Rosen R, Seftel A, Roehrborn C G
New England Research Institutes, Watertown, MA 2472, USA.
Int J Impot Res. 2007 Sep-Oct;19(5):480-5. doi: 10.1038/sj.ijir.3901554. Epub 2007 Aug 23.
We evaluated the effects of extended-release alfuzosin HCl 10 mg once daily (q.d.) on sexual function in men with lower urinary tract symptoms associated with benign prostatic hyperplasia (BPH). In a randomized, double-blind, placebo-controlled study of men aged > or = 50 years, after a 28-day placebo run-in period, patients were randomized to receive alfuzosin 10 mg q.d. or matching placebo for 28 days. The mean change from baseline (day 1) in sexual function on day 29 was assessed using the Danish Prostate Symptom Score Sex (DAN-PSSsex) questionnaire. A total of 372 patients were randomized to receive alfuzosin (n=186) or placebo (n=186), with 355 completing the study. At baseline, 64% of the patients reported erectile dysfunction (ED) and 63% reported ejaculatory dysfunction (EjD). For the 320 patients who completed the DAN-PSSsex, alfuzosin treatment was associated with a significant improvement in the mean change from baseline in erectile function on day 29 compared with placebo (P=0.02). No significant difference was observed between the two treatment groups in the mean change from baseline in ejaculatory function on day 29. For patients with ED at baseline, a marginal improvement in erectile function was demonstrated with alfuzosin treatment (P=0.09 vs placebo). For patients with EjD at baseline, the mean change from baseline in ejaculatory function with alfuzosin was comparable to that with placebo. Dizziness was the most common adverse event with alfuzosin treatment (5 vs 0% with placebo), with other adverse events reported with comparable frequency in both treatment groups. After 1 month of treatment, alfuzosin 10 mg q.d. significantly improved erectile function in men with lower urinary tract symptoms/ benign prostatic hypertrophy and had no adverse effect on ejaculatory function.
我们评估了每日一次口服10毫克缓释盐酸阿夫唑嗪对伴有良性前列腺增生(BPH)的下尿路症状男性性功能的影响。在一项针对年龄大于或等于50岁男性的随机、双盲、安慰剂对照研究中,经过28天的安慰剂导入期后,患者被随机分配接受每日一次10毫克阿夫唑嗪或匹配的安慰剂,为期28天。使用丹麦前列腺症状评分性(DAN - PSSsex)问卷评估第29天性功能相对于基线(第1天)的平均变化。共有372名患者被随机分配接受阿夫唑嗪(n = 186)或安慰剂(n = 186),355名患者完成了研究。基线时,64%的患者报告有勃起功能障碍(ED),63%的患者报告有射精功能障碍(EjD)。对于完成DAN - PSSsex的320名患者,与安慰剂相比,阿夫唑嗪治疗使第29天勃起功能相对于基线的平均变化有显著改善(P = 0.02)。在第29天射精功能相对于基线的平均变化方面,两个治疗组之间未观察到显著差异。对于基线时有ED的患者,阿夫唑嗪治疗显示勃起功能有轻微改善(与安慰剂相比,P = 0.09)。对于基线时有EjD的患者,阿夫唑嗪治疗后射精功能相对于基线的平均变化与安慰剂相当。头晕是阿夫唑嗪治疗最常见的不良事件(5% vs安慰剂为0%),两个治疗组报告的其他不良事件频率相当。治疗1个月后,每日一次10毫克阿夫唑嗪显著改善了伴有下尿路症状/良性前列腺增生男性的勃起功能,且对射精功能无不良影响。