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Factors influencing the presence of potentially explosive gases during colonoscopy: Results of the SATISFACTION study.

Marino CarnovaliCristiano SpadaPeter UebelPaolo BocusRenato CannizzaroFlaminia CavallaroBruno Mario CesanaPaola CesaroGuido CostamagnaDhanai Di PaoloAngelo Paulo FerrariCarsten HinkelSergey KashinArianna MassellaEkaterina MelnikovaAnna OrsattiThierry PonchonAlberto PradaFranco RadaelliSandro SferrazzaPietro SoruPier Alberto TestoniGian Eugenio TontiniMaurizio VecchiGiancarla Fiorinull null
Published in: Clinical and translational science (2023)
This study tested the hypothesis that bowel preparation with mannitol should not affect the colonic concentration of H 2 and CH 4 . Therefore, the SATISFACTION study, an international, multicenter, randomized, parallel-group phase II-III study investigated this issue. The phase II dose-finding part of the study evaluated H 2 , CH 4 , and O 2 concentrations in 179 patients randomized to treatment with 50 g, 100 g, or 150 g mannitol. Phase III of the study compared the presence of intestinal gases in 680 patients randomized (1:1) to receive mannitol 100 g in single dose or a standard split-dose 2 L polyethylene glycol (PEG)-Asc preparation (2 L PEG-Asc). Phase II results showed that mannitol did not influence the concentration of intestinal gases. During phase III, no patient in either group had H 2 or CH 4 concentrations above the critical thresholds. In patients with H 2 and/or CH 4 levels above detectable concentrations, the mean values were below the risk thresholds by at least one order of magnitude. The results also highlighted the effectiveness of standard washing and insufflation maneuvers in removing residual intestinal gases. In conclusion, bowel cleansing with mannitol was safe as the concentrations of H 2 and CH 4 were the same as those found in patients prepared with 2 L PEG-Asc. In both groups, the concentrations of gases were influenced more by the degree of cleansing achieved and the insufflation and washing maneuvers performed than by the preparation used for bowel cleansing. The trial protocol was registered with ClinicalTrials.gov (https://clinicaltrials.gov/ct2/show/NCT04759885) and with EudraCT (eudract_number: 2019-002856-18).
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