The study was designed to evaluate 5 major parameters in IBS patients during colonoscopy procedure and compare them with those of non-IBS patients; the parameters were pain severity, quality of colon preparation, duration of the procedure, technical difficulty of the procedure, and the success rate of the colonoscopy (cecal intubation).
During January and May 2016, adult patients who referred for colonoscopy to one academic centre in Shiraz University of Medical Sciences enrolled in this study and were categorized into IBS and non- IBS groups.
All IBS patients, for whom colonoscopy was requested to rule out the presence of any organic disease, fulfilled the ROME III criteria. This study was conducted before the implication of the new update release of ROME IV criteria.
Exclusion criteria for both groups were as follow: history of bowel surgery and altered GI anatomy; renal failure, which influences the amount of water consumption; current hospital admission or bed ridden/wheelchair bound condition, which limits the mobility of the patient; and confirmed diagnosis of colonic hypomotility disorders.
Colonoscopy procedures were conducted by 3 qualified attending gastroenterologists.
Demographic data were collected from the questionnaires. All patients had bowel preparation according to the standard protocol, which included polyethylene glycol bowel preparation powder, syrup of Senna, and bisacodyl tablets.
Duration of the procedure, time to pass the splenic flexure, time to reach the cecum, and successful intubation of terminal ileum were recorded.
Among the different bowel preparation scoring systems such as Aronchick BPS, Ottawa BPS, Boston BPS (
11), and Chicago BPS (
12), Boston bowel preparation scoring system (BPS) was selected as a practical and appreciable scoring system (
11) for evaluation of the quality of bowel preparation in this study. The patient’s pain sensation during the colonoscopy was measured by visual analogue scale (VAS), which is a 10 cm horizontal line with 2 anchors at each end with the words “No pain” and “Very severe pain”. Sedation was administered as needed using slow intravenous administration of midazolam with maximum dose of 2.5 mg.
The success of colonoscopy was evaluated based on a 6-point scoring. Score 1 was assigned to the left colon and 2 to the splenic flexure, 3 to the transverse colon, 4 to the right colon, 5 to the cecum, and 6 to the terminal ileum.
To objectively assess the difficulty of the colonoscopy for the colonoscopists, we used the visual analogue scale (VAS), with one end “very easy” and the other end “very difficult”.
Statistical analyses were conducted using statistical package for social sciences (SPSS, Chicago, IL, USA) release 16.0 for Windows. Independent t test was used to compare means and chi squared test was used for categorical variables. All P value levels less than 0.05 were considered as significant.