Implementation of optical diagnosis with a "resect and discard" strategy in clinical practice: DISCARD3 study.


Journal

Gastrointestinal endoscopy
ISSN: 1097-6779
Titre abrégé: Gastrointest Endosc
Pays: United States
ID NLM: 0010505

Informations de publication

Date de publication:
12 2022
Historique:
received: 10 03 2022
revised: 09 06 2022
accepted: 11 06 2022
pubmed: 21 6 2022
medline: 23 11 2022
entrez: 20 6 2022
Statut: ppublish

Résumé

Optical diagnosis (OD) of polyps can be performed with advanced endoscopic imaging. For high-confidence diagnoses, a "resect and discard" strategy could offer significant histopathology time and cost savings. The implementation threshold is a ≥90% OD-histology surveillance interval concordance. Here we assessed the OD learning curve and feasibility of a resect and discard strategy for ≤5-mm and <10-mm polyps in a bowel cancer screening setting. In this prospective feasibility study, 8 bowel cancer screening endoscopists completed a validated OD training module and performed procedures. All <10-mm consecutive polyps had white-light and narrow-band images taken and were given high- or low-confidence diagnoses until 120 high-confidence ≤5-mm polyp diagnoses had been performed. All polyps had standard histology. High-confidence OD errors underwent root-cause analysis. Histology and OD-derived surveillance intervals were calculated. Of 565 invited patients, 525 patients were included. A total of 1560 <10-mm polyps underwent OD and were resected and retrieved (1329 ≤5 mm and 231 6-9 mm). There were no <10-mm polyp cancers. High-confidence OD was accurate in 81.5% of ≤5-mm and 92.8% of 6-9-mm polyps. Sensitivity for OD of a ≤5-mm adenoma was 93.0% with a positive predictive value of 90.8%. OD-histology surveillance interval concordance for ≤5-mm OD was 91.3% (209/229) for U.S. Multi-Society Task Force, 98.3% (225/229) for European Society of Gastrointestinal Endoscopy, and 98.7% (226/229) for British Society of Gastroenterology guidelines, respectively. A resect and discard strategy for high-confidence ≤5-mm polyp OD in a group of bowel cancer screening colonoscopists is feasible and safe, with performance exceeding the 90% surveillance interval concordance required for implementation in clinical practice. (Clinical trial registration number: NCT04710693.).

Sections du résumé

BACKGROUND AND AIMS
Optical diagnosis (OD) of polyps can be performed with advanced endoscopic imaging. For high-confidence diagnoses, a "resect and discard" strategy could offer significant histopathology time and cost savings. The implementation threshold is a ≥90% OD-histology surveillance interval concordance. Here we assessed the OD learning curve and feasibility of a resect and discard strategy for ≤5-mm and <10-mm polyps in a bowel cancer screening setting.
METHODS
In this prospective feasibility study, 8 bowel cancer screening endoscopists completed a validated OD training module and performed procedures. All <10-mm consecutive polyps had white-light and narrow-band images taken and were given high- or low-confidence diagnoses until 120 high-confidence ≤5-mm polyp diagnoses had been performed. All polyps had standard histology. High-confidence OD errors underwent root-cause analysis. Histology and OD-derived surveillance intervals were calculated.
RESULTS
Of 565 invited patients, 525 patients were included. A total of 1560 <10-mm polyps underwent OD and were resected and retrieved (1329 ≤5 mm and 231 6-9 mm). There were no <10-mm polyp cancers. High-confidence OD was accurate in 81.5% of ≤5-mm and 92.8% of 6-9-mm polyps. Sensitivity for OD of a ≤5-mm adenoma was 93.0% with a positive predictive value of 90.8%. OD-histology surveillance interval concordance for ≤5-mm OD was 91.3% (209/229) for U.S. Multi-Society Task Force, 98.3% (225/229) for European Society of Gastrointestinal Endoscopy, and 98.7% (226/229) for British Society of Gastroenterology guidelines, respectively.
CONCLUSIONS
A resect and discard strategy for high-confidence ≤5-mm polyp OD in a group of bowel cancer screening colonoscopists is feasible and safe, with performance exceeding the 90% surveillance interval concordance required for implementation in clinical practice. (Clinical trial registration number: NCT04710693.).

Identifiants

pubmed: 35724693
pii: S0016-5107(22)01770-9
doi: 10.1016/j.gie.2022.06.019
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04710693']

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1021-1032.e2

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American Society for Gastrointestinal Endoscopy. Published by Elsevier Inc. All rights reserved.

Auteurs

Ahmir Ahmad (A)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Morgan Moorghen (M)

Pathology Department, St Mark's Hospital, Harrow, London, UK.

Ana Wilson (A)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Ioannis Stasinos (I)

NIMTS Hospital, Athens, Greece.

Adam Haycock (A)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Adam Humphries (A)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Kevin Monahan (K)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Noriko Suzuki (N)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Siwan Thomas-Gibson (S)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Margaret Vance (M)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Kowshika Thiruvilangam (K)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

Angad Dhillon (A)

Gastroenterology Department, Queen Elizabeth Hospital, Lewisham and Greenwich NHS Trust, London, UK.

Brian P Saunders (BP)

Wolfson Unit for Endoscopy, St Mark's Hospital, Harrow, London, UK.

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