Integrating large language models in systematic reviews: a framework and case study using ROBINS-I for risk of bias assessment.
Bashar HasanSamer SaadiNoora S RajjoubMoustafa HegaziMohammad Al-KordiFarah FletiMagdoleen FarahIrbaz B RiazImon BanerjeeZhen WangMohammad Hassan MuradPublished in: BMJ evidence-based medicine (2024)
Large language models (LLMs) may facilitate and expedite systematic reviews, although the approach to integrate LLMs in the review process is unclear. This study evaluates GPT-4 agreement with human reviewers in assessing the risk of bias using the Risk Of Bias In Non-randomised Studies of Interventions (ROBINS-I) tool and proposes a framework for integrating LLMs into systematic reviews. The case study demonstrated that raw per cent agreement was the highest for the ROBINS-I domain of 'Classification of Intervention'. Kendall agreement coefficient was highest for the domains of 'Participant Selection', 'Missing Data' and 'Measurement of Outcomes', suggesting moderate agreement in these domains. Raw agreement about the overall risk of bias across domains was 61% (Kendall coefficient=0.35). The proposed framework for integrating LLMs into systematic reviews consists of four domains: rationale for LLM use, protocol (task definition, model selection, prompt engineering, data entry methods, human role and success metrics), execution (iterative revisions to the protocol) and reporting. We identify five basic task types relevant to systematic reviews: selection, extraction, judgement, analysis and narration. Considering the agreement level with a human reviewer in the case study, pairing artificial intelligence with an independent human reviewer remains required.
Keyphrases
- systematic review
- endothelial cells
- artificial intelligence
- randomized controlled trial
- induced pluripotent stem cells
- machine learning
- clinical trial
- meta analyses
- pluripotent stem cells
- big data
- deep learning
- autism spectrum disorder
- computed tomography
- type diabetes
- magnetic resonance imaging
- adipose tissue
- study protocol
- metabolic syndrome
- diffusion weighted imaging
- open label
- skeletal muscle