Evidence map›Paper›PMID 41368579›Full record

ArticleFrontiers in pharmacology2025

Large language models management of complex medication regimens: a case-based evaluation.

Aaron Chase, Amoreena Most, Shaochen Xu, Erin Barreto, Brian Murray, Kelli Henry, Susan Smith, Tanner Hedrick, Xianyan Chen, Sheng Li and 2 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Aaron ChaseDepartment of Pharmacy, Wellstar MCG Health, Augusta, GA, United States.
Amoreena MostDepartment of Pharmacy, UNM Health System, Albuquerque, NM, United States.
Shaochen XuDepartment of Computer Science, University of Georgia, Athens, GA, United States.
Erin BarretoDepartment of Pharmacy, Mayo Clinic, Rochester, MN, United States.
Brian MurrayDepartment of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy, Aurora, CO, United States.
Kelli HenryDepartment of Pharmacy, Wellstar MCG Health, Augusta, GA, United States.
Susan SmithDepartment of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Athens, GA, United States.
Tanner HedrickDepartment of Pharmacy, University of North Carolina Medical Center, Chapel Hill, NC, United States.
Xianyan ChenDepartment of Epidemiology & Biostatistics, University of Georgia College of Public Health, Athens, GA, United States.
Sheng LiSchool of Data Science, University of Virginia, Charlottesville, VA, United States.
Tianming LiuDepartment of Computer Science, University of Georgia, Athens, GA, United States.
Andrea SikoraDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, CO, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Large language models (LLMs) have shown the ability to diagnose complex medical cases, but only limited studies have evaluated the performance of LLMs in the development of evidence-based treatment plans. The purpose of this evaluation was to test four LLMs on their ability to develop safe and efficacious treatment plans on complex patients managed in the intensive care unit (ICU). Methods: Eight high-fidelity patient cases focusing on medication management were developed by critical care clinicians including history of present illness, laboratory values, vital signs, home medications, and current medications. Four LLMs [ChatGPT (GPT-3.5), ChatGPT (GPT-4), Claude-2, and Llama-2-70b] were prompted to develop an optimized medication regimen for each case. LLM generated medication regimens were then reviewed by a panel of seven critical care clinicians to assess safety and efficacy, as defined by medication errors identified and appropriate treatment for the clinical conditions. Appropriate treatment was measured by the average rate of clinician agreement to continue each medication in the regimen and compared using analysis of variance (ANOVA). Results: Clinicians identified a median of 4.1-6.9 medication errors per recommended regimen, and life-threatening medication recommendations were present in 16.3%-57.1% of the regimens, depending on LLM. Clinicians continued LLM-recommended medications at a rate of 54.6%-67.3%, with GPT-4 having the highest rate of medication continuation among all LLMs tested (p < 0.001) and the lowest rate of life-threatening medication errors (p < 0.001). Conclusion: Caution is warranted using present LLMs for medication regimens given the number of medication errors that were identified in this pilot study. However, LLMs did demonstrate potential to serve as clinical decision support for the management of complex medication regimens given the need for domain specific prompting and testing.

Indexed as

artificial intelligencelarge language modelmedication regimen complexitynatural language processing (NLP)pharmacy

Identifiers

PMID41368579
PMCPMC12682882

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.