Department of Healthcare Management, Eulji University, Seongnam, South Korea.
Global Health Unit, Department of Health Sciences, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Int Urol Nephrol. 2019 Sep;51(9):1459-1471. doi: 10.1007/s11255-019-02209-y. Epub 2019 Jun 26.
Anticholinergics have been established for their efficacy and safety in adults with idiopathic overactive bladder syndrome (OAB-s) but not in children and adolescents. This study was aims to investigate the efficacy and safety of anticholinergics in children and adolescents with idiopathic OAB-s.
A total of nine studies with 11 trials comprising of 1801 subjects (1116 experimental and 685 controls) were included. Inclusion criteria were idiopathic OAB-s in children or adolescents. Overall SMD of change in diurnal urge incontinence per week, change in mean voiding frequency per 24 h, change in mean voided volume, and incidence of adverse events compared with placebo were investigated.
Overall SMD of diurnal urge incontinence per week for the anticholinergic group (experimental group) vs. the placebo group (control group) was - 0.15 (95% CI - 0.31, 0.01). Overall SMD of mean voiding frequency per 24 h was - 0.16 (95% CI - 0.33, 0.02). Overall SMD of mean voided volume was 0.49 (95% CI 0.10, 0.88). The overall incidence of any AEs of anticholinergics compared with placebo was OR = 1.06 (95% CI 0.84-1.34) (p = 0.637). Among each AEs, the only incidence of urinary tract infection showed a higher incidence rate for anticholinergics (OR = 1.92, 95% CI 1.06-3.49) than for placebo.
Apart from oxybutynin, other anticholinergics showed efficacy including an increase in mean voided volume. Moreover, there was no significant difference in the incidence of overall adverse events between anticholinergics and placebo.
抗胆碱能药物已被证实对成人特发性膀胱过度活动症(OAB-s)有效且安全,但在儿童和青少年中尚未得到验证。本研究旨在探讨抗胆碱能药物在儿童和青少年特发性 OAB-s 中的疗效和安全性。
共纳入 9 项研究,其中包括 11 项试验,共纳入 1801 例受试者(1116 例试验组,685 例对照组)。纳入标准为儿童或青少年特发性 OAB-s。研究比较了抗胆碱能药物组(试验组)与安慰剂组(对照组)在日间急迫性尿失禁每周变化、24 小时平均排尿频率变化、平均排尿量变化和不良反应发生率方面的总体标准化均数差(SMD)。
抗胆碱能药物组(试验组)与安慰剂组(对照组)在日间急迫性尿失禁每周变化方面的总体 SMD 为-0.15(95%置信区间-0.31,0.01)。24 小时平均排尿频率变化的总体 SMD 为-0.16(95%置信区间-0.33,0.02)。平均排尿量变化的总体 SMD 为 0.49(95%置信区间 0.10,0.88)。与安慰剂相比,抗胆碱能药物的总体不良反应发生率为 OR=1.06(95%置信区间 0.84-1.34)(p=0.637)。在每种不良反应中,只有尿路感染的发生率显示抗胆碱能药物(OR=1.92,95%置信区间 1.06-3.49)的发生率高于安慰剂。
除奥昔布宁外,其他抗胆碱能药物也显示出疗效,包括平均排尿量增加。此外,抗胆碱能药物与安慰剂之间的总体不良反应发生率无显著差异。