ArticleJournal of the Canadian Association of Gastroenterology2026
Human-machine interaction in optical polyp diagnosis: decision-making after CADx polyp diagnosis.
Article in Journal of the Canadian Association of Gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06822816 (Creation of a Video/Image Library of Annotated Full-length Endoscopy Procedures for the Development of Artificial Intelligence-empowered Endoscopy Quality Reporting and Educational Modules), which is not on this map. Not yet cited in PubMed.
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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.
Creation of a Video/Image Library of Annotated Full-length Endoscopy Procedures for the Development of Artificial Intelligence-empowered Endoscopy Quality Reporting and Educational Modules
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Artificial intelligence (AI)-based computer-aided diagnosis (CADx) systems are increasingly used to classify colorectal polyps during colonoscopy, but their impact depends on how endoscopists interpret AI predictions. This study aimed to evaluate endoscopists' decision-making after reviewing CADx outputs, using histopathology diagnosis as ground truth. Patients and methods: We performed a secondary analysis of a prospective study (NCT06822816) conducted at our centre between 2022 and 2025. All patients and polyps ≤10 mm with documented CADx output and endoscopist diagnosis were included. Endoscopists either accepted CADx classifications (neoplastic vs hyperplastic) or provided alternatives. Our primary outcome was the accuracy of accepted CADx diagnoses; secondary outcomes assessed reclassification patterns after CADx output rejection. Results: Our cohort included 754 polyps <10 mm from 367 patients. Accepted CADx diagnoses were correct for 89.1% of neoplastic and 68.7% of hyperplastic CADx predictions. Endoscopists accepted incorrect CADx classifications more frequently when these were neoplastic compared to hyperplastic (64.9% vs 26.5%). Upon rejecting correct CADx neoplastic predictions, endoscopists misclassified 23.4% as sessile serrated lesions (SSLs). Similarly, 29.5% of rejected correct CADx hyperplastic predictions were incorrectly reassigned as SSLs. Conclusions: Endoscopists exhibit a diagnostic bias toward neoplasia, particularly misclassifying hyperplastic polyps as SSLs. While this may enhance safety, it may risk unnecessary surveillance colonoscopies and increase costs.
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