The performance of covidence: an artificial intelligence-based tool for title and abstract screening in a breast cancer evidence-based clinical practice guideline

Clinical practice guidelines (CPGs) support evidence-based care but are time-consuming to develop. This study aimed to compare artificial intelligence (AI)-assisted versus manual title and abstract screening (Stage I) in Covidence using data from a published breast-cancer CPG. This systematic review (SR) included 8,774 articles identified through a medical literature search, after removing duplicates. Three article subsets ( n =500, 1,000, and 2,000) were randomly selected from 8,774 articles to perform 30, 30, and 10 trials, respectively, independent Stage I, AI-assisted trials. The primary outcome of each trial is workload savings achieved through AI-assisted identification of 95% and 100% relevant articles (i.e., sensitivity), and 100% of finally-included articles. The secondary outcome is missed finally-included articles when the sensitivity of 95% was reached for each subset. At the sensitivity of 95%, 100% relevant articles and 100% finally-included articles were identified, median (minimum, maximum) workload savings are 40.7% (4.4%, 59.4%), 25.0% (0.4%, 55.2%), 57.6% (6.2%, 76.4%) for n =500; 38.3% (6.2%, 54.0%), 17.3% (0.0%, 39.1%), 63.9% (0.4%, 77.5%) for n =1,000; 16.6% (10.8%, 41.8%), 4.4% (0.3%, 20.9%), 17.9% (0.8%, 64.6%) for n =2,000 respectively. Covidence’s performance does not improve as the size of the subsets increases for a CPG with multiple complicated research questions. A potential positive correlation between the proportion of relevant articles in initial training of Covidence and workload savings at Stage I across all 70 trials. At 95% sensitivity, 5 trials missed 1 article ( n =500); 2 trials missed 2 articles and 1 trial missed 1 article ( n =1,000); 1 trial missed 3 articles, and 5trials missed 1 article ( n =2,000). AI-assistance in Covidence for Stage I screening shows both promise and pitfalls in the SR for a breast cancer CPG on a complex topic. Further prospective research is needed to better understand the performance of AI-assistance in Covidence and the intricacies of CPG topics.

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Publication Details

Journal
Intelligent Medicine
Published
2025-12-01
DOI
https://doi.org/10.1016/j.imed.2025.12.008
Primary Topic
Clinical practice guidelines implementation
Type
article
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article

The performance of covidence: an artificial intelligence-based tool for title and abstract screening in a breast cancer evidence-based clinical practice guideline

Jonathan Sussman, Ashley Low, Xiaomei Yao, Ashirbani Saha et al.
Intelligent Medicine
Clinical practice guidelines implementation
article

The performance of covidence: an artificial intelligence-based tool for title and abstract screening in a breast cancer evidence-based clinical practice guideline

Jonathan Sussman, Ashley Low, Xiaomei Yao, Ashirbani Saha, Shakil Ahmed, Aditya Misra, Mariam Abdelmalek, Samya Ali, Sharan Saravanan
article en

Abstract

Clinical practice guidelines (CPGs) support evidence-based care but are time-consuming to develop. This study aimed to compare artificial intelligence (AI)-assisted versus manual title and abstract screening (Stage I) in Covidence using data from a published breast-cancer CPG. This systematic review (SR) included 8,774 articles identified through a medical literature search, after removing duplicates. Three article subsets ( n =500, 1,000, and 2,000) were randomly selected from 8,774 articles to perform 30, 30, and 10 trials, respectively, independent Stage I, AI-assisted trials. The primary outcome of each trial is workload savings achieved through AI-assisted identification of 95% and 100% relevant articles (i.e., sensitivity), and 100% of finally-included articles. The secondary outcome is missed finally-included articles when the sensitivity of 95% was reached for each subset. At the sensitivity of 95%, 100% relevant articles and 100% finally-included articles were identified, median (minimum, maximum) workload savings are 40.7% (4.4%, 59.4%), 25.0% (0.4%, 55.2%), 57.6% (6.2%, 76.4%) for n =500; 38.3% (6.2%, 54.0%), 17.3% (0.0%, 39.1%), 63.9% (0.4%, 77.5%) for n =1,000; 16.6% (10.8%, 41.8%), 4.4% (0.3%, 20.9%), 17.9% (0.8%, 64.6%) for n =2,000 respectively. Covidence’s performance does not improve as the size of the subsets increases for a CPG with multiple complicated research questions. A potential positive correlation between the proportion of relevant articles in initial training of Covidence and workload savings at Stage I across all 70 trials. At 95% sensitivity, 5 trials missed 1 article ( n =500); 2 trials missed 2 articles and 1 trial missed 1 article ( n =1,000); 1 trial missed 3 articles, and 5trials missed 1 article ( n =2,000). AI-assistance in Covidence for Stage I screening shows both promise and pitfalls in the SR for a breast cancer CPG on a complex topic. Further prospective research is needed to better understand the performance of AI-assistance in Covidence and the intricacies of CPG topics.

Intelligent Medicine
Population Health Research Institute (CA), Impact (CA), Hamilton Health Sciences (CA), McMaster University (CA)
Openalex Percentile: Top 26%
Clinical practice guidelines implementation
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