Suppr超能文献

每日一次 5 毫克索利那新与每日三次 5 毫克奥昔布宁速释制剂的耐受性比较:VECTOR 试验结果。

Tolerability of 5 mg solifenacin once daily versus 5 mg oxybutynin immediate release 3 times daily: results of the VECTOR trial.

机构信息

Department of Surgery/Urology, University of Toronto, Toronto, Ontario, Canada.

出版信息

J Urol. 2010 May;183(5):1892-8. doi: 10.1016/j.juro.2010.01.012. Epub 2010 Mar 29.

Abstract

PURPOSE

Although antimuscarinic treatment is indicated for overactive bladder, many patients discontinue it because of dry mouth. Of available antimuscarinics oxybutynin is associated with the highest dry mouth rate. We compared the safety and tolerability of 5 mg solifenacin vs 15 mg oxybutynin immediate release.

MATERIALS AND METHODS

At 12 Canadian centers a total of 132 patients with overactive bladder symptoms (greater than 1 urgency episode per 24 hours, and 8 or greater micturitions per 24 hours) were randomized to 5 mg solifenacin once daily or 5 mg oxybutynin 3 times daily for 8 weeks. The primary end point was the incidence and severity of dry mouth reported after direct questioning. Efficacy end points (3-day diary documented changes in urgency, frequency, incontinence, nocturia and voided volume), and changes on the Patient Perception of Bladder Condition scale and the Overactive Bladder Questionnaire were evaluated secondarily.

RESULTS

Of patients on solifenacin vs oxybutynin immediate release 35% vs 83% reported dry mouth (p <0.0001). Of patients reporting dry mouth severity was graded moderate by 13% and 42% of those on solifenacin and oxybutynin immediate release, and severe by 13% and 28%, respectively (p = 0.001). Patients in each group showed improvements in efficacy end points, and Patient Perception of Bladder Condition scale and Overactive Bladder Questionnaire scores from baseline to treatment end.

CONCLUSIONS

Significantly fewer patients on 5 mg solifenacin once daily reported dry mouth vs those receiving 5 mg oxybutynin immediate release 3 times daily. Significantly fewer patients on solifenacin reported moderate/severe dry mouth. Significantly fewer patients on solifenacin withdrew from study due to dry mouth and there were significantly fewer overall adverse events. Solifenacin and oxybutynin immediate release were efficacious in decreasing efficacy end points, and improved Patient Perception of Bladder Condition scale and Overactive Bladder Questionnaire results from baseline to treatment end.

摘要

目的

尽管抗毒蕈碱药物治疗适用于膀胱过度活动症,但许多患者因口干而停止治疗。在现有的抗毒蕈碱药物中,奥昔布宁与最高的口干发生率相关。我们比较了 5mg 索利那新与 15mg 奥昔布宁速释片的安全性和耐受性。

材料和方法

在 12 个加拿大中心,共有 132 名膀胱过度活动症症状患者(24 小时内超过 1 次尿急发作,24 小时内超过 8 次排尿)被随机分为每天一次 5mg 索利那新或每天 3 次 5mg 奥昔布宁速释片治疗 8 周。主要终点是直接询问后报告的口干发生率和严重程度。次要终点评估了疗效终点(3 天日记记录的尿急、频率、失禁、夜尿和排尿量的变化)以及患者对膀胱状况量表和膀胱过度活动症问卷的感知变化。

结果

在接受索利那新和奥昔布宁速释片治疗的患者中,分别有 35%和 83%报告口干(p<0.0001)。报告口干严重程度为中度的患者分别有 13%和 42%,严重程度为重度的患者分别有 13%和 28%(p=0.001)。两组患者的疗效终点、患者对膀胱状况量表和膀胱过度活动症问卷评分均从基线改善到治疗结束。

结论

每天一次 5mg 索利那新治疗的患者报告口干的比例明显低于每天 3 次 5mg 奥昔布宁速释片治疗的患者。报告口干中度/重度的患者明显少于索利那新治疗组。因口干而退出研究的患者明显少于索利那新治疗组,总的不良事件明显少于奥昔布宁速释片治疗组。索利那新和奥昔布宁速释片均能有效降低疗效终点,从基线到治疗结束均能改善患者对膀胱状况量表和膀胱过度活动症问卷的结果。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验