Singh-Franco Devada, Machado Caridad, Tuteja Sony, Zapantis Antonia
Pharmacy Practice, Nova Southeastern University, Fort Lauderdale, FL 33328, USA.
Clin Ther. 2005 May;27(5):511-30. doi: 10.1016/j.clinthera.2005.05.008.
Urinary incontinence is caused by an overactive bladder, leading to symptoms of urgency, frequency, and incontinence. Urge incontinence occurs predominantly in women as they age.
This article reviews the current primary literature concerning the efficacy and tolerability of the anticholinergic agent trospium chloride (TCl) in the treatment of overactive bladder with symptoms of urge incontinence, urgency, and frequency. The pharmacokinetics of TCl are also reviewed.
Pertinent articles in English were identified through a search of MEDLINE (1966-present), EMBASE Drugs & Pharmacology (1980-third quarter 2004), Current Contents/Clinical Medicine (week 42, 2003-week 41, 2004), Cochrane Database of Systematic Reviews, MICROMEDEX Healthcare Series, and International Pharmaceutical Abstracts (1970-present). The search terms were overactive bladder, urinary incontinence, trospium, randomized controlled clinical trial, oxybutynin, tolterodine, scopolamine, imipramine, desipramine, and propantheline.
TCl, a quaternary amine, exhibits high solubility in water but low oral bioavailability (9.6%) and poor central nervous system penetration. Approximately 80% of the absorbed fraction is renally eliminated as unchanged drug via active tubular secretion, with approximately 15% hepatically metabolized into a spiroalcohol and hydrolysis/oxidation products. In 3 placebo-controlled studies, patients who received TCl had an increase in maximum bladder filling capacity and bladder compliance, with a reduction in maximum cystometric capacity (P < 0.005); however, only 1 of these studies showed an increase in bladder compliance, with reductions in maximum detrusor pressure (P < 0.001), number of voids/d (P < or = 0.001), and incontinence episodes/d (P < or = 0.001). In another placebo-controlled study, TCl reduced the number of voids/d and incontinence episodes/d (both, P < or = 0.001). In 2 double-blind studies, TCl and oxybutynin were similarly effective in significantly increasing maximum cystometric capacity and bladder compliance, and in significantly reducing maximum detrusor pressure compared with baseline (all, P < 0.001); there were no significant differences between the 2 treatments at end point. In a third double-blind study comparing TCl and tolterodine with placebo, only TCl significantly reduced the frequency of micturitions/d (P = 0.01). Commonly reported adverse effects in patients receiving TCl included dry mouth, constipation, and headache.
In the 7 studies reviewed, TCl was effective and well tolerated in patients with urge incontinence caused by idiopathic detrusor muscle overactivity or neurogenic detrusor overactivity resulting from spinal cord injury. However, this agent was associated with anticholinergic adverse effects similar to those of other anticholinergic agents; careful monitoring of tolerability is required.
尿失禁由膀胱过度活动症引起,导致尿急、尿频和失禁症状。急迫性尿失禁在女性中随着年龄增长而更为常见。
本文综述了关于抗胆碱能药物氯化托烷司琼(TCl)治疗伴有急迫性尿失禁、尿急和尿频症状的膀胱过度活动症的疗效和耐受性的当前主要文献。还综述了TCl的药代动力学。
通过检索MEDLINE(1966年至今)、EMBASE药物与药理学(1980年 - 2004年第三季度)、《临床医学当前内容》(2003年第42周 - 2004年第41周)、Cochrane系统评价数据库、MICROMEDEX医疗保健系列以及《国际药学文摘》(1970年至今)来确定相关英文文章。检索词为膀胱过度活动症、尿失禁、托烷司琼、随机对照临床试验、奥昔布宁、托特罗定、东莨菪碱、丙咪嗪、地昔帕明和丙胺太林。
TCl是一种季铵盐,在水中具有高溶解度,但口服生物利用度低(9.6%)且中枢神经系统穿透力差。吸收部分的约80%通过主动肾小管分泌以原形药物经肾脏消除,约15%经肝脏代谢为螺醇及水解/氧化产物。在3项安慰剂对照研究中,接受TCl的患者最大膀胱充盈容量和膀胱顺应性增加,最大膀胱测压容量降低(P < 0.005);然而,这些研究中只有1项显示膀胱顺应性增加,最大逼尿肌压力降低(P < 0.001),每日排尿次数(P < 或 = 0.001)和每日失禁发作次数(P < 或 = 0.001)减少。在另一项安慰剂对照研究中,TCl减少了每日排尿次数和每日失禁发作次数(两者均P < 或 = 0.001)。在2项双盲研究中,与基线相比,TCl和奥昔布宁在显著增加最大膀胱测压容量和膀胱顺应性以及显著降低最大逼尿肌压力方面同样有效(所有P < 0.001);在终点时两种治疗之间无显著差异。在第三项比较TCl、托特罗定与安慰剂的双盲研究中,只有TCl显著降低了每日排尿频率(P = 0.01)。接受TCl的患者常见的不良反应包括口干、便秘和头痛。
在所综述的7项研究中,TCl对特发性逼尿肌过度活动或脊髓损伤导致的神经源性逼尿肌过度活动引起的急迫性尿失禁患者有效且耐受性良好。然而,该药物与其他抗胆碱能药物类似,会产生抗胆碱能不良反应;需要仔细监测耐受性。