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盐酸丙哌维林对比奥昔布宁治疗膀胱过度活动症导致急迫性尿失禁儿童的疗效、耐受性和安全性:一项多中心观察性队列研究的结果。

Efficacy, tolerability and safety of propiverine hydrochloride in comparison to oxybutynin in children with urge incontinence due to overactive bladder: Results of a multicentre observational cohort study.

机构信息

Department of Urology and Paediatric Urology, Krankenhaus Neunkirchen GmbH, Germany.

出版信息

BJU Int. 2010 Aug;106(4):550-6. doi: 10.1111/j.1464-410X.2009.09129.x. Epub 2009 Dec 11.

Abstract

OBJECTIVE

To compare, in a retrospective observational cohort study, the efficacy, tolerability and safety of propiverine and oxybutynin in children with urge incontinence (UI) due to overactive bladder.

PATIENTS AND METHODS

Medical records were scrutinized for children with UI. As a primary efficacy outcome variable the achievement of continence after treatment with variable doses of propiverine or oxybutynin was assessed. Weekly UI episodes and daily voiding frequency were evaluated as secondary efficacy outcomes. Tolerability was evaluated by the rate of adverse events, adverse drug reactions caused by antimuscarinics and premature treatment termination.

RESULTS

At 16 study centres, 621 children aged 5-14 years with UI due to overactive bladder were enrolled. After anticholinergic treatment (437 propiverine, 184 oxybutynin) continence was achieved in 61.6% and 58.7% of the patients after 186 and 259 days, respectively. There were clinically relevant improvements in voiding frequency across treatment groups. Daily doses of propiverine were markedly below the recommendations (0.54 vs 0.8 mg/kg body weight), daily doses of oxybutynin were according to the recommendations (0.31 vs 0.2-0.4 mg/kg body weight) at treatment initiation. There was a significantly more favourable tolerability to propiverine than oxybutynin for the overall rate of adverse events (3.9% vs 16.3%, odds ratio 4.813), adverse drug reactions caused by propiverine or oxybutynin (2.8% vs 9.2%) and premature treatment termination due to adverse drug reactions (1.6% vs 4.4%).

CONCLUSION

Propiverine and oxybutynin are effective in children with UI due to overactive bladder. Sufficient treatment periods of at least 2, preferably 3-4, months are the crucial factors for a successful treatment. The tolerability profile of propiverine is better than for oxybutynin.

摘要

目的

在一项回顾性观察队列研究中比较索利那新和奥昔布宁治疗膀胱过度活动症导致急迫性尿失禁(UI)儿童的疗效、耐受性和安全性。

患者和方法

仔细查阅患有 UI 的儿童的病历。将治疗后达到持续性(以变量剂量的索利那新或奥昔布宁治疗)作为主要疗效变量进行评估。每周 UI 发作次数和每日排尿频率作为次要疗效指标进行评估。通过不良事件发生率、抗毒蕈碱药物引起的不良反应和提前终止治疗来评估耐受性。

结果

在 16 个研究中心,共有 621 名 5-14 岁因膀胱过度活动症导致 UI 的儿童入组。接受抗胆碱能治疗(437 名索利那新,184 名奥昔布宁)后,186 天和 259 天后,分别有 61.6%和 58.7%的患者达到持续性。治疗组的排尿频率均有显著改善。索利那新的日剂量明显低于推荐剂量(0.54 与 0.8mg/kg 体重),奥昔布宁的日剂量在治疗开始时符合推荐剂量(0.31 与 0.2-0.4mg/kg 体重)。索利那新的总体不良事件发生率(3.9%比 16.3%,优势比 4.813)、索利那新或奥昔布宁引起的不良反应发生率(2.8%比 9.2%)和因不良反应提前终止治疗的发生率(1.6%比 4.4%)均显著优于奥昔布宁。

结论

索利那新和奥昔布宁治疗膀胱过度活动症导致的 UI 有效。至少 2 个月,最好是 3-4 个月的充分治疗期是成功治疗的关键因素。索利那新的耐受性优于奥昔布宁。

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