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米拉贝隆治疗小儿膀胱过度活动症的前瞻性初步研究。

Prospective Pilot Study of Mirabegron in Pediatric Patients with Overactive Bladder.

机构信息

Division of Urology, CHU de Québec-Université Laval, Québec, Québec, Canada.

Division of Urology, CHU de Québec-Université Laval, Québec, Québec, Canada.

出版信息

Eur Urol. 2016 Jul;70(1):9-13. doi: 10.1016/j.eururo.2016.02.007. Epub 2016 Feb 11.

Abstract

BACKGROUND

Antimuscarinics are the pharmacologic mainstay of overactive bladder (OAB) management, but side effects limit their use. Mirabegron, a new molecule with a distinct mechanism of action (β3-adrenoreceptor agonist), was recently approved as monotherapy for idiopathic OAB in adults but has not been studied in the pediatric population.

OBJECTIVE

To evaluate the efficacy and safety of mirabegron to treat urinary incontinence in children with idiopathic OAB who were refractory to and/or intolerant of antimuscarinics.

DESIGN, SETTING, AND PARTICIPANTS: A prospective off-label study using mirabegron was conducted. Pediatric patients without symptom improvement under behavioral and medical therapies and/or with significant side effects with at least two different antimuscarinic agents were recruited.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS

Our primary outcome was better reported efficacy than with the use of prior anticholinergic medication. Secondary end points were tolerability, safety, and satisfaction. Efficacy and tolerability were assessed with voiding diaries, postvoid residuals, urine cultures, electrocardiogram, and vital signs. Families were questioned for continence, side effects, compliance, and Patient Perception of Bladder Condition (PPBC) questionnaire. The Wilcoxon rank sum test and Wilcoxon signed rank test were used for statistical analysis.

RESULTS AND LIMITATIONS

A total of 58 patients were recruited at a median age of 10.1 yr and were on mirabegron for a median of 11.5 mo. Median bladder capacity improved from 150ml to 200ml (p<0.001). Continence improved in 52 of 58, with 13 being completely dry. Median PPBC improved from 4.0 to 2.0 (p<0.001). Eight patients reported mild or moderate side effects. Absence of a placebo group is a limitation of the study.

CONCLUSIONS

Mirabegron, a novel first-in-class therapy, appeared as a safe and effective alternative for children with idiopathic OAB refractory to antimuscarinics.

PATIENT SUMMARY

We evaluated the efficacy and safety of mirabegron to treat incontinence in pediatric patients. Continence, median voided volumes, and quality of life were improved after the introduction of mirabegron, and few side effects were reported.

摘要

背景

抗毒蕈碱药物是治疗膀胱过度活动症(OAB)的主要药物,但副作用限制了其使用。米拉贝隆是一种新型药物,作用机制独特(β3-肾上腺素能受体激动剂),最近被批准用于成人特发性 OAB 的单药治疗,但尚未在儿科人群中进行研究。

目的

评估米拉贝隆治疗对抗毒蕈碱药物不耐受或无效的特发性 OAB 儿童尿失禁的疗效和安全性。

设计、地点和参与者:进行了一项使用米拉贝隆的前瞻性非适应证研究。招募了接受行为和药物治疗后症状无改善或至少两种不同的抗毒蕈碱药物有明显副作用的儿科患者。

观察指标和统计分析

我们的主要观察指标是与使用前一种抗胆碱能药物相比,报告的疗效更好。次要终点是耐受性、安全性和满意度。通过排尿日记、残余尿量、尿液培养、心电图和生命体征评估疗效和耐受性。询问家属关于控尿、副作用、依从性和膀胱状况患者感知问卷(PPBC)。采用 Wilcoxon 秩和检验和 Wilcoxon 符号秩检验进行统计分析。

结果和局限性

共招募了 58 例患者,中位年龄为 10.1 岁,中位米拉贝隆治疗时间为 11.5 个月。中位膀胱容量从 150ml 增加到 200ml(p<0.001)。58 例中有 52 例控尿改善,其中 13 例完全干燥。PPBC 中位数从 4.0 分改善至 2.0 分(p<0.001)。8 例患者报告有轻度或中度副作用。研究的局限性在于没有安慰剂组。

结论

米拉贝隆,一种新型的首创疗法,似乎是一种安全有效的治疗抗毒蕈碱药物难治性特发性 OAB 的替代方法。

患者总结

我们评估了米拉贝隆治疗儿童膀胱过度活动症的疗效和安全性。引入米拉贝隆后,控尿、中位排尿量和生活质量得到改善,且报告的副作用很少。

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