Evidence map›Paper›PMID 40841953›Full record

ArticleCritical care (London, England)2025

Evaluating the o1 reasoning large language model for cognitive bias: a vignette study.

Or Degany, Sahar Laros, Daphna Idan, Sharon Einav

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Article in Critical care (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Or Degany *Gray School of Medicine, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel. ordegany@gmail.com.
Sahar Laros *Gray School of Medicine, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Daphna IdanMedint Medical Intelligence, Tel Aviv, Israel.
Sharon EinavMaccabi Healthcare Services, Sharon Region, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCognitive biases, systematic deviations from logical judgment, are well documented in clinical decision-making, particularly in clinical settings characterized by high decision load, limited time, and diagnostic uncertainty-such as critical care. Prior work demonstrated that large language models, particularly GPT-4, reproduce many of these biases, sometimes to a greater extent than human clinicians.

methodsWe tested whether the o1 model (o1-2024-12-17), a newly released AI system with enhanced reasoning capabilities, is susceptible to cognitive biases that commonly affect medical decision-making. Following the methodology established by Wang and Redelmeier [15], we used ten pairs of clinical scenarios, each designed to test a specific cognitive bias known to influence clinicians. Each scenario had two versions, differed by subtle modifications designed to trigger the bias (such as presenting mortality rates versus survival rates). The o1 model generated 90 independent clinical recommendations for each scenario version, totalling 1,800 responses. We measured cognitive bias as systematic differences in recommendation rates between the paired scenarios, which should not occur with unbiased reasoning. The o1 model's performance was compared against previously published results from both the GPT-4 model and historical human clinician studies.

resultsThe o1 model showed no measurable cognitive bias in seven of the ten vignettes. In two vignettes, the o1 model showed significant bias, but its absolute magnitude was lower than values previously reported for GPT-4 and human clinicians. In a single vignette, Occam's razor, the o1 model exhibited consistent bias. Therefore, although overall bias appears less frequent overall with the reasoning model than with GPT-4, it was worse in one vignette. The model was more prone to bias in vignettes that included a gap-closing cue, seemingly resolving the clinical uncertainty. Across eight vignette versions, intra‑scenario agreement exceeded 94%, indicating lower decision variability than previously described with GPT‑4 and human clinicians.

conclusionReasoning models may reduce cognitive bias and random variation in judgment (i.e., "noise"). However, our findings caution that reasoning models are still not entirely immune to cognitive bias. These findings suggest that reasoning models may impart some benefits as decision-support tools in medicine, but they also imply a need to explore further the circumstances in which these tools may fail.

Indexed as

Clinical Decision-MakingCognitionLanguageAdultBiasFemaleHumansLarge Language ModelsMaleMiddle AgedArtificial intelligenceClinical decision-makingCognitive biasCritical careDiagnostic errorHeuristicsLarge language modelsNoise (decision variability)Observer variationStep-by-step reasoning

Identifiers

PMID40841953
PMCPMC12372181

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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.