Evidence map›Paper›PMID 42664251›Full record

ArticlePLOS digital health2026

Artificial intelligence-driven study selection in systematic reviews of randomized controlled trials, emulated trials and economic evaluation studies using large language models.

Panu Looareesuwan, Wanchana Ponthongmak, Amarit Tansawet, Cholatid Ratanatharathorn, Habib Ur Rehman Owasi, Gareth J McKay, John Attia, Takehiko Oami, Ammarin Thakkinstian

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Panu LooareesuwanDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Wanchana PonthongmakDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-9896-1349
Amarit TansawetFaculty of Medicine, Research Affairs, Chulalongkorn University, Bangkok, Thailand.
Cholatid RatanatharathornDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Habib Ur Rehman OwasiDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Gareth J McKayCentre for Public Health, Queen's University Belfast, Belfast, United Kingdom.ORCID https://orcid.org/0000-0001-8197-6280
John AttiaCentre for Clinical Epidemiology and Biostatistics, School of Medicine and Public Health, University of Newcastle, Newcastle, NSW, Australia.ORCID https://orcid.org/0000-0001-9800-1308
Takehiko OamiDepartment of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Ammarin ThakkinstianDepartment of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systematic reviews (SRs) are key to evidence-based medicine but are often labor-intensive, especially in the study selection step. This study assessed the use of large language models (LLMs) to automate SR study screening and selection. Five SR projects were included: two published therapeutic SRs (SR1-2), two ongoing emulated-trial SRs (SR3-4), and one economic evaluation SR (SR5). The total number of studies screened for each SR was 3,966, 3,147, 695, 3,096 and 485, respectively, with 20, 24, 46, 32 and 70 eligible studies. Three LLMs-Gemini 2.0 Flash, Llama 3.1, and Qwen 2.5-were evaluated using training sets (five studies), title/abstract datasets, and full-text datasets predicted as relevant. Prompts based on the PICOS framework were iteratively refined using a recall-first strategy. Outputs were compared with human reviewer classifications using recall, number needed to screen (NNS), and percentage reduced workload with 95% confidence intervals. In the title/abstract screening phase, Llama 3.1 and Gemini 2.0 Flash achieved consistently high recall (90.00%-100.00% and 90.48%-100.00%), with workload reduction of 61.92%-97.10% and 65.21%-97.03%, respectively. Qwen 2.5 achieved the highest workload reduction (76.16%-99.19%) but showed the lowest recall (76.67%-88.89%). In the full-text selection phase, Llama 3.1 achieved the highest recall (93.33%-100.00%) with workload reductions of 73.15%-97.41%, but slower processing time (approximately 2.3-3.6 minutes per document). Qwen 2.5 yielded lower recall (66.67%-89.71%), despite the highest workload reduction (80.82%-99.44%) and similarly slow inference times (approximately 3.0-4.2 minutes per document). Gemini 2.0 Flash balanced high recall (83.33%-100.00%) with substantial workload reduction (76.71%-98.91%) and markedly faster inference (approximately 4-8 seconds per document). LLMs-particularly Llama 3.1 and Gemini 2.0 Flash-can substantially reduce SR screening workload while maintaining high recall when guided by a recall-first prompting framework. Remaining challenges include reproducibility in closed-source models and generalizability across diverse SR topics.

Identifiers

PMID42664251
PMCPMC13524291

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Registered trials

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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.