Efficacy and tolerability of high and low-volume bowel preparation compared: A real-life single-blinded large-population study.

Bisacodyl Bowel preparation volume Colonic adenomas Colonoscopy Polyethylene glycol Tolerability

Journal

World journal of gastrointestinal endoscopy
ISSN: 1948-5190
Titre abrégé: World J Gastrointest Endosc
Pays: United States
ID NLM: 101532474

Informations de publication

Date de publication:
16 Dec 2021
Historique:
received: 24 04 2021
revised: 25 06 2021
accepted: 02 12 2021
entrez: 24 1 2022
pubmed: 25 1 2022
medline: 25 1 2022
Statut: ppublish

Résumé

Low-volume preparations for colonoscopy have shown similar efficacy compared to high-volume ones in randomized controlled trials (RCT). However, most RCTs do not provide data about clinical outcomes including lesions detection rate. Moreover, real-life comparisons are lacking. To compare efficacy (both in terms of adequate bowel preparation and detection of colorectal lesions) and tolerability of a high-volume (HV: 4 L polyethylene glycol, PEG) and a low-volume (LV: 2 L PEG plus bisacodyl) bowel preparation in a real-life setting. Consecutive outpatients referred for colonoscopy were prospectively enrolled between 1 December 2014 and 31 December 2016. Patients could choose either LV or HV preparation, with a day-before schedule for morning colonoscopies and a split-dose for afternoon procedures. Adequate bowel preparation according to Boston Bowel Preparation Scale (BBPS), clinical outcomes including polyp detection rate (PDR), adenoma detection rate (ADR), advanced adenoma detection rate (AADR), sessile/serrated lesion detection rate (SDR) and cancer detection rate and self-reported tolerability of HV and LV were blindly assessed. Total 2040 patients were enrolled and 1815 (mean age 60.6 years, 50.2% men) finally included. LV was chosen by 52% of patients (50.8% of men, 54.9% of women). Split-dose schedule was more common with HV (44.7% In a real-life setting, PEG-based low-volume preparation with bisacodyl showed similar efficacy and tolerability compared to standard HV preparation. However, with higher PDR and ADR, HV should still be considered as the reference standard for clinical trials and the preferred option in screening colonoscopy, especially when colonoscopy is performed with standard resolution imaging.

Sections du résumé

BACKGROUND BACKGROUND
Low-volume preparations for colonoscopy have shown similar efficacy compared to high-volume ones in randomized controlled trials (RCT). However, most RCTs do not provide data about clinical outcomes including lesions detection rate. Moreover, real-life comparisons are lacking.
AIM OBJECTIVE
To compare efficacy (both in terms of adequate bowel preparation and detection of colorectal lesions) and tolerability of a high-volume (HV: 4 L polyethylene glycol, PEG) and a low-volume (LV: 2 L PEG plus bisacodyl) bowel preparation in a real-life setting.
METHODS METHODS
Consecutive outpatients referred for colonoscopy were prospectively enrolled between 1 December 2014 and 31 December 2016. Patients could choose either LV or HV preparation, with a day-before schedule for morning colonoscopies and a split-dose for afternoon procedures. Adequate bowel preparation according to Boston Bowel Preparation Scale (BBPS), clinical outcomes including polyp detection rate (PDR), adenoma detection rate (ADR), advanced adenoma detection rate (AADR), sessile/serrated lesion detection rate (SDR) and cancer detection rate and self-reported tolerability of HV and LV were blindly assessed.
RESULTS RESULTS
Total 2040 patients were enrolled and 1815 (mean age 60.6 years, 50.2% men) finally included. LV was chosen by 52% of patients (50.8% of men, 54.9% of women). Split-dose schedule was more common with HV (44.7%
CONCLUSION CONCLUSIONS
In a real-life setting, PEG-based low-volume preparation with bisacodyl showed similar efficacy and tolerability compared to standard HV preparation. However, with higher PDR and ADR, HV should still be considered as the reference standard for clinical trials and the preferred option in screening colonoscopy, especially when colonoscopy is performed with standard resolution imaging.

Identifiants

pubmed: 35070027
doi: 10.4253/wjge.v13.i12.659
pmc: PMC8716982
doi:

Types de publication

Journal Article

Langues

eng

Pagination

659-672

Informations de copyright

©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: The authors declare that there is no conflict of interest.

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Auteurs

Vincenzo Occhipinti (V)

Digestive Endoscopy and Gastroenterology Unit, A. Manzoni Hospital, ASST Lecco, Lecco 23900, Italy.

Paola Soriani (P)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Francesco Bagolini (F)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Valentina Milani (V)

Scientific Directorate, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Emanuele Rondonotti (E)

Gastroenterology Unit, Ospedale Valduce, Como 22100, Italy.

Maria Laura Annunziata (ML)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Flaminia Cavallaro (F)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Sara Vavassori (S)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Maurizio Vecchi (M)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Luca Pastorelli (L)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Gian Eugenio Tontini (GE)

Gastro-enterology Unit, IRCCS Policlinico San Donato, San Donato Milanese 20097, Italy.

Classifications MeSH