Department of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Department of Urology, Handa Municipal Hospital, Handa, Japan.
Department of Urology, Nagoya University Graduate School of Medicine, Nagoya, Japan; Department of Urology, Miyoshi Municipal Hospital, Miyoshi, Japan.
J Urol. 2017 Feb;197(2):452-458. doi: 10.1016/j.juro.2016.08.111. Epub 2016 Sep 8.
We investigated the efficacy of 2 α1-blockers with different affinities for the α1-adrenoceptor subtypes silodosin and naftopidil in the treatment of benign prostatic enlargement complicated by overactive bladder.
This was a prospective, open label, randomized, multicenter study of 350 outpatients with untreated benign prostatic enlargement associated with urinary urgency at least once per week and an OABSS (Overactive Bladder Symptom Score) of 3 or greater. Patients were randomly assigned to receive silodosin 8 mg per day or naftopidil 75 mg per day. Changes in parameters from baseline to 4 and 12 weeks were assessed based on I-PSS (International Prostate Symptom Score), I-PSS quality of life, OABSS and voiding functions measured by uroflowmetry.
On efficacy analysis a total of 314 patients were included in the 2 groups. No significant difference in adverse effects was observed between the groups. Mean I-PSS and I-PSS quality of life scores, and OABSS significantly improved in both groups. Statistically significantly greater improvement in the silodosin group than in the naftopidil group was observed in total OABSS (p = 0.03), I-PSS quality of life score (p = 0.005) and OABSS urgency score (p <0.001) at 12 weeks. In regard to voiding function the maximum urinary flow rate showed significant improvements in both groups but the change in the maximum flow rate in the silodosin group at 12 weeks was significantly greater than in the naftopidil group (3.6 vs 2.1 ml per second).
Silodosin, a pure α1A-adrenoceptor blocker, showed greater improvement in overactive bladder symptoms along with the urinary flow rate in patients with benign prostatic enlargement complicated by overactive bladder compared to naftopidil, an α1D>A-adrenoceptor blocker.
我们研究了两种对 α1-肾上腺素受体亚型亲和力不同的 2α1 阻滞剂——西洛多辛和萘哌地尔,在治疗伴有膀胱过度活动症的良性前列腺增生中的疗效。
这是一项前瞻性、开放标签、随机、多中心研究,纳入了 350 名未经治疗的良性前列腺增生伴至少每周一次尿急和 OABSS(膀胱过度活动症症状评分)≥3 的门诊患者。患者被随机分配接受西洛多辛 8mg/天或萘哌地尔 75mg/天治疗。根据 I-PSS(国际前列腺症状评分)、I-PSS 生活质量评分、OABSS 和尿流率测量的排尿功能,评估从基线到 4 周和 12 周的参数变化。
在疗效分析中,共有 314 名患者被纳入两组。两组之间的不良反应无显著差异。两组的 I-PSS 评分和 I-PSS 生活质量评分以及 OABSS 均显著改善。在总 OABSS(p=0.03)、I-PSS 生活质量评分(p=0.005)和 OABSS 急迫评分(p<0.001)方面,西洛多辛组的改善明显大于萘哌地尔组,在 12 周时观察到。在排尿功能方面,两组的最大尿流率均有显著改善,但在 12 周时西洛多辛组的最大尿流率变化明显大于萘哌地尔组(3.6 比 2.1ml/秒)。
与 α1D>A-肾上腺素受体阻滞剂萘哌地尔相比,纯 α1A-肾上腺素受体阻滞剂西洛多辛可显著改善伴有膀胱过度活动症的良性前列腺增生患者的膀胱过度活动症症状和尿流率。