Evidence map›Paper›PMID 41363762›Full record

ArticleClinical and translational gastroenterology2026

Effect of Combination of a Mucosal Exposure Device and Computer-Aided Detection in Diagnostic, Screening, and Surveillance Colonoscopy: An International, Multicenter Study.

Michiel H J Maas, Milou L M van Riswijk, Timo Rath, Paola Cesaro, Daniele Salvi, Peter D Siersema, DISCOVERY III study group

Abstract readMulticenter Study
In one paragraph

Article in Clinical and translational gastroenterology, 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
–field-weighted citation impact
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

7 authors.

Michiel H J MaasDepartment of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0009-0000-6382-1656
Milou L M van RiswijkDepartment of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, the Netherlands.
Timo RathDivision of Gastroenterology, Department of Medicine I, Universitätsklinikum Erlangen, Erlangen, Germany.
Paola CesaroDepartment of Gastroenterology and Endoscopy, Fondazione Poliambulanza Istituto Ospedaliero, Brescia, Italy.
Daniele SalviDepartment of Gastroenterology and Endoscopy, Fondazione Poliambulanza Istituto Ospedaliero, Brescia, Italy.
Peter D SiersemaDepartment of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, the Netherlands.
DISCOVERY III study group

Funding

European Society of Gastrointestinal Endoscopy, PENTAX Medical the ESGE Research Champions' Den 2022
6 · The paper itself

Abstract

introductionMucosal exposure devices (MEDs) and computer-aided detection (CADe) systems may both improve adenoma detection through distinct mechanisms: expanding mucosal visualization and highlighting lesions, respectively. This study investigated the efficacy of combining CADe-assisted colonoscopy with a MED compared with CADe-assisted colonoscopy alone.

methodsThis international, multicenter, prospective, nonrandomized, single-arm study (NTC05220345) was conducted at 3 centers that also participated in the previous DISCOVERY II randomized controlled trial, comparing CADe-assisted with conventional colonoscopy. Eligible participants were patients referred for diagnostic, nonfecal immunochemical test screening, or surveillance colonoscopy and underwent CADe-assisted colonoscopy (DISCOVERY, PENTAX Medical) with a MED using an integrated inflatable balloon (G-EYE, SMART Medical Systems). The primary outcome was adenoma detection rate (ADR); secondary outcomes included sessile serrated lesion detection rate and withdrawal time without interventions. Outcomes were compared with historical controls of the CADe-arm of the DISCOVERY II study.

resultsOf 196 enrolled participants, 182 were included in the final analysis and compared with 250 participants from the historical CADe-arm. ADR was 47.3% in the CADe + MED-group vs 38.4% in the CADe-group ( P = .066; absolute difference: 8.9%, 95% confidence interval: 0.6-18.3). Mixed-effects logistic regression model adjusting for clustering and confounders calculated an odds ratio of 1.16 (95% confidence interval: 0.74-1.81). Median withdrawal time was slightly longer with CADe + MED compared with CADe-only (10.0 vs 9.2 minutes, P = 0.004), whereas sessile serrated lesion detection rate was not significantly different (12.6% vs 18.4%, P = 0.11). DISCUSSION: In this study using historical controls, CADe-assisted colonoscopy combined with a MED did not significantly increase ADR compared with CADe alone, suggesting limited synergistic benefit.

Indexed as

AdenomaColonic PolypsColonoscopyColorectal NeoplasmsDiagnosis, Computer-AssistedEarly Detection of CancerAgedColonFemaleHumansIntestinal MucosaMaleMiddle AgedProspective Studiesadenomasartificial intelligencecolonoscopycomputer-aided detection

Identifiers

PMID41363762
PMCPMC12922936

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.