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Peripherally acting μ-opioid receptor antagonists for treatment of opioid-induced constipation in children

机译:外围作用μ-ApiOID受体拮抗剂,用于治疗儿童阿片类药物诱导的便秘

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Background and Objective Opioid-induced constipation (OIC) is a common and important problem in paediatric palliative care, critical care, and postoperative settings. Treatment for OIC is often ineffective and limited by enteral intake. A new class of drugs called peripherally acting mu-opioid receptor antagonists (PAMORAs) have been shown to be effective treatments of OIC in adults, including the agents methylnaltrexone and naloxegol. Data in children are limited to several small case reports, mostly in the palliative care setting. The goal of this study was to evaluate the effectiveness and safety of methylnaltrexone and naloxegol in hospitalized children, including those with critical illness. Methods We conducted a retrospective study of all children admitted to the Stollery Children’s Hospital in Edmonton (Canada) who received either methylnaltrexone or naloxegol for OIC. The primary outcome was median time to first bowel movement (BM) after the first dose of PAMORA. Results A total of 27 patients were included in the study. Kaplan–Meier survival analysis showed the median time to the first BM after the first dose of PAMORA was 15.5 hours. Seventeen (63%) patients had laxation within 24 hours of first dose. No significant adverse events were observed. Conclusion This study is the largest to date to evaluate efficacy and safety of PAMORAs in children. Future studies should be prospective and include larger numbers of patients with critical illness and postoperative OIC as indications for treatment.
机译:背景和目的阿片类药物诱发的便秘(OIC)是小儿姑息治疗,关键护理和术后设置的共同和重要的问题。对OIC的处理通常是无效和受肠内摄入量的限制。已经显示出一种叫外围作用的穆阿片类受体拮抗剂(Pamoras)的新类药物是在成人中有效治疗,包括甲基肠酮和纳洛克醇。儿童的数据仅限于几个小案报告,主要是在姑息治疗环境中。本研究的目标是评估住院儿童的甲基肠酮和纳洛烯醇的有效性和安全性,包括患有危重疾病的儿童。方法对埃德蒙顿(加拿大)的所有儿童进行了回顾性研究,他接受了OIC的甲基Naltrexone或Naloxegol。主要结果是在第一次服用Pamora之后的第一个肠运动(BM)的中值时间。结果共有27名患者纳入该研究。 Kaplan-Meier存活分析显示第一剂Pamora后的第一个BM的中位时间为15.5小时。十七(63%)患者在第一剂的24小时内泻药。没有观察到明显的不良事件。结论本研究是评估儿童Pamoras疗效和安全性的最大日期。未来的研究应该是前瞻性的,包括更多患有危重疾病和术后OIC的患者作为治疗的适应症。

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