丁溴海莨菪碱与氯他弗林缓解儿童急性非特异性腹痛的疗效——一项非随机试验

Pradip Kumar Paudel, S. Basnet, Merina Shreshtha
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引用次数: 0

摘要

简介:急性腹痛是儿童在急诊科(ED)常见的主诉。本研究的目的是比较海莨菪碱和海莨菪碱缓解ED患儿急性非特异性腹痛的疗效。方法:2017年12月至2018年6月,共有52名6岁至16岁的儿童参加了一项非随机试验,随机分配到海莨菪碱组或海莨菪碱组;每组26人。采用面部疼痛评分修正工具测量药物的疗效。主要结果是在摄入研究干预后60分钟测量面部疼痛评分(自我报告)减少至少2 / 10。其他结果为抢救性镇痛需求及药物不良反应。结果:海莨菪碱组20例(77%)、罗他弗林组21例(81%)在口服给药60 min后出现应答,差异无统计学意义(p=0.808)。呕吐是唯一的不良反应,分别有5例(19%)盐酸组和2例(8%)盐酸组。结论:在这项单中心随机对照试验中,发现海莨菪碱和氯他弗林对缓解儿童急性非特异性腹痛同样有效。
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Efficacy of Hyoscine Butylbromide Versus Drotaverine in Relieving Acute Nonspecific Abdominal Pain in Children- A Non - Randomized Trial
Introduction: Acute abdominal pain is a very common complaint for children presenting to the emergency department (ED). The purpose of this study was to compare efficacy of hyoscine and drotaverine for relieving acute nonspecific abdominal pain in children presenting to ED. Methods: Total of 52 children aged six years to 16 years were enrolled in a non-randomized trial at Paediatric ED of TUTH from Dec 2017 to June 2018, and randomly allocated to drotaverine or hyoscine groups; 26 in each group. Face pain score-revised tool was used to measure the efficacy of the drug. The primary outcome was to measure the reduction of face pain score (Self-reported) by at least 2 / 10 at 60 minutes after ingestion of study intervention. Other outcomes were requirement of rescue analgesia and adverse effects of drugs. Results: A total of 20 (77%) in hyoscine and 21 (81%) in drotaverine group responded to oral medication at the end of 60 minutes of oral administration and the difference was not statistically significant (p=0.808). Vomiting was only adverse event present in five (19%) in drotaverine and two (8%) in hyoscine groups, respectively. Conclusions: In this single center randomized controlled trial, both hyoscine and drotaverine were found to be equally efficacious for relieving acute non-specific abdominal pain in children.
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来源期刊
Journal of Nepal Paediatric Society
Journal of Nepal Paediatric Society Medicine-Pediatrics, Perinatology and Child Health
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审稿时长
12 weeks
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