首页> 外文期刊>Archives of disease in childhood >Polyethylene glycol 3350 plus electrolytes for chronic constipation in children: a double blind, placebo controlled, crossover study.
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Polyethylene glycol 3350 plus electrolytes for chronic constipation in children: a double blind, placebo controlled, crossover study.

机译:用于儿童慢性便秘的聚乙二醇3350和电解质:一项双盲,安慰剂对照,交叉研究。

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OBJECTIVES: To assess the efficacy and safety of polyethylene glycol 3350 plus electrolytes (PEG+E) for the treatment of chronic constipation in children. DESIGN: Randomised, double blind, placebo controlled crossover trial, with two 2-week treatment periods separated by a 2-week placebo washout. SETTING: Six UK paediatric departments. PARTICIPANTS: 51 children (29 girls, 22 boys) aged 24 months to 11 years with chronic constipation (lasting > or =3 months), defined as < or =2 complete bowel movements per week and one of the following: pain on defaecation on 25% of days; > or =25% of bowel movements with straining; > or 25% of bowel movements with hard/lumpy stools. 47 children completed the double blind treatment. MAIN OUTCOME MEASURES: Number of complete defaecations per week (primary efficacy variable), total number of complete and incomplete defaecations per week, pain on defaecation, straining on defaecation, faecal incontinence, stool consistency, global assessment of treatment, adverse events and physical examination. RESULTS: The mean number of complete defaecations per week was significantly higher for children on PEG+E than on placebo (3.12 (SD 2.05) v 1.45 (SD 1.20), respectively; p<0.001). Further significant differences in favour of PEG+E were observed for total number of defaecations per week (p = 0.003), pain on defaecation (p = 0.041), straining on defaecation (p<0.001), stool consistency (p<0.001) and percentage of hard stools (p = 0.001). Treatment related adverse events (all mild or moderate) occurred in similar numbers of children on PEG+E (41%) and placebo during treatment (45%). CONCLUSIONS: PEG+E is significantly more effective than placebo, and appears to be safe and well tolerated in the treatment of chronic constipation in children.
机译:目的:评估聚乙二醇3350加电解质(PEG + E)治疗儿童慢性便秘的疗效和安全性。设计:随机,双盲,安慰剂对照的交叉试验,其中两个2周的治疗期被2周的安慰剂冲刷隔开。地点:英国六个儿科。参与者:年龄在24个月至11岁之间的51名儿童(29名女孩,22名男孩),患有慢性便秘(持续时间≥3个月),定义为每周<或= 2次完全排便,且以下一项: 25%的天数; >或=肠蠕动的25%带有拉力; >或大便硬块状时排便的25%。 47名儿童完成了双盲治疗。主要观察指标:每周完全排便的数量(主要疗效变量),每周完全排便和不完全排便的总数,排便时的疼痛,排便时的压力,粪便失禁,大便稠度,整体治疗评估,不良事件和身体检查。结果:PEG + E患儿每周完全排便的平均数显着高于安慰剂组(分别为3.12(SD 2.05)v 1.45(SD 1.20); p <0.001)。在每周排便总数(p = 0.003),排便时疼痛(p = 0.041),排便时劳损(p <0.001),大便稠度(p <0.001)和硬粪百分比(p = 0.001)。与治疗相关的不良事件(所有轻度或中度)发生在接受治疗的不良反应事件中(44%),使用PEG + E(41%)和安慰剂的儿童数量相似。结论:PEG + E比安慰剂有效得多,并且在治疗儿童慢性便秘方面似乎是安全且耐受性良好的。

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