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Randomized Controlled Trial Comparative Study
Evaluating the efficacy of current treatments for reducing postoperative ileus: a randomized clinical trial in a single center.
- S Bonventre, A Inviati, V Di Paola, P Morreale, S Di Giovanni, P Di Carlo, D Schifano, G Frazzetta, G Gulotta, and G Scerrino.
- Department of Surgical and Oncological Sciences University of Palermo, Palermo, Italy - surgeryangela@hotmail.it.
- Minerva Chir. 2014 Feb 1;69(1):47-55.
AimPostoperative ileus has been considered an inevitable consequence of abdominal surgery. The aim of the study was to investigate the efficacy of same treatments in resolving postoperative ileus in various surgical approaches.MethodsA total of 360 patients underwent abdominal surgery, and was divided into four groups: videolaparoscopic cholecystectomy, laparotomic colo-rectal surgery, laparotomic Hartmann procedure, laparotomic gastric surgery. In each group, patients received different postoperative treatments: chewing gum, olive oil, both, and water. Each group was compared with a control group.ResultsIn patients who underwent videolaparoscopic cholecystectomy, median postoperative first passage of flatus and stool in the water group was 10 and 34 hours, respectively (P=0.006, P=0.021) and significantly earlier than in the control group (median postoperative 24 and 72 hours). Postoperative stay for the water group was lower (median day 1, 3rd interquartile 2.5) compared with control (median day 3; 3rd interquartile 7.0, P=0.01). In patients who underwent gastric surgery, median postoperative first passage of stool in the olive oil and chewing gum group was 48 hours, significantly earlier than in the control (median postoperative hour 120, P=0.04). Median time to first passage of flatus and stool was also earlier in the other groups compared with the control group, though this difference was not significant.ConclusionChewing gum, olive oil or both do not induce a relevant reduction of ileus after surgery. Water may be a safe and inexpensive option in reducing ileus. (United States National Institutes of Health, www.clinicaltrial.gov, number NCT01869231).
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