首页> 外文期刊>The Journal of Urology >Intravesical electromotive administration of oxybutynin in patients with detrusor hyperreflexia unresponsive to standard anticholinergic regimens.
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Intravesical electromotive administration of oxybutynin in patients with detrusor hyperreflexia unresponsive to standard anticholinergic regimens.

机译:对膀胱逼尿肌反射亢进的患者行膀胱电动施药对标准抗胆碱能疗法无反应。

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PURPOSE: About 15% to 20% of patients with detrusor hyperreflexia do not benefit from oral oxybutynin regimens, frequently because of unpleasant side effects. Several reports indicate that intravesical oxybutynin is effective in many of these patients but there are some who still fail to respond. MATERIALS AND METHODS: A select group of 10 adults with detrusor hyperreflexia unresponsive to standard oral and intravesical oxybutynin regimens were treated at weekly intervals with 5 mg. oxybutynin orally, or 5 mg. oxybutynin in 100 ml. intravesically for 60 minutes of passive diffusion and for 30 minutes with 5 mA. electrical current. Each treatment (plus oral placebo and 2 intravesical controls) was associated with an 8-hour, full urodynamic monitoring session, and periodic blood and bladder content sampling. RESULTS: There was no significant objective improvement with oral or intravesical passive diffusion oxybutynin. Conversely there was significant improvement in 5 of 6 objective urodynamic measurements with intravesical electromotive oxybutynin. Plasma profiles were a single peak and decay following oral oxybutynin and 2 distinct peaks with intravesical passive diffusion and electromotive oxybutynin. Area under the curve for intravesical passive diffusion were 709 ng. per 8 hours versus oral 1,485 (p <0.05) versus intravesical electromotive 2,781 (p <0.001). Bladder content samples confirmed oxybutynin absorption. Oral oxybutynin caused anticholinergic side effects in 7 of 10 patients. There were no side effects with intravesical passive diffusion or electromotive administrations. CONCLUSIONS: Accelerated intravesical administration results in greater bioavailability and increased objective benefits without side effects in previously unresponsive patients compared with oral and intravesical passive diffusion oxybutynin administration.
机译:目的:逼尿肌反射亢进的患者中约有15%至20%不能从口服奥昔布宁方案中获益,这通常是由于不良的副作用所致。几篇报道表明,膀胱内奥昔布宁对其中许多患者有效,但仍有一些患者仍无反应。材料与方法:选择的10名成人对逼尿肌反射亢进对标准口服和膀胱奥昔布宁疗法无反应的成年人,每周间隔5 mg治疗。奥昔布宁口服,或5 mg。 100毫升中的奥昔布宁。膀胱内进行60分钟的被动扩散,并在5 mA下进行30分钟。电流。每种治疗(加上口服安慰剂和2个膀胱内对照)都需要进行8小时的完整尿动力学监测,并定期进行血液和膀胱内容物采样。结果:口服或膀胱内被动扩散奥昔布宁没有明显的客观改善。相反,使用膀胱内电动奥昔布宁进行的6个客观尿动力学测量结果中有5个显着改善。血浆分布为口服奥昔布宁后的单个峰和衰减,以及2个具有膀胱内被动扩散和电动奥昔布宁的不同峰。膀胱内被动扩散曲线下面积为709 ng。每8小时对比口服1,485(p <0.05)对比膀胱内电动2,781(p <0.001)。膀胱内容物样本证实了奥昔布宁的吸收。 10例患者中有7例口服奥昔布宁引起抗胆碱能副作用。膀胱内被动扩散或电动给药没有副作用。结论:与口服和膀胱内被动扩散奥昔布宁给药相比,先前无反应的患者加速膀胱内给药可产生更高的生物利用度并增加客观益处,而无副作用。

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