Background and Aims: Adequate bowel cleansing is critical to ensure quality and safety of a colonoscopy. A novel 1-L polyethylene glycol plus ascorbate (1L-PEG+ASC) regimen was previously validated against low-volume regimens but was never compared with high-volume regimens.Methods: In a phase IV study, patients undergoing colonoscopy were randomized 1:1 to receive split-dose 1L PEG+ASC or a split-dose 4-L PEG-based regimen (4L-PEG) in 5 Italian centers. Preparation was assessed with the Boston Bowel Preparation Scale (BBPS) by local endoscopists and centralized reading, both blinded to the randomization arm. The primary endpoint was noninferiority of 1L-PEG+ASC in colon cleansing. Secondary endpoints were superiority of 1L-PEG+ASC, patient compliance, segmental colon cleansing, adenoma detection rate, tolerability, and safety.Results: Three hundred eighty-eight patients (median age, 59.8 years) were randomized between January 2019 and October 2019: 195 to 1L-PEG+ASC and 193 to 4L-PEG. Noninferiority of 1L-PEG+ASC was demonstrated for cleansing in both the entire colon (BBPS >= 6: 97.9% vs 93%; relative risk [RR], 1.03; 95% confidence interval [CI], 1.001-1.04; P superiority=.027) and in the right-sided colon segment (98.4% vs 96.0%; RR, 1.02; 95% CI, .99-1.02; P noninferiority=.013). Compliance was higher with 1L-PEG+ASC than with 4L-PEG (178/192 [92.7%] vs 154/190 patients [81.1%]; RR, 1.10; 95% CI, 1.05-1.12), whereas no difference was found regarding safety (moderate/severe side effects: 20.8% vs 25.8%; P=.253). No difference in adenoma detection rate (38.8% vs 43.0%) was found.Conclusions: One-liter PEG+ASC showed noninferiority compared with 4L-PEG in achieving adequate colon cleansing and provided a higher patient compliance. No differences in tolerability and safety were detected.

BACKGROUND AND AIMS: An adequate bowel cleansing is critical to assure quality and safety of colonoscopy. A novel 1L-PEG plus ascorbate(PEG+ASC) regimen was previously validated against low-volume regimens, but it was never compared with high-volume regimens. METHODS: In a Phase IV study, patients undergoing colonoscopy were randomized 1:1 to receive split-dose 1L PEG+ASC or a split-dose 4L PEG-based regimen in 5 Italian centers. Preparation was assessed with the Boston Bowel Preparation Scale (BBPS) by the local endoscopists and centralized reading, both blinded to the randomization arm. Primary endpoint was noninferiority of 1L PEG+ASC in colon cleansing. Secondary endpoints were superiority of 1L PEG+ASC, patient compliance, segmental colon cleansing, adenoma detection rate (ADR), tolerability and safety. RESULTS: A total of 388 patients (59.8 years) were randomized between January 2019 and October 2019: 195 to 1L PEG+ASC and 193 to 4L-PEG. Noninferiority of 1L PEG+ASC was demonstrated for cleansing in both the whole colon (BBPS>6: 97.9% vs 93%; RR, 1.03; 95% CI, 1.001-1.04; p-superiority=0.027) and in the right colon segment (98.4% vs 96.0%; RR, 1.02; 95% CI, 0.99-1.02; p noninferiority=0.013). Compliance was higher with 1L PEG+ASC than 4L-PEG (178/192, 92.7% vs 154/190 patients, 81.1%; RR, 1.10; 95% CI, 1.05-1.12), whereas no difference was found regarding safety (moderate/severe side-effects: 20.8% vs 25.8%; p=0.253). No difference in ADR (38.8% vs 43.0%) was found. CONCLUSION: 1L PEG+ASC showed noninferiority compared with 4L-PEG in achieving adequate colon cleansing, as well as a higher patient compliance. No differences in tolerability and safety were detected.

Novel 1-L polyethylene glycol + ascorbate versus high-volume polyethylene glycol regimen for colonoscopy cleansing: a multicenter, randomized, phase IV study

Repici, Alessandro;Maselli, Roberta;Hassan, Cesare
2021-01-01

Abstract

Background and Aims: Adequate bowel cleansing is critical to ensure quality and safety of a colonoscopy. A novel 1-L polyethylene glycol plus ascorbate (1L-PEG+ASC) regimen was previously validated against low-volume regimens but was never compared with high-volume regimens.Methods: In a phase IV study, patients undergoing colonoscopy were randomized 1:1 to receive split-dose 1L PEG+ASC or a split-dose 4-L PEG-based regimen (4L-PEG) in 5 Italian centers. Preparation was assessed with the Boston Bowel Preparation Scale (BBPS) by local endoscopists and centralized reading, both blinded to the randomization arm. The primary endpoint was noninferiority of 1L-PEG+ASC in colon cleansing. Secondary endpoints were superiority of 1L-PEG+ASC, patient compliance, segmental colon cleansing, adenoma detection rate, tolerability, and safety.Results: Three hundred eighty-eight patients (median age, 59.8 years) were randomized between January 2019 and October 2019: 195 to 1L-PEG+ASC and 193 to 4L-PEG. Noninferiority of 1L-PEG+ASC was demonstrated for cleansing in both the entire colon (BBPS >= 6: 97.9% vs 93%; relative risk [RR], 1.03; 95% confidence interval [CI], 1.001-1.04; P superiority=.027) and in the right-sided colon segment (98.4% vs 96.0%; RR, 1.02; 95% CI, .99-1.02; P noninferiority=.013). Compliance was higher with 1L-PEG+ASC than with 4L-PEG (178/192 [92.7%] vs 154/190 patients [81.1%]; RR, 1.10; 95% CI, 1.05-1.12), whereas no difference was found regarding safety (moderate/severe side effects: 20.8% vs 25.8%; P=.253). No difference in adenoma detection rate (38.8% vs 43.0%) was found.Conclusions: One-liter PEG+ASC showed noninferiority compared with 4L-PEG in achieving adequate colon cleansing and provided a higher patient compliance. No differences in tolerability and safety were detected.
2021
BACKGROUND AND AIMS: An adequate bowel cleansing is critical to assure quality and safety of colonoscopy. A novel 1L-PEG plus ascorbate(PEG+ASC) regimen was previously validated against low-volume regimens, but it was never compared with high-volume regimens. METHODS: In a Phase IV study, patients undergoing colonoscopy were randomized 1:1 to receive split-dose 1L PEG+ASC or a split-dose 4L PEG-based regimen in 5 Italian centers. Preparation was assessed with the Boston Bowel Preparation Scale (BBPS) by the local endoscopists and centralized reading, both blinded to the randomization arm. Primary endpoint was noninferiority of 1L PEG+ASC in colon cleansing. Secondary endpoints were superiority of 1L PEG+ASC, patient compliance, segmental colon cleansing, adenoma detection rate (ADR), tolerability and safety. RESULTS: A total of 388 patients (59.8 years) were randomized between January 2019 and October 2019: 195 to 1L PEG+ASC and 193 to 4L-PEG. Noninferiority of 1L PEG+ASC was demonstrated for cleansing in both the whole colon (BBPS>6: 97.9% vs 93%; RR, 1.03; 95% CI, 1.001-1.04; p-superiority=0.027) and in the right colon segment (98.4% vs 96.0%; RR, 1.02; 95% CI, 0.99-1.02; p noninferiority=0.013). Compliance was higher with 1L PEG+ASC than 4L-PEG (178/192, 92.7% vs 154/190 patients, 81.1%; RR, 1.10; 95% CI, 1.05-1.12), whereas no difference was found regarding safety (moderate/severe side-effects: 20.8% vs 25.8%; p=0.253). No difference in ADR (38.8% vs 43.0%) was found. CONCLUSION: 1L PEG+ASC showed noninferiority compared with 4L-PEG in achieving adequate colon cleansing, as well as a higher patient compliance. No differences in tolerability and safety were detected.
Ascorbic Acid
Colonoscopy
Humans
Laxatives
Middle Aged
Cathartics
Polyethylene Glycols
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11699/66147
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