This quasi - experimental hospital - based study was conducted between March 01 - July 27, 2017 on General Surgery Clinic patients who were scheduled for MBP in preoperative period at Adnan Menderes University Hospital, Turkey. The inclusion criteria were as follows: voluntary participation in the study, aged ≥ 18, conscious and oriented to place, time, and person, mobilized and not global or received aphasia patients. The exclusion criteria were as follows: fever (body temperature ≥ 38.3°C) in preoperative period, receive any inotropic or cardiac agent in preoperative period, and transport to operation room during 1 hour following MBP. For sample size, the results of Advanced Repeated Measures ANOVA Power Analysis with power set as 0.85, effect size 0.74 and standard deviation 4.95, a selection of 32 patients were sufficient for this study. The total research sample comprised of 64 patients without the control group.
Written approvals were obtained from the Ethics Board of a University Faculty of Medicine E. 124125, University Hospital Chief Physician, General Surgery Head of Department and Directorate of Nursing Services of the University Hospital. Informed consent was obtained from all patients after explaining the objectives of the research in preoperative period. For the collection of data, a modified socio - demographic, patients follow-up, and patients complaints associated with MBP forms were used. The forms were developed based on the literature. For mechanical bowel preparation fleet enema 133 solution (Monobasic Sodium Phosphate 19 g, Dibasic Sodium Phosphate 7 g) was used. Additionally, for pain NRS-V (
20), Visual Analogue Scale for Fatigue was used for fatigue (
21) and Pittsburgh Sleep Quality Index (PSQI) for sleep quality (
22,
23) were used. Patients socio - demographic data and nutrition risk score were assessed after patients admission. Patients were assessed for pain, fatigue, and sleep quality 1 hour before MBP. After preparing of MBP devices and providing of patients privacy, anal region were assessed in terms of irritation, wound, infection or etc. Patients were placed in the left- lateral position and fleet enema applied slowly for 2-3 minutes, then, patients were placed in semi-Fowler’s position. Patients mobilized for bowel contents evacuation after 8-10 minutes at the end of the procedure. Then, patients were placed in semi-Fowler’s position after taking the bed. Patients were assessed in terms of nausea, vomiting, change of taste in mouth, abdomen cramp, abdomen pain, bloating, stomach ache, sweating, palpitation, dyspnea, and vertige 1 hour before, just before, right after, at the end of 20, 40, and 60 minutes after MBP.
For statistical analysis, SPSS version 21 (SPSS Inc., Chicago, IL, USA) was used. The Shapiro - Wilk test was employed to test the normality of the distribution of data. The descriptive characteristics were expressed as percentages in the categorical variables and as means, standard deviation and medians. The Friedman’s Test was used to compare patients complaints in different periods. Statistical significance was set at P < 0.05, as appropriate.