ArticleCochrane evidence synthesis and methods2025
Assessing the Feasibility and Acceptability of a Bespoke Large Language Model Pipeline to Extract Data From Different Study Designs for Public Health Evidence Reviews.
Article in Cochrane evidence synthesis and methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Using full agreement across multiple large language models for title-and-abstract screening in systematic reviews: a proof-of-concept.Systematic reviews · 2026Article
- Assessing the Feasibility and Acceptability of a Bespoke Large Language Model Pipeline to Extract Data From Different Study Designs for Public Health Evidence Reviews.Cochrane evidence synthesis and methods · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Data extraction is a critical but resource-intensive step of the evidence review process. Whilst there is evidence that artificial intelligence (AI) and large language models (LLMs) can improve the efficiency of data extraction from randomized controlled trials, their potential for other study designs is unclear. In this context, this study aimed to evaluate the performance of a bespoke LLM model pipeline (Retrieval-Augmented Generation pipeline utilizing LLaMa 3-70B) to automate data extraction from a range of study designs by assessing the accuracy and reliability of the extractions measured as error types and acceptability. Methods: Accuracy was assessed by retrospectively comparing the LLM extractions against human extractions from a review previously conducted by the authors. A total of 173 data fields from 24 articles (including experimental, observational, qualitative, and modeling studies) were assessed, of which three were used for prompt engineering. Reliability was assessed by calculating the mean maximum agreement rate (the highest proportion of identical returns from 10 consecutive extractions) for 116 data fields from 16 of the 24 studies. An evaluation framework was developed to assess the accuracy and reliability of LLM outputs measured as error types and acceptability (acceptability was assessed on whether it would be usable in real-world settings if the model acted as one reviewer and a human as a second reviewer). Results: Of the 173 data fields evaluated for accuracy, 68% were rated by human reviewers as acceptable (consistent with what is deemed to be acceptable data extraction from a human reviewer). However, acceptability ratings varied depending on the data field extracted (33% to 100%), with at least 90% acceptability for "objective," "setting," and "study design," but 54% or less for data fields such as "outcome" and "time period." For reliability, the mean maximum agreement rate was 0.71 (SD: 0.28), with variation across different data fields. Conclusion: This evaluation demonstrates the potential for LLMs, when paired with human quality assurance, to support data extraction in evidence reviews that include a range of study designs. However, further improvements in performance and validation are required before the model can be introduced into review workflows.
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Registered trials
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.