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Macrogol (polyethylene glycol) laxatives in children with functional constipation and faecal impaction: a systematic review.

机译:功能性便秘和粪便压迫儿童的聚乙二醇(聚乙二醇)轻泻剂:系统评价。

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As the evidence base supporting the use of laxatives in children is very limited, we undertook an updated systematic review to clarify the issue. A comprehensive literature search was carried out to identify randomised controlled trials of polyethylene glycol (PEG) versus either placebo or active comparator, in patients aged <18 years with primary chronic constipation. Outcomes were assessed as either global assessments of effectiveness or differences in defaecation rates. Seven qualifying studies involving 594 children were identified. Five were comparisons of PEG with lactulose, one with milk of magnesia and one with placebo. Study duration ranged from 2 weeks to 12 months. PEG was significantly more effective than placebo and either equivalent to (two studies) or superior to (four studies) active comparator. Differences in study design precluded meaningful meta-analysis. Lack of high quality studies has meant that the management of childhood constipation has tended to rely on anecdote and empirical treatment choice. Recent publication of well designed randomised trials now permits a more evidence-based approach, with PEG-based treatments having been proven to be effective and well-tolerated first-line treatment.
机译:由于支持在儿童中使用泻药的证据基础非常有限,我们进行了更新的系统评价以澄清该问题。对年龄<18岁的原发性慢性便秘患者进行了全面的文献检索,以确定聚乙二醇(PEG)与安慰剂或活性比较剂的随机对照试验。结果被评估为有效性的全球评估或排便率的差异。确定了涉及594名儿童的七项合格研究。五是PEG与乳果糖的比较,一是氧化镁牛奶,另一是安慰剂的比较。研究持续时间从2周到12个月不等。 PEG比安慰剂有效得多,并且等效于(两项研究)或优于(两项研究)活性比较剂。研究设计的差异排除了有意义的荟萃分析的可能。缺乏高质量的研究意味着对儿童便秘的管理往往依赖于轶事和经验疗法的选择。经过精心设计的随机试验的最新发表现在允许使用更多基于证据的方法,基于PEG的治疗已被证明是有效且耐受性良好的一线治疗。

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