ChatGPT and Other Large Language Models in Inflammatory Arthritis: A Systematic Review Across Clinical Tasks

医学 指南 银屑病性关节炎 一致性 炎性关节炎 关节炎 可读性 类风湿性关节炎 物理疗法 梅德林 痹症科 临床试验 痛风 替代医学 重症监护医学 内科学 系统回顾 青少年类风湿关节炎 强直性脊柱炎 临床实习 循证医学 个性化医疗 可解释性 病人教育 荟萃分析 生物仿制药 临床判断 抗风湿药
作者
Yosef Adiniaev,Mahmud Omar,Tohar M. Timor,Yiftach Barash,Olga R. Brook,Mohammad E. Naffaa,Alon Gorenshtein,Eyal Klang
出处
期刊:The Journal of Rheumatology [The Journal of Rheumatology Publishing Company Limited]
卷期号:: jrheum.2026-0444
标识
DOI:10.3899/jrheum.2026-0444
摘要

OBJECTIVE: Large language models (LLMs) are increasingly evaluated for rheumatology tasks, but their performance in inflammatory arthritis remains unclear. We systematically reviewed LLM performance across clinical tasks in inflammatory arthritis. METHODS: We conducted a systematic review (PROSPERO: CRD420261359100), searching PubMed, Scopus, and PubMed Central (January 2022 to April 2026) for studies evaluating LLM performance on clinical tasks in inflammatory arthritis. Two reviewers (Y.A., A.G.) screened 113 records. RESULTS: Eighteen studies covered rheumatoid arthritis (n=3), ankylosing spondylitis/axial spondyloarthritis (n=7), psoriatic arthritis (n=2), gout (n=1), juvenile idiopathic arthritis (n=1), and multiple diseases (n=4). Most diseases and tasks were represented by only one to a few studies, and the evidence base remains earlystage and uneven across conditions. Over 20 distinct LLMs were evaluated, including ChatGPT-3.5 to ChatGPT-4o, Gemini 2.0, DeepSeek-R1/V3, Claude, and Perplexity; ChatGPT/GPT variants were the most frequently tested models (16 of 18 studies), so the current evidence base is predominantly GPT/ChatGPT-based. Findings spanned patient education (n=11), guideline adherence (n=6), clinical reasoning (n=3), and other applications (n=1). All readability assessments exceeded recommended thresholds. Guideline concordance ranged from 48% to 96%. Accuracy was lower for case-based clinical scenarios (4.24/6) than FAQ and guideline-based questions (5.32-5.36/6; p=0.044). When compared with real clinical data, agreement was poor (Cohen and Fleiss κ ≈ 0). CONCLUSION: LLMs may support patient education, factual medication queries, and structured guideline questions when used under clinician review, but should not be used for case-based reasoning, treatment selection, or autonomous clinical decisions. None of the 18 included studies evaluated retrieval-augmented or agent-based systems, and none prospectively validated LLMs in clinical workflows. Safe integration in rheumatology will require purpose-built, knowledge-grounded systems and prospective evaluation before routine clinical use.

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