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Pragmatic real-world evaluation of computer-aided detection in colonoscopy: A within-endoscopist comparative study.

Created on 14 Aug 2026

Authors

Carlos Bernardes, Manuel Rocha, Jaime Rodrigues, Pedro Bastos, Raquel Ortigão, Ricardo Veloso, Teresa Moreira, Liliana Rafael, Cláudia Lourenço, Márcia Pinto, Lígia Prado, Pedro Pimentel-Nunes

Published in

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver. Aug 13, 2026. Epub Aug 13, 2026.

Abstract

Computer-aided detection (CADe) improves adenoma detection rate (ADR) in randomised trials; however, translation into routine practice remains uncertain, with real-world studies showing inconsistent results.
To evaluate CADe in a pragmatic multicentre setting using a within-endoscopist design, with endoscopists serving as their own comparators under routine clinical conditions.
Pragmatic multicentre observational study analysing prospectively recorded data from 13 units. Six endoscopists performed procedures in a unit with routine CADe use and in units without CADe, enabling within-operator comparisons under naturalistic conditions. The primary outcome was ADR. Secondary outcomes included combined adenoma plus clinically significant serrated polyp detection rate (A+CSSPDR) and additional polyp-related metrics.
Of 3161 colonoscopies, 2973 were analysed (947 CADe; 2026 non-CADe). ADR was higher with CADe (34.4%vs 30.7%; p = 0.042). A+CSSPDR was also higher (40.3%vs 35.8%; p = 0.018), with consistent improvements across other metrics. In multivariable analysis, CADe remained independently associated with higher ADR (aOR 1.31, 95%CI 1.11-1.55; p = 0.002) and A+CSSPDR (aOR 1.33, 95%CI 1.13-1.56; p = 0.001), with attenuation after adjustment for endoscopist.
In a pragmatic real-world setting, CADe improved detection of colorectal neoplasia. This within-endoscopist design provides a balanced estimate of effectiveness by minimising behavioural bias affecting both trial and real-world studies.

PMID:
42595629
Bibliographic data and abstract were imported from PubMed on 14 Aug 2026.

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