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Safety and efficacy of milk and molasses enemas compared with sodium phosphate enemas for the treatment of constipation in a pediatric emergency department.

机译:乳和糖蜜灌肠剂与磷酸钠灌肠剂在小儿急诊科治疗便秘的安全性和有效性。

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OBJECTIVES: The purpose of this study was to determine the safety and efficacy of routine milk and molasses enemas (MME) compared with sodium phosphate enemas for the treatment of constipation in the pediatric emergency department (ED). A secondary objective included the identification of factors associated with enema selection in the pediatric ED. METHODS: This study was approved by the University of Texas Southwestern Medical Center Institutional Review Board. The study design was a retrospective comparative chart review. Medical records of patients who presented to the ED and received either MME or sodium phosphate enema for constipation between November 1, 2007, and November 1, 2008, were identified and reviewed for data collection. The following data were collected to determine safety and efficacy: baseline demographics, chief complaint, medical history, radiographic imaging, enema type, treatment dose, adverse effects, improvement in symptoms, time until defecation, failure of initial therapy requiring additional intervention, and time from treatment until disposition. RESULTS: Both treatment groups had similar baseline characteristics. No statistically significant differences in treatment effect were noted between MME and sodium phosphate enemas. Several clinically significant trends were noted including the need for additional rectal treatment after administration of sodium phosphate enemas versus oral therapy after MME. In addition, there were 6 cases of treatment failure with sodium phosphate enemas versus 1 case with MME. CONCLUSIONS: No statistically significant differences were found between MME and sodium phosphate enemas. Based on our results, the 2 treatment options were found to be equally safe and effective.
机译:目的:本研究的目的是确定常规牛奶和糖蜜灌肠剂(MME)与磷酸钠灌肠剂相比在儿科急诊室(ED)治疗便秘的安全性和有效性。次要目标包括确定与小儿急诊室灌肠选择相关的因素。方法:本研究得到德克萨斯大学西南医学中心机构审查委员会的批准。研究设计是回顾性比较图表审查。确定并审查了在2007年11月1日至2008年11月1日之间接受急诊就诊并接受MME或磷酸钠灌肠治疗便秘的患者的病历,并进行了数据收集。收集以下数据以确定安全性和有效性:基线人口统计学,主要诉求,病史,放射影像学,灌肠类型,治疗剂量,不良反应,症状改善,排便时间,需要额外干预的初始治疗失败和时间从治疗到处置。结果:两个治疗组的基线特征相似。在MME和磷酸钠灌肠剂之间未观察到治疗效果的统计学显着差异。注意到一些临床上重要的趋势,包括与MME后口服磷酸钠灌肠相比,口服磷酸钠灌肠后需要额外的直肠治疗。此外,磷酸钠灌肠治疗失败6例,而MME治疗1例。结论:MME和磷酸钠灌肠剂之间无统计学差异。根据我们的结果,发现这两种治疗方案同样安全有效。

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