delirium in the ICU: Management with Valproic Acid
Maddie Treadway; Sarah Wyatt; Robert Steed; Steve Lindley
Background: Agitation and delirium are common complications in critically ill patients, with delirium occurring in up to 80% of mechanically ventilated patients in the intensive care unit (ICU) setting. These conditions are associated with an increased cost to healthcare systems due to prolonged hospital and ICU length of stay, long-term cognitive impairment, and increased morbidity and mortality. Pharmacological management of delirium and agitation in the ICU often involves antipsychotics or sedatives, which are limited by their arrhythmogenic and deliriogenic side effects. Due to the lack of improvement in clinically meaningful patient-centered outcomes, the Society of Critical Care Medicine’s focused guideline update could not make a recommendation for or against the use of antipsychotics over usual care. More recently, valproic acid (VPA), has emerged as a potential alternative for the management of delirium and agitation in the ICU. Despite promising preliminary data for VPA, evidence remains limited, and institutional practices vary widely. The purpose of this study was to evaluate the efficacy and safety of VPA for the management of agitation and delirium in ICU patients.

Methods: This single-center, retrospective descriptive analysis evaluated 60 adult patients admitted to a medical, surgical-trauma, or cardiovascular ICU from 1/1/2022-7/1/2025. Patients were included if they were ≥ 18 years old, admitted to an ICU for ≥ 24 hours, and received scheduled VPA for the management of delirium or agitation for ≥ 3 days. Patients were excluded if they received VPA for any other indication (i.e., seizures), were pregnant, had a critical care pain observation tool score ≥ 3 immediately before VPA initiation, or were prescribed VPA prior to admission. The primary outcome was the overall change in the Intensive Care Delirium Screening Checklist (ICDSC) and Riker Sedation-Agitation Scale (SAS) scores. The secondary outcomes were the incidence of agitation (SAS > 4) and delirium (ICDSC ≥ 4) for up to 7 days and the change in concurrent psychoactive medications over 7 days. The safety outcome was the incidence of adverse events.

Results: A total of 988 VPA orders were identified, corresponding to 182 patients after removal of duplicate orders. Ninety patients met initial screening criteria, with 60 patients included in the outcomes analysis based on availability of ICDSC and SAS scores. Following initiation of VPA, the incidence of agitation decreased from 80% on days 0–1 to 18.3% on days 3–7 (z = - 5.8, P < 0.001). The incidence of delirium decreased from 46.7% on days 0–1 to 25% during days 3–7 (z = - 2.9, P = 0.003). The median concurrent psychoactive medication use was 3 (IQR 1-5) vs. 3 (IQR 1.75-4.25) on day 1 vs. day 7, respectively. Thrombocytopenia (platelets < 100 10*3/µL) occurred in 4 (6.7%) patients, elevated AST (> 80 IU/L) in 12 (20%) patients, elevated ALT (> 80 IU/L) in 8 (13.3%) patients, and hyperammonemia (> 60 µmol/L) in 7 (11.7%) patients.

Conclusion: In this retrospective analysis, initiation of VPA was associated with statistically significant reductions in agitation and delirium scores among critically ill patients. However, interpretation of these results should be made cautiously given the retrospective design, documentation variability, and the complex nature of critically ill patient populations. Further prospective studies are needed to compare VPA to the standard of care for agitation and delirium treatment in the ICU and establish optimal dosing strategies.


Moderators
avatar for Devin Lavender

Devin Lavender

Clinical Assistant Professor, UGAA1University of Georgia College of Pharmacy (Ambulatory Care)PGY2
Ambulatory Care, Scholarship of Teaching and Learning, Resident and Student Development.
Presenters
avatar for Maddie Treadway

Maddie Treadway

PGY1 Pharmacy Resident - Acute Care, Spartanburg Medical Center
I'm currently a PGY1 resident with a passion for critical care and emergency medicine and will be continuing my training next year as a PGY2 Critical Care resident. I enjoy discussing complex ICU pharmacotherapy, reviewing literature and working through challenging patient cases... Read More →
Evaluators
Friday May 1, 2026 9:30am - 9:50am EDT
Parthenon 1

9:30am EDT

Comparison of Nicardipine and Labetalol for Peri-Thrombolysis Blood Pressure Management in Acute Ischemic Stroke - Olivia Klassa
Friday May 1, 2026 9:30am - 9:50am EDT
Title: Comparison of Nicardipine and Labetalol for Peri-Thrombolysis Blood Pressure Management in Acute Ischemic Stroke
Authors: Olivia Klassa, Braiden Sorgenfrei, Michael Wagner, Alex Ewing, Lauren McAbee 
Background:  
Acute ischemic stroke requires rapid thrombolytic therapy to restore cerebral blood flow and optimize outcomes; however, safe administration depends on effective blood pressure control. Current AHA/ASA guidelines recommend reducing blood pressure to less than 185/110 mmHg prior to tenecteplase and maintaining less than 180/105 mmHg for 24 hours after administration. Elevated blood pressure may delay thrombolytic administration and increase hemorrhagic risk. Labetalol and nicardipine are commonly used first-line agents, though limited evidence supports a preferred option. This study aims to compare labetalol and nicardipine for their impact on door-to-needle time and 24-hour blood pressure control in patients receiving tenecteplase for acute ischemic stroke. 
Methods:  
A retrospective chart review was conducted at an 864-bed academic medical center in Greenville, South Carolina, between January 1, 2021, and October 31, 2025. Adults with acute ischemic stroke who received tenecteplase and required pre-thrombolysis blood pressure management with nicardipine or labetalol were included. Eligible patients were identified using a report from the Get With The Guidelines–Stroke database. Patients with hemorrhagic stroke, pregnancy, or receipt of alternative antihypertensives were excluded. The primary outcome was door-to-needle time. Secondary outcomes included time to blood pressure control, 24-hour blood pressure variability, antihypertensive utilization, and clinical outcomes including bleeding, mortality, and functional and neurologic status. 
Results:  
A total of 100 patients met inclusion criteria and were included in the final analysis. Of these, 38 received labetalol alone, 25 received nicardipine alone, 31 required escalation from labetalol to nicardipine, and 6 required escalation from nicardipine to labetalol prior to TNK administration. Baseline characteristics were similar between groups, though the nicardipine group had a higher prevalence of hypertension and greater outpatient antihypertensive use. Median door-to-needle time was similar between groups (28 vs. 33 minutes, p=0.09), and a similar proportion of patients achieved a door-to-needle time less than or equal to 30 minutes. However, a greater proportion of patients receiving labetalol achieved door-to-needle times less than or equal to 15 minutes (15.8% vs. 0%, p=0.02). Door-to-CT times were also similar across groups. Time to blood pressure control differed significantly between strategies, with labetalol achieving faster control compared to nicardipine (4 minutes vs. 8 minutes, p=0.001). Patients requiring escalation between agents experienced longer times to blood pressure control. Blood pressure parameters during the first 24 hours, as well as safety and functional outcomes, were similar across treatment strategies. 
Conclusions:  
The findings of this study demonstrate that antihypertensive strategy prior to TNK administration did not significantly impact door-to-needle time in patients presenting with acute ischemic stroke. While labetalol achieved faster time to blood pressure control compared with nicardipine, this difference did not translate into meaningful differences in treatment timing or clinical outcomes. Safety and functional outcomes were also similar between treatment strategies. These findings should be interpreted in the context of the retrospective single-center design and small sample sizes.
Moderators Presenters
avatar for Olivia Klassa

Olivia Klassa

PGY1 Acute Care Resident, Prisma Health - Upstate
Olivia Klassa, PharmD, is originally from Springfield, VA. She attended the University of South Carolina in Columbia, SC, where she earned her Bachelor of Science in Pharmaceutical Sciences and her Doctor of Pharmacy. Olivia is currently completing her PGY-1 Acute Care Pharmacy Residency... Read More →
Evaluators
avatar for Anh Nguyen

Anh Nguyen

Clinical Pharmacy Specialist, Emory Decatur Hospital
I’m a Board‑Certified Critical Care Pharmacy Specialist with a passion for taking care of some of the sickest patients in the hospital. I’ve worked in both intermediate and intensive care settings, where every day brings a new challenge and a new opportunity to make a meaningful... Read More →
Friday May 1, 2026 9:30am - 9:50am EDT
Athena H

9:30am EDT

Evaluation Of Intra-Procedural Blood Pressure In Acute Ischemic Stroke Patients Undergoing Mechanical Thrombectomy
Friday May 1, 2026 9:30am - 9:50am EDT
Sarah Layne, Chelsea Mitchell, Sterling Torian, Austin Roberts
TriStar Centennial Medical Center – Nashville, Tennessee

Background: Blood pressure (BP) control is an essential component in management of patients with acute ischemic stroke (AIS). Significant reductions in BP can lead to hypoperfusion and worsened cerebral injury, whereas uncontrolled hypertension can increase the risk of hemorrhage and cerebral edema. In patients undergoing mechanical thrombectomy (MT), current guidelines recommend a pre-procedure BP less than 185/110 mmHg, but intra-procedural goals have yet to be established. Literature evaluating intra-procedural BP goals in patients undergoing mechanical thrombectomy is lacking. Current randomized controlled trials have evaluated the use of anesthesia, which may impact hemodynamics. Further studies are needed to determine if there is an ideal blood pressure target to prevent neurologic deterioration and worse functional outcomes. The purpose of this study was to evaluate the effect of intra-procedural blood pressure on clinical and safety outcomes in acute ischemic stroke patients undergoing mechanical thrombectomy.

Methods: This was a single-center retrospective cohort study conducted through chart review from October 1, 2022, to June 30, 2025. Patients who underwent MT within the study timeframe were included. Exclusion criteria consisted of any intra-procedural hemorrhagic complication, lack of successful reperfusion (TICI score 0-2a), missing baseline Glasgow Coma Scale (GCS), or patients aged less than 18 years old. Patients were divided into two groups, those who had an intra-procedural systolic blood pressure (SBP) less than 140 mmHg or a drop in SBP by at least 40 mmHg (group 1) and those who did not meet the criteria (group 2). The primary outcome was incidence of neurologic deterioration at 24 hours post-mechanical thrombectomy, defined as a decrease in GCS score of at least 2 from the baseline score. The secondary outcome was incidence of intracranial hemorrhage at 48 hours. Subgroup analyses were performed for patients who received intravenous (IV) fibrinolytics and those who did not, and separately for patients with any intra-procedural SBP less than 120 mmHg compared with those who had SBP greater than 120 mmHg.

Results: Fifty-four patients were screened. Five patients did not meet inclusion criteria, and thirteen patients were excluded (n=5 lack of successful reperfusion, n=1 intra-procedural hemorrhagic complication, n=7 missing baseline GCS). This resulted in a final sample size of thirty-six. All patients met criteria for group 1 (n=36). Six patients (16.7%) developed neurologic deterioration at 24 hours. Eighteen patients (50%) had some degree of intracranial hemorrhage, as determined by any mention of hemorrhage on brain imaging. In the subgroup analysis comparing patients who received IV fibrinolytics with those who did not, 1 of 9 patients (11%) in the fibrinolytic group had neurologic deterioration, compared with 5 of 27 patients (18.5%) in the non-fibrinolytic group. Neurologic deterioration occurred in all six (100%) patients in the SBP less than 120 mmHg subgroup.
 
Conclusions: Our study found that 16.7% of patients had neurologic deterioration 24 hours post-procedure. All patients who received MT had an intra-procedural SBP less than 140 mmHg or a drop by 40 mmHg; therefore, we were unable to detect differences between groups for our original analysis. While not powered for significance, patients who did not receive fibrinolytic therapy as well as those with intra-procedural SBP less than 120 mmHg had numerically higher percentages of neurologic deterioration at 24 hours. Further research is warranted to determine the optimal intra-procedural SBP goal for patients undergoing MT.
 
This research was supported (in whole or in part) by HCA Healthcare and/or an HCA Healthcare affiliated entity. The views expressed in this publication represent those of the author(s) and do not necessarily represent the official views of HCA Healthcare or any of its affiliated entities.
Moderators
CW

Cassandra Wade

Pharmacy Procurement Coordinator, John D Archbold Memorial Hospital
Presenters
avatar for Sarah Layne

Sarah Layne

Sarah is a 2025 graduate of Belmont University School of Pharmacy. She is currently a PGY-1 resident at TriStar Centennial Medical Center in Nashville, TN. Sarah will be completing a PGY-2 Critical Care Residency Program next year with plans of becoming a Critical Care Clinical P... Read More →
Evaluators
avatar for Madison Yates

Madison Yates

Clinical Pharmacist Practitioner, PGY1 Ambulatory Residency Program Coordinator, Cone Health
Friday May 1, 2026 9:30am - 9:50am EDT
Athena G

9:30am EDT

Evaluation of Phenobarbital Dosing for the Management of Alcohol Withdrawal Syndrome
Friday May 1, 2026 9:30am - 9:50am EDT
Background: Alcohol withdrawal syndrome (AWS) results from the sudden cessation of heavy alcohol use, causing symptoms such as tremors, anxiety, and agitation. Benzodiazepines remain first-line for alcohol withdrawal management according to American Society of Addition Medicine (ASAM) guidelines. Phenobarbital has a half-life of about 80 to 120 hours which allows for adequate control of withdrawal symptoms, and its self-tapering effect reduces the risk of medication abuse seen with benzodiazepines. The initial dosing of phenobarbital varies across institutions, typically starting at 130 mg or 260 mg, based on recommendations derived from clinical practice and studies such as Hendey et al. However, weight-based dosing strategies (ex. 10 mg/kg) have emerged with aims of achieving therapeutic serum concentrations and optimizing symptom control, as opposed to repeated smaller doses. The purpose of this study was to compare outcomes between patients that received an initial phenobarbital dose higher than 260 mg versus those that got a lower dose of 260 mg or less.

Methods: This IRB approved, retrospective chart review was conducted at a 711-bed academic medical center from 1/1/2020 to 9/26/2025. Adult patients who received phenobarbital were identified through a report from the electronic medical record. Patients were included if they had alcohol withdrawal documented within the chart. Patients were excluded if they were pregnant, incarcerated, had phenobarbital listed as a home medication, had a urine drug screen positive for barbiturates, any history of seizures not related to alcohol withdrawal, or were mechanically ventilated prior to phenobarbital administration. The primary outcome was stable or improved CIWA and/or RASS scores from baseline within the first 24 hours, defined as two consecutive CIWA and/or RASS scores equal to or below baseline. The secondary outcomes were the change in CIWA and/or RASS score after the first dose, improved or stable CIWA and/or RASS scores from 24-48 hours and 48-72 hours, cumulative benzodiazepine requirements, adjunctive medication requirements, hospital and ICU length of stay, and escalation of care. Comparative analyses of the primary and secondary outcomes were conducted using t-tests. Other appropriate statistical tests were utilized as needed.

Results: Of the 395 patients screened, 187 met inclusion criteria and were enrolled in the final analysis. Patients were grouped by initial phenobarbital dose; 118 received low-dose phenobarbital (≤260 mg) and 69 received high-dose phenobarbital (>260 mg). The primary outcome was achieved in 81 (80%) patients in the low-dose group compared with 59 (90%) in the high-dose group (p=0.111). No significant differences were found between the low-dose group and high-dose group for stable or improved CIWA and/or RASS scores at 24-48 hours (87% vs 90%; p=0.53) or 48-72 hours (94% vs 97%; p=0.71). Cumulative benzodiazepine requirements, adjunctive medication requirements, hospital length of stay, ICU length of stay, and escalation of care were similar between groups. Patients in the high-dose group demonstrated statistically significant greater reductions in CIWA scores following the initial dose compared to the low-dose group at 6 hours (mean change: 6.24 vs 0; p=0.005) and 24 hours (mean change: 8.05 vs 2.25; p=0.002).

Conclusions: Based on the results of this study, both low-dose and high-dose phenobarbital appear to have similar outcomes in the management of alcohol withdrawal. This study also found that higher initial phenobarbital doses were associated with more rapid symptom control in the first 24 hours without resulting in any additional complications or safety concerns. Establishing evidence-based protocols could improve standardization of care and optimize outcomes for patients with alcohol withdrawal.

Moderators
avatar for Aayush Patel

Aayush Patel

Clinical Pharmacy Specialist, Emergency Medicine, Piedmont Columbus Regional Midtown
Presenters Evaluators
Friday May 1, 2026 9:30am - 9:50am EDT
Athena A

9:30am EDT

Evaluation of Updates to the Rabies Post-Exposure Prophylaxis Order Set
Friday May 1, 2026 9:30am - 9:50am EDT
Evaluation of Updates to the Rabies Post-Exposure Prophylaxis Order Set
R. Tye Fobbs, Rachael Weingarten, Rachel Rumbarger
Cone Health at Moses Cone Hospital – Greensboro, NC
Background:
Rabies is a vaccine-preventable zoonotic viral disease affecting the central nervous system. The World Health Organization (WHO) recommends giving human rabies immune globulin (HRIG) to patients exposed to rabies if they have broken or punctured skin, or if their mucous membranes were contaminated with saliva from a mammal confirmed to have rabies or if the animal is not up to date on rabies vaccinations or the animal is unavailable for quarantine and observation. In the last 10 years, the utilization of rabies immunoglobulin and vaccinations has more than doubled in Cone Health emergency departments. There is no attributable cause to this increase in vaccination across our health systems. Inappropriate use of rabies post-exposure prophylaxis results in unnecessary costs and medical risks. A recent medication use evaluation explored the use of HRIG and rabies vaccines at Cone Health. Results showed that rabies post-exposure prophylaxis use in the emergency departments was not in accordance with WHO guidelines approximately 31% of the time.  In May 2025, Cone Health introduced a rabies post-exposure prophylaxis order set to help guide providers in assessing the need for post-exposure prophylaxis for individual patients who meet criteria as well as providing a dose rounding protocol to decrease waste. This study aims to evaluate the implementation of the new rabies post-exposure prophylaxis order set in relation to the recommended WHO guidelines.
Methods:
This was an IRB-reviewed, determined exempt retrospective, pre-post comparator study of patients who received human rabies immune globulin (HRIG) in Cone Health emergency departments. Data was collected between January to June 2024 for the pre-intervention group and June to December 2025 for the post-intervention group. Patients were excluded if they received immune globulin at an urgent care center, did not meet inclusion criteria for dose rounding or weighed less than 37.5 kg. The primary outcome was appropriate use of HRIG. Secondary outcomes included amount of HRIG given, amount that would have been given based on weight-based dosing, amount of waste saved, cost savings incurred, number of patients that received < 90% or > 110% of their weight-based dose, and re-presentation within 30 days for a suspected adverse reaction to HRIG.
Results: A total of 170 patients were screened with 70 patients in the pre-protocol group and 100 patients in the post-protocol group. The post protocol group was associated with a higher proportion of appropriate administration of HRIG when compared to the pre-protocol group [90 (90%) vs. 48 (68.5%); p = 0.0005]. There were no patients who represented within 30 days for a suspected adverse reaction to HRIG.
Conclusions: Implementation of a rabies post-exposure prophylaxis order set resulted in increased compliance with administration of HRIG per WHO guidelines. Dose rounding did not result in representation within 30 days for a suspected adverse reaction to HRIG and decreased overall waste. These findings suggest that having an established order set and dose rounding protocol increases compliance with WHO guidelines while decreasing waste.
 
  
Moderators
avatar for Brittany NeSmith

Brittany NeSmith

PGY1 Residency Program Director, BSSFBon Secours St. Francis DowntownPGY1
Presenters Evaluators
BB

Brooke Bibb

Ascension Saint Thomas Hospital West
Friday May 1, 2026 9:30am - 9:50am EDT
Athena J

9:30am EDT

Resident Presentation - Terence Natt
Friday May 1, 2026 9:30am - 9:50am EDT
Evaluation of Alternative Dosing of Tranexamic Acid in Adults with Traumatic Injuries 
Terence Natt, Madison Schwartz, Kevin Lynch, Dana Thorvilson 

CaroMont Regional Medical Center - Gastonia, NC 

Background/Purpose: Timely and proper dosing of tranexamic acid (TXA) in traumatic bleeding is imperative to reduce patient mortality. There is limited literature evaluating alternative dosing strategies to ensure TXA is consistently administered to patients that meet criteria. The purpose of this study is to determine if alternative dosing of TXA 2-grams administered intravenously over 10 minutes improves survival outcomes compared to standard dosing of a 1-gram intravenous (IV) bolus over 10 minutes followed by a 1-gram infusion over 8 hours.   

Methodology: Eligible patients were those >18 years old who met traumatic hemorrhage protocol criteria and were provided TXA by Gastonia Emergency Medical Services (GEMS) or in CaroMont Regional Medical Center’s emergency department (ED). The retrospective phase included patients who received standard dosing of TXA. Following protocol changes enacted in January 2026, the prospective phase included patients who received a 1-gram IV bolus of TXA in the ED following a 1-gram TXA administration by GEMS or received 2- grams of TXA as an IV bolus administered over 10 minutes in the ED. A chart review was completed to determine the primary endpoint of patient survival at 28 days, and secondary endpoints including change in heart rate and systolic blood pressure from initial presentation to 1 hour after TXA administration, blood product administration, ICU and hospital length of stay, and adverse drug events related to TXA administration). 

Results: In progress 

Conclusion: In progress 



Moderators
avatar for Abigayle Campbell

Abigayle Campbell

Clinical Specialist, Psychiatry; PGY1 Acute Care RPC, Self Regional Healthcare
For the past 6 years, I have served as the Clinical Pharmacy Specialist within the Inpatient Behavior Health Center at Self Regional Healthcare in Greenwood, SC. Recently, I have transitioned into a new role as the Medication Utilization and Quality Coordinator. I completed my bachelor's... Read More →
Presenters Evaluators
Friday May 1, 2026 9:30am - 9:50am EDT
Athena B

9:30am EDT

Antibiotic escalation strategies after ceftriaxone failure in culture-negative spontaneous bacterial peritonitis (SBP): a single-center retrospective cohort study
Friday May 1, 2026 9:30am - 9:50am EDT
Background: Spontaneous bacterial peritonitis (SBP) is the most common bacterial infection among patients with decompensated cirrhosis. Ceftriaxone remains a widely used first line empiric therapy; however, shifts in epidemiology and rising antimicrobial resistance have raised concerns regarding treatment failure in this population. A key challenge in SBP management is that up to 60% of cases are culture negative, necessitating reliance on peritoneal fluid cytology for diagnosis and assessment of therapeutic response. In patients with culture negative SBP who fail to respond to ceftriaxone, evidence-based guidance for antibiotic escalation is lacking, resulting in substantial variability in clinical practice. Evaluation of outcomes in patients with culture negative SBP empirically treated with ceftriaxone may help identify risk factors for treatment failure and inform the effectiveness of commonly employed escalation strategies.
Objective: This study aims to determine the success rates of the following antibiotic escalation strategies used after ceftriaxone failure: carbapenem-sparing regimens (cefepime, or piperacillin-tazobactam), carbapenem regimens, carbapenem-sparing + broad gram-positive coverage (vancomycin, linezolid, or daptomycin), or carbapenem + broad gram-positive coverage. A secondary aim is to identify risk factors associated with ceftriaxone treatment failure in the patient population.
Methods: This is a retrospective cohort study conducted at a tertiary referral hospital from June 2022 to December 2025. Adult patients were included if they had culture negative SBP, defined as an ascitic polymorphonuclear (PMN) count ≥250 cells/µL, were primarily treated with ceftriaxone, and underwent a repeat paracentesis ≥48 hours later to assess treatment response (or had resolution of ascites). Patients were excluded if they had secondary peritonitis, non-cirrhotic peritonitis, or received ≥ 24 hours of alternative antibiotics prior to ceftriaxone. For the primary outcome, we evaluated response rates across the 4 antibiotic escalation groups. Treatment success was defined as a ≥25% reduction in PMN count on repeat paracentesis. For the secondary endpoint, we planned to evaluate risk factors associated with treatment failure and compare patient outcomes.
Results: A total of 69 patients with culture-negative SBP were included. The median age was 55 years (IQR 47–66), 67% were male, and the most common etiology of cirrhosis was alcohol-related (41%). Median MELD-Na score was 22 (IQR 17–28). The median time from admission to SBP diagnosis was 20 hours (IQR 1–69), and 86% of patients received ceftriaxone 2g. Ceftriaxone failure occurred in 5 patients (7.2%). All five received antibiotic escalation: four were treated with a carbapenem-based regimen, and one received cefepime with metronidazole. Among patients with documented PMN response data, reductions ranged from 31% to 89%. Two patients in the ceftriaxone failure group died in-hospital (40%) compared to 4 patients (6%) in the success group. Median hospital length of stay was longer in the failure group (14 days [IQR 10–16] vs. 8 days [IQR 6–18]), as was duration of antibiotic therapy (9 days [IQR 7–13] vs. 5 days [IQR 4–6]). In an exploratory analysis of potential risk factors, nosocomial SBP was identified in 20% of failures and 27% of successes. Prior anti-pseudomonal antibiotic exposure within 90 days was more prevalent among ceftriaxone failures compared to successes (40% vs. 23%). The small sample size precluded formal statistical comparison for all outcomes.
Conclusion: Ceftriaxone failure was uncommon in our cohort of culture-negative SBP, occurring in approximately 7% of patients. Ceftriaxone failure was associated with prolonged hospitalization, extended antibiotic exposure, and higher in-hospital mortality. Prior broad-spectrum antibiotic use emerged as a potential risk factor warranting further investigation in larger cohorts. These findings underscore the need for larger prospective studies to establish evidence-based escalation strategies.
Moderators
JK

Joseph Kohn

PRIS2Prisma Health Richland-University of South CarolinaPGY1
Presenters
MA

Maryam Alarfaj

PGY-1 Resident, AdventHealth Orlando
Evaluators
avatar for Jolie Gallagher

Jolie Gallagher

Clinical Pharmacy Specialist, Critical Care, Emory University Hospital
I am the clinical pharmacy manager at Emory University Hospital.  My background training is in critical care.  My current areas of interest are optimization of transitions of care and pharmacist burnout and resilience.
Friday May 1, 2026 9:30am - 9:50am EDT
Athena I

9:30am EDT

Evaluation of the Implementation of a Cardiothoracic Surgery Pre-Operative Anemia Treatment Protocol 
Friday May 1, 2026 9:30am - 9:50am EDT
Evaluation of the Implementation of a Cardiothoracic Surgery Pre-Operative Anemia Treatment Protocol  

Alyan Saeed, Brendon Banes, Rebecka Hazelwood 
 
Background/Purpose: Patients undergoing cardiothoracic surgery (CTS) frequently present with baseline anemia, which has been associated with increased transfusion requirements, acute kidney injury (AKI), and higher postoperative morbidity and mortality. Prior studies suggest that pre-operative anemia optimization using intravenous iron, erythropoiesis-stimulating agents, and vitamin supplementation may reduce transfusion needs and improve surgical outcomes. In November 2023, Wellstar Kennestone Regional Medical Center (WKRMC) implemented a pre-operative anemia protocol for CTS patients with hemoglobin <12 g/dL; however, its clinical impact has not been formally evaluated. This study aimed to assess the efficacy and safety of the CTS pre-operative anemia protocol.  

Methods: This was an observational, retrospective chart review conducted at WKRMC evaluating adult patients (≥18 years) who underwent CTS between December 1, 2023 and September 1, 2025. Patients with a baseline hemoglobin <12 g/dL were grouped based on whether they received the pre-operative anemia treatment protocol prior to surgery. Patients were followed from three days prior to surgery through seven days post-operatively, hospital discharge, or death, whichever occurred first.   
The primary endpoint was the difference in post-operative hemoglobin levels between patients managed under the protocol and those in the non-protocol group. Secondary endpoints included number of post-operative red blood cell (RBC) units transfused and incidence of AKI within seven days. Safety outcomes included venous thromboembolism, stroke, post-operative infection, and hypersensitivity reactions to IV iron.  
Statistical analyses included paired and independent t-tests, along with Fisher’s exact test for categorical variables.  

Results: A total of 100 patients were included (protocol n=50, non-protocol n=50). Post-operative hemoglobin was similar between patients managed under the protocol and those receiving usual care (8.80 g/dL vs 9.07 g/dL, p=0.25). The mean number of RBC units transfused did not differ significantly between patients managed under the protocol and those receiving usual care (2.28 units vs 2.26 units, p=0.98). Post-operative AKI occurred less frequently in the protocol group compared to the non-protocol group (20% vs 36%, p=0.037). No significant differences were observed regarding the safety end points. There were no cases of IV iron hypersensitivity reactions in the protocol group.  

Conclusion: The pre-operative anemia protocol was associated with a lower incidence of post-operative acute kidney injury in CTS patients, while post-operative hemoglobin levels were similar between groups. These findings suggest that pre-operative anemia management may contribute to improved renal outcomes, despite comparable perioperative hematologic values.  
 

Moderators
avatar for Brian Leith

Brian Leith

Clinical Pharmacist, VA Medical Center
I am currently the emergency medicine and antimicrobial stewardship pharmacist at the VA Medical Center in Fayetteville, NC.
Presenters
avatar for Alyan Saeed

Alyan Saeed

PGY1 Pharmacy Resident, Wellstar Kennestone Regional Medical Center
Evaluators
BK

Brian Knott

Clinical Pharmacy Manager, AdventHealth Winter Park
Friday May 1, 2026 9:30am - 9:50am EDT
Olympia 2

9:30am EDT

Impact of GLP-1 and GLP-1/GIP Receptor Agonists on Perioperative Glycemic Control in Arthroplasty
Friday May 1, 2026 9:30am - 9:50am EDT
Impact of GLP-1 and GLP-1/GIP Receptor Agonists on Perioperative Glycemic Control in Arthroplasty

Authors: Julia Sitek, Charles Hartis, Zachary Klick, Minal Patel, Amit Saha, Ashley Talbott, Sarah Kittner, Emily Schaefer 

Objective: Describe the effect of GLP-1 and GLP-1/GIP receptor agonists on perioperative blood glucose levels. 

Background:  
Obesity and type 2 diabetes (T2DM) are well-established risk factors for osteoarthritis, a leading cause of joint degeneration requiring arthroplasty. Both conditions, along with perioperative hyperglycemia, have been associated with worse postprocedural outcomes and increased risk of mortality.  Glucose-like peptide-1 (GLP-1) and GLP-1/glucose-dependent insulinotropic polypeptide receptor agonists (GLP-1/GIP RA) are becoming increasingly popular due to their indications for T2DM and weight management. Perioperative management of GLP-1 and GLP-1/GIP RAs, specifically the optimal holding duration in surgery, remains controversial. Case reports describing intraoperative aspiration events have prompted recommendations to hold these agents before surgery. Conversely, emerging evidence suggests potential benefits of continuing these medications preoperatively, including improved metabolic outcomes. Given their long-half-lives, these agents may continue to confer glycemic benefits even when held; however, withholding them may increase the risk of perioperative hyperglycemia. Therefore, the purpose of this study is to determine the effect of GLP-1 and GLP-1/GIP RAs on perioperative glycemic control in patients undergoing arthroplasty.  

Methods
This multicenter, retrospective, cohort study compared the incidence of perioperative hyperglycemia in patients with T2DM with or without a GLP-1 or GLP-1/GIP RA. Patients 18 years and older with T2DM who underwent primary elective total knee or hip arthroplasty and had available preoperative and postoperative blood glucose data were included in this study. Those with type 1 diabetes, an operative diagnosis of periarticular knee or lower extremity fracture, an American Society of Anesthesiologists classification of 4 or higher, or a need for general anesthesia were excluded. The primary outcome was the percentage of patients with preoperative and postoperative blood glucose levels of 180 mg/dL or greater. Secondary outcomes include any incidence of a hyperglycemic event during admission, 30-day incidence of prosthetics joint infections (PJI) and surgical site infections, incidence of aspiration or regurgitation during procedure, postoperative nausea and vomiting, and 30-day all-cause mortality. Data collection includes baseline demographics, hospitalization characteristics, and drug characteristics, specifically the agent, dose, and time withheld before surgery. Descriptive statistics were used to summarize the incidence of the primary outcome. Inferential statistics were analyzed using Student-t tests for continuous endpoints and Chi-square tests for categorical endpoints. 

Preliminary Results: Among patients undergoing total knee or hip arthroplasty across five hospitals between March 2, 2024 and September 1, 2025, 104 patients were included in the analysis. The cohort was 53.8% female with a mean age of 69 years, mean A1c of 6.5%, and mean BMI of 32.65 kg/m². Preoperatively, 42.3% were on a GLP‑1 or GLP‑1/GIP RA preoperatively. The primary outcome occurred in one (2.3%) patient on a GLP‑1 RA and one (1.7%) patient not receiving a GLP‑1 or GLP‑1/GIP RA preoperatively [OR of 1.37 (95% CI : 0.08 – 22.55, P-Value 0.82)]. The secondary outcome of any event of hyperglycemia during admission occurred in 19 (43.2%) patients receiving a GLP‑1 or GLP-1/GIP RA and 24 (40%) patients not receiving a GLP‑1 or GLP‑1/GIP RA [OR 1.14 ( 95% CI : 0.51 – 2.51, P- Value 0.74)]. Among GLP‑1 or GLP‑1/GIP RA users, the mean duration of medication hold prior to surgery was 10 days. No patients experienced a surgical site infection, PJI, or aspiration/regurgitation event during the study period.  

Conclusion: Holding GLP-1 or GLP-1/GIP RAs for elective total knee or hip arthroplasties does not affect perioperative glycemic control. The benefit of holding GLP-1 or GLP-1/GIP RAs for primary elective arthroplasty may outweigh the risk as no statistically significant increase in incidence of hyperglycemia was observed.
Moderators
avatar for Christele Robinson

Christele Robinson

Emergency Medicine Clinical Pharmacy Specialist, Emory University Hospital
Christele Robinson, PharmD, is board certified in pharmacotherapy. She is a member of the Department of Pharmacy at Emory University Hospital and currently practicing as an Emergency Medicine Clinical Pharmacy Specialist. Dr. Robinson obtained a Bachelor of Science degree at the... Read More →
Presenters
avatar for Julia Sitek

Julia Sitek

PGY1 Pharmacy Resident, Atrium Health Wake Forest Baptist
Evaluators
avatar for Cody Parker

Cody Parker

Clinical Pharmacy Specialist, St. Joseph's/Candler
Dr. Cody Parker is the PGY1 Pharmacy Residency Program Director at St. Joseph's/Candler in Savannah, GA. He received his Doctor of Pharmacy from the University of Georgia and completed a Postgraduate Year One (PGY1) Pharmacy Practice Residency at St. Joseph’s/Candler. Dr. Parker is a Clinical Pharmacy Sp... Read More →
Friday May 1, 2026 9:30am - 9:50am EDT
Athena D

9:30am EDT

Safety of Intravenous Push Lacosamide Compared with Intravenous Piggyback at a Community Hospital
Friday May 1, 2026 9:30am - 9:50am EDT
Authors: Lauren Baugh, Karen Babb 

Background:
Lacosamide is an FDA approved medication for the treatment of focal onset seizures and primary generalized tonic-clonic seizures and is also used off-label for status epilepticus.1 The Neurocritical Critical Care Guidelines for the Evaluation and Management of Status Epilepticus propose 200 mg lacosamide given over 15 minutes as an alternative for rapid administration, while acknowledging the risk for possible adverse effects, such as hypotension or QT prolongation.2 Recent studies suggest an increased incidence of cardiovascular, neurological, and infusion site related adverse events with intravenous push as compared to intravenous piggyback administration.4

This study will assess the incidence of adverse events associated with intravenous push compared to intravenous piggyback lacosamide within our institution.

Methodology:
This was a single-center retrospective cohort analysis. Chart review was utilized to compare patients that received lacosamide via intravenous piggyback or push administration. Included in the study were adult patients 18 years old or older that received at least one dose of IV push or IV piggyback lacosamide from May 1, 2024 - October 31, 2024 and December 1, 2024 - May 31, 2025. Exclusion criteria was doses greater than 400 milligrams. The primary outcome was incidence of adverse drug events (hypotension, bradycardia, infusion site reactions, sedation) in patients receiving intravenous push lacosamide compared to those that receive intravenous piggyback lacosamide. Secondary outcomes reviewed time to administration of intravenous push lacosamide compared to that of intravenous piggyback lacosamide.

Results:
A total of 110 patients were included in the study, with 50 in the intravenous piggyback group and 60 in the intravenous push group. Baseline characteristics, such as age, sex, weight, race, home lacosamide use, and pre-existing comorbidities, were comparable between the two cohorts. Of the 110 patients, a total of 747 doses were observed, with 379 doses given intravenous push and 368 given intravenous piggyback. Of the primary outcomes, incidence of bradycardia, hypotension, medication related sedation, and administration site reaction, there were no statistically significant differences. The median time to first dose administration was 50 minutes in the intravenous push group and 62 minutes in the intravenous piggyback group.

Conclusion:
This study highlights the advantages of administering intravenous push lacosamide without increased risk of adverse events. The findings indicate that the incidence of adverse events was not higher than that seen in the intravenous piggyback administration, while providing shorter time to first dose administration. However, limitations of the study should be considered in the interpretation of the results. The primary limitation of this study was the missing documentation of heart rate, blood pressure, and sedation scores with each dose of lacosamide given. Furthermore, findings should be interpreted in light of the fact that patients requiring hospitalization are often critically ill and exposed to a multitude of factors which could independently contribute to adverse outcomes rather than solely lacosamide administration. In the future, the findings should be presented to the pharmacy and therapeutics committee to further support the current implemented practice. The results of this study should also encourage education on the importance of standardized nursing documentation.

[email protected]
Moderators Presenters
avatar for Lauren Baugh

Lauren Baugh

PGY1 Pharmacy Resident, CommonSpirit Memorial
My name is Lauren Baugh. I am currently a PGY1 resident at CHI Memorial in Chattanooga, Tennessee. I graduated from the University of Georgia College of Pharmacy with my PharmD in 2025. I will be staying on as clinical pharmacist at Memorial after completion of my PGY1 residency.
... Read More →
Evaluators
avatar for Allie Hale

Allie Hale

Clinical Pharmacist and Residency Program Director, Parkridge Health System
Friday May 1, 2026 9:30am - 9:50am EDT
Athena C

9:30am EDT

Pharmacist Led COPD Medication Recommendations During Discharge Medication Review
Friday May 1, 2026 9:30am - 9:50am EDT
Title: Pharmacist Led COPD Medication Recommendations During Discharge Medication Review

Authors: Bridget Arellano, Ali Diaz, Dahlia Kaiser
AdventHealth Orlando, Orlando, FL

Background/Purpose: Chronic obstructive pulmonary disease (COPD) remains a leading cause of morbidity, with national 30-day readmission rates near 30%. To reduce rates of readmission, the Center for Medicare and Medicaid Services (CMS) implemented a Hospital Readmission Reduction Program, incentivizing improved communication and coordination for patients at discharge. Currently our COPD readmission rate is approximately 20%. To address this, our hospital initiated a pharmacist-led discharge medication reconciliation (DMR) workflow to optimize COPD therapy with a goal to maintain readmission rates below 16%. However, the clinical reach of this program and the rate of provider acceptance of these recommendations is not well established. This study aimed to evaluate physician acceptance of pharmacist-driven COPD therapy recommendations and its association with 30-day readmission rates.

Methods: This retrospective chart review included patients ≥65 years of age with COPD, discharged home from AdventHealth Orlando between January and September of 2025. Data collected included demographics, pharmacist interventions, recommendation types, provider response, and 30-day readmission outcomes. Descriptive statistics were used to evaluate intervention frequency, acceptance rates, and readmission outcomes.

Results: A total of 168 patient encounters and 119 unique patients were analyzed. Pharmacist interventions were made in 14 (8.3%) patient encounters, and the majority (n=10; 71.4%) were to recommend adding an additional agent to the patient’s current regimen. Of the 14 pharmacist interventions, 9 (64.3%) were accepted by the provider. Overall, 30-day readmissions occurred in 22 (18.5%) patients and 59 (35.1%) encounters. Out of the nine encounters with accepted interventions, 4 (44.4%) had a 30-day readmission. Due to the low intervention rate, comparative analysis between accepted and non-accepted recommendations was limited.

Conclusions: Pharmacist interventions during discharge medication reconciliation were very limited in this dataset of elderly patients with COPD. Although readmission rates in this specific population remained above goal, the low number of interventions restricts conclusions regarding the impact of recommendation acceptance on patient readmission rates. Future efforts should focus on the DMR workflow and evaluate various barriers surrounding pharmacist interventions on optimizing COPD therapy.

Moderators
AQ

April Quidley

PGY1 Residency Program Director, ECU Health Medical Center
Presenters Evaluators
AJ

Audrey Johnson

Surgical/Trauma Critical Care Pharmacist, Memorial Health University Medical Center
Friday May 1, 2026 9:30am - 9:50am EDT
Olympia 1

9:50am EDT

Impact of Embedded Clinical Pharmacy Services on Glycemic Control in an Internal Medicine Clinic
Friday May 1, 2026 9:50am - 10:10am EDT
Title: Impact of Embedded Clinical Pharmacy Services on Glycemic Control in an Internal Medicine Clinic 

Authors: Kisara Thompson, Tacorya Adewodu, Andrew Bundeff, Molly Hinely, Danielle Baker, Michael DeWitt 

Objective: Evaluate the effect of clinical pharmacy services on A1c reduction in patients with type 2 diabetes and a baseline A1c of ≥ 8%, compared with patients who were managed by usual care, defined as a primary care provider acting as the sole responsible diabetes managing provider. 

Background: Uncontrolled type 2 diabetes results in serious health complications. Hemoglobin A1c is used to measure average blood glucose over the past three months and is used to guide optimal treatment plans. Studies have demonstrated an improvement in microvascular and macrovascular complications in patients with improved glycemic control in those with type 2 diabetes. 

The Winston-Salem East Clinic, a part of Atrium Health Wake Forest Baptist, is the primary study site. It is a medical resident-run internal medicine clinic that serves a large population of underserved and uninsured patients. Since March of 2023, a clinical pharmacist practitioner (CPP), has been integrated into the clinic two days of the week working under collaborate practice agreements with supervising physicians. Patients with uncontrolled type 2 diabetes are referred to the CPP to provide medication management.  

Methods: This single-center, retrospective, cohort study compared mean percent change of A1c managed by a primary care provider (PCP) versus A1c managed by a CPP. Patient data was collected between July 1st, 2023 and October 31st, 2025. Patients included were ≥ 18 years of age, diagnosed with type 2 diabetes, and those who had completed at least two follow-up visits with their PCP or clinical pharmacist. Patients excluded were the following: type 1 diabetes, managed by endocrinology, seen by non-network PCPs, pregnant, lost to follow-up – defined as no additional follow-up appointments or A1c labs drawn within the study time frame. Demographic information such as sex assigned at birth, age at encounter, race and ethnicity and primary payor were collected. The primary outcome assessed was mean percent change in A1c at 90- and 180- days with and without established clinical pharmacy management. Secondary outcomes included clinical interventions made, number of continuous glucose monitors (CGMs) prescribed, and incidence of diabetes related emergency department visits and/or hospitalizations during the study time frame. Patients were identified through a data sorting platform within the electronic health record.  

Results: A total of 144 patients were enrolled in the study, with 72 patients per study group. The primary endpoints were statistically analyzed by linear regression. Adjusting for baseline A1c, there is an average reduction of 1.2 percentage points in A1c measured at 90-days in patients managed by a pharmacist, compared to patients managed by usual care (95% CI: -2.0 – (-0.36), p-value: 0.005). Adjusting for baseline A1c, there is an average reduction of 1.3 percentage points in A1c measured at 180-days in patients managed by a pharmacist, compared to patients managed by usual care (95% CI: -2.1 – (-0.46), p-value: 0.003). Pharmacist managed patients were approximately eight times more likely to have their insulin therapy changed compared to patients who were managed by usual care (95% CI: 1.3 – 2.9, p-value: 0.001). There were no differences associated with rates of change in other medication therapy changes. During the study period, pharmacy managed patients had approximately a 53-point higher prescription rate for a CGM than those managed by usual care. There were no differences detected in the incidence rates between pharmacy managed and usual care patients in regard to ED and/or hospitalizations related to type 2 diabetes within the study period.

Conclusions: Among patients with type 2 diabetes and a baseline A1c ≥ 8%, clinical pharmacy management was associated with a statistically significant greater reduction in A1c compared with usual care management with mean reduction of 1.2 and 1.3 percentage points at 90-days and 180-days, respectively. 
Moderators
avatar for Aayush Patel

Aayush Patel

Clinical Pharmacy Specialist, Emergency Medicine, Piedmont Columbus Regional Midtown
Presenters Evaluators
Friday May 1, 2026 9:50am - 10:10am EDT
Athena A

9:50am EDT

Utility of ZOLL Heart Failure Management System (HFMS) in the management of chronic heart failure
Friday May 1, 2026 9:50am - 10:10am EDT
Title: Utility of ZOLL Heart Failure Management System (HFMS) in the management of chronic heart failure 

Authors: Emily Rudisell, Laura Jane Straw, James Ampadu, Melissa Redmond, Joseph Bates, Lauren Lyons   

Background: Heart failure with reduced ejection fraction (HFrEF) remains a burdensome disease in which patients experience progressive neurohormonal activation leading to worsening symptoms, fluid retention, and recurrent exacerbations. Guideline-directed medical therapy (GDMT), as recommended by the 2022 AHA/ACC/HFSA Heart Failure Guidelines, has been shown to significantly reduce morbidity and mortality in these patients; however, timely medication titration remains challenging. Non-invasive remote monitoring offers the opportunity to detect changes in fluid status earlier, allowing expedited interventions and potentially supporting optimization of GDMT. The ZOLL Heart Failure Monitoring System (HFMS) is a first-in-class non-invasive wearable patch-based device that utilizes a transdermal radiofrequency sensor to monitor pulmonary fluid levels. This system generates alerts when predefined fluid thresholds are exceeded, prompting clinical evaluation and treatment. Despite increasing clinical use, real-world data describing HFMS and its role in supporting GDMT optimization remain limited. This study aims to characterize the impact of outpatient HFMS utilization and to evaluate its potential to decrease time to GDMT optimization and reduce HF-related morbidity and readmissions. 

Methods: This single-center, retrospective cohort study included adult patients with HFrEF who were prescribed HFMS by an advanced heart failure provider. The primary endpoint was time to GDMT optimization following HFMS initiation, defined as the number of days to achieve maximally tolerated dose of GDMT, compared with patients who were prescribed HFMS but were unable to receive it due to insurance denial. Secondary endpoints included HF related readmission rates at 30 and 90 days after HFMS use discontinuation, comparison of HF readmission rates 6 months before and after HFMS utilization, frequency of thoracic fluid index alerts, and the presence of clinical interventions in response to alerts. Data was collected from the electronic health record and HFMS monitoring system. Primary outcomes were analyzed using generalized estimating equations and descriptive analyses. Secondary outcomes were interpreted using a McNemar test, Wilcoxon signed ranked test with Hodges-Lehmann estimator, and descriptive analyses.  

Results: In progress.  

Conclusions: In progress. 

Moderators
avatar for Abigayle Campbell

Abigayle Campbell

Clinical Specialist, Psychiatry; PGY1 Acute Care RPC, Self Regional Healthcare
For the past 6 years, I have served as the Clinical Pharmacy Specialist within the Inpatient Behavior Health Center at Self Regional Healthcare in Greenwood, SC. Recently, I have transitioned into a new role as the Medication Utilization and Quality Coordinator. I completed my bachelor's... Read More →
Presenters Evaluators
Friday May 1, 2026 9:50am - 10:10am EDT
Athena B

9:50am EDT

Evaluating the Accuracy of Medication Histories of Behavioral Health Patients in the Emergency Department
Friday May 1, 2026 9:50am - 10:10am EDT
Background: Accurate medication histories reduce the likelihood of medication errors in patients being admitted to the hospital. Medication histories can inform inpatient providers of what medications the patient is taking prior to the emergency department encounter. Existing literature corroborates that pharmacist involvement in the medication history process leads to less discrepancies. Regarding patients in the emergency department with behavioral health problems, pharmacists are ideally qualified to collect accurate medication histories in this patient population. At our institution, medication histories for behavioral health patients are nursing-led. The purpose of this study is to determine the accuracy of medication histories collected for behavioral health patients in the emergency department.   
 
Methodology: Over a specified 4-month period, patients admitted to the behavioral health units of CaroMont Regional Medical Center’s emergency department (ED) had their medication histories performed by a member of the pharmacy team following completion by nursing staff. Patients aged 18 years or older roomed in behavioral health areas of the ED with a medication history completed by nursing staff were eligible for inclusion. Pregnant and incarcerated patients were excluded. For each patient, investigators utilized interviews with the patient or patient’s caregiver(s), prior to encounter medication lists, medication dispense histories, facility medication administration records, and telephone consultations with primary care providers, pharmacies, or facilities to collect information regarding a patient’s prior to encounter medications. Investigators then compared findings from the pharmacist-completed medication histories to the medication history completed by nursing staff. Any discrepancies between medication histories were collected as data and corrected in the electronic medical record. Additional data collected included patient demographics, reason for emergency department visit, and time taken to complete each medication history. Primary endpoint data were reported descriptively for the number of discrepancies across the cohort. Secondary endpoint data were reported descriptively for number of prior to encounter medications per patient, number of discrepancies per patient, and types of discrepancies (including omissions/erroneous exclusions, commissions/erroneous inclusions, drug name errors, drug formulation errors, drug dose errors, and drug regimen errors).
 
Results: During the specified data collection period, 92 patients were screened. Thirty patients had prior to encounter medications reviewed. Female sex accounted for 53.3% of patients and median age was 34 years. Reasons for exclusion are described below.  

Exclusion Reason n (%) 
Chief Complaint not Psychiatric 51 (82.1) 
Patient Admitted 5 (8.3)
Patient Discharged 2 (3.2)
Patient Condition 2 (3.2)
Prior to Encounter Medications Reviewed by PTA Technician 1 (1.6) 
Prior to Encounter Medications Not Reviewed by Nursing During Encounter 1 (1.6)

Across the 30 patients whose prior to encounter medications were reviewed, 71 discrepancies were identified- an average of 2.33 discrepancies per patient. Patients had an average of 6.23 prior to encounter medications, and the average time for medication history completion was 6.13 minutes. The specific type of discrepancies among the 71 identified are broken down in the table below. 

Discrepancy Type n (%) 
Commission 31 (43.1)
Omission 21 (29.9)
Regimen 9 (12.8)
Dose 8 (11.4)
Formulation 2 (2.8)
Name 0 (0)
 
Conclusion: Based on our findings, pharmacy personnel are in a position to optimize the detection and correction of discrepancies following an initial nursing driven review of behavioral health patients’ prior to encounter medications. Due to the nature of how the study was conducted, limitations of this study include that it cannot be determined how many discrepancies were already corrected by nursing personnel, or how many discrepancies were not identified by investigators. Additional limitations are that the mental state of patients may have contributed to inadequate histories, as well as previous medication changes having gone undetected during transfers to other care areas. 

Moderators
CW

Cassandra Wade

Pharmacy Procurement Coordinator, John D Archbold Memorial Hospital
Presenters Evaluators
avatar for Madison Yates

Madison Yates

Clinical Pharmacist Practitioner, PGY1 Ambulatory Residency Program Coordinator, Cone Health
Friday May 1, 2026 9:50am - 10:10am EDT
Athena G

9:50am EDT

Evaluation of the use of 3% sodium chloride in traumatic brain injury
Friday May 1, 2026 9:50am - 10:10am EDT
Authors: Yasmeen A. Ettrick, Kelly M. Bodine, John Patka, Shauntrell Johnson
Background: Traumatic brain injury (TBI) is a major cause of morbidity and mortality and is frequently complicated by cerebral edema and elevated intracranial pressure. Osmotic therapy with hypertonic saline is a key intervention to mitigate secondary brain injury; clinical guidelines, however, recommend its use for symptomatic neurologic deterioration rather than prophylactic administration. At Grady Memorial Hospital, 3% sodium chloride is commonly used in the emergency department (ED), often prior to neuroimaging due to clinical urgency.
Methods: This single-center, retrospective cohort study was conducted at Grady Memorial Hospital, a Level I trauma center in Atlanta, Georgia. Adult patients (≥18 years) presenting to the emergency department with traumatic brain injury who received at least one dose of 3% sodium chloride between January 1 and June 30, 2024, were included. Patients were excluded for pregnancy, incarceration, non-traumatic indications, transfer from outside facilities, or initial administration after hospital admission. The primary outcome was appropriateness of 3% sodium chloride use, defined by the presence of clinical findings and radiographic evidence of herniation or midline shift. Secondary outcomes included total volume administered and changes in serum sodium and osmolarity.
Results: A total of 65 patients met inclusion criteria, of whom 57 received 3% hypertonic saline prior to CT imaging and 8 received it after imaging. Patients treated prior to CT were younger (median age 40 vs 62 years, p = 0.056) and had lower Glasgow Coma Scale scores (median 4 vs 11, p = 0.013), while hemodynamic parameters were similar between groups. Appropriateness of 3% sodium chloride use was observed in 54.4% of pre-CT administrations compared with 25% post-CT, though this difference was not statistically significant (p = 0.149). Median total volume administered was 500 mL prior to CT and 250 mL after CT, with no significant difference. Median serum sodium increased by 5 mEq/L in the pre-CT group and 4 mEq/L in the post-CT group (p = 0.635), while median serum osmolarity increased by 8 mOsm/L and 3 mOsm/L, respectively (p = 0.45).
Conclusion: In this cohort, 3% hypertonic saline was most often administered before CT imaging, typically in patients with more severe neurologic impairment. Pre-CT administrations were more frequent and more likely to meet guideline criteria than post-CT hypertonic administration, though some still lacked clinical or radiographic indications. Neither pre-CT nor post-CT administration was associated with harmful changes in serum sodium or osmolarity, suggesting that early use may be safe when clinically justified.
Objective: To evaluate the timing, utilization patterns, and physiologic effects of 3% sodium chloride administration in adult ED patients with TBI.
Self-Assessment Question: Identify the recommended indication for hypertonic saline use in adult patients with traumatic brain injury. 
Moderators
avatar for Brittany NeSmith

Brittany NeSmith

PGY1 Residency Program Director, BSSFBon Secours St. Francis DowntownPGY1
Presenters
avatar for Yasmeen Ettrick

Yasmeen Ettrick

PGY-2 Emergency Medicine Resident, Grady Memorial Hospital
Yasmeen Ettrick, PharmD, is a PGY-2 Emergency Medicine Pharmacy Resident at Grady Memorial Hospital. She earned her Doctor of Pharmacy degree from Midwestern University and completed her PGY-1 residency at Cook County Hospital in Chicago, IL. Upon completion of her PGY-2 training... Read More →
Evaluators
BB

Brooke Bibb

Ascension Saint Thomas Hospital West
Friday May 1, 2026 9:50am - 10:10am EDT
Athena J

9:50am EDT

Evaluation of Two Four-Factor Prothrombin Concentrates for Anticoagulant Reversal
Friday May 1, 2026 9:50am - 10:10am EDT
Title: Evaluation of Two Four-Factor Prothrombin Concentrates for Anticoagulant Reversal   
Authors: Mary G. Johnson, Jessica Hernandez, Annmarie Vallomthail, Kristina Larizadeh, Nina Casanova, Feras Akbik
Background: Vitamin K antagonists (VKAs) and factor Xa inhibitors are oral anticoagulants used for the treatment and prevention of thromboembolic events. Bleeding is the most common adverse effect of oral anticoagulants, and rapid reversal may be required in cases of severe hemorrhage or when urgent surgery is indicated. Four-factor prothrombin complex concentrates (4F-PCCs), including Kcentra® and Balfaxar®, are standard treatments for reversal of VKAs and factor Xa inhibitors. Emory University Hospital recently changed formulary agents from Kcentra® to Balfaxar®. In one clinical trial, Balfaxar® was found to be non-inferior to Kcentra® for the reversal of warfarin for urgent surgery; however, there is a paucity of data directly comparing these agents for VKA and factor Xa inhibitor-related bleeding. Limited data and lack of guideline recommendations for a preferred 4F-PCC contribute to clinical uncertainty in selecting an optimal reversal agent. The objective of this study is to evaluate the safety and efficacy of Balfaxar® vs. Kcentra® for reversal of VKAs and factor Xa inhibitors.   
Methods: This study is an Institutional Review Board-approved, single-center, retrospective chart review of patients who received 4F-PCC from December 4, 2024 to August 1, 2025. Patients were included if they were at least 18 years of age, presented to Emory University Hospital, and received at least one dose of 4F-PCC for reversal of a VKA or factor Xa inhibitor. Patients were excluded if they received 4F-PCC at an outside hospital or for procedural use, were concomitantly taking a P2Y12 inhibitor, had a history of a congenital bleeding disorder, or were pregnant, nursing, or incarcerated. The primary outcome was hemostatic efficacy. Hemostatic efficacy in intracerebral hemorrhage (ICH) patients was defined as change in hematoma volume ≤ 20% or 21-35% within 24 hours of baseline without a repeat 4F-PCC dose or surgical intervention within 24 hours. In non-ICH patients, hemostatic efficacy was defined as a hemoglobin drop ≤ 2g/dL within 24 hours, or transfusion of < 2 units of packed red blood cells without a repeat 4F-PCC dose or surgical intervention within 24 hours. Secondary outcomes include in-hospital mortality, thrombotic events, ICU length of stay, hospital length of stay, and number of repeat doses within 48 hours. Descriptive statistics will be used to summarize the continuous and categorical variables. Chi-squared tests will assess differences in outcomes between treatment groups.  
Results: Out of 71 patients, 37 patients were included in the Kentra® group and 34 in the Balfaxar® group. Baseline characteristics were similar between the groups except BMI of 25-29.9 kg/m2 was notably different (45.9% vs. 14.7%, p=0.004). A total of 20 patients in the Kcentra® group and 19 in the Balfaxar® group met the primary outcome of hemostatic efficacy (54.1% vs. 50.0%, p=0.877). There were notable differences between in-hospital mortality (13.5% vs. 32.4%, p=0.058) and number of repeat doses (0.0% vs. 8.8%, p=0.065), but these findings, along with the other secondary outcomes, were not statistically significant. However, there was a significant increase in thrombotic events (ischemic stroke) in the Balfaxar® group (0.0% vs. 14.7%, p=0.016).  
Conclusion: There was no significant difference in hemostatic efficacy between Kcentra® and Balfaxar®. While no difference in efficacy was observed, ischemic stroke, in-hospital mortality, and repeat doses within 48 hours were more notable in the Balfaxar® group. Larger studies are needed to validate these results and further guide the selection of the optimal reversal agent.

Moderators Presenters Evaluators
avatar for Allie Hale

Allie Hale

Clinical Pharmacist and Residency Program Director, Parkridge Health System
Friday May 1, 2026 9:50am - 10:10am EDT
Athena C

9:50am EDT

Optimizing Rabies Post-Exposure Management: Assessing Immunoglobulin Use and Vaccination Follow Up
Friday May 1, 2026 9:50am - 10:10am EDT
Optimizing Rabies Post-Exposure Management: Assessing Immunoglobulin Use and Vaccination Follow Up   

Quartney Gilliam, Mckenzie Hodges, Bianca Rivera-Ramirez, Aayush Patel 

Piedmont Columbus Regional Midtown, Columbus, GA 

Background: Rabies is a viral infection that is fatal without timely and proper intervention. Transmission most commonly occurs through the bite of an infected animal, with dogs representing the predominant source of human exposure. Current guidelines emphasize rapid and comprehensive post-exposure prophylaxis (PEP), which includes immediate wound cleansing, prompt administration of human rabies immunoglobulin (HRIG), and initiation of the vaccine series. Although PEP is highly effective when given appropriately and on time, its real-world implementation is often challenged by system level and institutional barriers. These include delays in starting treatment, late or missed doses of HRIG or vaccines, variability in provider adherence to protocols, poor patient follow-up, as well as significant strain on both patients and the healthcare system when navigating multiple visits across different facilities, possibly leading to confusion and fragmented care. To help reduce unnecessary repeat emergency department visits and improve continuity of care, patients presenting to Piedmont Columbus Regional Midtown (PCRM) or Piedmont Columbus Northside (PCN) emergency departments may be referred to Midtown Medical Clinic (MMC), a transitional care clinic, for follow-up rabies vaccinations. This study aims to evaluate the effectiveness of the current institutional rabies PEP protocols implemented at both PCRM as well as PCN, identify gaps in its application, and explore strategies to improve adherence, timeliness, and patient outcomes after a potential rabies exposure. 

Methodology:
We conducted an IRB‑approved retrospective chart review of patients presenting to the emergency departments of PCRM or PCN from January 1, 2025, to December 31, 2025. This review included all patients who presented with a chief complaint of an animal-related bite or scratch. Patients were excluded if they transferred to another facility after evaluation or PEP initiation, left against medical advice, refused vaccination, or had insufficient documentation to determine exposure type, treatment, or follow‑up. The primary outcome measured adherence to CDC rabies PEP guidelines by determining whether eligible patients received indicated HRIG and/or vaccine and identifying both missed treatment and treatment given to patients who did not meet criteria. The secondary outcomes evaluated instances where clinical criteria for initiating rabies PEP were not met, follow-up compliance, and the rate and factors associated with referral to MMC for follow-up care. The outcomes were assessed using descriptive statistics.

Results: Among 200 screened patients (157 adults and 43 pediatric patients), eligibility for rabies post‑exposure prophylaxis (PEP) was identified in 42% of adults and 56% of pediatric patients. Among eligible patients, 77% of adults and 50% of pediatric patients were initiated on PEP, while 9% of ineligible adults and 10% of ineligible pediatric patients received PEP. Follow‑up after PEP initiation varied, with 25% of adults and 43% of pediatric patients completing the full vaccination series, and differences in follow‑up location observed based on the site of initial presentation.

Conclusions: In this evaluation adult rabies PEP initiation largely aligned with CDC guidance with most eligible adults receiving therapy and minimal use among those without indications. In contrast, initiation among pediatric patients meeting eligibility criteria was inconsistent. Across both age groups completion of the rabies vaccination series remained challenging, highlighting persistent barriers to follow‑up after initial PEP initiation.

Contact: [email protected]
Moderators
JK

Joseph Kohn

PRIS2Prisma Health Richland-University of South CarolinaPGY1
Presenters
avatar for Quartney Gilliam

Quartney Gilliam

PGY-1 Pharmacy Resident, Piedmont Columbus Regional Midtown
Quartney K. Gilliam, PharmD, is a PGY-1 Pharmacy Resident at Piedmont Columbus Regional Midtown in Columbus, Georgia. She is originally from Orlando, Florida and obtained her Doctor of Pharmacy degree from the University of South Florida Taneja College of Pharmacy. Her clinical interests... Read More →
Evaluators
avatar for Jolie Gallagher

Jolie Gallagher

Clinical Pharmacy Specialist, Critical Care, Emory University Hospital
I am the clinical pharmacy manager at Emory University Hospital.  My background training is in critical care.  My current areas of interest are optimization of transitions of care and pharmacist burnout and resilience.
Friday May 1, 2026 9:50am - 10:10am EDT
Athena I

9:50am EDT

Valproic Acid for Seizure Prophylaxis and Reduction of Headache Burden Following Subarachnoid Hemorrhage - Kristin Lanier
Friday May 1, 2026 9:50am - 10:10am EDT
Valproic Acid for Seizure Prophylaxis and Reduction of Headache Burden Following Subarachnoid Hemorrhage
Michael Wagner, Kristin Lanier, Jenna Sorgenfrei

Background:  
Aneurysmal subarachnoid hemorrhage (aSAH) management includes possible surgical intervention, blood pressure control, management of hydrocephalus, vasospasm prevention, and seizure prophylaxis. Guidelines do not currently recommend a specific seizure prophylaxis agent for aSAH. Levetiracetam is commonly selected in favor of the benign side effect profile and overall patient tolerability, yet it does not address any additional symptoms of aSAH. Valproic acid not only provides seizure prophylaxis but has demonstrated benefits in both migraine prophylaxis and headache treatment. The objective of this study is to determine if switching from levetiracetam to valproic acid reduces headache burden in patients based on utilization of pain medication for breakthrough symptoms  

Methods: 
A single-center, retrospective, cohort study identified adult patients admitted to the neurological intensive care unit of Prisma Health-Upstate between September 1, 2023 to September 1, 2025 with a diagnosis of aneurysmal subarachnoid hemorrhage. Seizure prophylaxis with levetiracetam was compared to valproic acid to determine the difference in overall headache burden based on breakthrough pain medication administration. Secondary outcomes include seizure incidence, intensive care unit length of stay, transcranial doppler changes, and incidence of adverse effects 

Results: 
A total of 115 patients were included with 66 in the levetiracetam group and 49 in the valproic acid group. Patients were prescribed similar pain regimens including scheduled gabapentin, lidocaine patches, and acetaminophen as needed in both the valproic acid group and levetiracetam (39.4% vs. 67.3%). For the primary outcome of daily headache incidence, there was a statically significant difference in favor of the levetiracetam group (3.0 vs. 2.4, P = 0.02). Additionally, patients in the valproic acid group demonstrated more frequent use of both as needed and breakthrough pain medication utilization. No differences were found in adverse effects.  

Conclusions:
Seizure prophylaxis with valproic acid did not reduce headache incidence or pain medication utilization following nontraumatic subarachnoid hemorrhage. These findings support the use of either valproic acid or levetiracetam as seizure prophylaxis, with no added benefit seen in the valproic acid group.  


Resident Contact: [email protected]
Moderators
avatar for Christele Robinson

Christele Robinson

Emergency Medicine Clinical Pharmacy Specialist, Emory University Hospital
Christele Robinson, PharmD, is board certified in pharmacotherapy. She is a member of the Department of Pharmacy at Emory University Hospital and currently practicing as an Emergency Medicine Clinical Pharmacy Specialist. Dr. Robinson obtained a Bachelor of Science degree at the... Read More →
Presenters
avatar for Kristin Lanier

Kristin Lanier

PGY2 Critical Care Resident, Prisma Health Upstate
Kristin Lanier, PharmD, is originally from Laurinburg, NC. She attended Wake Forest University in Winston-Salem, NC, where she earned a bachelor's degree in Biology and minored in Chemistry. She then attended Campbell University in Buies Creek, NC where she earned her Doctor of Pharmacy... Read More →
Evaluators
avatar for Cody Parker

Cody Parker

Clinical Pharmacy Specialist, St. Joseph's/Candler
Dr. Cody Parker is the PGY1 Pharmacy Residency Program Director at St. Joseph's/Candler in Savannah, GA. He received his Doctor of Pharmacy from the University of Georgia and completed a Postgraduate Year One (PGY1) Pharmacy Practice Residency at St. Joseph’s/Candler. Dr. Parker is a Clinical Pharmacy Sp... Read More →
Friday May 1, 2026 9:50am - 10:10am EDT
Athena D

9:50am EDT

Improving Timeliness and Sequencing of Empiric Antibiotics in Sepsis Through a Standardized Order-Set
Friday May 1, 2026 9:50am - 10:10am EDT
BACKGROUND: Sepsis is a leading cause of hospital morbidity and mortality. While current Surviving Sepsis Guidelines emphasize early broad-spectrum antibiotic administration, they do not address sequencing. Evidence suggests that delays in gram negative coverage, against Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa, are associated with increased mortality, and administration of broad-spectrum beta lactams prior to vancomycin may improve survival. In practice, initiation of antibiotic therapy is delayed due to lack of IV access, blood culture collection, medication verification, and absence of standardized order sets. These limitations are greater among spinal cord (SCI) and traumatic brain injury (TBI) patients who have atypical presentations complicating early sepsis recognition. The aim of this study is to assess the order of appropriate antibiotic administration, delays in administration from lack of intravenous (IV) access, and timing of blood culture collection to support creation of a sepsis order set.

METHODS: This is a single-center, retrospective, quality improvement project performed at a rehabilitation center. Patients (≥18 years) admitted between July 1, 2023, and July 31, 2025, who met systemic inflammatory response (SIRS) criteria and received IV vancomycin and one gram-negative agent for sepsis or neutropenic indications were included. Patients were excluded if antibiotic timing was inadequately documented.
Data collected included patient demographics, injury type (SCI or TBI), sepsis indicators, timing of sepsis recognition, antibiotic timing and sequencing, blood culture collection, lactate measurement, IV fluid resuscitation, and IV access placement.  

The primary outcome was sequencing, including gram-negative coverage first followed by gram-positive coverage antibiotics. Secondary outcomes included time between gram-negative and gram-positive therapy, percentage of patients with cultures drawn before antibiotic administration, frequency of IV-related delays, and type of IV line. Data was analyzed using descriptive statistics. 

RESULTS: A total of 65 patients meeting SIRS inclusion criteria were evaluated. The median age was 34 years old (SD 18.8), with males comprising 81.5% of the cohort (n=53). Injury classifications included SCI (n=24, 37%), TBI (n=26, 41.5%), and dual (n=14, 21.5%) diagnoses.
When vancomycin was administered prior to gram-negative therapy, the mean delay to gram-negative coverage was 141 minutes. Upon further analysis, vancomycin was administered first in 15.4% of encounters, while gram negative agents were more frequently administered first, including piperacillin-tazobactam (57%), cefepime (20%), and meropenem (7.6%).  

In 20% of encounters, blood cultures were either obtained after the first antibiotic dose or not obtained. IV access was not established prior to antibiotic ordering in 46.2% of patients. Antibiotics were administered via peripheral IV (75%), midline (11%), or peripherally inserted central catheter (14%). 

CONCLUSIONS: Administering vancomycin first resulted in an expected delay of more than two hours before effective gram-negative coverage. This delay was likely due to the standard vancomycin infusion time at this facility. Because delays in antibiotic administration increase mortality in sepsis, education on Y-site compatibility is essential to allow compatible agents to be administered simultaneously and facilitate faster, more efficient antibiotic delivery. Moreover, 20% of blood cultures were collected inappropriately, compromising diagnostic accuracy and limiting targeted antibiotic therapy, highlighting the need for reinforcement of proper culture collection.

Additionally, nearly half of patients meeting sepsis criteria at the time of antibiotic ordering did not have IV access, reflecting a challenge unique to rehabilitation settings, where the goal is early discontinuation of IV lines to enhance mobility, minimize line associated complications, and support functional recovery. However, for sepsis, a delay in IV access inadvertently leads to a delay in antibiotic administration. 
These findings show inconsistent sepsis workflows and clinically relevant delays which can impact patient outcomes, highlighting the need for a standardized sepsis order set in rehabilitation hospitals to streamline IV access, culture collection, and appropriate antibiotic prioritization. 

Moderators
avatar for Devin Lavender

Devin Lavender

Clinical Assistant Professor, UGAA1University of Georgia College of Pharmacy (Ambulatory Care)PGY2
Ambulatory Care, Scholarship of Teaching and Learning, Resident and Student Development.
Presenters Evaluators
Friday May 1, 2026 9:50am - 10:10am EDT
Parthenon 1

9:50am EDT

Improving Pharmacy Inventory Management with Real-Time Barcode Scanning
Friday May 1, 2026 9:50am - 10:10am EDT
Background:
Accurate inventory management is essential for operational efficiency, yet traditional models relying on periodic third-party counts limit real-time visibility and delay error correction. Over the previous years, several audit processes have been trialed, each with varying trade-offs related to ease of use, time requirements, utility, and interruption of standard workflows. A significant amount of time was spent after the counts were completed, reconciling discrepancies in the third party data including medications that could not be accurately identified based on barcode scans. Our institution recently transitioned from a biannual, vendor-supported inventory process to an internally managed model, revealing workflow inefficiencies and gaps in issue identification due to reliance on delayed data systems and fragmented scanning processes. To improve workflow and data integrity, a real-time barcode scanning tool was developed and iteratively refined to facilitate live inventory validation.

Methods:
The tool enables immediate feedback during both full inventory counts and targeted audits. Key development considerations included optimizing data refresh processes, accommodating large and variable datasets, and enhancing usability through simplified visual indicators to reduce user fatigue.  Over time, improvements focused on minimizing error rates and improving workflow integration.

Results:
Implementation of the tool improved operational efficiency by reducing the need for dual auditors and minimizing workflow interruptions. The system enhanced auditor autonomy by removing the need for individual assignments and enabling users to validate counts independently in real time. It also decreased duplication of counts and enabled immediate identification and correction of discrepancies, reducing the number of recounts required.

Conclusions:
A real-time barcode scanning approach to inventory management enhances efficiency, accuracy, and staff autonomy. This solution addresses key limitations of traditional inventory processes and supports proactive discrepancy resolution. Ongoing evaluation during a full live-count inventory will further quantify its impact on time savings and error reduction.

Moderators
AQ

April Quidley

PGY1 Residency Program Director, ECU Health Medical Center
Presenters
avatar for Lauren Flick

Lauren Flick

PGY-2 Informatics Resident, AdventHealth
PGY-1 Informatics Resident at AdventHealth Orlando
Evaluators
AJ

Audrey Johnson

Surgical/Trauma Critical Care Pharmacist, Memorial Health University Medical Center
Friday May 1, 2026 9:50am - 10:10am EDT
Olympia 1

9:50am EDT

Impact of Integrating the BioFire® Meningitis/ Encephalitis Panel (MEP) with Antimicrobial Stewardship in a Non-Teaching Community Hospital
Friday May 1, 2026 9:50am - 10:10am EDT
Title: Title: Impact of Integrating the BioFire® Meningitis/ Encephalitis (ME) Panel with Antimicrobial Stewardship in a Non-Teaching Community Hospital

Investigators: Ashtyn Keller; Brad Crane; Emily Duncan; Stephanie Grimes; Joy (Abby) Bussey 

Study Location: Prisma Health Blount Memorial Hospital, Maryville, TN – Department of Pharmacy 

Background: Limited data exists on the clinical and financial impact of rapid cerebrospinal fluid (CSF) diagnostic testing in non-academic community hospitals. This study evaluated the effect of implementing the BioFire® MEP on patient outcomes and hospital resource utilization.  

Methods: This IRB-approved, single-center, retrospective cohort study included adults hospitalized from July 2020 through June 2025 with an identified CSF culture ordered. Exclusion criteria were if less than 18 years old, test cancellation or non-completion, transfer to another facility, repeat CSF specimens from the same patient or infection, or treated outpatient only. The primary outcome was time to optimal antimicrobial therapy in patients without the BioFire® MEP or with the BioFire® MEP. Secondary outcomes compared duration of antimicrobial therapy, hospital length of stay, and hospital costs per visit. Student’s t-tests were used with significance defined as p < 0.05. 

Results: A total of one hundred and twenty-one patients were included: eighty-seven patients (72%) did not utilize the BioFire® MEP, and thirty-four patients (28%) utilized the BioFire® MEP. Median time to optimal antimicrobial therapy without the BioFire® MEP was 3.0 days compared to 2.0 days with the BioFire® MEP (absolute difference 1 day; 95% CI 0.004 to 1.96; p=0.04). Mean duration of antimicrobial therapy without the BioFire® MEP was 4.0 days compared to 2.9 days with the BioFire® MEP (absolute difference 1.1; 95% CI -2.72 to 0.56; p=0.19). Median hospital length of stay without the BioFire® MEP was 6.0 days compared to 4.5 days with the BioFire® MEP (absolute difference 1.5; 95% CI -1.74 to 4.74; p=0.36). Median hospital costs per visit without the BioFire® MEP were $8,456 compared to $9,854 with the BioFire® MEP (absolute difference $1,398). 

Conclusion: In conclusion, this retrospective cohort study in a non-academic, community hospital, demonstrated that the implementation of the BioFire® MEP was associated with a significantly significant reduction in time to optimal antimicrobial therapy and potentially shorter antimicrobial duration and hospital length of stay. Additional large-scale studies are recommended to confirm these findings.

Moderators Presenters Evaluators
CT

Christina Thurber

PGY-1 Residency Program Coordinator
Friday May 1, 2026 9:50am - 10:10am EDT
Parthenon 2

9:50am EDT

Impact of the Intravenous Lorazepam Shortage on Alcohol Withdrawal Treatment in the ICU
Friday May 1, 2026 9:50am - 10:10am EDT
Background: The American Society of Addiction Medicine guidelines recommend benzodiazepines as first-line treatment for moderate-severe alcohol withdrawal syndrome (AWS). Intravenous (IV) lorazepam is a first-line therapy for AWS at Emory Healthcare (EHC) to prevent complications such as seizures and delirium tremens. The quick onset, half-life, and lack of metabolites make IV lorazepam a desirable agent for AWS. There have been intermittent shortages of IV lorazepam, with the most recent shortage beginning in May 2025. In response, EHC built an electronic alert as a soft stop for all IV lorazepam orders to notify providers of the shortage and recommend alternatives. In addition, the AWS order set was modified to replace IV lorazepam with IV midazolam. The goal of this study was to understand medication utilization patterns during this shortage and provide guidance for future shortages.  

Methods: This study was a multi-center, retrospective chart review of adult patients receiving treatment for moderate-severe AWS from 1/30/2025 to 9/7/2025 in the ICU. Pre-shortage and post-shortage groups were determined based on IV lorazepam shortage alerts, which began in EPIC on 5/20/2025. The primary objective was to examine medication utilization patterns of AWS before and after the alert was implemented. Evaluation of this endpoint was determined by medication name, strength, route, frequency, and duration for 48 hours after the alcohol withdrawal order set was active. Secondary objectives measured safety and clinical outcomes and included respiratory rates, hypotension, and changes in scores of Clinical Institute Withdrawal Assessment Alcohol Scale (CIWA), length of stay, mortality, 30-day readmissions, respectively. Data was analyzed using descriptive statistics, t-test, and Mann-Whitney U test.

Results: There were 127 patients in the pre-shortage group and 152 patients in the post-shortage group. Baseline characteristics were similar between groups. The average baseline CIWA scores were similar with first CIWA ≥8 13.44 pre-shortage versus 12.86 post-shortage. IV lorazepam doses were higher in the first 12 hours of the AWS order set ordering time. In the post-shortage group, there was a greater decrease in IV lorazepam dose 12-24 hours post-alert (63.14% versus 43.72%). IV lorazepam orders trended down (57% versus 47%, p-value 0.097), and patients prescribed oral lorazepam trended up (23% versus 32%, p-value 0.081). More patients in the post-shortage group were prescribed chlordiazepoxide (5 versus 16 patients, p-value 0.038) and midazolam (20 versus 45 patients, p-value 0.006). Phenobarbital use did not change significantly (86 versus 89 patients, p-value 0.115). First CIWA <8, was similar at 4.37 pre-shortage versus 3.84 post-shortage. The average time to CIWA score <8 from the first score ≥8 was greater in the pre-shortage group 9 hours and 13 minutes compared to 8 hours and 37 minutes (p-value 0.205). Average hospital length of stay (12.39 versus 11.07 days, p-value 0.290), average ICU length of stay (5.28 versus 5.44 days, p-value 0.725), and mortality (5 versus 7 patients, p-value 0.784) were similar between the two groups. Readmission within 30 days and respiratory depression were higher in the post-shortage group (12% versus 18%, p-value 0.166 and 67% versus 73%, p-value 0.267, respectively).

Conclusion: Following IV lorazepam alerts, medication utilization shifted towards chlordiazepoxide and midazolam. The average cumulative dose of IV lorazepam decreased more in the post-shortage group after the first 12 hours. Phenobarbital use may not have changed due to provider practice styles and the recommended alternatives. This was a retrospective study, alerts for alternative agents could be bypassed, and medications listed may have been used for other indications. Future direction includes evaluating alternative medication usage patterns with a developed phenobarbital order set. A comparative analysis focused on adverse drug events and efficacy may further shape treatment.

Moderators
avatar for Brian Leith

Brian Leith

Clinical Pharmacist, VA Medical Center
I am currently the emergency medicine and antimicrobial stewardship pharmacist at the VA Medical Center in Fayetteville, NC.
Presenters
AL

Anatolia Legaspi

PGY-1 Resident, Emory University Hospital Midtown
Evaluators
BK

Brian Knott

Clinical Pharmacy Manager, AdventHealth Winter Park
Friday May 1, 2026 9:50am - 10:10am EDT
Olympia 2

9:50am EDT

Resident Presentation - Katherine Albus
Friday May 1, 2026 9:50am - 10:10am EDT
Linezolid as Empiric Therapy for Methicillin-Resistant Staphylococcus aureus (MRSA) Bacteremia: A Retrospective Cohort Analysis of Clinical Outcomes  
Katherine Albus, Kellee Geren, Samantha Walker, Brandon Hawkins 
The University of Tennessee Medical Center, Knoxville, TN 
 
Background/Purpose: Methicillin-resistant Staphylococcus aureus (MRSA) remains one of the most difficult-to-treat Staphylococcus species worldwide, with mortality exceeding 20%. Vancomycin (VAN) or daptomycin (DAP) are considered first-line empiric therapies for MRSA bacteremia.  Small subgroup analyses have suggested improved survival and faster bacteremia clearance with linezolid (LZD) versus glycopeptides, yet its role is largely unclear. This study aimed to compare the effectiveness of LZD versus VAN or DAP in patients with MRSA bacteremia.   
 
Methodology: This single-center, retrospective, observational cohort study included hospitalized between December 2017 and June 2024. The primary outcome was a composite of 60-day all-cause mortality and bacteremia persisting greater than 7 days. Secondary outcomes included the individual components of the composite outcome, duration of antimicrobial therapy, duration of bacteremia, and ICU admission. Eligible patients were 18 years of age or older, had at least one MRSA-positive blood culture, and received empiric LZD, VAN, or DAP for at least 48 hours from culture collection. VAN and DAP were assessed as composite groups. Exclusion criteria included death or transition to hospice within 48 hours of culture collection, failure to receive a study antibiotic within 3 hours of culture, receipt of a comparator antimicrobial for more than 24 hours, or lack of susceptibility to the empiric agent. 
 
Results: There was no difference in patients receiving LZD or VAN/DAP in the primary composite outcome (0% LZD vs. 43.8% VAN/DAP; P = 0.074) or the individual components of 60-day all-cause mortality (0%  LZD vs. 19.8%  VAN/DAP; P = 0.580) and persistent bacteremia greater than 7 days (0% LZD vs. 32.6% VAN/DAP; P = 0.319). The median duration of antimicrobial therapy was numerically shorter in the LZD group compared with the VAN/DAP group (19.5 days vs. 43 days, respectively), though this was not significant (P = 0.143). ICU admission rates during treatment were comparable between groups (20% LZD vs. 38% VAN/DAP; P = 0.646). The duration of bacteremia was significantly shorter among patients treated with LZD compared to VAN/DAP, with median durations of 2.4 days and 5.5 days, respectively (P = 0.036). 
 
Conclusions: In a small sample, empiric LZD for MRSA bacteremia demonstrated comparable rates of 60-day mortality and persistent bacteremia compared with VAN or DAP. LZD demonstrated a significantly shorter duration of bacteremia than VAN/DAP, although these findings may be due to LZD use in less complicated infections. These results, when considered alongside existing clinical and pharmacologic evidence, support further investigation of LZD as a potential first-line option for MRSA bacteremia. Larger, prospective studies are needed to better define the role of LZD in uncomplicated, Gram positive infections with Gram negative coverage where appropriate.  

Link: https://docs.google.com/document/d/e/2PACX-1vQzRhZffUvSQUgtz-e88XOkxVPWlCJON2KHAtHhLXttKCpq05YARaPn9673tC8gAzP64x3Ss3WU3wYN/pub
Moderators Presenters
KA

Katherine Albus

Katie Albus, PharmD is a PGY1 at the University of Tennessee Medical Center in Knoxville, Tennessee. She completed her pharmacy schooling at Virginia Commonwealth University and plans to continue her education through a PGY2 in critical care at Carilion Roanoke Memorial Hospital in... Read More →
Evaluators
avatar for Anh Nguyen

Anh Nguyen

Clinical Pharmacy Specialist, Emory Decatur Hospital
I’m a Board‑Certified Critical Care Pharmacy Specialist with a passion for taking care of some of the sickest patients in the hospital. I’ve worked in both intermediate and intensive care settings, where every day brings a new challenge and a new opportunity to make a meaningful... Read More →
Friday May 1, 2026 9:50am - 10:10am EDT
Athena H

10:20am EDT

UNFILLED SLOT
Friday May 1, 2026 10:20am - 10:40am EDT

Friday May 1, 2026 10:20am - 10:40am EDT
Parthenon 1
  • global Y

10:20am EDT

UNFILLED SLOT
Friday May 1, 2026 10:20am - 10:40am EDT
Friday May 1, 2026 10:20am - 10:40am EDT
Parthenon 2

10:20am EDT

UNFILLED SLOT
Friday May 1, 2026 10:20am - 10:40am EDT

Friday May 1, 2026 10:20am - 10:40am EDT
Olympia 1
  • global Y

10:20am EDT

UNFILLED SLOT
Friday May 1, 2026 10:20am - 10:40am EDT
Friday May 1, 2026 10:20am - 10:40am EDT
Olympia 2

10:20am EDT

Evaluation of Pharmacist-Led Intervention to Improve Statin Utilization Metrics in a Value-Based Care Model - A. Garrett Allegra
Friday May 1, 2026 10:20am - 10:40am EDT
Background: Value-based care models are growing in popularity. These models follow the logic that healthcare organizations should receive a higher level of reimbursement for providing more effective care. Reimbursement rates are determined by the health systems’ performance on pre-determined patient care metrics. Health organizations can achieve better outcomes while lowering costs through a value-based care model.1 Examples of commonly measured outcomes include A1c, blood pressure, and statin-utilization. Value-based care starts with understanding the shared health needs of your patients and then implementing an interdisciplinary team approach to meet those needs.1 AdventHealth Hendersonville (AHH) is a non-profit health system in Western North Carolina comprising 13 primary care clinics and one main hospital campus. AHH participates in value-based care for patients insured by Medicare through an organization called CHESS, which deploys clinical pharmacists to aid in monitoring their metrics. One metric AHH focused on for 2025 is statin utilization for people with diabetes or atherosclerotic cardiovascular disease (ASCVD) history. Prior studies have demonstrated that cardiovascular disease is the number one cause of death in the world and that statins are largely underutilized by populations that would benefit from them.2 The most common barrier to initiation is patient refusal.2 Pharmacist-led interventions can improve statin utilization metrics.2 The objective of this quality improvement project was to improve statin utilization metrics via pharmacist-led clinic visits at AHH. Methods: A pre-existing registry of 161 Medicare Advantage patients not meeting statin utilization metrics was analyzed for intervention opportunity. The patients included had either a diagnosis of diabetes or history of ASCVD and were not currently taking a statin. Exclusion criteria included prior refusal of service by patient or provider, statin already on medication list, appropriate chart documentation of statin intolerance, and not being a patient of the clinic site anymore. Prior refusal of service was documented in the pre-existing patient registry by CHESS pharmacists. A pharmacy resident reached out via phone to each patient a maximum of three times to attempt to schedule an in person or virtual visit focused on statin initiation or appropriate documentation of statin intolerance. At these pharmacy visits, the pharmacy resident discussed hyperlipidemia, statin use history, and potential adverse effects and use clinical decision making to either initiate a statin or appropriately document true statin intolerance in the record. Results: After removing patients that met exclusion criteria, 30 patients with diabetes and 4 patients with ASCVD history were included (n=34). Of the 30 patients in the diabetes group, 19 were able to be reached by phone (63.3%). After an appointment with pharmacy clinic, 15 of these (78.9%) were able to meet the quality metric, with 2 patients initiated on statin therapy and 13 having statin intolerance appropriately documented in their chart. Of the other 4 patients reached, 1 patient declined statin therapy despite counseling, 1 patient’s primary care provider declined statin initiation, and 2 patients were not indicated for statin therapy. In the ASCVD group, all 4 patients were able to be reached (100%). After an appointment with pharmacy clinic, 2 of these patients (50%) were able to meet the quality metric, with both patients having statin intolerance appropriately documented in their chart. The other 2 patients reached both declined meeting with a pharmacist to discuss cholesterol management. Combining the datasets gives 17 patients updated to meeting the quality metric of 23 patients reached (73.9%) and 34 patients overall (50%). Conclusion: Pharmacist intervention can improve statin utilization metrics for patients with diabetes or ASCVD. Integrating clinical pharmacy into a value-based care model can be beneficial to organizational reimbursement rates due to this improvement in metrics.
Moderators Presenters
avatar for Garrett Allegra

Garrett Allegra

PGY2 Ambulatory Care Pharmacy Resident, Mountain Area Health Education Center
Garrett is from Winchester, Virginia and completed undergraduate education at Virginia Tech before going to pharmacy school at Virginia Commonwealth University. At VCU, he developed a strong interest in ambulatory care, particularly in the areas of cardiology, diabetes, and substance... Read More →
Evaluators
avatar for Don Tyson

Don Tyson

Director of Pharmacy, Piedmont Athens Regional Medical Center
Friday May 1, 2026 10:20am - 10:40am EDT
Athena B

10:20am EDT

Clinical Outcomes Associated with Aspirin Dose in Traumatic Blunt Cerebrovascular Injury
Friday May 1, 2026 10:20am - 10:40am EDT
Background: Stroke complicates up to 20% of traumatic blunt cerebrovascular injuries (BCVI), with the highest risk occurring within 72 hours of injury, underscoring the importance of prompt antithrombotic therapy. Current guidelines from the Eastern Association for the Surgery of Trauma and the Western Trauma Association recommend antithrombotic therapy but differ in preferred agents and dosing strategies. Prisma Health Richland’s (PHR) institutional guideline recommends aspirin monotherapy for BCVI grades I–III without specifying dose. Data comparing aspirin dosing in BCVI are limited. One retrospective study reported a 3.5% stroke rate with aspirin 81 mg, compared with previously reported rates of 2–8% using aspirin 325 mg. We sought to compare the incidence of ischemic stroke among patients with traumatic BCVI treated with aspirin 81 mg versus 325 mg. 
  
Methods: We conducted a retrospective cohort study of adult patients with traumatic BCVI treated with aspirin monotherapy at PHR from February 27, 2021 to September 30, 2025. Patients with stroke prior to aspirin initiation during index admission, inconsistent aspirin dosing within the first 7 days, or grade V BCVI were excluded. The primary outcome was ischemic stroke within 90 days of injury. Secondary outcomes included time to aspirin initiation, adherence to repeat imaging guidelines, worsening intracerebral hemorrhage (ICH), worsening solid organ injury, gastrointestinal (GI) bleeding, and in-hospital mortality. Baseline characteristics were compared using appropriate univariate analyses. Multivariable logistic regression was performed to evaluate the association between aspirin dose and ischemic stroke, adjusting for BCVI grade and time to aspirin initiation. 
  
Results: This study included 130 patients with a traumatic BCVI who were treated with aspirin therapy for stroke prevention. Of those included, 106 patients (81.5%) received aspirin 325 mg and 24 patients (18.5%) received aspirin 81 mg. Baseline characteristics were similar between the two treatment groups, with the majority being African American males. The most common mechanism of injury was motor vehicle collision (73.8%), followed by injury due to a fall (16.2%) and assault (1.5%). Concomitant traumatic brain injury was present in 46.2% of patients, while 13.8% of patients also had a solid organ injury. During the study period, 12 patients (9.2%) experienced an ischemic stroke. Ten of these patients received aspirin 325 mg, while 2 patients received aspirin 81 mg (p=1). Multivariate logistic regression with covariates BCVI grade and time to aspirin initiation demonstrated no different in the incidence of ischemic stroke with aspirin 325 mg (aOR 0.831, 95% CI 0.951-1.003). The majority of patients (94.6%) had repeat imaging completed within the 7-day timeframe indicated in our local BCVI guidelines. A new or worsening ICH occurred in 22 patients, the majority being in the aspirin 325 mg group (n=19; p=0.764), and a GI bleed occurred in 5 patients, all of whom received aspirin 325 mg (p=0.584). The overall mortality rate was 9.2% with 8 patients in the aspirin 325 mg group and 4 patients in the aspirin 81 mg group dying during the study period (p=0.225) 
 
Conclusion: This retrospective cohort study found that patients with a traumatic BCVI were more frequently treated with aspirin 325 mg compared to 81 mg, however, there was no significant difference in the primary outcome comparing the incidence of ischemic stroke between these two treatment groups. There was a non-significantly higher incidence of new or worsening ICH and GI bleed in the aspirin 325 mg group. These findings suggest that a larger study with more variance in aspirin treatment may be beneficial to validate a correlation between aspirin dose and incidence of ischemic stroke. 


Moderators
avatar for Stephanie Lesslie

Stephanie Lesslie

PGY-2 Critical Care Residency Director, Memorial University Medical Center
Presenters
avatar for Kendall Jolly

Kendall Jolly

PGY1 Pharmacy Resident, Prisma Health Richland - University of South Carolina
Kendall Jolly is a PGY1 Pharmacy Resident at Prisma Health Richland. She completed her Bachelor of Science and Doctor of Pharmacy degrees at the University of Georgia. After PGY1, she will be staying at Prisma Health Richland to complete a PGY2 in pediatrics.
Evaluators
avatar for Jonathan Alligood

Jonathan Alligood

Residency Program Director, Phoebe Putney Memorial Hospital
Friday May 1, 2026 10:20am - 10:40am EDT
Athena I

10:20am EDT

Comparison of Tenecteplase versus Alteplase for Pulmonary Embolism During In-Hospital Cardiac Arrest 
Friday May 1, 2026 10:20am - 10:40am EDT
Comparison of Tenecteplase versus Alteplase for Pulmonary Embolism During In-Hospital Cardiac Arrest  
Authors: Paola Reyes-Serrano, Jason Vilar, Emily To 
Background: Pulmonary embolism (PE) accounts for approximately 2–5% of in-hospital cardiac arrests (IHCA) and is associated with high mortality despite advanced resuscitative efforts. Current guidelines recommend systemic thrombolysis when PE is suspected or confirmed during cardiac arrest; however, evidence supporting thrombolytic use in this setting remains limited. Alteplase has historically been the most commonly used thrombolytic agent for PE, while tenecteplase offers potential advantages, including greater fibrin specificity, longer half-life, and administration as a single intravenous bolus. This study aimed to compare clinical outcomes and safety of tenecteplase versus alteplase for suspected or confirmed PE during IHCA following a system-wide formulary change. 

Methods: A retrospective cohort study was conducted across AdventHealth facilities. Adult patients who experienced IHCA and received systemic thrombolysis with alteplase or tenecteplase for suspected or confirmed PE between January 2024 and January 2026 were included. Suspected PE was defined by provider clinical assessment at the time of arrest. Baseline demographic characteristics, arrest characteristics, laboratory values, and PE risk factors were collected from the electronic health record. The primary outcome was return of spontaneous circulation (ROSC). Secondary outcomes included time from arrest to thrombolytic administration, time from thrombolytic administration to ROSC, cardiopulmonary resuscitation (CPR) duration, ICU and hospital length of stay, in-hospital mortality, and neurologic outcomes at discharge. Sustained ROSC was defined as ROSC maintained for at least 20 minutes. Safety outcomes included major bleeding events and blood transfusion requirements. Continuous variables were compared using Mann–Whitney U tests, and categorical variables using chi-square or Fisher’s exact tests. 

Results: A total of 48 patients met inclusion criteria, 26 received alteplase and 22 received tenecteplase. ROSC occurred in 16 patients (33%), 10 patients (38.5%) in the alteplase group and 6 patients (27.3%) in the tenecteplase group. Sustained ROSC occurred in 7 patients (15.4%), 4 patients (15.4%) in alteplase group and 3 patients (13.6%) in tenecteplase group. Median time from thrombolytic administration to ROSC was 9.5 minutes (IQR 1.75–12.75) with alteplase and 13.5 minutes (IQR 5.75–16.25) with tenecteplase. Median total CPR duration was 41.0 minutes (IQR 22.5–54.0) with alteplase and 33.5 minutes (IQR 22.0–48.8) with tenecteplase. CPR duration following thrombolytic administration was similar between groups (16.5 minutes in both groups). Median time from arrest to thrombolytic administration was 18.5 minutes (IQR 11–31.3) with alteplase and 14.5 minutes (IQR 6.75–27.3) with tenecteplase. In-hospital mortality occurred in 24 patients (92.3%) who received alteplase and 22 patients (100%) who received tenecteplase. Neurologic outcomes were similar, with a median modified Rankin Scale (mRS) score of 6 (IQR 6–6) in both groups. Major bleeding occurred in 2 patients (7.7%) in the alteplase group and 2 patients (9.1%) in the tenecteplase group. Blood transfusion requirements were low, occurring in 1 patient (3.8%) in the alteplase group and 2 patients (9.1%) in the tenecteplase group. Baseline characteristics differed between groups in several variables. Patients who received tenecteplase were older (66.5 vs 58.5 years) and had lower median weight (73.9 vs 99.5 kg). Tenecteplase dosing was appropriate based on weight in 19 of 22 patients (86%), while 3 patients (14%) received doses outside of recommended weight-based ranges.  

Conclusion: In this multicenter retrospective cohort of patients receiving systemic thrombolysis for suspected pulmonary embolism during in-hospital cardiac arrest, tenecteplase demonstrated clinical and safety outcomes comparable to alteplase. Rates of ROSC, bleeding events, and mortality were similar between treatment groups despite baseline differences in patient characteristics. Given its single intravenous bolus administration and comparable outcomes observed in this cohort, tenecteplase may represent a practical alternative to alteplase for thrombolytic therapy during cardiac arrest when pulmonary embolism is suspected. Larger prospective studies are needed to better define optimal thrombolytic selection in this high-risk population.
Moderators Presenters
avatar for Paola Reyes Serrano

Paola Reyes Serrano

PGY1 Pharmacy Resident, AdventHealth Orlando
Evaluators
avatar for Jessica Sterchi

Jessica Sterchi

Clinical Pharmacy Supervisor and Acute Care PGY1 RPD, BMHT1Blount Memorial HospitalPGY1
Friday May 1, 2026 10:20am - 10:40am EDT
Athena J

10:20am EDT

Development of an Ongoing Quality Metric for Vancomycin Dosing
Friday May 1, 2026 10:20am - 10:40am EDT
Elena Galagan, Joy Peterson, Karen Barlow
Wellstar Kennestone Regional Medical Center, Marietta, GA

Background

Vancomycin has a narrow therapeutic index, requiring individualized pharmacokinetic dosing to maintain trough levels between 10–20 mcg/mL while minimizing the risk of acute kidney injury (AKI). Despite its common use, many institutions lack formal metrics to assess vancomycin dosing appropriateness. This quality assurance project at Wellstar Kennestone Regional Medical Center (WKRMC) aimed to create a sustainable, ongoing quality metric and real-time monitoring system for vancomycin dosing practices.

Objectives/Methods

The project was conducted in two parts. The primary objective was to develop an ongoing quality metric that evaluates vancomycin dosing quality by monitoring therapeutic trough levels and AKI in adult patients. The secondary objective was to use this metric and Microsoft® Power BI dashboard to enhance decision-making and increase the proportion of patients achieving therapeutic targets.
Part 1 (establishing a baseline) was a retrospective quality assurance project including data from three fiscal years (July 1, 2021, through June 30, 2024). Adult patients who received intravenous vancomycin during an inpatient admission at WKRMC, had vancomycin dosed by a clinical pharmacist, and had at least one vancomycin trough level were included; pediatric patients under 18 years were excluded. The baseline percentage of patients with therapeutic vancomycin levels (10–20 mcg/mL) was calculated to establish the goal for the metric.
Baseline AKI incidence was determined by collecting up to three serum creatinine values around the time of trough collection and measuring the frequency of AKI as defined by Kidney Disease: Improving Global Outcome (KDIGO) criteria. A random sample of 123 patients was selected by choosing every 100th patient from each fiscal year for detailed review to validate the dashboard, estimate data capture performance, identify opportunities for improvement, and refine variables.
Part 2 (implementation) focused on developing a sustainable, ongoing quality metric and monitoring dashboard. Core metric components included the percentage of patients achieving therapeutic trough levels and the incidence of AKI, with stratification by key risk factors. Data elements were mapped to automated reports from Epic®, aggregated in a secure environment, and visualized in Microsoft® Power BI to create an interactive dashboard for clinical pharmacists. The dashboard was designed to support ongoing monitoring, early detection of trends, and continuous optimization of vancomycin dosing practices.
 
Results

The 123-patient review validated data accuracy, assessed variable performance, and guided refinement of the quality metric. This process led to adjustments in data capture, including the addition, modification, and removal of specific variables to enhance clinical relevance and reliability. Variables related to trough timing, serum creatinine trends, and AKI risk factors were refined to improve clarity and support clinical decision-making.
Findings from the review were used to validate automated Epic® data feeds, ensuring accurate representation of therapeutic trough attainment and AKI indicators. Based on these insights, targeted education was provided to clinical pharmacists on interpreting dashboard metrics and using the tool for ongoing dosing evaluation. The finalized dashboard enables monitoring of vancomycin dosing, supports trend and outlier identification, and provides a foundation for continuous quality improvement.

Conclusion

This project developed and validated a sustainable, ongoing quality metric for vancomycin dosing, supported by an interactive Power BI dashboard. Although this project was conducted around vancomycin troughs, the concept is also applicable to Area Under the Curve (AUC) targets. The goal of this initiative is to provide actionable information to clinical pharmacists to assess and improve vancomycin dosing accuracy, with the intent of increasing the proportion of trough levels within the therapeutic range while supporting ongoing renal safety surveillance.

Contact: [email protected]
Moderators Presenters
avatar for Elena Galagan

Elena Galagan

PGY1 Pharmacy Resident/ Staff Clinical Pharmacist, Wellstar Kennestone Regional Medical Center
Non-Traditional PGY1
Staff Clinical Pharmacist at Wellstar Kennestone
Mercer University Class of 2017
Evaluators
avatar for Liz Oglesby

Liz Oglesby

Pharmacy Clinical Coordinator, PGY-1 Residency Program, Mobile Infirmary
Liz Oglesby, PharmD, BCPS, is the Pharmacy Clinical Coordinator and PGY-1 Residency Program Director at Mobile Infirmary in Mobile, Alabama. She obtained her doctorate of pharmacy from Auburn University in 2017 and completed PGY-1 training at Baptist Health Princeton Hospital in 2018. Her primary practice foc... Read More →
Friday May 1, 2026 10:20am - 10:40am EDT
Athena A

10:20am EDT

Evaluating the Impact of ACEi or ARB Reinitiation versus Discontinuation Post Hospitalization with Acute Kidney Injury on Patient Outcomes
Friday May 1, 2026 10:20am - 10:40am EDT
Angiotensin converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARBs) provide cardiovascular and renal protections across hypertension, chronic kidney disease, and heart failure populations, yet are often held during episodes of acute kidney injury (AKI). Optimal timing of post-AKI reinitiation remains uncertain. We aimed to compare outcomes among patients whose ACEi or ARB therapy was restarted at different times.   
 
We conducted a single center, retrospective cohort study of adult inpatients with AKI whose ACEi, ARB, or ARNI therapy was held ≥24 hours during hospitalization. Patients were categorized into 3 groups depending on whether therapy was restarted during hospitalization, restarted upon discharge, or not continued at discharge. The primary endpoint was complete renal recovery at 90 days. Secondary endpoints were AKI readmission rates within 90 days of discharge, cardiovascular events and all-cause mortality at 12 months, and time to treatment reinitiation in group 3. 
 
Among 148 patients (Group 1, n=41; Group 2, n=52; Group 3, n=55), there was no significant difference across groups in renal recovery at 90 days (73.2%, 59.6%, 67.3%, respectively; p=0.13). AKI readmission rates within 90 days (9.8%, 19.2%, 9.1%, respectively; p=0.25), cardiovascular events within 12 months (17.1%, 7.7%, 18.2%, respectively; p=0.22), and all-cause mortality within 12 months (12.2%, 5.8%, 7.3%, respectively; p=0.53) were similar across groups. Median (SD) time to reinitiation in group 3 was 60 ±94 days (p=0.049). 
 
Early reinitiation of ACEi or ARB after AKI did not worsen renal recovery at 90 days or increase adverse events. These findings support timely reinitiation with appropriate monitoring.  

Moderators Presenters
avatar for Leslie Phillips

Leslie Phillips

PGY-2 Pharmacotherapy Pharmacy Resident, University of Tennessee Medical Center
Dr. Leslie A. Phillips is a PGY-2 Pharmacotherapy resident at the University of Tennessee Medical Center. Originally from Atlanta, Georgia, she earned her Bachelor of Science in Chemistry from Kennesaw State University and a Doctor of Pharmacy degree from The University of Georgia... Read More →
Evaluators
avatar for Yona Roberts

Yona Roberts

RPD/Clinical Pharmacy Manager, WSGA1Wellstar Cobb HospitalPGY1
Yona Roberts earned a Doctor of Pharmacy degree from Florida Agricultural and Mechanical University in Tallahassee, Florida.  She went on to complete a Pharmacy Practice Residency through Mercer University at DeKalb Medical Center in Atlanta, Georgia.  After completion of her residency... Read More →
Friday May 1, 2026 10:20am - 10:40am EDT
Athena H

10:20am EDT

Evaluating the Outcomes of Pharmacist Driven Interventions in a Geographic Rounding Pilot at a Large Community Hospital
Friday May 1, 2026 10:20am - 10:40am EDT
Oksana Buksa, PharmD, April Williams, PharmD, BCPS, Michele Moseley, PharmD, BCPS, Anna Cross, PharmD, Erik Roberts, CPhT
Huntsville Hospital – Huntsville, Alabama

Purpose/Background:
Huntsville Hospital has announced the implementation of a hospitalist-led geographic rounding pilot that began on October 1st, 2025, which was designed to allow providers to care for patients within the same inpatient unit, thereby maximizing efficiency and improving continuity of care, with the goal of decreasing hospital length of stay. The service currently spans three inpatient floors and encourages hospitalists to prioritize rounding on patients who are discharging home first, followed by those discharging to post-acute care facilities, and subsequently, all other patients remaining.  In addition, Huntsville Hospital has a robust Transitions of Care team that includes pharmacists who play an integral role in facilitating patient discharges by reviewing discharge medication reconciliation and communicating with providers to clarify medication orders as needed, as well as providing essential medication education to patients. The purpose of this research is to evaluate the outcomes of pharmacist-driven interventions within a hospitalist-led geographic rounding model focused on improving patient outcomes and coordination of care. If the results from this pilot demonstrate positive outcomes and are well received by participating rounding physicians, then the program may be expanded to additional inpatient units within the hospital.

Methodology:
This single center, Institutional Review Committee (IRC)–approved pre and post analysis was designed to evaluate the primary outcome, defined as the time from discharge order placement to patient discharge from the hospital. Secondary outcomes include hospital length of stay, total number of discharge reconciliations reviewed by the Transitions of Care pharmacy team per month, average time required to complete individual discharge interventions, and the total number of discharges classified as having significant clinical impact. Pre-implementation data was collected from the following dates: July 1st-September 30th, 2025. Post implementation data was collected from patients discharged by physicians participating in the rounding pilot between November 1st, 2025 and January 31st, 2026. Outcomes were compared between the three month pre and post implementation periods. Baseline characteristics include age, race, sex, and discharge disposition. Statistical analysis was conducted to evaluate categorical and continuous data using descriptive statistics. These analyses aim to evaluate the potential impact of the rounding pilot and pharmacist-driven discharge processes on the timeliness of hospital discharge and overall patient care outcomes.

Results:
A total of 1,201 discharges occurred during the post-implementation period, of which 418 patients (75.3%) were included in the rounding pilot with documented Transitions of Care (TOC) discharge notes. The primary outcome, the time from discharge order placement to patient discharge from facility, decreased overall in the post-implementation period. However, when stratified by discharge disposition, this time increased for home/self-care patients but not for facility discharges, which may be attributable to the higher proportion of facility discharges in the post period, requiring more complex coordination of care. Additionally, duplicate discharge orders were identified, which may have prolonged discharge timing, as these patients were not ready for discharge at the time of initial order placement. For secondary outcomes, patient length of stay did not decrease in the post-implementation period, which could be impacted by seasonal variability and differences in patient acuity between the pre- and post-implementation groups. The average time to complete TOC discharge notes and the number of interventions with significant clinical impact remained similar between groups.  

Conclusion:
Although the results from this study did not demonstrate a consistent improvement in the primary outcome across all discharge dispositions, geographic rounding can still enhance patient care through improved coordination and interdisciplinary communication. The integration of Transitions of Care pharmacists into geographic rounding supports earlier involvement in the discharge process and facilitates optimized medication reconciliation, discharge planning, and patient education.
Moderators Presenters Evaluators
Friday May 1, 2026 10:20am - 10:40am EDT
Athena G

10:20am EDT

Impact of Education on Subcutaneous Electronic Glucose Management System Usage in a Community Hospital - Makenzie Foster
Friday May 1, 2026 10:20am - 10:40am EDT
Impact of Education on Subcutaneous Electronic Glucose Management System Usage in a Community Hospital
Makenzie Foster & Taylor Riedel-Rogers

Background:
The American Diabetes Association recommends using basal/bolus insulin for the management of hyperglycemia in non-critically ill hospitalized patients.1 The incidence of hypoglycemia while on a basal/bolus insulin regimen in the hospital setting can be as high as 33%.2 A hypoglycemic event during admission has been shown to increase mortality rates, complications, and hospital length of stay.1 The use of electronic glucose management systems (eGMS) in hospitalized patients has been shown to decrease incidence of hypoglycemia compared to those managed solely by providers.3 Additionally, patients managed by eGMS were found to have a higher percentage of blood glucose levels within target range compared to traditional provider management.4 Baptist Health Lexington implemented a subcutaneous glucose management system in 2022. This study aims to assess the duration of subcutaneous eGMS use prior to and following a single session of subcutaneous eGMS education to pharmacists and nurses at Baptist Health Lexington.

Methods:
This study is an IRB-approved study where a pre-post analysis of subcutaneous eGMS duration is conducted following a single session of eGMS education. A retrospective review of patient charts will be conducted on patients who received blood glucose management through eGMS at Baptist Health Lexington prior to implementing a single session of pharmacist and nurse education from 03/01/2025 to 08/31/2025. Additionally, a retrospective review of patient charts will be conducted following the implementation of eGMS education from 10/01/2025 to 03/31/2026 for those managed by subcutaneous eGMS. The primary endpoint of this study is the duration of subcutaneous eGMS use following a single session of pharmacist and nurse eGMS education. The secondary endpoints are the number of patients transitioning from intravenous to subcutaneous eGMS, the incidence of hypoglycemic events and the total number of patients managed by subcutaneous eGMS.

Results: 
The retrospective analysis identified 101 patients in the pre-intervention group and 66 patients in the post-intervention group. Following a single session of pharmacist and nurse subcutaneous eGMS education, the duration of subcutaneous eGMS was found to be statistically significant (p-value 0.025). The incidence of hypoglycemic events was 7 out of 101 patients in the pre-intervention group and 3 out of 66 patients in the post-intervention group (p-value 0.73). The number of patients transitioning from intravenous to subcutaneous therapy was 33 out of 101 in the pre-intervention group and 19 out of 66 in the post-intervention group. 

Conclusion: 
Pharmacist and nurse subcutaneous eGMS education resulted in a statistically significant increase in the duration of subcutaneous eGMS therapy. However, a statistically significant difference was not found for the incidence of hypoglycemic events or number of patients transitioning from intravenous to subcutaneous therapy following a single session of pharmacist and nurse education. There are still opportunities for improvement in the utilization of subcutaneous eGMS at Baptist Health Lexington and further education on eGMS is currently being pursued at a system level.

References:
1. El Sayed, Nuha A., et al. “16. diabetes care in the hospital: standards of care indiabetes—2024.” Diabetes Care, vol. 47, no. Supplement_1, 11 Dec. 2023, https://doi.org/10.2337/dc24-s016.
2. Aloi, Joseph, et al. “Comparison of an electronic glycemic management system versus provider-managed subcutaneous basal bolus insulin therapy in the hospital setting.” Journal of Diabetes Science and Technology, vol. 11, no. 1, 25 Sept. 2016, pp.12–16, https://doi.org/10.1177/1932296816664746.
3. Bouldin, Mary Grace, et al. “Evaluation of the efficacy and safety of an EGLYCEMIC management system in a community hospital setting.” Journal of Diabetes Science and Technology, vol. 15, no. 2, 16 Dec. 2020, pp. 236–241, https://doi.org/10.1177/1932296820980026.

Resident Contact Information:
Makenzie Foster, PGY1 Pharmacy Resident
Email: [email protected]
Moderators Presenters
avatar for Makenzie Foster

Makenzie Foster

PGY1 Pharmacy Resident
My name is Makenzie Foster, and I am a PGY1 pharmacy resident at Baptist Health Lexington. I graduated with my Doctor of Pharmacy from the University of Kentucky College of Pharmacy in 2025, and I completed my pre-pharmacy education at the University of Kentucky in 2021. I will be... Read More →
Evaluators
avatar for Carrie Callahan

Carrie Callahan

Internal Medicine (IM) Specialist, PGY2 IM RPD, Emory University Hospital


Friday May 1, 2026 10:20am - 10:40am EDT
Athena D

10:20am EDT

Optimizing Postoperative Pain Management in Total Hip Arthroplasty with Liposomal Bupivacaine
Friday May 1, 2026 10:20am - 10:40am EDT
Primary Author: Jessica Kennedy

Co-Authors: Taylor Burich; Michael Brandon Hardison; Jeremy Walley

Title: Optimizing Postoperative Pain Management in Total Hip Arthroplasty with Liposomal Bupivacaine

Background: Total hip arthroplasty (THA) is associated with significant postoperative pain, prolonged hospitalizations, early mobilization, and increased opioid utilization.  In the United States, over 500,000 THA occur every year and can often lead to opioid over prescribing. Effective postoperative pain control is critical in THA to facilitate early mobilization, reduce opioid consumption, and support recovery. Liposomal bupivacaine is Food and Drug Administration (FDA) approved as a long-acting local and regional anesthetic. The purpose of this study is to assess liposomal bupivacaine utilization as a part of a multimodal analgesia approach to improve pain control and reduce opioid consumption following THA.

Methods: This study aims to evaluate the efficacy of liposomal bupivacaine as a part of a multimodal analgesic approach in patients undergoing THA. Data will be collected through patient interviews via a standardized questionnaire to determine opioid utilization, pain score, and time to regain mobility and sensation. Patients included in this study are those 18 years or older who underwent THA with liposomal bupivacaine utilization. Exclusion criteria will be patients receiving liposomal bupivacaine for any other indication and those with a documented hypersensitivity or allergic reaction to liposomal bupivacaine or any of its analogs. The primary objective of this study is to examine opioid requirements after surgery as well as pain scores in patients who received liposomal bupivacaine. Secondary objectives will include the time to regain mobility and sensation post-operatively, as well as cost savings from a reduction in length of stay.  

Results: The primary endpoint saw the pain scores of those who received liposomal bupivacaine 17 individuals fell within mild pain scores (0-3), and 5 within the moderate pain scores (4-6). Compared to the standard of care group who had 13,16,13 in their mild, moderate, and severe pain scores. As for opioid requirements there was change of an increase in usage within both groups, however, those who received liposomal bupivacaine required19 mg compared to standard of care which required on average 27.1 mg. As for secondary endpoints  there was no difference within the mobility and sensation as both groups were moving about every hour at a minimum. Analysis for cost is still in progress. 

Conclusion: Utilization of liposomal bupivacaine provides a multimodal approach for postoperative pain management in THA. Those individuals who received liposomal bupivacaine had a reduction in pain scores and opioid usage when compared to the standard of care. 

Moderators Presenters Evaluators
Friday May 1, 2026 10:20am - 10:40am EDT
Athena C

10:40am EDT

UNFILLED SLOT
Friday May 1, 2026 10:40am - 11:00am EDT
Friday May 1, 2026 10:40am - 11:00am EDT
Parthenon 2

10:40am EDT

UNFILLED SLOT
Friday May 1, 2026 10:40am - 11:00am EDT

Friday May 1, 2026 10:40am - 11:00am EDT
Olympia 1
  • global Y

10:40am EDT

UNFILLED SLOT
Friday May 1, 2026 10:40am - 11:00am EDT
Friday May 1, 2026 10:40am - 11:00am EDT
Olympia 2
  • global Y

10:40am EDT

UNFILLED SLOT
Friday May 1, 2026 10:40am - 11:00am EDT

Friday May 1, 2026 10:40am - 11:00am EDT
Parthenon 1
  • global Y

10:40am EDT

Resident Presentation - McKenzie Lane - Assessing the Real-World Impact of Inclisiran in an Outpatient Cardiology Clinic
Friday May 1, 2026 10:40am - 11:00am EDT
McKenzie Lane, Savannah Owen, Elizabeth Egawa, Erika McDonald, Amy Moore, Danielle Yates

Purpose: Inclisiran has demonstrated effective lipid-lowering effects when combined with statins; however, the effects of inclisiran monotherapy on low-density lipoprotein (LDL) in patients with a history of atherosclerotic cardiovascular disease have not been thoroughly evaluated in a real-world setting. Additionally, data to support that inclisiran reduces the risk of major adverse cardiac events (MACE) does not yet exist. 

Methods: In an East Tennessee cardiology clinic, 68 patients were included for evaluation of inclisiran’s lipid-lowering effects. A retrospective chart review was completed for each patient to identify several key factors, including LDL levels, documentation of MACE, and documentation of adverse effects. REDCap™ and Microsoft Excel™ were utilized as the data collection software. Statistical analysis for the primary outcome included chi square; unpaired t-test was utilized for the secondary outcome. 

Results: Forty-eight percent of patients had an LDL reduction of greater than or equal to fifty percent. The primary outcome was also evaluated in patients who were using inclisiran as monotherapy for LDL lowering, patients on high intensity statins in addition to inclisiran, and non-adherent patients, defined as at least 3 months past due for an inclisiran dose. Thirty-four patients were on inclisiran monotherapy, and fifteen of those patients achieved an LDL lowering of at least fifty percent. Nine patients were on inclisiran in addition to a high intensity statin, and five of those patients achieved an LDL lowering of at least fifty percent. Nineteen patients were non-adherent, and ten of those patients achieved an LDL lowering of at least fifty percent. Additionally, fourteen patients reached an LDL of twenty-five or less. There were three patients with documented occurrences of major adverse cardiac events and seven documented adverse events. The average reduction in LDL was forty-one percent.   

Conclusions: Approximately half of the patients evaluated met an LDL reduction of at least fifty percent. There was no statistically significant difference in the primary outcome based on the subgroups evaluated. However, patients who were on high intensity statins in addition to inclisiran were more likely to achieve very low LDL levels. Results for patients who were non-adherent were similar to the total population.
Moderators Presenters
avatar for McKenzie Lane

McKenzie Lane

PGY1 Resident, Prisma Health Blount Memorial Hospital
Evaluators
avatar for Don Tyson

Don Tyson

Director of Pharmacy, Piedmont Athens Regional Medical Center
Friday May 1, 2026 10:40am - 11:00am EDT
Athena B

10:40am EDT

Sustained Virologic Response Rates in Hepatitis C Treatment with Concomitant Acid Suppressive Therapy
Friday May 1, 2026 10:40am - 11:00am EDT
Introduction:   
Hepatitis C (HCV) remains a significant public health concern in the United States, with an estimated 2.4 million people living with chronic infection. Untreated HCV is a leading cause of chronic liver disease, and a major contributor to the development of cirrhosis, hepatic carcinoma and death. HCV management has been revolutionized by direct-acting antivirals (DAAs). Regimens such as sofosbuvir/velpatasvir (Epclusa™), glecaprevir/pibrentasvir (Mavyret™), ledipasvir/sofosbuvir (Harvoni™), and sofosbuvir/velpatasvir/voxilaprevir (Vosevi™) achieve cure rates exceeding 95%  with short, well-tolerated treatment courses.1Treatment success is assessed by sustained virologic response (SVR), assessed 4–12 weeks after therapy completion and indicated by an undetectable HCV RNA level. Treatment failure was a detectable HCV RNA during the same post-treatment assessment window. 
 
A key consideration in DAA therapy, Mavyret excluded, is their requirement for an acidic gastric pH, raising concerns for patients prescribed acid-suppressive agents such as proton-pump inhibitors (PPI) and histamine-2-receptor antagonists (H2RA). Guidelines recommend modifying PPI dose when they exceed 20 mg of omeprazole or an equivalent, as pharmacokinetic studies demonstrate reduced DAA exposure at higher doses.  H₂RAs have a less pronounced interaction, with coadministration permitted up to 40 mg twice daily of famotidine or an equivalent. Although the clinical impact is not fully established, reduced exposure may affect efficacy. PPIs remain among the most commonly prescribed medication classes in the United States, with many available over the counter, increasing the risk of unreported use and overlooked interactions. This study evaluates virologic response rates in patients treated for HCV with and without concurrent acid-suppressive therapy at Grady Memorial Hospital. 
 
 
Study Design and Methods:  
A retrospective analysis was conducted to compare SVR achievement in patients who did and did not receive acid suppressive therapy during HCV treatment. Patients were included if they are ≥18 years of age, diagnosed with HCV, completed treatment and had a documented post-treatment HCV RNA level. Patients were excluded if they had an incomplete treatment course for HCV, were lost to follow up or had no documented viral load 4-12 weeks after completion of therapy. Patients were stratified by use of acid suppressive therapy. The primary outcome was the rate of SVR achievement after treatment of HCV between groups. Secondary outcomes include differences in SVR between PPI’s including the drug and dose, differences in SVR between PPI and H2RA and differences in SVR based on cirrhosis state. Descriptive statistics were utilized for baseline characteristics, and demographic information. Chi Square test was used to analyze the rates of SVR between groups. 
Results:  
Among 736 adults who completed HCV treatment and had follow-up viral load testing, 359 (48.8%) received concomitant acid-suppressant therapy and 377 (51.2%) did not. Baseline characteristics were similar between groups. SVR rates were high overall and did not differ significantly between the two groups (96% vs 95%; p = 0.578). SVR differed by specific acid-suppressant agent (p < 0.001). Among patients receiving acid suppression, SVR was highest in those receiving omeprazole (98%) and ranitidine (98%), followed by famotidine (97%) and pantoprazole (94%). Patients receiving esomeprazole had the lowest SVR rate at 87%, corresponding to a higher proportion of treatment failures (13%) compared with other agents (2–6%). Overall, cure rates remained above 90% for all agents except esomeprazole. Patients receiving guideline-recommended acid-suppressant dosing achieved higher SVR compared with those receiving non-recommended dosing (97% vs 74%; p < 0.001). 
 
Conclusion:  
Concomitant acid-suppressant use was not associated with reduced SVR achievement, supporting current guideline recommendations that PPIs and H2RAs, when used at guideline recommended doses, can be safely continued during HCV therapy. 

Moderators Presenters Evaluators
avatar for Jessica Sterchi

Jessica Sterchi

Clinical Pharmacy Supervisor and Acute Care PGY1 RPD, BMHT1Blount Memorial HospitalPGY1
Friday May 1, 2026 10:40am - 11:00am EDT
Athena J

10:40am EDT

Evaluating Predictive Value and Stewardship of Methicillin-Resistant Staphylococcus aureus Nasal Swab in Mechanically Ventilated Trauma Patients
Friday May 1, 2026 10:40am - 11:00am EDT
Background: 
Methicillin-resistant Staphylococcus aureus (MRSA) nasal swabs are commonly used to safely discontinue empiric MRSA coverage in patients due to their high negative predictive value (NPV) of greater than 98% for MRSA infections. While MRSA nasal swabs have a high NPV, they are not well studied to guide de-escalation in mechanically ventilated patients. Limited guidance exists on de-escalation in mechanically ventilated patients prior to respiratory culture results leading to continuation of empiric antibiotics for an extended duration. This study aims to evaluate the predictive value and stewardship of MRSA nasal swabs in mechanically ventilated trauma patients with ventilator associated pneumonia (VAP). 

Methods:  
This is a single-center, retrospective prevalence study of adults admitted to the Surgical Critical Care (SCC) service with a traumatic injury who were mechanically ventilated for greater than or equal to 48 hours from January 2020 through January 2025. Patients who received a MRSA nasal swab, bronchoalveolar lavage (BAL), and empiric antibiotics for MRSA pneumonia were included in the study. The primary outcome is to establish positive predictive value (PPV), negative predictive value (NPV), sensitivity, and specificity of MRSA nasal swab results. 

Results: MRSA nasal swabs demonstrated a PPV of 58.3% (95% CI 30.4%-86.2%) while the NPV was 97.1% (95% CI 91.4%-100%), a sensitivity of 87.5% (95% CI 64.6%-100%), and a specificity of 86.8% (95% CI 76.1%-97.6%). The median turnaround time for MRSA nasal swab results was 26.4 hours (IQR 25.5,27.6), compared to 48.7 hours (IQR 44.6,64.3) for BAL culture results. 

Conclusions: This study demonstrates that MRSA nasal swabs possess a high NPV in mechanically ventilated trauma patients with VAP and the rapid turnaround time for MRSA nasal swab results compared to BAL cultures provides a clinical advantage for timely antibiotic de-escalation. 

Moderators Presenters
JS

Jessica Schuchardt

PGY2 Critical Care Pharmacy Resident, University of Tennessee Medical Center
Jessica Schuchardt, PharmD is a current PGY-2 Critical Care Pharmacy Resident at the University of Tennessee Medical Center in Knoxville, TN. Prior to residency she earned her Doctor of Pharmacy from the University of Maryland School of Pharmacy. After the completion of her PharmD... Read More →
Evaluators
avatar for Yona Roberts

Yona Roberts

RPD/Clinical Pharmacy Manager, WSGA1Wellstar Cobb HospitalPGY1
Yona Roberts earned a Doctor of Pharmacy degree from Florida Agricultural and Mechanical University in Tallahassee, Florida.  She went on to complete a Pharmacy Practice Residency through Mercer University at DeKalb Medical Center in Atlanta, Georgia.  After completion of her residency... Read More →
Friday May 1, 2026 10:40am - 11:00am EDT
Athena H

10:40am EDT

Evaluation of an Institutional Multimodal Analgesia Protocol- Kira Mike
Friday May 1, 2026 10:40am - 11:00am EDT
Purpose/Background: Previously, Huntsville Hospital implemented several multimodal analgesia order sets intended to enhance postoperative outcomes by reducing opioid utilization, leading to reduced hospital length of stay, early ambulation, and improved overall outcomes. Although initial findings were favorable, the emergence of new evidence necessitates re-evaluation of the protocol to ensure continued alignment with current best practices. This project will compare the utilization and effectiveness of the previous order sets with the development and implementation of updated order sets incorporating current literature.
Methodology: This was a single-center, Institutional Review Committee (IRC)–approved, pre–post analysis conducted at Huntsville Hospital to evaluate existing multimodal analgesia protocols. The primary objective was to reduce opioid usage by optimizing multimodal regimen. The secondary objective was to characterize utilization patterns of the order sets by order set and prescriber type. Data was reviewed for patients receiving select order sets following surgery between February 1, 2025, and August 31, 2025.
Baseline demographic variables, including sex, age, gender, and related allergies, were obtained from the electronic health record. Literature review was conducted, and associated findings was utilized to update the respective order sets.  Opioid use in morphine equivalents and length of stay will be compared between the two groups. Descriptive analyses were performed to assess adherence to the existing multimodal order set and to identify discrepancies between current practice and recommendations described in the literature.
Results: Pre-intervention data analysis demonstrated that multimodal analgesia utilization varied across specialties, with acetaminophen being the most consistently used agent. Additionally, existing order sets were not aligned with current primary literature recommendations.
Conclusion: Guided by pre-intervention data analysis and literature review, recommendations for order set modifications were developed. Post-intervention data assessing primary and secondary outcomes are currently pending.
Moderators Presenters Evaluators
avatar for Liz Oglesby

Liz Oglesby

Pharmacy Clinical Coordinator, PGY-1 Residency Program, Mobile Infirmary
Liz Oglesby, PharmD, BCPS, is the Pharmacy Clinical Coordinator and PGY-1 Residency Program Director at Mobile Infirmary in Mobile, Alabama. She obtained her doctorate of pharmacy from Auburn University in 2017 and completed PGY-1 training at Baptist Health Princeton Hospital in 2018. Her primary practice foc... Read More →
Friday May 1, 2026 10:40am - 11:00am EDT
Athena A

10:40am EDT

Evaluation of Serum Phosphate Levels in ICU Patients Undergoing Continuous Renal Replacement Therapy
Friday May 1, 2026 10:40am - 11:00am EDT

Evaluation of Serum Phosphate Levels in ICU Patients Undergoing Continuous Renal Replacement Therapy
Katherine Fonfara, Eric Pyles, Rebecca Falter
AdventHealth Orlando, Orlando, FL
Background: Severe hypophosphatemia is associated with serious adverse effects such as skeletal muscle weakness, respiratory insufficiency, cardiac rhythm disturbances, and delirium. These complications have been linked to worsening clinical outcomes including failed extubations, increased time on mechanical ventilation, and increased intensive care unit (ICU) and hospital length of stay. Patients on continuous renal replacement therapy (CRRT) are at increased risk of experiencing hypophosphatemia and the corresponding complications.

Iatrogenic hypophosphatemia represents a modifiable risk factor that may potentially improve patient outcomes. This study aims to evaluate phosphate replacement strategies in critically ill patients on CRRT and characterize incidence and severity of hypophosphatemia. 

Methods: This evaluation was a single-center, retrospective study comparing rates of hypophosphatemia in adult patients requiring CRRT and those not on CRRT admitted to the ICU at a large community hospital. Patients who were admitted to an ICU and receiving CRRT for 24 hours or more were included in the treatment group. The control group included patients admitted to an ICU and not requiring CRRT. Patients with end-stage renal disease on chronic dialysis, nocturnal CRRT/sustained low-efficiency dialysis (SLED), or with confounding metabolic conditions were excluded from either group. The primary outcome was the percentage of hypophosphatemic levels, defined as serum phosphate level less than 1.9 mg/dL. Secondary outcomes included percentage of severe hypophosphatemic levels, defined as serum phosphate level less than 1.0 mg/dL, in-hospital mortality, hospital length of stay, ICU length of stay, and time requiring mechanical ventilation. A post-hoc subgroup analysis was conducted to compare the primary outcome based on average CRRT flow rates. 

Results: A total of 100 patients were included in the study, with 50 patients included in each group. The baseline demographics were similar between both groups except home diuretic use, and baseline phosphorus and serum creatinine levels. In the control group, the median baseline phosphorus level was 3.1 mmol/L (IQR 2.6-3.8), and the median baseline serum creatinine was 1.0 mg/dL (IQR 0.8-1.2). In the CRRT group, the median baseline phosphorus level was 5.4 mmol/dL (IQR 4.2-6.4), and the median baseline serum creatinine was 2.9 mg/dL (IQR 2.2-4.1). 

Regarding the primary outcome, the CRRT group had a significantly higher median percentage of hypophosphatemic levels compared with the control group (10.8% [0-29.3] vs 0% [0], p < 0.001). For the secondary outcomes, there was no difference in the median percentage of severely hypophosphatemic levels between groups (0% [0] in both groups, p = 0.317). The median hospital length of stay was longer in the CRRT group compared with the control group (14 days [7-24.8] vs 4.5 days [3-9.5], p < 0.001). Similarly, the median ICU length of stay was longer in the CRRT group (8 days [5-14] vs 3 days [2-7], p < 0.001). The median ventilator duration was also significantly longer in the CRRT group (4 days [3-8] vs 1 day [1-2], p < 0.001). In-hospital mortality was significantly higher in the CRRT group with 62% of patients dying during admission compared with 18% in the control group (p < 0.001). In the subgroup analysis of the CRRT group, there was no difference in percentage of hypophosphatemic levels across flow rate groups (< 20 ml/kg/h, 20-25 ml/kg/h, and > 25 ml/kg/h). 

Conclusions: Patients receiving CRRT were associated with a significantly greater percentage of hypophosphatemic phosphate measurements compared with control group. The CRRT group had higher phosphate levels at baseline and was associated with increased phosphate depletion. No association was observed between CRRT dialysate flow rate and the percentage of hypophosphatemic levels. These findings support the need for close phosphorus monitoring as well as early phosphorus supplementation.




Moderators
avatar for Stephanie Lesslie

Stephanie Lesslie

PGY-2 Critical Care Residency Director, Memorial University Medical Center
Presenters Evaluators
avatar for Jonathan Alligood

Jonathan Alligood

Residency Program Director, Phoebe Putney Memorial Hospital
Friday May 1, 2026 10:40am - 11:00am EDT
Athena I

10:40am EDT

Evaluating Pharmacist Monitoring in Patients with Euglycemic Diabetic Ketoacidosis Prescribed Sodium-Glucose Cotransporter-2 inhibitors Prior to Admission
Friday May 1, 2026 10:40am - 11:00am EDT
Purpose/Background: Euglycemic diabetic ketoacidosis (EDKA) falls under the umbrella of diabetic ketoacidosis (DKA) and can occur in patients with type 1 or type 2 diabetes mellitus. EDKA is thought to be caused by a renal threshold for glucosuria that is lower due to increased gluconeogenesis and free fatty acid metabolism. A common medication class prescribed to patients with diabetes mellitus, sodium-glucose cotransporter-2 (SGLT2) inhibitors, are thought to inhibit both glucose and sodium resorption at the renal proximal tubule which leads ultimately to glucosuria and negative fluid balances. These mechanisms lead to a loss of bicarbonate and cause ketogenesis, which ultimately leads to EDKA. The purpose of this study is to evaluate the effect of pharmacy monitoring on the appropriate clinical courses in patients on sodium-glucose cotransporter-2 inhibitors who are admitted for euglycemic diabetic ketoacidosis in a regional medical center.
Methodology: Data will be collected based on a pre- and post-evaluation of the electronic medical record. Prospective data collection will be done through a daily report of patients that are greater than or equal to 18 years old, admitted to CaroMont Regional Medical center, have an SGLT2 inhibitor on their prior to admission medication list, and have a diagnosis of diabetes on their hospital problem list. Patients will be excluded if they are less than 18 years old, have no diagnosis of diabetes mellitus, have a glucose on admission that is > 250 mg/dL, are pregnant or incarcerated. Once the daily report is run, the clinical pharmacist will ensure the correct lab values and medications are ordered. If a patient meets EDKA criteria, a clinical pharmacist will evaluate the need for additional evaluation, including β-hydroxybutyrate, to strengthen diagnostic criteria and guide potential treatment. Retrospective data collection will be done through the collection of pre-specified criteria and analysis of the treatment course in patients that presented with EDKA. Both data sets will be taken from the same months, one year apart. The data sets will be compared to assess the effectiveness of pharmacy interventions. The primary endpoint of the study will be the time to resolution of euglycemic diabetic ketoacidosis. Time to insulin infusion, length of stay, number of admissions, and number of clinical pharmacist interventions will also be assessed.  
Results: Pending 
Conclusions: Pending
Presentation Objective: To describe the benefit of pharmacy interventions in the treatment course of patients that present with euglycemic diabetic ketoacidosis secondary to receiving sodium-glucose cotransporter-2 inhibitors for management of their diabetes prior to admission.  
Self-Assessment: What are the criteria for a diagnosis of euglycemic diabetic ketoacidosis?
Authors: Rylee Williams, Joe Norton, Joanna Nixon
Moderators Presenters
avatar for Rylee Williams

Rylee Williams

PGY-1 Resident, CaroMont Regional Medical Center
Evaluators
avatar for Carrie Callahan

Carrie Callahan

Internal Medicine (IM) Specialist, PGY2 IM RPD, Emory University Hospital


Friday May 1, 2026 10:40am - 11:00am EDT
Athena D

10:40am EDT

Evaluation of Prophylactic Anticoagulation usage within the Central Alabama Veterans Health Care System Inpatient Setting
Friday May 1, 2026 10:40am - 11:00am EDT
Primary Author: Charles Pitts
Co-Authors: Hope Allen, Brittany Till, Morgan Moulton, Perry Thompson, Walter Minger, Tiffany Lyght

Background: Venous thromboembolism (VTE) is a common cardiovascular diagnosis, with many cases linked to recent hospitalizations. Prophylactic anticoagulation is used to prevent VTE, guided by patient risk factors. Risk Assessment Models (RAMs), such as the Padua VTE RAM, help determine when VTE prophylaxis is appropriate or should be avoided due to bleed risk, as recommended by the American Society of Hematology. This project was designed to evaluate the current utilization of prophylactic anticoagulation using the Padua VTE RAM to determine its appropriateness in patients admitted to the inpatient setting. According to the Padua RAM, scores of 4 or more are indicative of high VTE risk and should receive anticoagulation.

Methods: This project was a retrospective, observational review of Veterans' charts who received prophylactic anticoagulation in the inpatient setting within the Central Alabama Veterans Health Care System (CAVHCS). Data collected included Veteran demographics, active prescriptions, ICD codes, recent surgeries, age, body mass index (BMI), birth sex, kidney function, presence of a central venous catheter, critical care admissions, liver function tests, platelet counts, and recent bleeding events. The data was compiled in a de-identified Microsoft Excel spreadsheet for analysis. The primary outcome assessed was the percentage of Veterans appropriately placed on prophylactic anticoagulation based on inclusion/exclusion criteria. Secondary outcomes included the number of admitted Veterans receiving prophylactic anticoagulation who experienced bleeding-related events and thrombosis-related events.

Results: One hundred Veteran charts were evaluated for this project. Of the evaluated charts, prophylactic anticoagulation was appropriately administered or withheld in 53 Veterans and prophylactic anticoagulation was inappropriately administered or withheld in 47 Veterans based on their individual Padua RAM scores. Of the 47 Veterans, 45 received inappropriate prophylactic anticoagulation and two Veterans had prophylactic anticoagulation withheld inappropriately. None of the Veterans evaluated experienced bleed or thrombosis-related events.

Conclusions: Nearly 50% of Veterans reviewed had anticoagulation inappropriately administered or withheld while admitted. While this evaluation did not find any bleed or thrombosis-related events, the current anticoagulation prescribing trends leave room for improvement. The creation of a policy to standardize the criteria for VTE prophylaxis could increase appropriate anticoagulation prescribing patterns within the CAVHCS inpatient setting. This project also exposes an area of Veteran healthcare that Clinical Pharmacy Practitioners could assist in optimizing and monitoring.
Moderators Presenters
avatar for Charles Pitts

Charles Pitts

PGY1 Pharmacy Resident, Central Alabama Veterans Healthcare System
Charlie Pitts is currently a PGY1 pharmacy resident with the Central Alabama Veterans Healthcare System in Montgomery, Alabama. He is originally from Hopkinsville, Kentucky, but has been a resident of Alabama since starting pharmacy school at the Samford University McWhorter School... Read More →
Evaluators
Friday May 1, 2026 10:40am - 11:00am EDT
Athena C

10:40am EDT

Evaluation of the Impact of Lower Extremity Wound Order Set Revision
Friday May 1, 2026 10:40am - 11:00am EDT
Title: Evaluation of the impact of lower extremity wound order set revision

Authors: Katie Hindman, Adesuwa Utomwen, Dustin Zeigler, Jeremy Frens

Objective: Discuss the utilization of an updated lower extremity wound order set

Self-Assessment Question: 
  • True or False: The updated lower extremity wound order set had numerically increased adherence compared to the prior order set.

Background: Diabetic foot infections (DFIs) pose a significant threat to quality of life, being a leading cause of non-traumatic lower extremity amputations. Therefore, it is essential to utilize effective antibiotics to treat these infections. The International Working Group on the Diabetic Foot (IWGDF) and Infectious Diseases Society of America (IDSA) published updated guidelines in 2023, advising that empiric coverage for Pseudomonas aeruginosa is not necessary in Western countries and temperate climates. A prior systematic review on the epidemiology of P. aeruginosa in DFIs found a global prevalence of 16.6%, with the lowest prevalence of 11.1% being in Western countries. A review of patients at our institution, Cone Health, with toe and/or foot amputation(s), supported these findings with only 1.7% of cultures identifying P. aeruginosa. The most isolated pathogens were Staphylococcus aureus and coagulase-negative Staphylococcus species. The lower extremity wound order set at Cone Health was modified, removing empiric P. aeruginosa coverage due to its low incidence. The purpose of this study is to evaluate prescriber compliance with the updated order set and assess microbiological concordance between prescribed empiric therapy and cultured pathogens following the modifications.

Methods: This was an IRB approved, determined exempt, retrospective cohort analysis of individuals with diabetic foot infections at a single health system encompassing four community hospitals. The revised order set went live in February 2025. The review spanned a pre-intervention cohort from June to December 2024 and a post-intervention cohort from June to November 2025. Adults aged 18 years or older with confirmed DFI with or without osteomyelitis were included in this study. Those individuals admitted to the intensive care unit or with the presence of chronic foot ulceration were excluded. Infection-related information collected included wound classification, utilization of order set, inpatient antibiotics utilized, duration of antibiotics, type of amputation, culture results, pathology results and discharge antibiotics. The primary outcome of this study is adherence to order set recommendations, defined as aligning with the antibiotic recommendations per infection severity. Secondary outcomes include proportion of patients with microbiological match to empiric antibiotics, 30-day mortality rate and 30-day readmission rate.

Results: The post-intervention cohort demonstrated a modest increase in adherence to lower extremity wound order set recommendations compared to the pre-intervention cohort (34% vs 30%, p=0.55). Among patients with available culture data, all 17 individuals in the pre-intervention cohort received empiric antibiotics concordant with culture results compared to 26 of 30 patients (87%) in the post-cohort (p=0.075). Streptococcus species were the most commonly isolated gram-positive organisms in both cohorts (10 cases in the pre-cohort and 11 in the post-cohort). There was a higher prevalence of Proteus mirabilis and Enterobacter cloacae in the post-cohort, but these organisms demonstrated minimal resistance to penicillins and cephalosporins. The use of vancomycin and cefepime decreased from the pre- to post-intervention period, while utilization of linezolid and ampicillin/sulbactam increased.

Conclusion: The revised lower extremity wound order set was associated with a numerically higher rate of adherence compared to the prior version, with approximately half of providers in each cohort utilizing the order set. Empiric antibiotics demonstrated microbiological match in most cases. The organisms cultured in this study align with those typically observed in DFIs in the United States. The updated order set represents an advancement in antimicrobial stewardship in DFIs through the inclusion of preferred alternatives. Limitations of this study include variability in obtainment of pathology and cultures between providers as well as a small sample size. Future directions include reinforcing appropriate utilization of the DFI order set and evaluating discharge antibiotic therapy to assess the potential benefit of creating standardized recommendations.
Moderators Presenters
avatar for Katie Hindman

Katie Hindman

PGY1 Acute Care Pharmacy Resident
I am a PGY1 Acute Care Pharmacy Resident at Moses Cone Hospital in Greensboro, NC. I went to the University of South Carolina College of Pharmacy in Columbia, SC. I am excited to be staying at Cone Health to complete a PGY2 Infectious Diseases Pharmacy Residency next year!
Evaluators
Friday May 1, 2026 10:40am - 11:00am EDT
Athena G

11:00am EDT

UNFILLED SLOT
Friday May 1, 2026 11:00am - 11:20am EDT
Friday May 1, 2026 11:00am - 11:20am EDT
Parthenon 2
  • global Y

11:00am EDT

UNFILLED SLOT
Friday May 1, 2026 11:00am - 11:20am EDT

Friday May 1, 2026 11:00am - 11:20am EDT
Olympia 1
  • global Y

11:00am EDT

UNFILLED SLOT
Friday May 1, 2026 11:00am - 11:20am EDT
Friday May 1, 2026 11:00am - 11:20am EDT
Olympia 2
  • global Y

11:00am EDT

UNFILLED SLOT
Friday May 1, 2026 11:00am - 11:20am EDT

Friday May 1, 2026 11:00am - 11:20am EDT
Parthenon 1
  • global Y

11:00am EDT

Optimizing Shingrix Immunization in Veterans on Immunosuppressive Therapy
Friday May 1, 2026 11:00am - 11:20am EDT
Background & Purpose:
Herpes zoster, commonly known as shingles, results from reactivation of latent varicella zoster virus and is associated with substantial morbidity, particularly among older adults and immunocompromised populations. Veterans receiving immunosuppressive therapy are at increased risk for severe disease, including postherpetic neuralgia and hospitalization. The recombinant herpes zoster vaccine (Shingrix) is a non-live, adjuvanted vaccine with efficacy exceeding 90% and is recommended for adults aged ≥50 years and immunocompromised adults aged ≥19 years. Despite these recommendations, vaccination rates among immunocompromised Veterans remain suboptimal. Within the Veterans Health Administration, Shingrix administration requires provider ordering and coordination of nurse clinic visits, which may introduce logistical barriers and contribute to delayed vaccination or incomplete series. Pharmacist-led interventions that incorporate patient education and care coordination may improve vaccine uptake by addressing hesitancy and streamlining the vaccination process.

Methods:
A pharmacist-led telephone intervention was conducted at the Ralph H. Johnson Veterans Affairs Health Care System in Charleston, South Carolina. Veterans prescribed immunosuppressive therapy who lacked one or both doses of the recombinant zoster vaccine were identified using a National VA Rheumatology Immunization Population Management Tool. Eligible patients were those enrolled in specialty clinics and prescribed a biologic, conventional synthetic, or targeted synthetic disease-modifying antirheumatic drug or systemic glucocorticoid. A random sample of 100 patients was selected. A PGY1 pharmacy resident conducted structured telephone outreach using motivational interviewing techniques to assess vaccine acceptance, explore concerns, and provide tailored education regarding shingles risk and vaccine safety. For patients who agreed to vaccination, orders for Shingrix and nurse clinic appointment were placed for one or both doses, if applicable. Vaccination outcomes and documented reasons for acceptance or refusal were tracked through the electronic medical record.

Results:
Sixty-six of 100 patients contacted agreed to receive Shingrix following pharmacist intervention, 30 declined, and 4 were previously vaccinated without documentation. Thirty-nine patients (59.1%) completed the vaccination series during the project period. Completion rates were higher among patients requiring one dose compared to two doses (72.2% vs 54.2%, p = 0.18). No significant differences in completion were observed by sex or ethnicity. Among patients who did not complete vaccination, over half were due to appointment-related barriers, including cancelled visits or failure to schedule.
Vaccine acceptance was most commonly associated with improved awareness, perceived benefit and risk reduction, and provider engagement that addressed questions, misinformation, and resolved logistical barriers. Patients frequently cited increased understanding of the need to complete the two-dose series and elevated herpes zoster risk in the setting of immunosuppressive therapy as key drivers of acceptance. Reasons for vaccine decline included vaccine hesitancy, low perceived risk, desire for additional time, information, or provider input, and scheduling barriers.

Conclusion:
Pharmacist-led outreach improved willingness to receive Shingrix among immunocompromised Veterans; however, series completion remained variable and was frequently impacted by logistical barriers. These findings highlight the importance of coordinated workflows and multidisciplinary collaboration to support vaccination beyond initial patient agreement. Addressing patient-specific concerns and streamlining scheduling processes can improve vaccine uptake and series completion while reinforcing the pharmacist’s role in vaccine stewardship.
Moderators Presenters
avatar for Taylor Boothe

Taylor Boothe

PGY1 Pharmacy Resident, Ralph H. Johnson VA Healthcare System
Evaluators
avatar for Liz Oglesby

Liz Oglesby

Pharmacy Clinical Coordinator, PGY-1 Residency Program, Mobile Infirmary
Liz Oglesby, PharmD, BCPS, is the Pharmacy Clinical Coordinator and PGY-1 Residency Program Director at Mobile Infirmary in Mobile, Alabama. She obtained her doctorate of pharmacy from Auburn University in 2017 and completed PGY-1 training at Baptist Health Princeton Hospital in 2018. Her primary practice foc... Read More →
Friday May 1, 2026 11:00am - 11:20am EDT
Athena A

11:00am EDT

Similar but not the Same: Patient Reported Outcomes when Switching to Biosimilar Adalimumab - Hayleigh Hallam
Friday May 1, 2026 11:00am - 11:20am EDT
Background: Adalimumab was one of the first monoclonal antibodies to have biosimilar agents commercially available. With its extensive list of indications, the market for adalimumab biosimilars has grown rapidly, and ten products have approved interchangeability in the United States. While the definition for biologic interchangeability includes demonstrated efficacy, safety, and immunogenicity comparable to the reference product, biosimilars can contain different inactive ingredients, preservatives, and administration types. These characteristics led to the development of studies exploring potential discrepancies in the efficacy and safety of adalimumab biosimilars as measured via validated tools by disease-state. Most concluded that there are no significant differences between clinical outcomes with the use of an adalimumab biosimilar compared to the reference product. Despite these findings, there are incidences of patients reporting differences in practice. This study will aim to identify patient-reported differences in efficacy and adverse effects related to switching from the adalimumab reference product (Humira®) to a biosimilar agent.

Methods: This study used a unique retrospective-prospective design of patients followed by Prisma Health Specialty Pharmacy on adalimumab for an FDA approved use. First, a retrospective chart review was conducted of patients from January 2024 through September 2025 who received at least 3 months of Humira® and at least one month of a biosimilar. Patients who discontinued adalimumab for any reason before adequate trials were completed or filled with another pharmacy were excluded. Patients meeting these criteria had their upcoming refill phone calls flagged for survey participation. At the end of this workflow completion, patients were asked if they would like to participate in a survey related to their experience with switching to an adalimumab biosimilar. This featured 10 multiple-choice questions using Likert-scale responses to achieve validity, and patients could decline any response at any time. Primary endpoints of this study included perceived efficacy and safety of Humira® and biosimilar as documented in the patient chart and obtained via patient survey. Secondary endpoints were differences between the former, including between biosimilar agents.

Results: A total of 324 patient charts were screened, and 46 patients met inclusion criteria. Patients with rheumatoid or psoriatic arthritis made up 58.7% of the study population. A majority of patients (95.7%) were transitioned to an adalimumab biosimilar due to a non-medical, insurance-mandated switch. Most patients were changed to adalimumab-adaz (Hyrimoz®; 60.9%) or adalimumab-adbm (Cyltezo®; 28.3%).

A majority of patients completed the survey (71.7%), and most were still on an adalimumab product (75.8%). At baseline, many patients thought that Humira® worked above average (27.3%) or excellent (54.6%), and almost two-thirds of patients claimed it worked better than the biosimilar. Of these patients, those who completely agreed (30.3%) were generally on Hyrimoz® (90%), and those who mostly agreed (30.3%) were generally on Cyltezo® (70%). After switching to the biosimilar, around half (48.5%) of patients experienced a delay in symptom management, which included active disease flares.

Per patient chart review, there were minimal differences in side effects reported with both Humira® and the biosimilar products (9.9% and 6.5%, respectively). This was similar in the patient survey; however, side effects were reported more frequently, occurring in 27.4% of patients in each group. The most common side effect experienced was injection site reactions. If given the chance, 61% of patients said they would switch back to Humira® from their biosimilar.

Conclusions: There are considerable patient-perceived differences in efficacy but minimal differences in safety experienced when switching from Humira® to a biosimilar. While most patients prefer Humira®, their switch is typically mandated by insurance. Support from pharmacists and other healthcare team members is imperative to try and keep patients on an efficacious biologic regimen.
Moderators Presenters
avatar for Hayleigh Hallam

Hayleigh Hallam

PGY1 Pharmacy Resident, Ambulatory Care, Prisma Health-Upstate
Hayleigh Hallam, PharmD is a current PGY1 Ambulatory Care Resident at Prisma Health-Upstate in Greenville, SC. Originally from Marietta, GA, she obtained a bachelor's degree in biomedical sciences and a minor in Leadership Studies from Auburn University before going on to complete... Read More →
Evaluators
avatar for Don Tyson

Don Tyson

Director of Pharmacy, Piedmont Athens Regional Medical Center
Friday May 1, 2026 11:00am - 11:20am EDT
Athena B

11:00am EDT

Impact of hydrocortisone weaning on the duration of septic shock
Friday May 1, 2026 11:00am - 11:20am EDT
Background:
Sepsis is a life-threatening condition caused by a dysregulated host response to infection, and septic shock represents its most severe form, carrying a high mortality risk. Intravenous (IV) hydrocortisone is recommended by the Surviving Sepsis Guidelines for patients requiring ongoing vasopressor support despite adequate fluid resuscitation. However, the optimal discontinuation strategy remains unclear as current guidelines do not specify whether hydrocortisone should be tapered or abruptly discontinued. Existing literature is limited and conflicting, and practice variability persists. This study evaluates the impact of hydrocortisone tapering versus abrupt discontinuation on recurrence of septic shock.
Methods:
This single-center, retrospective cohort study was conducted at Atrium Health Wake Forest Baptist Medical Center. Adult patients admitted to the Medical Intensive Care Unit (ICU) between September 2024 and August 2025 who received ≥ 8 doses or ≥48 hours of IV hydrocortisone for septic shock were included. Patients were categorized into two groups: taper (any dose reduction prior to discontinuation) or no taper (abrupt discontinuation). Resolution of shock was defined as maintaining a mean arterial pressure ≥65 mmHg without vasopressor support for ≥12 hours.
The primary outcome was recurrence of septic shock, defined as vasopressor reinitiation within 72 hours or escalation in vasopressor or hydrocortisone therapy. Secondary outcomes included duration of vasopressor therapy, ICU length of stay, hospital length of stay, and incidence of hyperglycemia (≥180 mg/dL). Continuous variables were analyzed using Wilcoxon rank-sum tests, and categorical variables using chi-square or Fisher’s exact tests, as appropriate.
Results:
A total of 43 patients were included (no taper n=30; taper n=13). Baseline characteristics were similar between groups, with no statistically significant differences in age, sex, vasopressor requirements, or severity markers.
Recurrence of septic shock occurred in 30% of the no-taper group and 38% of the taper group (p=0.7), demonstrating no statistically significant difference between strategies. Median duration of vasopressor therapy was similar (136 hours vs 123 hours; p=0.6).
There were no significant differences in secondary outcomes, including ICU length of stay (8 vs 7 days; p>0.9), hospital length of stay (18 vs 16 days; p=0.8), or incidence of hyperglycemia (70% vs 69%; p>0.9).
Conclusions:
In this retrospective cohort study, tapering of hydrocortisone did not reduce the recurrence of septic shock compared to abrupt discontinuation. No differences were observed in vasopressor duration, length of stay, or hyperglycemia. These findings suggest that routine tapering of hydrocortisone may not provide clinical benefit in this population. Prospective studies are warranted to confirm these findings and inform guideline recommendations.
Moderators
avatar for Stephanie Lesslie

Stephanie Lesslie

PGY-2 Critical Care Residency Director, Memorial University Medical Center
Presenters
avatar for Riley Montague

Riley Montague

PGY1 Pharmacy Resident, Atrium Health Wake Forest Baptist Medical Center
Hello, my name is Riley Montague. I am originally from a very small rural town in North Western Kentucky. I completed my PhamD degree at the University of Kentucky College of Pharmacy in Lexington, Kentucky. I am currently a PGY1 pharmacy resident at Atrium Health Wake Forest Baptist... Read More →
Evaluators
avatar for Jonathan Alligood

Jonathan Alligood

Residency Program Director, Phoebe Putney Memorial Hospital
Friday May 1, 2026 11:00am - 11:20am EDT
Athena I

11:00am EDT

Incidence of Chronic Opioid Use Post-Surgical Exposure in Opiate Naïve Patients
Friday May 1, 2026 11:00am - 11:20am EDT
  • Title: Incidence of Chronic Opioid Use Post-Surgical Exposure in Opiate Naïve Patients 
  • Authors: Rachel Peña, PharmD, Caitlin Thomas, PharmD, BCCCP, James Neilen, PharmD
  • Objective: The purpose of this study was to evaluate the association between discharge opioid supply ( ≤3 days vs ≥7 days) and the development of chronic opioid use in opioid naive post-surgical patients. 
  • Background: Opioids are used as an effective treatment for post-operative management, trauma, or chronic pain, but can be limited by their side effects and undesirable dependence if dosed improperly or lead to recreational misuse. Current literature states that by limiting opioid supply to 3 or fewer days post-operatively after discharge, there are fewer conversions to long term opioid users among opioid naïve patients.  Evaluating similar opioid prescribing practices as in the literature may help to inform safer prescribing practices at our institution.  
  • Methods: A single center retrospective study was performed in a large acute care community teaching hospital from January 1, 2024 through December 31, 2025. Patients were identified between January 1, 2024 to December 31, 2024, with follow up Prescription Drug Monitoring Program (PDMP) data collected for up to one year post discharge through December 31, 2025 to track prescription opioid fills.  Adults admitted to the hospital who underwent surgery and were opiate naïve (defined  as patients who have not filled an opioid prescription in the previous 6 months prior to surgery) were included in the study. Patients were excluded if they had a history of substance abuse, had cancer or chronic pain, had a cardiac, spinal, or oncological related surgery, and if they underwent another surgery within the 1-year study period after the initial surgery. Patients who were discharged with an opioid supply of 3 days or less were compared to patients discharged with an opioid supply of 7 days or more. Chronic opioid use was defined as having filled 10 or more prescriptions or 90 days of continuous use within a 1-year period after surgery. The primary endpoint was the incidence of new, persistent opioid use defined as more than 10 opioid prescription fills or more than 90 days of continuous use. Secondary endpoints included the types of opioids prescribed, inpatient and outpatient MME (daily and total), type of surgery, 3-month, 6-month, and 1 year prescription fill quantities post discharge.  
  • Results: Of the 676 patients screened, a total of 332 patients (281 in comparator group, 51 in study group) met inclusion criteria. Of this population, 229 (69%) were male, the average hospital length of stay was 3.31 days, the average opioid supply in days on discharge was 7.02, average morphine milligram equivalent (MME) for discharge opioid supply was 35.56. The most prescribed opioid on discharge was oxycodone 5 mg immediate release tablet (42.2%) and most common surgery type among the population was cesarean section (26.5%). Of the 332 patients, 4 (1.2%) filled more than 10 opioid prescriptions within 1 year after discharge, and 4 (1.2%) had more than 90 days of continuous use of opioids within 1 year after discharge. Of the patients who filled more than 10 opioid prescriptions and had more than 90 days of continuous use of opioids, all 4 of the patients were from the comparator group that had been discharged with 3 days or less supply of opioid upon discharge (P=1.000) . None of the patients in the study group filled more than 10 opioid prescriptions or had more than 90 days of continuous opioid use after discharge. The average number of fills at 3 months after discharge was 1.09, at 6 months was 1.18, and after 1 year was 1.36. 
  • Conclusion: Patients who were prescribed ≥ 3 days of opioids post-operatively at discharge did not have an increase in long term usage of opioids after 1 year.  

Moderators Presenters Evaluators
avatar for Jessica Sterchi

Jessica Sterchi

Clinical Pharmacy Supervisor and Acute Care PGY1 RPD, BMHT1Blount Memorial HospitalPGY1
Friday May 1, 2026 11:00am - 11:20am EDT
Athena J

11:00am EDT

Evaluating the Impact of Provider Education on Empiric Antibiotic Use for Low-Risk Intra-abdominal Infections at a Community Hospital​
Friday May 1, 2026 11:00am - 11:20am EDT
Background: 
  • Intra-abdominal infections (IAIs) are a frequent cause of hospitalization which occasionally require empiric broad-spectrum antibiotic use. Despite current guidelines indicating that P. aeruginosa is uncommon in low-risk, community-acquired IAI, antipseudomonal agents remain frequently prescribed. This unnecessary use increases risks of nephrotoxicity, resistance, and higher healthcare costs.2 For low-risk patients without significant comorbidities, healthcare exposure, or septic shock, narrower regimens are recommended.1 Persistent inappropriate prescribing highlights an opportunity for targeted antimicrobial stewardship interventions to optimize empiric therapy, improve patient outcomes, and reduce unnecessary broad-spectrum exposure. 
Objectives: 
  • Evaluate the impact of pharmacy-led provider education on reducing inappropriate antipseudomonal antibiotic use in patients with low-risk intra-abdominal infections 
  • Primary outcome: Percentage difference of patients receiving antipseudomonal antibiotics before and after the intervention 
  • Secondary outcomes: Days of therapy (DOT) per 1,000 patient days, hospital length of stay, incidence of C. difficile infection, and identification of P. aeruginosa on culture during hospitalization, impact of infectious disease (ID consult) on de-escalation 
Methods: 
  • Retrospective chart review approved by the local Institutional Review Board (IRB) 
  • Chart review to evaluate empiric antibiotic use in adult patients with low-risk intra-abdominal infections (IAIs), as defined by the 2024 Surgical Infection Society guidelines. 
  • During the pre-intervention period between May 1st, 2025 and September 30th, 2025, patients are assessed for documented infection diagnosis and empiric antibiotic selection to determine the frequency of antipseudomonal antibiotic use. Data gathered from this review is used to develop an educational presentation for hospitalist providers to highlight recommended therapy for low-risk IAI. 
  • A post-intervention chart review between November 1st, 2025 and March 30th,  2026 will be performed to reassess prescribing practices 
  • Inclusion criteria 
  • Age ≥18 
  • Admitted to Baptist Health Lexington with primary diagnosis of diverticulitis, peritonitis, cholecystitis, cholangitis, pancreatitis, or appendicitis 
  • Received antimicrobial therapy 
  • Exclusion criteria 
  • Pregnant or incarceration. Met criteria for high-risk infection (admitted to ICU during hospital stay, required surgical intervention, received IV antibiotics in previous 90 days, recent Pseudomonas culture, immunocompromised, post-operative infection or inadequate source control, age ≥ 80) 
Results: 
  • Baseline characteristics were similar between pre- and post-intervention groups, with diverticulitis most common. The educational intervention did not significantly reduce inappropriate antipseudomonal use, which remained high. A numerical decrease in overall antimicrobial exposure was observed but was not statistically significant. No C. difficile testing or P. aeruginosa cultures were identified. Antimicrobial use shifted overall, driven by reduced ertapenem use, while other broad-spectrum agents remained common. Infectious disease consultation was associated with higher rates of de-escalation. 
Conclusions: 
  • Provider education alone did not significantly reduce inappropriate antipseudomonal use in low-risk IAI. Persistent broad-spectrum prescribing suggests the need for more active stewardship strategies. The absence of P. aeruginosa supports guideline recommendations, and the impact of ID consultation highlights the value of multidisciplinary involvement. 
References 
  1. The Surgical Infection Society Guidelines on the Management of Intra-Abdominal Infection: 2024 Update Jared M. Huston, Philip S. Barie, E. Patchen Dellinger, Joseph D. Forrester, Therese M. Duane, Jeffrey M. Tessier, Robert G. Sawyer, Miguel A. Cainzos, Kemal Rasa, Jeffrey G. Chipman, Lillian S. Kao, Frederic M. Pieracci, Kristin P. Colling, Daithi S. Heffernan, Janice Lester, and Therapeutics and Guidelines Committee  
  1. Lodise TP, Izmailyan S, Olesky M, Lawrence K. An Evaluation of Treatment Patterns and Associated Outcomes Among Adult Hospitalized Patients With Lower-Risk Community-Acquired Complicated Intra-abdominal Infections: How Often Are Expert Guidelines Followed? Open Forum Infect Dis. 2020 Jun 19;7(7):ofaa237. doi: 10.1093/ofid/ofaa237. PMID: 32676511; PMCID: PMC7353956. 



Moderators Presenters
avatar for Taylor Walker

Taylor Walker

Pharmacy Resident, Baptist Health Lexington
Taylor Walker is a current PGY1 resident at Baptist Health Lexington (BHL) in Lexington, Kentucky. Taylor graduated from the University of Kentucky College of Pharmacy with her PharmD in 2025. After residency, Taylor plans to continue her pharmacy career as a clinical staff pharmacist... Read More →
Evaluators
Friday May 1, 2026 11:00am - 11:20am EDT
Athena G

11:00am EDT

Evaluating Vancomycin AUC Monitoring in Adult Cystic Fibrosis Patients
Friday May 1, 2026 11:00am - 11:20am EDT
Title 
Evaluating Vancomycin AUC Monitoring in Adult Cystic Fibrosis Patients 
 
Authors 
Taylor J. Merritt, Carrie Tilton Callahan, Kelly Soyeong Ko, Cynthia Shin-Yee Tsai, Heidi King Berman, Nicole L. Metzger  
 
Practice Site 
Emory University Hospital 
 
Objective  
Audience members will be able to evaluate the impact of AUC-based vancomycin monitoring on therapeutic target attainment and safety outcomes compared with traditional trough-based monitoring in adult patients with cystic fibrosis (CF)  
 
Background  
Area under the curve (AUC)–based vancomycin monitoring is recommended to improve efficacy and reduce nephrotoxicity. However, evidence supporting its use in adult people with cystic fibrosis (PwCF) remains limited.  
 
Methods  
This single-center, retrospective observational study included hospitalized adults with CF who received intravenous vancomycin and at least one appropriately drawn vancomycin level. Patients were excluded if they were pediatric, pregnant, incarcerated, had unstable renal function, or did not have vancomycin for > 48 hours. Encounters were grouped based on strategy: AUC or trough-based monitoring. Therapeutic targets were defined as: AUC of 400–600 mg·hr/L or trough of 15–20 mg/dL. Primary outcome was the proportion of encounters achieving therapeutic targets at first appropriate level. Secondary outcomes included time to therapeutic target attainment, number of regimen adjustments, length of hospital stay, and incidence of acute kidney injury. An exploratory analysis was conducted by reclassifying patients in the trough-based group who met institutional AUC-dosing criteria and assessing whether therapeutic targets would have been achieved when using an institutional AUC calculator.   
 
Results  
A total of 43 encounters representing 27 patients met inclusion criteria, with 16 encounters in the AUC-based group and 27 in the trough-based group. Therapeutic exposure targets at first level draw were achieved in 37.5% of AUC-monitored encounters compared to 14.8% of trough-monitored (p-value 0.14). Mean time to therapeutic target attainment was similar between groups, and no cases of acute kidney injury occurred in the AUC group compared to 7.4% in the trough-based group. Length of hospital stay and number of vancomycin levels collected were comparable between strategies. In the exploratory analysis, patients regrouped from trough to AUC demonstrated 48.3% therapeutic targets at initial draw compared to 0% in the trough-based group. 
 
Conclusions  
AUC-based vancomycin monitoring did not demonstrate a statistically significant improvement over trough-based monitoring in adults with cystic fibrosis; however, a trend toward improved therapeutic target attainment and no increase in nephrotoxicity was observed. These findings support consideration of AUC-based monitoring in this population and add to the limited data available for adult patients with cystic fibrosis. 
 
Self-Assessment Question 
Which statement best reflects the findings from this study?  
A) AUC-based monitoring significantly reduced AKI in PwCF   
B) AUC-based monitoring significantly improved target attainment   
C) Trough-based monitoring resulted in fewer regimen changes   
D) AUC-based monitoring demonstrated a trend toward improved target attainment without increasing AKI 
 
 
Contact Email 
[email protected] 

Moderators Presenters
avatar for Taylor Merritt

Taylor Merritt

PGY2 Internal Medicine Pharmacy Resident, Emory University Hospital
Dr. Taylor Merritt is from West Green, Georgia. She received her Bachelor of Science in Pharmaceutical Sciences and Doctor of Pharmacy degrees from Mercer University College of Pharmacy in Atlanta, Georgia. She is currently a PGY2 Internal Medicine Pharmacy Resident at Emory University... Read More →
Evaluators
avatar for Carrie Callahan

Carrie Callahan

Internal Medicine (IM) Specialist, PGY2 IM RPD, Emory University Hospital


Friday May 1, 2026 11:00am - 11:20am EDT
Athena D

11:00am EDT

Impact of a Pharmacist-Led IV Iron Referral Pathway on Outpatient Referrals and IV Iron Administration - Vanna Labi
Friday May 1, 2026 11:00am - 11:20am EDT
Background: Intravenous (IV) iron is an effective therapy for iron deficiency anemia, and growing evidence supports outpatient administration when clinically appropriate. Despite this, hospitalized patients frequently receive IV iron without a standardized process to ensure therapy completion after discharge. To address this gap, the adult iron replacement order set was updated to better facilitate ambulatory infusion referrals and incorporate a pharmacist consult. The consult prompts inpatient clinical pharmacists to review indication for IV iron with the ordering provider and determine whether remaining doses can be safely administered in the outpatient setting or if additional inpatient doses are medically necessary. The purpose of this study was to evaluate the impact of these order set changes on outpatient IV iron referral rates. 

Methods: This multi-center, IRB-reviewed determined exempt, retrospective cohort study evaluated adult patients receiving IV iron across four Cone Health hospitals and affiliated outpatient infusion centers. Patients with IV iron orders placed through the inpatient infusion order set during the study period were included. The primary outcome was the proportion of hospitalized patients receiving IV iron who were referred for outpatient infusion. Chi-square test was utilized to compare pre-intervention (September 17, 2024–May 12, 2025) and post-intervention (May 13, 2025–October 31, 2025) cohorts for the primary outcome. Secondary outcomes included the proportion of referred patients who received at least one outpatient IV iron dose, the proportion who completed their planned outpatient IV iron treatment course, median time from discharge to first outpatient IV iron administration, median time from discharge to first outreach for infusion scheduling, and reasons for incomplete outpatient IV iron treatment among referred patients. Descriptive statistics were used to summarize baseline characteristics. 

Results: Data on 201 patients were collected from both the pre- and postimplementation phases. During the pre-intervention period, 1,430 hospitalized patients received inpatient IV iron, with 36 patients (2.5%) referred for outpatient infusion. In the post-intervention period, 1,131 hospitalized patients received inpatient IV iron, and 168 patients (14.6%) were referred for outpatient infusion (p < 0.001).  Among referred patients, 31 of 36 patients (86.1%) in the pre-intervention group and 99 of 165 patients (60.0%) in the post-intervention group received at least one outpatient IV iron dose (p = 0.0029). Overall, 24 of 36 patients (66.7%) in the pre-intervention group and 88 of 165 patients (53.3%) in the post-intervention group completed their planned IV iron treatment course (p = 0.1445). Median time from hospital discharge to first outreach for infusion scheduling was 4 days (range 0–81) in the pre-intervention group and 3 days (range 0–30) in the post-intervention group. Median time from discharge to first outpatient IV iron administration was 13 days (range 5–91) in the pre-intervention group and 11 days (range 8–18) in the post-intervention group. The most frequently identified barriers to treatment completion were no-shows, inability to contact patients, rehospitalization, patient-directed delays, and documentation gaps. 

Conclusions: Implementation of an updated IV iron order set incorporating pharmacist review significantly increased referrals for outpatient IV iron therapy. Standardizing referral workflows at hospital discharge may improve continuity of care, support timely outpatient iron repletion, and optimize utilization of inpatient and ambulatory infusion resources.


Moderators Presenters
avatar for Vanna Labi

Vanna Labi

PGY1 Acute Care Pharmacy Resident, Cone Health - Moses H. Cone Memorial Hospital
Evaluators
avatar for Yona Roberts

Yona Roberts

RPD/Clinical Pharmacy Manager, WSGA1Wellstar Cobb HospitalPGY1
Yona Roberts earned a Doctor of Pharmacy degree from Florida Agricultural and Mechanical University in Tallahassee, Florida.  She went on to complete a Pharmacy Practice Residency through Mercer University at DeKalb Medical Center in Atlanta, Georgia.  After completion of her residency... Read More →
Friday May 1, 2026 11:00am - 11:20am EDT
Athena H

11:00am EDT

Impact of Midodrine on Optimization of Guideline-Directed Medical Therapy in Patients with Heart Failure with Reduced Ejection Fraction
Friday May 1, 2026 11:00am - 11:20am EDT
Title: Impact of Midodrine on Optimization of Guideline-Directed Medical Therapy in Patients with Heart Failure with Reduced Ejection Fraction
Authors: Isabelle Perling, Jessica Starr, Nathan Pinner, Alyssa Osmonson, Kenda Germain
Objective: Discuss whether the addition of midodrine in patients with heart failure with reduced ejection fraction (HFrEF) facilitates optimization of Step 1 guideline-directed medical therapy (GDMT)
Self-Assessment Question: True or false, the addition of midodrine for HFrEF patients led to optimization of GDMT compared to those not started on midodrine.
Background: Heart failure is a complex syndrome that results from impairment of ventricular filling or blood ejection from the heart. It is classified by ejection fraction with the most common types being heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction.
Guideline-directed medical therapy (GDMT) for HFrEF includes four step 1 agents: renin-angiotensin system inhibition with an angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, or angiotensin receptor-neprilysin inhibitors, beta blockers, mineralocorticoid receptor antagonists, and sodium-glucose cotransporter 2 inhibitors. These treatments prolong patient life, improve symptoms, and reduce hospitalizations for HFrEF patients. Due to the notable blood pressure lowering effects of many of these agents, some patients cannot tolerate full GDMT.
Midodrine is a peripheral alpha-1 agonist that increases arterial and venous tone resulting in increased BP. It is FDA approved for symptomatic orthostatic hypotension but has been used off-label for vasopressor weaning in the intensive care unit and hemodialysis associated hypotension. Because combining multiple agents of GDMT can lower BP, some clinicians are beginning to use midodrine to counteract hypotension and ensure full optimization of GDMT.
Methods: This is a single center, IRB approved, retrospective chart review in patients with HFrEF and at least one Step 1 GDMT agent(s) on their home medication list. Patients with ≥3 normotensive blood pressure readings, contraindications to GDMT, mixed heart failure, end stage kidney disease, liver failure, and addition of midodrine for vasopressor de-escalation or no prescription fill data post-discharge were excluded. The primary endpoint was optimization of Step 1 GDMT, including addition of further agents or dose increases in current. Secondary outcomes include addition of GDMT, dose increase in current GDMT, reduction of GDMT, dose decreases in current GDMT, 30-day re-admission, mortality within a year, ability to come off midodrine, and improvement in ejection fraction.
Results: 28 patients were analyzed, 14 on midodrine and 14 without midodrine. There was no difference in optimization of Step 1 GDMT between the midodrine and matched control group. 3/14 patients in the midodrine group were optimized on step 1 GDMT compared to 6/14 in the control group (p=0.225). There was a meaningful difference in mortality within a year between the midodrine and control groups, 5/14 and 1/14, respectively (p=0.065).
Conclusion: Midodrine did not result in a difference in optimization of GDMT. Mortality was higher in the midodrine group, emphasizing the need for further studies evaluating the safety of the medication in HFrEF patients.
Moderators Presenters
IP

Isabelle Perling

PGY2 Internal Medicine Pharmacy Resident, Baptist Health Princeton Hospital
Isabelle (Izzy) Perling, PharmD, is a PGY2 Internal Medicine Pharmacy Resident from Atlanta, Georgia. She completed her undergraduate courses at Auburn University before receiving her PharmD from the University of Georgia College of Pharmacy. Izzy completed PGY1 at Baptist Health... Read More →
Evaluators
Friday May 1, 2026 11:00am - 11:20am EDT
Athena C

11:20am EDT

UNFILLED SLOT
Friday May 1, 2026 11:20am - 11:40am EDT

Friday May 1, 2026 11:20am - 11:40am EDT
Olympia 1
  • global Y

11:20am EDT

UNFILLED SLOT
Friday May 1, 2026 11:20am - 11:40am EDT
Friday May 1, 2026 11:20am - 11:40am EDT
Olympia 2
  • global Y

11:20am EDT

UNFILLED SLOT
Friday May 1, 2026 11:20am - 11:40am EDT
Friday May 1, 2026 11:20am - 11:40am EDT
Parthenon 2
  • global Y

11:20am EDT

UNFILLED SLOT
Friday May 1, 2026 11:20am - 11:40am EDT

Friday May 1, 2026 11:20am - 11:40am EDT
Parthenon 1
  • global Y

11:20am EDT

Evaluating the Risk Factors for Acute Kidney Injury Associated with Mannitol Therapy for Increased Intracranial Pressure
Friday May 1, 2026 11:20am - 11:40am EDT
Background:  
A common complication of traumatic and non-traumatic neurological injuries is elevated intracranial pressure (ICP). Preventing elevated ICP is critical for minimizing secondary neurologic injuries. First line pharmacologic therapies include hyperosmolar agents, such as hypertonic saline and mannitol. In the 2020 Neurocritical Care Society (NCS) Guidelines for Acute Treatment of Cerebral Edema, hypertonic saline and mannitol are both considered viable options, and there is little data to support one therapy over another, with many patients receiving both in clinical practice. Hypertonic saline is a plasma volume expander and may lead to hypernatremia; while mannitol is an osmotic diuretic and may not be preferred in patients due to risk of acute kidney injury (AKI). 
Increased serum concentrations of mannitol may be associated with AKI due to renal vasoconstriction. While most hospitals do not directly measure mannitol serum concentrations, osmolar gap monitoring has emerged as a surrogate marker for serum levels of mannitol. The NCS Guidelines recommend monitoring osmolar gap over serum osmolarity to assess the risk of AKI; however, the osmolar gap value at which to withhold mannitol remains unclear. The aim of this study is to determine risk factors for AKI among patients who receive mannitol for elevated ICP.  
 
Methods:  
This was a multi-center, retrospective, observational cohort study to identify the risk factors for AKI in patients who receive mannitol to manage elevated ICP. Patients were included if admitted to the Neurocritical Care or Trauma ICU between March 1st, 2024, and November 1st, 2025, received at least 1 g/kg of mannitol, and at least 2 doses of mannitol during admission. Patients were excluded if they had end-stage renal disease or have a baseline dependence on renal replacement therapy.  The primary outcome was identification of risk factors associated with AKI. Univariate logistic regression analysis was used to determine which variables are associated with AKI. We included variables such as peak osmolar gap, total mannitol dose administered, age, comorbid conditions, and number of nephrotoxic medications.  The secondary outcome was to compare characteristics of patients with AKI to those without AKI. Other statistical analyses were descriptive and inferential in nature.  
 
Results:   
A total of 230 patients who received mannitol between March 1st, 2024, and November 1st, 2025, were screened for inclusion. Of these, 102 patients met inclusion criteria and were included in the study cohort. The most common reason patients were not included was receiving less than 1 g/kg of mannitol and/or fewer than two doses of mannitol during admission. 
Baseline characteristics included patients that were predominantly male (56%) and White (53%), with a median age of 58 years. Most patients were admitted with a nontraumatic neurologic injury (94%) and were managed in the Neurocritical ICU (95%). Baseline serum creatinine was higher in patients who developed AKI compared to those who did not (1.02 mg/dL vs 0.79 mg/dL (p = 0.001). 
Among the 102 included patients, 28 developed AKI as defined by the Stage 1 AKI KDIGO Criteria. A univariate logistic regression analysis was conducted to evaluate differences between patients with and without AKI. Baseline serum creatinine (p = 0.010) and APACHE-II score (p = 0.032) were significantly associated with AKI. The median [IQR] peak serum creatinine among patients with AKI was 1.66 [1.41 - 2.46] mg/dL. 

Conclusions: 
In a univariate logistic regression analysis, higher baseline serum creatinine and APACHE II scores were associated with an increased risk of AKI. Factors associated with administration of mannitol, such as peak osmolar gap and total mannitol dose administered, were not associated with an increased risk of AKI.  
Moderators Presenters
avatar for Carly Mitchell

Carly Mitchell

PGY1 Pharmacy Resident, Atrium Health Wake Forest Baptist Medical Center
Evaluators
avatar for Liz Oglesby

Liz Oglesby

Pharmacy Clinical Coordinator, PGY-1 Residency Program, Mobile Infirmary
Liz Oglesby, PharmD, BCPS, is the Pharmacy Clinical Coordinator and PGY-1 Residency Program Director at Mobile Infirmary in Mobile, Alabama. She obtained her doctorate of pharmacy from Auburn University in 2017 and completed PGY-1 training at Baptist Health Princeton Hospital in 2018. Her primary practice foc... Read More →
Friday May 1, 2026 11:20am - 11:40am EDT
Athena A

11:20am EDT

Evaluation of Neurostimulants on Functional-Cognitive Capacity in Traumatic Brain Injury
Friday May 1, 2026 11:20am - 11:40am EDT
Introduction: Traumatic brain injury (TBI) is a major cause of long-term disability, with persistent cognitive and functional deficits affecting millions of survivors. Neurostimulants such as amantadine are recommended for disorders of consciousness after TBI; however, limited evidence exists evaluating the impact of combination neurostimulant therapy with methylphenidate on functional recovery. This study evaluated the effect of single versus dual neurostimulant therapy on functional-cognitive outcomes in patients with moderate to severe TBI.
Methods: A single-center retrospective observational study was conducted at a Level I trauma center from January 1 to December 31, 2024. Adult patients (age >16 years) with moderate to severe TBI, defined as a Glasgow Coma Score (GCS) < 12 within 72 hours of arrival, who received amantadine alone or amantadine plus methylphenidate for ≥3 days during intensive care unit (ICU) admission were included. The primary outcome was discharge functional-cognitive capacity measured by the Rancho Los Amigos Scale-Revised (RLAS-R). Secondary outcomes included change in GCS, ICU and hospital length of stay (LOS), and discharge disposition. Propensity matching (1:4) and multivariable analyses were performed.
Results: Seventy-six patients were included (amantadine n=57; dual therapy n=19). Baseline demographics and injury characteristics were similar between groups. Median discharge RLAS-R scores did not significantly differ between dual therapy and monotherapy groups (4 vs 5, p=0.12). ICU and hospital LOS were comparable between groups, and discharge disposition distributions were similar. Multivariable regression adjusting for initial GCS demonstrated no significant association between treatment strategy and discharge functional-cognitive outcomes (OR 0.73, 95% CI 0.30–1.81). ICU (21 vs 19 days, p = 0.20) and hospital LOS (29 vs 33 days, p = 0.10) were comparable between groups, and discharge disposition distributions were similar, with more than 50% of patients being discharged to an acute rehab facility.
Conclusions: Early initiation of dual neurostimulant therapy (amantadine plus methylphenidate) produced functional-cognitive outcomes comparable to amantadine monotherapy without decreasing resource utilization. These findings suggest no clear additive benefit of combination therapy in moderate to severe TBI and highlight the need for
Moderators Presenters
SK

Sydney Kisala

PGY-2 Critical Care Pharmacy Resident, Grady Memorial Hospital
Sydney Kisala is a PGY-2 Critical Care Pharmacy Resident at Grady Memorial Hospital in her hometown of Atlanta, GA, where she also completed her PGY-1 pharmacy residency. She earned her Doctor of Pharmacy degree from the University of Georgia in Athens, GA. Her current research project... Read More →
Evaluators
Friday May 1, 2026 11:20am - 11:40am EDT
Athena C

11:20am EDT

Evaluation of Prophylactic Antibiotic Usage in Patients with Open Fracture
Friday May 1, 2026 11:20am - 11:40am EDT

Moderators
avatar for Stephanie Lesslie

Stephanie Lesslie

PGY-2 Critical Care Residency Director, Memorial University Medical Center
Presenters
avatar for Zackery Moreo

Zackery Moreo

PGY-2 Emergency Medicine Pharmacy Resident, Grady Memorial Hospital

Evaluators
avatar for Jonathan Alligood

Jonathan Alligood

Residency Program Director, Phoebe Putney Memorial Hospital
Friday May 1, 2026 11:20am - 11:40am EDT
Athena I

11:20am EDT

Evaluation of Revisions to Pharmacist-Directed Heparin Infusion Protocol
Friday May 1, 2026 11:20am - 11:40am EDT
Evaluation of Revisions to Pharmacist-Directed Heparin Infusion Protocol 
Caylen Wouters, Samantha Sims, Kristy Williams, Andrew Revels, Jordana Champion 
East Alabama Medical Center

ABSTRACT

Purpose 
At our institution, patients requiring heparin infusions are managed by the pharmacy staff based on activated partial thromboplastin time (aPTTs) levels. In July 2024, revisions to our institution’s heparin protocol changed the way pharmacists modified heparin drips based on aPTT levels. These changes included updating the nomogram for heparin infusion rate adjustments and reducing the number of required boluses per protocol. The purpose of this study is to assess the effects of these revisions on the institution’s current heparin protocol. 

Methods 
This study was a single-center, retrospective chart review evaluating the electronic health records (EHR) of adult patients admitted to our institution who received heparin for at least 48 hours according to the institution’s revised pharmacist-driven heparin protocol. The primary outcome was the frequency of achieving two consecutive therapeutic aPTTs within 48 hours of heparin infusion initiation. Secondary outcomes included: bleeding occurrences, number of aPTT levels drawn within 48 hours, total number aPTT levels drawn during infusion, number of patients who received initial heparin boluses, number of patients who received additional heparin boluses, number of times heparin drips held for elevated aPTTs, sub-, supra- and therapeutic aPTTs, time to achieving two consecutive therapeutic aPTTs, and duration of heparin drip. Patients were identified using admission dates between January-June 2024 for the pre-revision group and January-June 2025 for the post-revision group and then randomized and evaluated for inclusion. The statistical analysis was done using IBM SPSS Statistics version 30.0.0.0 (IBM Corp., 2024). The chi-square method was used for the nominal data within the primary and secondary outcomes, and the student t-test was used for the continuous data in the secondary outcomes. P-value < 0.05 was considered statistically significant.

Results
One hundred patients were included in the final analysis of this study with 50 patients in the pre-revision group and 50 patients in the post-revision group. Baseline characteristics included men and women averaging about 65 years old, mostly of White/European descent, and a BMI of about 29 kg/m2. For the primary outcome, there was no statistically significant difference in the achievement of two consecutive therapeutic aPTTs within 48 hours between the pre-revision group and the post-revision group (50% and 56% respectively, P= 0.689). Overall, the secondary outcomes were similar between groups and were not statistically significant. The one secondary outcome that demonstrated a statistically significant difference was the amount of additional heparin boluses administered during heparin treatment, with 48% in the pre-revision group and 14% in the post-revision group.

Conclusions
The updated pharmacist-driven heparin protocol demonstrated comparable efficacy to the prior protocol revealing no significant decrease in time to therapeutic range. The significant decrease in the number of supplemental boluses between groups indicated improvement in the initial dosing accuracy and enhanced dose adjustments within the new protocol. A reduction in heparin boluses may ultimately lead to a decrease in the risk of supratherapeutic anticoagulation, nurse workload, and interruptions in therapy; therefore, these reductions could help improve overall patient safety and operational efficiency.
Moderators Presenters
avatar for Caylen Wouters

Caylen Wouters

PGY1 Pharmacy Resident, East Alabama Medical Center
Caylen Wouters is from Port Saint Lucie, FL. Caylen completed her undergraduate studies at the University of Florida in Animal Sciences with a minor in Agribusiness. She earned her PharmD from Auburn University Harrison College of Pharmacy. Her clinical interests are critical care... Read More →
Evaluators
avatar for Don Tyson

Don Tyson

Director of Pharmacy, Piedmont Athens Regional Medical Center
Friday May 1, 2026 11:20am - 11:40am EDT
Athena B

11:20am EDT

Outcomes of anticoagulation alone vs anticoagulation plus intervention in patients who present to the ED with massive pulmonary embolism.
Friday May 1, 2026 11:20am - 11:40am EDT
Purpose: The literature surrounding optimal treatment of massive pulmonary embolisms (PE) is unclear. Numerous studies have been published regarding treatment options including anticoagulation, fibrinolytic therapy, thrombectomies, catheter-directed fibrinolytic therapy, and surgical embolectomy with limited direct or combination therapy comparisons. This study aims to evaluate anticoagulation alone to anticoagulation plus intervention (fibrinolytics, thrombectomy, catheter-directed fibrinolytic therapy) in the treatment of massive PE in emergency department patients across Prisma Health. 

Methods: This study is a retrospective cohort study, evaluating patients diagnosed with massive PE presenting to a Prisma Health emergency department from May 1, 2021, to August 31, 2025. The primary outcomes will be time to first improvement in hemodynamic instability markers of either systolic blood pressure (≥ 120 mmHg without vasopressors), O2 saturation (≥ 94% on room air or 2 liters nasal cannula) or heart rate (≤ 100 beats per minute or patient’s baseline) as well as average time to composite improvement for those meeting at least 2 or more markers of hemodynamic instability. Additional variables collected and evaluated will include anticoagulant used, intervention if any, available imaging, in-hospital mortality, and readmission for PE. Outcomes will be evaluated using logistic regression for primary outcomes and other descriptive analyses. 

Results: Out of 860 patients screened, 41 patients were included in the anticoagulation + intervention and 22 were included in the anticoagulation only group. The median age was 62 years in the intervention group compared with 70.5 in the anticoagulation only group. 78% of patients vs 95.5% of patients presented with comorbid conditions such as heart failure, COPD, and cancer. All of the first documented vital signs in the emergency department were outside of our set thresholds. Of the 41 patients in the intervention group, 23 received fibrinolytics only, 4 received a thrombectomy only, 14 received a fibrinolytic plus a thrombectomy, and none received catheter-directed fibrinolytic therapy. Of the patients who received a fibrinolytic only, 19 received alteplase compared to 4 who received tenecteplase (p=0.002). There was no difference seen in which vital sign improved first between the intervention group and the anticoagulation only group, as well as our subgroup population: alteplase vs tenecteplase patients. The median time to vital sign improvement (in hours) was significantly lower at 5 hours vs 8.5 hours between our two major groups (p=0.024). The logistic regression showed that there was no vital sign that stood out as the main driving factor for the improvement seen. 34.1% of patients in the intervention group had a bleed compared to 9.1% in the anticoagulation group. There was no difference seen in terms of major bleeds, mortality, or readmission rates. 

Conclusion: Patients given anticoagulation plus an intervention had quicker time to vital sign improvement compared to patients given anticoagulation only. There was no difference in terms of mortality or readmission rates between the two primary groups and the two fibrinolytic subgroups. Future studies are needed to explore what kinds of interventions bring the best outcomes for massive pulmonary embolism patients.
Moderators Presenters
avatar for Dhruv Patel

Dhruv Patel

PGY1 Acute Care Pharmacy Resident, Prisma Health Richland
My name is Dhruv Patel, PharmD, and I am currently a PGY1 Acute Care Pharmacy Resident at Prisma Health Richland Hospital in Columbia, SC. I went to pharmacy school at Virginia Commonwealth University School of Pharmacy in Richmond, VA. I will be staying on at Prisma Health Richland... Read More →
Evaluators
Friday May 1, 2026 11:20am - 11:40am EDT
Athena G

11:20am EDT

Protocol Guided VTE Prophylaxis in Trauma Patients: A Retrospective Cohort Study
Friday May 1, 2026 11:20am - 11:40am EDT
Background: Venous thromboembolism (VTE) is a significant cause of morbidity and mortality following traumatic injury. Trauma patients are at an increased risk for VTE secondary to dysregulation of the coagulation system, reduced mobility, and the type of traumatic injury. Low molecular weight heparin (LMWH) is the drug of choice for VTE prophylaxis in this population because of its increased bioavailability, longer half-life, and predictable pharmacokinetics. Subcutaneous heparin is alternatively recommended for patients with a creatinine clearance less than 30 mL/min or with end stage renal disease on hemodialysis. Timely initiation of appropriate VTE prophylaxis is crucial to preventing fatal complications in trauma patients. VTE prophylaxis must be initiated early and continue throughout the admission without missing doses for orthopedic and most other surgical procedures. Limited guidance has been established and VTE prophylaxis strategies generally rely on institutional protocol and surgeon’s discretion. Given the challenges of balancing bleed risk and VTE prevention, there is a need for a standardized protocol guided VTE prophylaxis in trauma patients. The purpose of this study was to determine the impact of implementing a VTE prophylaxis protocol in trauma patients admitted to the intensive care unit.

Methods: This was an observational, pre-post study completed at Piedmont Columbus Regional Midtown in Columbus, GA during two independent time periods. The primary objective of this study was to determine rate of compliance with evidence based VTE prophylaxis in the pre-implementation group compared to the post-implementation group, including appropriate dose of VTE prophylaxis, time to administration of VTE prophylaxis, and time to perioperative re-initiation of VTE prophylaxis. The secondary objectives were incidence of VTE, incidence of major bleeding, number of initial anti-Xa levels in goal for patients who received LMWH, and days needed to achieve goal anti-Xa level for patients who received LMWH. The primary outcome was analyzed using Chi-square test and the secondary outcomes were analyzed using either Chi-square test or Fisher's exact test. Patients were excluded if their length of stay was less than 24 hours, they were pregnant, had coagulopathy on admission, clinical signs of ongoing hemorrhage, had an indication for therapeutic anticoagulation on admission, or traumatic brain injury meeting high-risk Modified Berne-Norwood Criteria.

Results: For the primary objective of protocol compliance for VTE prophylaxis, 25% of patients in the pre-group met compliance with the protocol versus 41% in the post-group. For secondary objectives, three patients in the pre-group had a VTE occurrence whereas none did in the post-group. Six patients in the pre-group had an incidence of major bleeding, compared to none in the post-group. Only 10 patients in the pre-group had anti-Xa level monitoring obtained and 13 patients in the post group. Of which, 40% had an initial anti-Xa at goal in the pre-group versus 54% in the post-group. The days needed to achieve anti-Xa goal was also not significantly different after implementation of the protocol.

Conclusion: Implementation of a standardized VTE prophylaxis protocol improved appropriate selection of dose and time to initiation without increasing frequency of bleeding.

Contact: [email protected]
Moderators Presenters
avatar for Emily Davis

Emily Davis

PGY-2 Critical Care Resident, Piedmont Columbus Regional Midtown
Emily is a current PGY-2 critical care resident at Piedmont Columbus Regional Midtown. She is originally from Columbus, GA and went to pharmacy school at the University of Georgia College of Pharmacy.
Evaluators
avatar for Carrie Callahan

Carrie Callahan

Internal Medicine (IM) Specialist, PGY2 IM RPD, Emory University Hospital


Friday May 1, 2026 11:20am - 11:40am EDT
Athena D

11:20am EDT

Medication-induced falls in hospitalized patients: assessing the impact of anticholinergic drugs and the predictability of fall risk scores - William W. Feese
Friday May 1, 2026 11:20am - 11:40am EDT
Introduction:    
Some of the most prescribed medications in the elderly population have potent anticholinergic properties, which are associated with potentially harmful side effects, such as an increased risk of falls. In addition, many elderly patients are on potentially inappropriate medications as defined by the Beers criteria, many of which can also increase fall risk. Pharmacists can play a pivotal role in preventing inpatient falls by proactively identifying patients taking potentially inappropriate medications and making recommendations related to de-prescribing or medication optimization. The objective of this study is to investigate if a causal relationship exists between inpatient falls and medication usage. 
Methods:  
This is a retrospective case-controlled study of adult patients aged 65 years or older admitted to The University of Tennessee Medical Center from January 2023 to May 2025. Patients were separated into two groups: the fall group, which included patients aged 65 years or older who had experienced an inpatient fall (as identified by ICD-10 codes for inpatient falls), and the control group, which included patients aged 65 years or older who had not experienced an inpatient fall. Patients were excluded if they were under 65 years old. The Anticholinergic Burden Score and the Beers Criteria scoring systems were utilized to assess the total number of potentially inappropriate medications the patients were taking at admission, during their hospital stay, and at discharge. The primary outcome is the median score on each scoring system at each time point: admission, during their hospital stay, and on discharge. Secondary outcomes are length of stay and discharge location. 
Results
A total of 310 participants met the inclusion criteria. Baseline characteristics were similar between groups except for a higher prevalence of atrial fibrillation in the no-fall group (P = 0.004). Both measures of potentially inappropriate medication exposure were significantly higher in patients who experienced a fall. Median Anticholinergic Burden scores were 4 vs 2 (P < 0.0001), and median Beers Criteria scores were 7 vs 5 (P < 0.0001) in the fall and no-fall groups, respectively. Despite no difference in admissions scores, the change in both metrics from admission to maximum inpatient values were significantly greater in the fall group (P < 0.0001). Patients who fell had a longer median length of stay (8 vs 4 days, P < 0.0001) and were more frequently discharged to skilled nursing facilities (P < 0.0001). A post-hoc analysis was conducted regarding past medical history for atrial fibrillation and Parkinson's disease, as they were significant or marginally non-significant, respectively. Each 1-point increase in Anticholinergic Burden Score increased fall risk by 26.9%, and each 1-point increase in Beers Criteria Score increased fall risk by 14.3% among patients with atrial fibrillation or Parkinson's disease. 
Conclusion
Patients who experienced an inpatient fall had significantly higher maximum Anticholinergic Burden and Beers Criteria scores than those who did not fall. Falls were also associated with longer hospital stays and a greater likelihood of discharge to a skilled nursing facility. Medication risk scores increased from admission through the time of the fall, suggesting an opportunity to improve inpatient medication optimization to prevent falls. Future research should evaluate high-risk medication combinations and dose-related effects within the Anticholinergic Burden and Beers Criteria to better guide prescribing for high-risk hospitalized patients. 

Moderators Presenters
avatar for William Feese

William Feese

PGY-2 Internal Medicine Pharmacy Resident, University of Tennessee Medical Center
Dr. Feese was born and raised in Lexington, Kentucky. He completed his Bachelor of Science in Pharmaceutical Sciences with an emphasis in Health Humanities from the esteemed St. Louis College of Pharmacy and his Doctor of Pharmacy from the University of Health Sciences and Pharmacy... Read More →
Evaluators
avatar for Yona Roberts

Yona Roberts

RPD/Clinical Pharmacy Manager, WSGA1Wellstar Cobb HospitalPGY1
Yona Roberts earned a Doctor of Pharmacy degree from Florida Agricultural and Mechanical University in Tallahassee, Florida.  She went on to complete a Pharmacy Practice Residency through Mercer University at DeKalb Medical Center in Atlanta, Georgia.  After completion of her residency... Read More →
Friday May 1, 2026 11:20am - 11:40am EDT
Athena H

11:20am EDT

Evaluation of Empiric Vancomycin Utilization in Febrile Neutropenia
Friday May 1, 2026 11:20am - 11:40am EDT
Lauryn Malone, Ben Casey, Darby Siler 
TriStar Centennial Medical Center – Nashville, TN 

Background: Febrile neutropenia (FN) is a common complication of cancer treatment and is considered to be an oncologic emergency. Vancomycin is primarily used to treat infections caused by methicillin-resistant Staphylococcus aureus. FN guidelines do not recommend routine use of MRSA coverage as empiric therapy for FN unless pre-specified criteria are fulfilled. Despite these recommendations, previous studies suggest vancomycin is often prematurely added to empiric antibiotic therapy regimens in patients with febrile neutropenia. Utilization of vancomycin empirically in FN has been increasing, though its clinical utility remains uncertain due to the lower incidence of resistant gram-positive organisms causing FN. The purpose of this study was to evaluate the utilization and prescribing patterns of empiric vancomycin for febrile neutropenia at our facility. 
 
Methods: Patients were identified based on having vancomycin ordered for the indication of febrile neutropenia. Patients were included if they had a fever and were neutropenic. Exclusion criteria consisted of patients ages 18 years of age or younger, patients receiving care under the pediatric oncology service, patients without a diagnosis of cancer, and patients with vancomycin ordered for less than 24 hours. The primary outcome was to evaluate the incidence of guideline-directed utilization of empiric vancomycin for febrile neutropenia. Secondary outcomes included the duration of fever, appropriateness of gram-positive and gram-negative coverage, incidence of positive blood cultures, and prescribing patterns among various specialties. Descriptive statistics were used to report outcomes. 
 
Results: A total of 153 patients were screened; 38 patients met inclusion criteria, and 115 patients were excluded due to receiving vancomycin for less than 24 hours. Of the 38 patients included, 89% (n =34) had hematologic malignancies, with a cohort age range of 28–80 years. Among the 38 patients evaluated, 26 (68%) received empiric MRSA coverage consistent with established FN guidelines. The most common indication for empiric vancomycin was concerns for pneumonia on imaging (13/38 patients; 34%). The average duration of MRSA coverage was 93.8 hours (SD: 63.7 hours). Emergency medicine providers initiated empiric vancomycin for 17/38 patients (45%). No adverse reactions were noted for included patients.
 
Conclusions: This study found that in patients presenting with FN who were empirically started on vancomycin, therapy was routinely discontinued within 24 hours. This study also found that in patients who received vancomycin for greater than 24 hours, vancomycin utilization was discordant with guideline recommendations for MRSA directed therapy in FN, highlighting the potential need for antimicrobial stewardship intervention for this patient population. 
 
This research was supported (in whole or in part) by HCA Healthcare and/or an HCA Healthcare affiliated entity. The views expressed in this publication represent those of the author(s) and do not necessarily represent the official views of HCA Healthcare or any of its affiliated entities.
Moderators Presenters
avatar for Lauryn Malone

Lauryn Malone

PGY-1 Pharmacy Resident, TriStar Centennial Medical Center
Lauryn is a 2025 graduate of Auburn University Harrison College of Pharmacy. She is currently a PGY-1 Resident at TriStar Centennial Medical Center in Nashville, TN. Lauryn will be completing a PGY-2 Oncology Residency Program next year with plans of becoming an Oncology Clinical... Read More →
Evaluators
avatar for Jessica Sterchi

Jessica Sterchi

Clinical Pharmacy Supervisor and Acute Care PGY1 RPD, BMHT1Blount Memorial HospitalPGY1
Friday May 1, 2026 11:20am - 11:40am EDT
Athena J

11:40am EDT

UNFILLED SLOT
Friday May 1, 2026 11:40am - 12:00pm EDT

Friday May 1, 2026 11:40am - 12:00pm EDT
Olympia 1
  • global Y

11:40am EDT

UNFILLED SLOT
Friday May 1, 2026 11:40am - 12:00pm EDT
Friday May 1, 2026 11:40am - 12:00pm EDT
Olympia 2
  • global Y

11:40am EDT

UNFILLED SLOT
Friday May 1, 2026 11:40am - 12:00pm EDT

Friday May 1, 2026 11:40am - 12:00pm EDT
Parthenon 1
  • global Y

11:40am EDT

UNFILLED SLOT
Friday May 1, 2026 11:40am - 12:00pm EDT
Friday May 1, 2026 11:40am - 12:00pm EDT
Parthenon 2
  • global Y

11:40am EDT

Optimizing Migraine Management in Veterans: A Pharmacist-Led Review of Triptan Use in Primary Care Clinics
Friday May 1, 2026 11:40am - 12:00pm EDT
Optimizing Migraine Management in Veterans: A Pharmacist-Led Review of Triptan Use in Primary Care Clinics
Justin Barnett, Jessica Parks, Stephanie Hopkins, Karyn Fabo
Fayetteville NC VA Coastal Health Care System – Fayetteville, NC

Background: Acute migraine headaches affect approximately 16% of the United States population. Triptans (e.g., sumatriptan, rizatriptan, etc.) are often the first-line option for acute migraine management. Triptans provide symptom relief by promoting vasoconstriction of intracranial blood vessels, and while this mechanism is the primary source of therapeutic benefit, it also increases cardiovascular risks, especially coronary vasospasm. As a result, the triptan class is contraindicated in patients with a history of cardiovascular disease, and use should be limited in patients with risk factors for cardiovascular disease. Nationwide prescribing patterns suggest that nearly 14% of patients using triptans meet at least one contraindication.


Methods: This quality improvement initiative identified adult Veterans at a Veterans Affairs (VA) Health Care Center who had an active prescription for a triptan medication. Patients qualified for review if they were managed by one of six designated primary care clinics and were disqualified if their migraine disorder was actively managed by a VA or private-sector neurologist.

Contraindications (including ischemic heart disease, arrhythmias, uncontrolled hypertension, history of gastrointestinal ischemia, history of stroke, peripheral vascular disease, and structural heart disease) and cardiovascular risk factors (including hypertension, hyperlipidemia, diabetes mellitus, hepatic or renal failure, obesity, age >65 years, and current tobacco use) were identified via electronic health record (EHR) review. The primary author attempted telephone contact with each identified Veteran to reconcile any potential discrepancies in EHR documentation.

At the conclusion of the patient encounter, the primary investigator recommended the following: no intervention, referral by primary care provider (PCP) to neurology service, referral by PCP to cardiology service, discontinuation of triptan prescription, or referral directly to clinical pharmacist practitioner (CPP) for chronic disease state management. Recommendations were assessed as “accepted” or “not accepted”, and the results were analyzed using descriptive statistics. Findings will be communicated to the designated primary care clinics in order to improve future prescribing practices.


Results: Of the 86 patients identified, 13 patients (15.1%) had at least one contraindication to triptan use, and the most frequent contraindication was uncontrolled hypertension (n=9, 10.4%). Interventions were recommended for 33 Veterans but were accepted for only 17. The most frequently recommended intervention was for a neurology consult (n=20). The most frequently accepted intervention (n=10) was for referral to a CPP for management of chronic disease states that can increase cardiovascular risk.


Conclusions: Data from this quality improvement initiative demonstrate that pharmacists should be actively engaged in monitoring triptans and counseling patients to ensure those with contraindications do not use this class of medications.

Moderators Presenters
avatar for Justin Barnett

Justin Barnett

PGY2 Ambulatory Care Pharmacy Resident, Fayetteville NC VA Coastal Health Care System
Dr. Justin Barnett was born and raised in Savannah, GA. He attended the University of Georgia to complete his pharmacy pre-requisites prior to earning his Doctor of Pharmacy degree from the UGA College of Pharmacy. He completed his PGY1 Pharmacy Residency at the James H. Quillen VA... Read More →
Evaluators
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena C

11:40am EDT

Use and Safety of Direct Oral Anticoagulants Immediately Following Bioprosthetic Valve Replacement in Patients with Atrial Fibrillation
Friday May 1, 2026 11:40am - 12:00pm EDT
Use and Safety of Direct Oral Anticoagulants Immediately Following Bioprosthetic Valve Replacement in Patients with Atrial Fibrillation
Boma Legg-Jack, William Kendrick, Kellie Ball, Jeff Lewis
 
Background: Direct oral anticoagulants (DOACs) are preferred for stroke prevention in atrial fibrillation (A-fib) patients. However, current American Heart Association guidelines suggest warfarin indefinitely for mechanical valves, at least 3 months after surgical bioprosthetic valve replacement, and possibly after transcatheter valve replacement with indication for anticoagulation. After 3 months, DOACs may be considered, though data during the initial 90 days after implantation is limited. This study assesses the efficacy of DOACs in patients who underwent surgical or transcatheter bioprosthetic valve replacement within the first 90 days after implantation.

Methods: This is an Institutional Review Board-approved retrospective chart review conducted within the University of Tennessee Medical Center Knoxville (UTMCK). Patients were included if they were ≥ 18 years old, had a surgical or transcatheter bioprosthetic valve replacement at UTMCK between January 2020 and February 2025, a-fib indication, and evidence of follow-up. The primary outcome was the composite of stroke, transient ischemic attack (TIA), systemic embolism (deep vein thrombosis or pulmonary embolism), valve thrombosis, intracardiac thrombus, or death from any cause during the first 90 days after initiating oral anticoagulation following bioprosthetic valve replacement. Secondary outcomes included major bleeding during the first 90 days after initiating oral anticoagulation, clinically relevant non-major bleeding, death from any cause, and 30-day and 90-day readmission rate.

Results: Among 191 patients, 5.8% of those receiving a DOAC experienced a thrombotic event[BK1] within 90 days of valve replacement. Nonmajor and major bleeding occurred in six and two patients, respectively. Readmissions occurred in 19 patients within 30 days of discharge, and 18 patients within 90 days of discharge.

Conclusion: Although thromboembolic and mortality events were observed, the overall event rate was 5.8% among 191 patients, lower than rates reported in existing literature. Given the limited sample size, further studies are needed to more fully evaluate the safety and efficacy of DOACs during the first 90 days after valve replacement.
  
Moderators Presenters Evaluators
avatar for Don Tyson

Don Tyson

Director of Pharmacy, Piedmont Athens Regional Medical Center
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena B

11:40am EDT

Comparing Time-to-target Mean Arterial Pressure with Weight-based vs. Non-weight-based Norepinephrine ​
Friday May 1, 2026 11:40am - 12:00pm EDT
COMPARING TIME-TO-TARGET MEAN ARTERIAL PRESSURE WITH WEIGHT BASED VS. NON-WEIGHT-BASED NOREPINEPHRINE
Logan Turner, PharmD; Brian Hairston, PharmD, MBA; Allison Jolley, PharmD, BCCCP; Andrew B. Watkins, PharmD, BCIDP

FMOL Health | St. Dominic- Jackson, MS

Background/Purpose: Septic shock is a life-threatening manifestation of sepsis characterized by persistent hypotension requiring vasopressor therapy to maintain a mean arterial pressure (MAP) ≥ 65 mmHg. Norepinephrine is the first-line vasopressor recommended in current guidelines; however, there is no standardized dosing strategy, and institutions utilize either weight-based (mcg/kg/min) or fixed (mcg/min) dosing protocols. At FMOL Health | St. Dominic, practice transitioned from fixed dosing to weight-based dosing in 2022. The purpose of this study is to compare time to goal MAP between weight-based and fixed norepinephrine dosing strategies in critically ill adults with septic shock.


Methodology: This quasi-experimental, retrospective cohort study will evaluate adult ICU patients treated for septic shock during two time periods: January 1, 2019 to December 31, 2019 (fixed dosing cohort) and January 1, 2023 to December 31, 2023 (weight-based dosing cohort). Patients will be identified using electronic health record data. Eligible patients will include adults ≥ 18 years of age admitted to the ICU during the study periods with a diagnosis of septic shock requiring initiation of norepinephrine infusion to maintain a goal MAP ≥ 65 mmHg. Septic shock will be defined using clinical documentation and qSOFA criteria. Patients will be excluded if norepinephrine was initiated for indications other than septic shock, if vasopressors were started prior to ICU admission, if they are pregnant or incarcerated, or if key norepinephrine infusion data are incomplete or missing.


Results: A total of 100 patients were included, with 50 patients in each group. There was no significant difference in median time to target MAP between the weight-based and non-weight-based groups (41 vs 46 minutes; p = 0.73). Weight-based dosing was associated with significantly higher initial and maximum norepinephrine infusion rates. No statistically significant differences were observed in secondary outcomes, including AKI, mortality, or ICU length of stay.


Conclusions: Weight-based norepinephrine dosing did not improve time to target MAP and resulted in higher infusion rates without clear clinical benefit, suggesting no advantage over non-weight-based dosing in patients with septic shock. Although the overall incidence of acute kidney injury did not differ between groups, patients who developed AKI in the weight-based group received higher maximum norepinephrine doses, highlighting a potential safety concern.


Moderators Presenters
avatar for Logan Turner

Logan Turner

Pharmacy Resident, FMOL Health | St. Dominic
Evaluators
avatar for Liz Oglesby

Liz Oglesby

Pharmacy Clinical Coordinator, PGY-1 Residency Program, Mobile Infirmary
Liz Oglesby, PharmD, BCPS, is the Pharmacy Clinical Coordinator and PGY-1 Residency Program Director at Mobile Infirmary in Mobile, Alabama. She obtained her doctorate of pharmacy from Auburn University in 2017 and completed PGY-1 training at Baptist Health Princeton Hospital in 2018. Her primary practice foc... Read More →
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena A

11:40am EDT

Intravenous Versus Subcutaneous Insulin Administration: Evaluation of Blood Glucose Control in the Critical Care Setting
Friday May 1, 2026 11:40am - 12:00pm EDT
Authors: Mikayla Texido, Jill Dunning, Caitlin Thomas
Purpose/Background: Hyperglycemia is commonly seen and associated with adverse outcomes among hospitalized patients, especially in the intensive care unit (ICU) because these patients are more vulnerable to poor outcomes. Previous trials demonstrate that improved glycemic management can reduce hospital complications, infections, and costs. In the critical care setting, guidelines recommend continuous intravenous (IV) insulin infusion as the preferred method for achieving specific glycemic goals while avoiding hypoglycemia. Despite these recommendations, there are limited studies that directly compare the safety and efficacy of IV insulin to subcutaneous (SubQ) insulin for glycemic management in the critical care setting. This study aims to evaluate patients who were eligible for IV insulin administration through an electronic glucose management system (eGMS) and compare those who were managed with IV insulin via eGMS versus those managed with SubQ insulin.
Methodology: This was a single center, retrospective chart review conducted at AdventHealth Orlando that evaluated patients in the ICU who received glycemic management with either IV or SubQ insulin from June 18, 2025, to August 18, 2025. Adult patients with either two consecutive blood glucose values ≥180 mg/dL or one blood glucose ≥300 while admitted to the cardiac, neuro, medical, surgical, or multi-system ICU were included. Patients were excluded if they were managed on IV insulin utilizing eGMS for less than 6 hours, were managed with IV insulin without eGMS, had cardiovascular surgery within 30 days prior to inclusion, or were being treated with insulin for diabetic ketoacidosis, hyperosmolar hyperglycemic state, or hyperkalemia. Patients managed with IV insulin through eGMS utilization were compared to those managed with SubQ insulin. The primary outcome was the percentage of blood glucose values within a goal range of 70-180 mg/dL. A total of 774 blood glucose values would provide 80% power to detect a 10% difference. Secondary efficacy endpoints included the time until blood glucose was in range, median blood glucose, and ICU length of stay in both groups, with time on eGMS and percent of successful transitions from IV to SubQ additionally evaluated in the IV group. Safety endpoints included the incidence of hypoglycemia (BG <70 mg/dL) and severe hypoglycemia (BG <40 mg/dL).
Results: Of the 431 patients screened, 149 patients met inclusion criteria and no exclusion criteria with 74 in the IV group and 75 in the SubQ group. The IV group had a total of 3,997 individual blood glucose values while the SubQ group had 1,599. Of the patients included, 82 (55.0%) were male, the median A1c was 6.7%, and the median blood glucose on ICU admission was 198 mg/dL. Blood glucose was within the goal range of 70-180 mg/dL in 79.9% of the measurements in the IV group versus 61.2% in the SubQ group (p<0.001). The median blood glucose in the IV group was 146 mg/dL versus 173 mg/dL in the SubQ group (p<0.001). Of patients who were able to maintain their blood glucose within goal range for at least 6 consecutive hours, the median time to blood glucose within goal range was 6.3 hours in the IV group (n=72) versus 14.0 hours in the SubQ group (n=60; U=1011; p<0.001). The patients in the IV group had a longer median ICU length of stay (7.5 days vs. 4.0 days; U=1877.5; p<0.001) and there were no incidences of severe hypoglycemia in either group.
Conclusion: Hyperglycemic patients admitted to the ICU had a higher percentage of blood glucose values within the goal range of 70-180 mg/dL with intravenous insulin administered via eGMS compared to patients managed with subcutaneous insulin.
Moderators
avatar for Stephanie Lesslie

Stephanie Lesslie

PGY-2 Critical Care Residency Director, Memorial University Medical Center
Presenters
avatar for Mikayla Texido

Mikayla Texido

PGY1 Pharmacy Resident, AdventHealth Orlando
Evaluators
avatar for Jonathan Alligood

Jonathan Alligood

Residency Program Director, Phoebe Putney Memorial Hospital
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena I

11:40am EDT

Outpatient Medical (OPM) Drug Formulary Expansion to Optimize Margin
Friday May 1, 2026 11:40am - 12:00pm EDT
Title: Outpatient Medical (OPM) Drug Formulary Expansion to Optimize Margin
Authors: William Siders, David Collette
Background:
Drug formularies for the Centers of Medicare & Medicaid Services and commercial insurers are updated regularly, which can create reimbursement challenges related to misalignment between prescribed therapies and payer-specific formulary preferences. Administering non-preferred agents can result in claim denials and increased administrative burden for providers and pharmacy staff. At Huntsville Hospital Outpatient Medical Services, variability in insurance coverage across commercial and government payers highlighted the need for a standardized approach to formulary management. The purpose of this pharmacoeconomics project was to expand and standardize the outpatient medical drug formulary to align with current insurance preferences and maximize reimbursement.
Methodology:
A comprehensive review of our current formulary workhorse agents along with formulary requirements and coverage criteria across major commercial and government insurers was conducted. Based on this review, the Outpatient Medical Services drug formulary was updated to reflect payer-preferred agents by insurance type. Standardized, provider-facing communications were developed, including formal educational letters distributed to providers outlining formulary changes and payer-specific drug preferences. Educational efforts emphasized appropriate product selection at the time of prescribing and appropriate documentation to ensure alignment with each patient’s insurance coverage. Additionally, education was also provided to administrative staff to reduce the number of denial claims through changes in the prior authorization process. The project team also worked in conjunction with the Finance and Information Technology teams at Huntsville Hospital to ensure appropriate billing codes were being used for each product. Pharmacy services were designated as a centralized resource to support therapeutic interchange, prior authorization confirmation, and transition planning during implementation.
Results:
In 2025, a total of 499 denial claims were identified, representing a potential loss of $402,832. The most common reasons for denial included submission or billing errors (n=157), lack of medical necessity (n=103), and duplication of payments (n=32). In 2026, only one denial claim had occurred as of March 1, 2026. Formulary optimization identified certain brands of ustekinumab, infliximab, and tocilizumab as the largest negative margin products. Transitioning to payer-preferred agents and biosimilars (Yesintek/Wezlana, Avsola/Inflectra, and Tofidence) resulted in a projected margin improvement of approximately $350,000 for 2026. The most profitable products included IVIG, bevacizumab, and rituximab. Overall, the total projected margin increase for outpatient medical services in 2026 is estimated at 7-10%.

Conclusion:
Implementation of an insurance-aligned outpatient formulary was associated with improved projected reimbursement margins and a marked reduction in claim denials. Alignment with payer-preferred agents and improved documentation contributed to decreased denial rates and an increase in overall margin. This pharmacist-supported, multidisciplinary approach may enhance financial stability and operational efficiency in outpatient infusion practices.
Moderators Presenters
avatar for William Casey Siders

William Casey Siders

PGY-1 Resident, Huntsville Hospital
Evaluators
avatar for Yona Roberts

Yona Roberts

RPD/Clinical Pharmacy Manager, WSGA1Wellstar Cobb HospitalPGY1
Yona Roberts earned a Doctor of Pharmacy degree from Florida Agricultural and Mechanical University in Tallahassee, Florida.  She went on to complete a Pharmacy Practice Residency through Mercer University at DeKalb Medical Center in Atlanta, Georgia.  After completion of her residency... Read More →
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena H

11:40am EDT

Comparative Evaluation of IV Push Versus IV Infusion Administration of Levetiracetam
Friday May 1, 2026 11:40am - 12:00pm EDT
Comparative Evaluation of IV Push Versus IV Infusion Administration of Levetiracetam 
Tavin Cook, Ashley Crisler, T.J. Henderson, Aayush Patel 
Piedmont Columbus Regional Midtown, Columbus GA

Background:
Levetiracetam is commonly administered as an IV infusion; however, IV push (IVP) administration has the potential to improve medication turnaround times, reduce nursing workload, and lower medication preparation costs without compromising safety. In January 2026, Piedmont Columbus Regional implemented IVP levetiracetam hospital wide. The objective of this study is to compare the timeliness of administration and cost difference associated with IVP levetiracetam versus IV infusion levetiracetam. 

Methods:
This study was a single-center, Institutional Review Board (IRB)–approved, retrospective chart review. The overall study timeframe spanned from October 13, 2025, to March 13, 2026. The pre-implementation period was October 13, 2025, to January 12, 2026, and the post-implementation period was January 14, 2026, to March 13, 2026. The study included adult patients aged 18 years or older who received intravenous levetiracetam at doses of less than 2 grams.  An EHR Slicer/Dicer data collection tool was used to collect points of time of order entry, order verification, and administration of medication. Cost analyses were conducted by integrating direct drug cost. The primary objective is to assess the difference in time from order verification to administration of once dose levetiracetam pre and post implementation. Secondary objectives include direct drug cost, time-critical medication compliance, and adverse drug reactions. Statistical analysis for the primary outcome used Mann-Whitney-U, secondary outcome descriptive analysis and chi-square testing. 

Results:
IV push levetiracetam demonstrated a numerically faster time to administration compared to IV infusion (19.7 vs 23.9 minutes), though this difference was not statistically significant (p=0.41). Time-critical medication compliance was significantly higher with IV push (85.7% vs 81.8%, p<0.001), and no adverse drug reactions were reported in either group. Additionally, IV push was associated with substantially lower direct drug costs, translating to significant projected annual savings.

Conclusions:
IV push levetiracetam is a cost-effective alternative to IV infusion that improves time-critical medication compliance while maintaining a comparable safety profile. Although a faster administration trend was observed, it did not reach statistical significance. Overall, IV push represents a practical and efficient strategy for levetiracetam administration within institutional practice.

Contact:
[email protected]   

Moderators Presenters Evaluators
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena G

11:40am EDT

Dalbavancin versus oral antibiotics for Staphylococcus aureus bone and joint infections
Friday May 1, 2026 11:40am - 12:00pm EDT
Authors: Mackenzie G. Pearsall, John Williamson, Mary Banoub, Charles Hartis, Elizabeth Palavecino, Vera Luther, Erin Barnes, Erika Swintosky, Michael DeWitt, Jennifer J. Wenner, Olivia Randazza

Background/Purpose: Staphylococcus aureus is a common organism associated with bone and joint infections (BJI).  Historically, the standard of care (SOC) treatment for BJIs is prolonged intravenous (IV) antibiotic therapy. Studies have compared alternative BJI treatments, including oral antibiotics and long acting lipoglycopeptides like dalbavancin, to SOC with no significant differences in clinical outcomes. This study aims to compare the clinical success of dalbavancin with or without an oral antibiotic versus oral antibiotics alone for the treatment of S. aureus BJI after IV lead-in.   
 
Methods: This is a multisite, retrospective, cohort study including adult patients with a documented S. aureus BJI. Patients were randomly identified using microbiologic culture data until there were 52 matched pairs on initial or recurrent infection. Eligible patients were those treated with dalbavancin with or without an oral antibiotic or an oral antibiotic alone who received 50% or less of the planned total treatment duration as IV lead-in. Patients were excluded if they had a polymicrobial BJI, concomitant endocarditis, valvular abscess, or infectious central nervous system involvement, if the S. aureus isolate was resistant to the antibiotic received, or if they had persistent bacteremia.  The primary outcome was clinical success at 90 days from the end of therapy. Secondary outcomes included identification of factors associated with clinical failure, incidence of adverse events, therapy discontinuation, incomplete therapy, and hospital readmission at 30 and 90 days. The results were analyzed using descriptive statistics. Categorical data was analyzed using Pearson’s chi-squared or Fisher’s exact test, and continuous data was analyzed using the Wilcoxon rank sum test. A univariate logistic regression was completed to identify factors associated with clinical failure. 
 
Results: In total, 1287 patients were screened, and 104 patients were included in the study with 52 patients in each cohort. The sample size was limited by the number of patients who received dalbavancin within the study period. 
  
The median age of the overall cohort was 50 years. There was a significant difference in the incidence of current or history of illicit intravenous drug use (IVDU) between the two cohorts, representing 19.2% of the oral cohort compared to 55.8% of the dalbavancin cohort (p<0.001).  Types of BJI were similar between the groups (dalbavancin vs. orals), including native osteomyelitis (37% vs. 50%, p=0.2), native joint septic arthritis (21% vs.17%, p=0.6), and prosthetic joint or hardware-associated infection (35% vs. 25%, p=0.3). However, the dalbavancin cohort contained significantly more cases of vertebral osteomyelitis (15% vs.1.9%, p=0.031) and MRSA isolates (77% vs. 52%, p=0.008). There was no difference in presence of source control (81% vs. 92%, p=0.085), however the dalbavancin group had significantly longer duration of IV lead-in (median 160 vs. 96 hours, p<0.001). 
 
The incidence of clinical success was 71% in the dalbavancin cohort compared to 69% in the oral cohort (p=0.8). There was a non-significant trend towards a higher rate of incomplete therapy in the dalbavancin cohort compared to the oral cohort (21% vs 9.6%, p=0.10). There were no significant differences in the rates of other secondary outcomes. The estimated cost savings were not significantly different between cohorts, with a median savings of $79006 in the dalbavancin cohort compared to $65580 in the oral cohort (p=0.5). 
 
None of the factors assessed in the univariate logistic regression (bacteremia, retained prosthetic material, IVDU, source control, incomplete therapy, isolate resistance to methicillin, and vertebral osteomyelitis) were significantly associated with clinical failure. Patients who obtained source control had a numerically lower rate of clinical failure (OR 0.36, p=0.084). 
 
Conclusions: In this cohort, there was no difference in clinical success between the oral antibiotic and dalbavancin treatment strategies after IV lead-in in S. aureus bone and joint infections. 


Moderators Presenters
avatar for Mackenzie Pearsall

Mackenzie Pearsall

PGY1 Pharmacy Resident, Atrium Health Wake Forest Baptist
Evaluators
avatar for Jessica Sterchi

Jessica Sterchi

Clinical Pharmacy Supervisor and Acute Care PGY1 RPD, BMHT1Blount Memorial HospitalPGY1
Friday May 1, 2026 11:40am - 12:00pm EDT
Athena J

11:40am EDT

Evaluation of Electronic Health Record Alerts for Heparin Use After Direct Oral Anticoagulant Exposure
Friday May 1, 2026 11:40am - 12:00pm EDT
Background: Anticoagulation therapy in hospitalized patients is inherently high-risk with complex dosing requirements and significant potential for drug interactions. Heparin is an anticoagulant that utilizes laboratory monitoring to target therapeutic concentrations, but accuracy of anti-Xa levels can be falsely elevated due to recent direct oral anticoagulant (DOAC) exposure. Our practice advisories (OPAs) are utilized within the electronic health record (EHR) to improve clinical decision-making and advance patient safety. The study site employs OPA alerts to identify elevated anti-Xa levels in patients who may have had recent exposure to a DOAC with the goal of helping practitioners decide if a reagent that removes DOAC effect on anti-Xa (DOAC-StopTM) should be utilized.  The objective of this study was to analyze the impact of an OPA for elevated anti-Xa levels in patients receiving heparin infusions with recent potential or known DOAC exposure, focusing on clinical appropriateness of DOAC-StopTM utilization and safety outcomes. 
Methods: This single center, retrospective cohort study analyzed patients with an elevated anti-Xa OPA alert(s) between January 1st and April 3rd, 2024 focusing on clinical appropriateness and safety outcomes. OPAs alerted for patients who were on a heparin infusion, had an elevated anti-Xa ≥ 1, and were within three days of admission or had documented receipt of a DOAC within the previous five days. Exclusion criteria included pregnancy, incarceration, switching between heparin protocols during the admission, and administration of enoxaparin within 24 hours of the elevated anti-Xa. The primary outcome assessed the appropriateness of subsequent actions in response to the OPA. Appropriateness was defined based on a treatment flowchart developed for study. Secondary outcomes included incidence of bleeding within 24 and 48 hours of the alert(s) per the International Society on Thrombosis and Haemostasias (ISTH) bleeding criteria and a subgroup analysis of DOAC-StopTM utilization by level of care and nursing shift. 
Results: A total of 100 patients were included in the final analysis. At baseline, 46% of patients were receiving apixaban, 6% rivaroxaban, and 48% were not receiving any anticoagulant within the 72 hours prior to heparin initiation. Clinical use of DOAC-StopTM following the first OPA was deemed appropriate for 92% of initial advisories and inappropriate for 8%. Inappropriate use, according to the study-developed flowchart, included administering DOAC-Stop™ to patients without prior DOAC exposure and omitting it in high-risk patients with prior exposure. There was no statistically significant difference between appropriate clinical use based on time of shift (p = 0.426) or by level of care (p = 0.119). Bleeding events were mostly attributable to clinically relevant non-major bleeding or major bleeding defined as a hemoglobin decrease of 2 mg/dL or more that required no clinical intervention. These events occurred within 0-24 hours in 11% of patients and within 0-48 hours in 18% of patients.  
Conclusions: While the true effect of this OPA is difficult to discern given lack of a control group, the high level of appropriate advisory response indicates that it was successful in identifying potential candidates for DOAC-StopTM and ensuring that high-risk patients received adequate anticoagulation evaluation. Practice advisories and protocols do not account for every scenario, and clinical judgement must be utilized to determine candidacy for DOAC-StopTM. 


Moderators Presenters Evaluators
avatar for Carrie Callahan

Carrie Callahan

Internal Medicine (IM) Specialist, PGY2 IM RPD, Emory University Hospital


Friday May 1, 2026 11:40am - 12:00pm EDT
Athena D
 

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