Impact of endoscopy system, high definition, and virtual chromoendoscopy in daily routine colonoscopy: a randomized trial.


Journal

Endoscopy
ISSN: 1438-8812
Titre abrégé: Endoscopy
Pays: Germany
ID NLM: 0215166

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 16 1 2019
medline: 21 4 2020
entrez: 16 1 2019
Statut: ppublish

Résumé

To improve detection of mucosal lesions during colonoscopy a number of imaging modalities have been suggested, including high definition and virtual chromoendoscopy. Given the theoretical advantage of these new imaging techniques, we aimed to investigate their use for the detection of polyps in patients referred for colonoscopy in a large tertiary hospital. Demographic, endoscopic, and histological data from 1855 consecutive patients undergoing colonoscopy were collected prospectively. Patients were randomly assigned to three endoscopy systems (Fujinon, Olympus, or Pentax) in combination with four modalities: conventional white-light colonoscopy (n = 505), high definition white-light colonoscopy (n = 582), virtual chromoendoscopy (n = 285) and high definition virtual chromoendoscopy (n = 483). The mean adenoma detection rate (ADR) was 34.9 %, and the adenoma per colonoscopy rate (APCR) was 2.1. No significant differences were noted between the three endoscopy systems. Moreover, no differences in ADR or APCR were observed between the four imaging modalities. High definition white-light colonoscopy resulted in a significantly higher detection of sessile serrated adenomas (8.2 % vs. 3.8 %; No significant differences in ADR or APCR between different endoscopy systems, high definition, and/or virtual chromoendoscopy could be observed in routine colonoscopies in the general population. High definition endoscopy was associated with a significantly higher detection rate of serrated adenomas and adenocarcinomas.

Sections du résumé

BACKGROUND
To improve detection of mucosal lesions during colonoscopy a number of imaging modalities have been suggested, including high definition and virtual chromoendoscopy. Given the theoretical advantage of these new imaging techniques, we aimed to investigate their use for the detection of polyps in patients referred for colonoscopy in a large tertiary hospital.
METHODS
Demographic, endoscopic, and histological data from 1855 consecutive patients undergoing colonoscopy were collected prospectively. Patients were randomly assigned to three endoscopy systems (Fujinon, Olympus, or Pentax) in combination with four modalities: conventional white-light colonoscopy (n = 505), high definition white-light colonoscopy (n = 582), virtual chromoendoscopy (n = 285) and high definition virtual chromoendoscopy (n = 483).
RESULTS
The mean adenoma detection rate (ADR) was 34.9 %, and the adenoma per colonoscopy rate (APCR) was 2.1. No significant differences were noted between the three endoscopy systems. Moreover, no differences in ADR or APCR were observed between the four imaging modalities. High definition white-light colonoscopy resulted in a significantly higher detection of sessile serrated adenomas (8.2 % vs. 3.8 %;
CONCLUSIONS
No significant differences in ADR or APCR between different endoscopy systems, high definition, and/or virtual chromoendoscopy could be observed in routine colonoscopies in the general population. High definition endoscopy was associated with a significantly higher detection rate of serrated adenomas and adenocarcinomas.

Identifiants

pubmed: 30646403
doi: 10.1055/a-0755-7471
doi:

Types de publication

Comparative Study Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

237-243

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© Georg Thieme Verlag KG Stuttgart · New York.

Déclaration de conflit d'intérêts

Dr. Bessissow has received research support from Pentax and speaker fees from Ferring and Pendopharm. Dr. Cuyle has received nonfinancial support (travel expenses) from Norgine. Dr. Ferrante has received consultancy fees from Ferring and speaker fees from Dr. Falk Pharma and Ferring. Dr. Van Assche has received speaker fees from Ferring. Dr. Vermeire has received consultancy fees from Ferring and speaker fees from Dr. Falk Pharma and Ferring. Dr. Bisschops has received speaker fees, consultancy fees, and/or research support from Boston Scientific, CDx Diagnostics, Cook Medical, Fujifilm, Olympus, Medtronic, and Pentax.Dr. Roelandt is supported by Clinical Mandate from Belgian Foundation against Cancer (Stichting tegen Kanker). Drs. Ferrante, Van Assche, and Vermeire are senior clinical investigators of the Research Foundation – Flanders (FWO). Dr. Bisschops is supported by a grant from the Research Foundation – Flanders (FWO).

Auteurs

Philip Roelandt (P)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Ingrid Demedts (I)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Hilde Willekens (H)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Talat Bessissow (T)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Lieve Braeye (L)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Georges Coremans (G)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Pieter-Jan Cuyle (PJ)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Marc Ferrante (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Anne-Marie Gevers (AM)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Martin Hiele (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Maggy Osselaer (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Jan Tack (J)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Sabine Tejpar (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Oncology, KU Leuven, Leuven, Belgium.

Marijke Ulenaers (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Gert Van Assche (G)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Eric Van Cutsem (E)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Oncology, KU Leuven, Leuven, Belgium.

Stijn Van Gool (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Jaarke Vannoote (J)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Severine Vermeire (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

Raf Bisschops (R)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), KU Leuven, Leuven, Belgium.

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