Evidence map›Paper›PMID 42712411›Full record

ArticleBMJ digital health & AI2026

Comparison of three large language models' ability to assess the risk of bias using ROBINS-I tool.

Samer Saadi, Farah Fleti, Omar H Rajjoub, Ayla Shamsi Basha, Mohammed Firwana, Zain Abideen, Tamim Rajjo, Zhen Wang, M Hassan Murad

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Article in BMJ digital health & AI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Samer Saadi *Evidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-9225-1197
Farah Fleti *Evidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.
Omar H RajjoubEvidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.
Ayla Shamsi BashaEvidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.
Mohammed FirwanaEvidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.
Zain AbideenDepartment of Family Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Tamim RajjoDepartment of Family Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Zhen WangEvidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.
M Hassan MuradEvidence-Based Practice Center, Mayo Clinic, Rochester, Minnesota, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aims to compare the reliability and accuracy of three large language models (LLMs) (Claude, Gemini and GPT) in assessing the risk of bias of nonrandomised studies using the ROBINS-I tool. Methods and analysis: We conducted a secondary analysis of 171 nonrandomised studies previously assessed with Risk Of Bias In Non-randomized Studies of Interventions (ROBINS-I) tool by two independent human review teams. Only studies with concordant human domain-level ratings were included. Each study was independently assessed twice by Claude, Gemini and Generative Pre-trained Transformer (GPT) using agent-based structured implementations of the ROBINS-I tool. Reliability (agreement between two runs of the same LLM) was evaluated using percent agreement and Gwet's AC1. Accuracy (agreement with human reviewers) was assessed only for studies with consistent LLM ratings, using the same metrics. Results: Claude demonstrated high reliability across all domains (79.5-98.0% agreement, AC1=0.729-0.975). Gemini showed moderate-to-high reliability (agreement 76.7-100%, AC1=0.680-1.0). GPT exhibited lower reliability overall, though domain-level agreement ranged from 70.9-95.6% (AC1=0.596-0.944). In terms of accuracy, Claude showed overall poor agreement with human reviewers (14.4-68.5% agreement; low AC1 values). Gemini demonstrated moderate-to-high accuracy in several domains, including deviations from intended interventions (79.6%, AC1=0.848) and measurement of outcomes (73.9%, AC1=0.702), with the highest overall agreement (40.0%, AC1=0.672). GPT showed variable accuracy, with the highest in measurement of outcomes (62.8%, AC1=0.571) and classification of interventions (57.8%, AC1=0.498), but poor performance in selection (14.3%, AC1 = -0.041) and overall agreement (23.0%, AC1=0.267). Conclusions: Claude was internally consistent but poorly aligned with human reviewers. Gemini achieved both high reliability and moderate-to-high accuracy, whereas GPT had lower reliability and mixed accuracy. Current off-the-shelf LLMs cannot reliably perform ROBINS-I risk of bias assessments.

Indexed as

Artificial intelligenceEvidence-Based Medicine

Identifiers

PMID42712411
PMCPMC13528376

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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.