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他达拉非对美国和波多黎各勃起功能障碍男性的疗效和安全性。

The efficacy and safety of tadalafil in United States and Puerto Rican men with erectile dysfunction.

作者信息

Seftel Allen D, Wilson Steven K, Knapp Peter M, Shin Janey, Wang W Christine, Ahuja Sanjeev

机构信息

University Hospitals, Case Western Reserve University, Cleveland VA Medical Center, Cleveland, Ohio 44106-5046, USA.

出版信息

J Urol. 2004 Aug;172(2):652-7. doi: 10.1097/01.ju.0000132857.39680.ce.

Abstract

PURPOSE

We evaluate the efficacy and safety of tadalafil, taken as needed, in men with mild to severe erectile dysfunction (ED) and assess sexual intercourse attempt patterns.

MATERIALS AND METHODS

In this multicenter, double-blind, placebo controlled, parallel study conducted in the United States and Puerto Rico 207 men with ED were randomized to placebo or 20 mg tadalafil for 12 weeks. The primary efficacy variables were changes from baseline in the mean International Index of Erectile Function erectile function domain score and mean per patient percentage of "yes" responses to Sexual Encounter Profile (SEP) diary questions 2 (successful penetration) and 3 (successful intercourse). The Global Assessment Question was a secondary end point and post hoc analyses on sexual intercourse attempt patterns were conducted.

RESULTS

Men treated with tadalafil compared with placebo reported greater mean changes from baseline on the erectile function domain score (9.3 vs 0.3 with placebo, p <0.001) and on the mean per patient percentage of successful penetration (SEP question 2, 31.6% vs 2.3% with placebo, p <0.001) and successful intercourse attempts (SEP question 3, 43.6% vs 3.5% with placebo, p <0.001). The per treatment group percentage of successful intercourse attempts during treatment was higher for tadalafil than placebo (67.6% vs 24.1%, respectively, p <0.001) and most successful intercourse attempts occurred between 4 and 36 hours after taking tadalafil. Of the men treated with tadalafil 82.8% reported improved erections versus 19.6% taking placebo (Global Assessment Question, p <0.001). The most common treatment emergent adverse events were headache (15.7% vs 6.3% with placebo), back pain (8.8% vs 0%), and dyspepsia (7.5% vs 0%).

CONCLUSIONS

Tadalafil (20 mg) significantly improved erectile function and patients did not closely temporally link sexual intercourse attempts with taking tadalafil. Tadalafil was also well tolerated in both groups of men with mild to severe ED.

摘要

目的

我们评估按需服用他达拉非对轻至重度勃起功能障碍(ED)男性的疗效和安全性,并评估性交尝试模式。

材料与方法

在这项在美国和波多黎各进行的多中心、双盲、安慰剂对照、平行研究中,207名ED男性被随机分为安慰剂组或20毫克他达拉非组,为期12周。主要疗效变量为国际勃起功能指数勃起功能领域平均得分相对于基线的变化,以及每位患者对性接触记录(SEP)日记问题2(成功插入)和问题3(成功性交)回答“是”的平均百分比。总体评估问题是次要终点,并对性交尝试模式进行了事后分析。

结果

与安慰剂组相比,服用他达拉非的男性在勃起功能领域得分相对于基线的平均变化更大(分别为9.3和安慰剂组的0.3,p<0.001),成功插入的平均每位患者百分比(SEP问题2,分别为31.6%和安慰剂组的2.3%,p<0.001)以及成功性交尝试(SEP问题3,分别为43.6%和安慰剂组的3.5%,p<0.001)。在治疗期间,他达拉非组成功性交尝试的每组治疗百分比高于安慰剂组(分别为67.6%和24.1%,p<0.001),且大多数成功性交尝试发生在服用他达拉非后4至36小时之间。在服用他达拉非的男性中,82.8%报告勃起功能改善,而服用安慰剂的为19.6%(总体评估问题,p<0.001)。最常见的治疗中出现的不良事件为头痛(分别为15.7%和安慰剂组的6.3%)、背痛(分别为8.8%和0%)以及消化不良(分别为7.5%和0%)。

结论

他达拉非(20毫克)显著改善了勃起功能,且患者并未在时间上紧密地将性交尝试与服用他达拉非联系起来。他达拉非在轻至重度ED的两组男性中耐受性均良好。

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