Zinner Norman, Gittelman Marc, Harris Richard, Susset Jacques, Kanelos Angelo, Auerbach Stephen
Department of Urology, University of California, Los Angeles, California, USA.
J Urol. 2004 Jun;171(6 Pt 1):2311-5, quiz 2435. doi: 10.1097/01.ju.0000127742.73136.0c.
Trospium chloride is an anticholinergic agent with predominantly peripheral nonselective antimuscarinic activity lacking central nervous system effects. It has no known drug-drug interactions, an advantage for patients taking many medications. Because these qualities may provide added benefit when treating patients with symptoms associated with overactive bladder (OAB) and urge incontinence, we studied the effectiveness of trospium in treating these conditions.
Patients with OAB with urge incontinence were randomized 1:1 to 20 mg trospium twice daily or placebo in this 12-week, multicenter, parallel, double-blind, placebo controlled trial. Dual primary end points were change in average number of toilet voids and change in urge incontinent episodes per 24 hours. Secondary efficacy variables were change in average of volume per void, voiding urge severity, urinations during day and night, time to onset of action and change in Incontinence Impact Questionnaire.
A total of 523 patients were entered at 51 sites. Trospium significantly decreased average frequency of toilet voids and urge incontinent episodes compared to placebo. It significantly increased average volume per void, and decreased average urge severity and daytime frequency. All effects occurred by week 1 and all were sustained throughout the study. Nocturnal frequency decreased significantly by week 4 and Incontinence Impact Questionnaire scores improved at week 12. Trospium was well tolerated.
Trospium was found to have sustained effectiveness beginning at the end of week 1 in decreasing the number of voids, urge incontinent episodes, total daily micturitions and urge severity, and in increasing volume per void. It also improved symptoms of OAB and quality of life.
氯化托烷司琼是一种抗胆碱能药物,主要具有外周非选择性抗毒蕈碱活性,无中枢神经系统作用。它不存在已知的药物相互作用,这对服用多种药物的患者来说是一个优势。由于这些特性在治疗膀胱过度活动症(OAB)和急迫性尿失禁相关症状的患者时可能会带来额外益处,我们研究了氯化托烷司琼治疗这些病症的有效性。
在这项为期12周的多中心、平行、双盲、安慰剂对照试验中,将伴有急迫性尿失禁的OAB患者按1:1随机分为每日两次服用20毫克氯化托烷司琼组或安慰剂组。两个主要终点是每日平均排尿次数的变化和每24小时急迫性尿失禁发作次数的变化。次要疗效变量包括每次排尿平均尿量的变化、排尿急迫严重程度、白天和夜间排尿次数、起效时间以及尿失禁影响问卷的变化。
共有51个研究点的523名患者入组。与安慰剂相比,氯化托烷司琼显著降低了平均排尿次数和急迫性尿失禁发作次数。它显著增加了每次排尿的平均尿量,降低了平均急迫严重程度和白天排尿频率。所有这些效果在第1周时就已出现,并且在整个研究过程中持续存在。夜间排尿频率在第4周时显著降低,尿失禁影响问卷得分在第12周时有所改善。氯化托烷司琼耐受性良好。
研究发现,从第1周结束时起,氯化托烷司琼在减少排尿次数、急迫性尿失禁发作次数、每日总排尿量和急迫严重程度以及增加每次排尿量方面具有持续的有效性。它还改善了OAB症状和生活质量。