Evidence map›Paper›PMID 39935064›Full record

ArticleClinical pharmacology and therapeutics2025

Chat GPT vs. Clinical Decision Support Systems in the Analysis of Drug-Drug Interactions.

Thorsten Bischof, Valentin Al Jalali, Markus Zeitlinger, Anselm Jorda, Michelle Hana, Karla-Nikita Singeorzan, Nikolaus Riesenhuber, Gunar Stemer, Christian Schoergenhofer

Abstract readComparative Study
In one paragraph

Article in Clinical pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Drug-drug interaction identification using large language models.medRxiv : the preprint server for health sciences · 2025
    Article
  10. Article
  11. Article
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

9 authors.

Thorsten BischofDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.ORCID 0009-0003-8288-8591
Valentin Al JalaliDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-9196-1936
Markus ZeitlingerDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Anselm JordaDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5500-5878
Michelle HanaDepartment for Medicines Information and Clinical Pharmacy, Pharmacy of the University Hospital Vienna, Vienna, Austria.
Karla-Nikita SingeorzanDepartment for Medicines Information and Clinical Pharmacy, Pharmacy of the University Hospital Vienna, Vienna, Austria.
Nikolaus RiesenhuberDepartment for Medicines Information and Clinical Pharmacy, Pharmacy of the University Hospital Vienna, Vienna, Austria.ORCID 0000-0001-5123-2280
Gunar StemerDepartment for Medicines Information and Clinical Pharmacy, Pharmacy of the University Hospital Vienna, Vienna, Austria.
Christian SchoergenhoferDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current standard method for the analysis of potential drug-drug interactions (pDDIs) is time-consuming and includes the use of multiple clinical decision support systems (CDSSs) and the interpretation by healthcare professionals. With the emergence of large language models developed with artificial intelligence, an interesting alternative arose. This retrospective study included 30 patients with polypharmacy, who underwent a pDDI analysis between October 2022 and August 2023, and compared the performance of Chat GPT and established CDSSs (MediQ®, Lexicomp®, Micromedex®) in the analysis of pDDIs. A multidisciplinary team interpreted the obtained results and decided upon clinical relevance and assigned severity grades using three categories: (i) contraindicated, (ii) severe, (iii) moderate. The expert review identified a total of 280 clinically relevant pDDIs (3 contraindications, 13 severe, 264 moderate) using established CDSSs, compared with 80 pDDIs (2 contraindications, 5 severe, 73 moderate) using Chat GPT. Chat GPT almost entirely neglected pDDIs with the risk to QTc prolongation (85 vs. 8), which could also not be sufficiently improved by using a specific prompt. To assess the consistency of the results provided by Chat GPT, we repeated each query and found inconsistent results in 90% of the cases. In contrast, Chat GPT provided acceptable and comprehensible recommendations for specific questions on side effects. The use of Chat GPT for the identification of pDDIs cannot be recommended currently, because clinically relevant pDDIs were not detected, there were obvious errors and results were inconsistent. However, if these limitations are addressed accordingly, it is a promising platform for the future.

Indexed as

Decision Support Systems, ClinicalAgedAged, 80 and overArtificial IntelligenceDrug InteractionsFemaleGenerative Artificial IntelligenceHumansMaleMiddle AgedPolypharmacyRetrospective Studies

Identifiers

PMID39935064
PMCPMC11924163

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Registered trials

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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.