WASh multicentre randomised controlled trial: water-assisted sigmoidoscopy in English NHS bowel scope screening

Abstract

Objectives The English Bowel Cancer Screening Programme invites 55 year olds for a sigmoidoscopy (Bowel Scope Screening (BSS)), aiming to resect premalignant polyps, thus reducing cancer incidence. A national patient survey indicated higher procedural pain than anticipated, potentially impacting on screening compliance and effectiveness. We aimed to assess whether water-assisted sigmoidoscopy (WAS), as opposed to standard CO₂ technique, improved procedural pain and detection of adenomatous polyps. Design The WASh (Water-Assisted Sigmoidoscopy) trial was a multicentre, single-blind, randomised control trial for people undergoing BSS. Participants were randomised to either receive WAS or CO₂ from five sites across England. The primary outcome measure was patient-reported moderate/severe pain, as assessed by patients on a standard Likert scale post procedure prior to discharge. The key secondary outcome was adenoma detection rate (ADR). The costs of each technique were also measured. Results 1123 participants (50% women, mean age 55) were randomised (561 WAS, 562 CO₂). We found no difference in patient-reported moderate/severe pain between WAS and CO₂ (14% in WAS, 15% in CO2; p=0.47). ADR was 15% in the CO₂ arm and 11% in the WAS arm (p=0.03); however, it remained above the minimum national performance standard in both arms. There was no statistical difference in mean number of adenomas nor overall polyp detection rate. There was negligible cost difference between the two techniques. Conclusion In the context of enema-prepared unsedated screening sigmoidoscopies performed by screening-accredited endoscopists, no difference in patient-reported pain was seen when using either a CO₂ or WAS intubation technique. Trial registration number ISRCTN81466870.