Endoscopy 2025; 57(10): 1180-1181
DOI: 10.1055/a-2651-7353
Letter to the editor

Same evidence but different recommendations – Dilemma in computer-aided detection in colonoscopy

1   Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy
2   Endoscopy Unit, IRCCS Humanitas Research Hospital, Rozzano, Italy
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3   Clinical Effectiveness Research Group, University of Oslo and Oslo University Hospital, Oslo, Norway
4   Gastroenterology Section, Transplantation Medicine, Oslo University, Oslo, Norway
5   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan (Ringgold ID: RIN220878)
› Institutsangaben

Gefördert durch: AIRC (Associazione Italiana per la Ricerca sul Cancro) IG 2022 - ID. 27843 project.
Gefördert durch: European Commission No. 101057099
Gefördert durch: Japan Society of Promotion of Science (No. 22H03357)
Preview

A recent Position Statement from the European Society of Gastrointestinal Endoscopy (ESGE) [1] highlights the paradoxes of modern guideline development. In March 2025, ESGE [1], the British Medical Journal (BMJ) [2], and the American Gastroenterological Association (AGA) [3] released guidelines on using computer-aided detection (CADe) during colonoscopy, all based on the same evidence from the EU-funded OperA project [4]. Despite this shared foundation, ESGE weakly recommended CADe, BMJ weakly recommended against it, and AGA made no recommendation.

This confusing discord was not due to differences in the evidence base, but to differing interpretations of it, driven by uncertainties of the data, different preferences and values, and selection of the panel members, all of which are considered core pillars when making trustworthy GRADE-based guidelines [5]. All three guidelines used a microsimulation model showing that CADe would prevent 111 colorectal cancers per 100 000 screened (0.1% absolute reduction), require 6366 additional colonoscopies (6.4% increase), and cause no change in harms [4]. Yet they reached contradictory conclusions.

Key uncertainties that shaped their judgments included limitations of microsimulation modelling, the unblinded nature of colonoscopy trials, variable CADe performance among endoscopists, opaque regulatory processes for CADe, and unclear patient values and preferences [2]. When benefits are marginal and evidence is imperfect, how a panel interprets these uncertainties plays a crucial role in the final recommendation. Panel composition also played a role: ESGE included only clinicians, BMJ included patient partners and methodologists, and AGA had clinicians and methodologists but not patients. These differences suggest that guideline outcomes are influenced not only by evidence but by who is interpreting it – and the values they bring to the table.

For clinicians, especially when recommendations are weak or conflicting, understanding this process is essential. In such cases, shared decision-making – openly discussing potential benefits, harms, and burdens with patients – is crucial to delivering patient-centered care.



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Artikel online veröffentlicht:
24. September 2025

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