Tolerance, safety, and efficacy of PEG3350 + bisacodyl bowel preparation: comparison between two treatments of different duration in pediatric patients

Ligia Marcela Portillo-Canizalez, G. Blanco-Rodríguez, Gustavo Teyssier-Morales, J. Penchyna-Grub, S. T. Mendieta, J. Zurita-Cruz
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Abstract

Background: Multiple bowel preparations have been used in children undergoing colonoscopy, with variable limitations due to acceptance, tolerance, and proper cleaning. The objective of this study was to compare the tolerability, safety, and efficacy of colonoscopy preparation with one-day of PEG 3350 (polyethylene glycol) (4 g/kg/day) + bisacodyl compared with two days of preparation with PEG 3350 (2 g/kg/day) + bisacodyl in pediatric patients. Methods: A clinical, randomized, single-blind trial was performed. Patients aged 2 to 18 years scheduled for colonoscopy were included. Patients were randomized into two groups: one day of preparation with PEG 3350 4 g/kg/day + bisacodyl and two days of preparation with PEG 3350 2 g/kg/day + bisacodyl. Through a questionnaire, a physical examination, and an endoscopic evaluation (Boston scale), the tolerance, safety and efficacy of both preparations evaluated were determined. Student’s t-test was performed for quantitative variables and χ2 for qualitative variables. Results: There were no significant differences in compliance rates, adverse effects, and extent of colonoscopic evaluation. Conclusions: Tolerance and safety between the intestinal preparation for 1-day colonoscopy with PEG 3350 (4 g/kg/day) + bisacodyl and the 2-day preparation with PEG 3350 (2 g/kg/day) + bisacodyl were similar. The quality of cleanliness was good in both groups, being partially more effective in the 1-day group with PEG
PEG3350 + bisacodyl肠道准备的耐受性、安全性和有效性:两种治疗方法在儿科患者中不同持续时间的比较
背景:在接受结肠镜检查的儿童中已经使用了多种肠道准备,由于接受、耐受和适当的清洁而存在不同的局限性。本研究的目的是比较儿科患者结肠镜检查准备1天PEG 3350(聚乙二醇)(4 g/kg/天)+比沙代碱与2天PEG 3350 (2 g/kg/天)+比沙代碱的耐受性、安全性和有效性。方法:采用临床、随机、单盲试验。年龄在2至18岁的患者计划进行结肠镜检查。患者被随机分为两组:1天的peg3350 4 g/kg/天+比萨科代,2天的peg3350 2 g/kg/天+比萨科代。通过问卷调查、体格检查和内镜评估(波士顿量表),确定两种评估制剂的耐受性、安全性和有效性。定量变量采用学生t检验,定性变量采用χ2检验。结果:两组患者在依从率、不良反应和结肠镜评估程度上无显著差异。结论:1天结肠镜下肠制剂PEG 3350 (4 g/kg/天)+比沙可代与2天制剂PEG 3350 (2 g/kg/天)+比沙可代的耐受性和安全性相似。两组的清洁质量都很好,在使用PEG的1天组中部分更有效
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