Blonde Lawrence
Ochsner Clinic Foundation, New Orleans, LA 70121, USA.
Curr Med Res Opin. 2006 Nov;22(11):2111-20. doi: 10.1185/030079906X148256.
Cardiovascular (CV) risk factors are associated with an increased risk of erectile dysfunction (ED). In men with diabetes mellitus (DM), pooled from clinical trials of sildenafil treatment for ED, this retrospective analysis determined efficacy and safety, overall and in subgroups with additional CV risk (i.e., hypertension, dyslipidemia, and smoking).
From the manufacturer's database of worldwide research, 12-week data from men with DM were pooled from randomized, double-blind, placebo-controlled trials of flexible-dose sildenafil (25, 50, or 100 mg, PRN) for ED.
Question 3 (achieving an erection), question 4 (maintaining an erection), and the Erectile Function domain of the International Index of Erectile Function; percentage of successful intercourse attempts according to patient event logs; and response to a global efficacy question (GEQ). Differences between groups were determined using logistic regression (percentage of responders according to GEQ) and analysis of covariance (all other outcomes).
Inclusion criteria were met by 11 trials and by 974 men with DM and ED who were randomized to placebo (n = 482) and sildenafil (n = 492) within the selected trials. For all outcomes, overall and regardless of additional CV risk, the benefit was greater for sildenafil versus placebo (p < or = 0.0001), including 3-fold more men responding that sildenafil treatment improved their erections (62% vs. 18%) and a more than doubling of the mean +/- standard error percentage of successful sexual intercourse attempts (52.6 +/- 5.0 vs. 22.4 +/- 5.1). Adverse events were mild to moderate and included (sildenafil vs. placebo) headache (5% vs. 2%), flushing (7% vs. 2%), and dyspepsia (4% vs. 0%), which is consistent with the profile in the general population of men treated with sildenafil for ED.
This retrospective analysis of pooled data showed that sildenafil was well tolerated and improved erectile function and intercourse success in men with ED and DM, regardless of additional CV risk factors.
心血管(CV)危险因素与勃起功能障碍(ED)风险增加相关。在糖尿病(DM)男性中,本回顾性分析从西地那非治疗ED的临床试验数据中汇总得出,确定了总体及具有其他心血管风险(即高血压、血脂异常和吸烟)亚组的疗效和安全性。
从制造商的全球研究数据库中,汇总了来自灵活剂量西地那非(25、50或100毫克,按需服用)治疗ED的随机、双盲、安慰剂对照试验中糖尿病男性的12周数据。
国际勃起功能指数的第3个问题(实现勃起)、第4个问题(维持勃起)以及勃起功能领域;根据患者事件记录得出的成功性交尝试百分比;以及对总体疗效问题(GEQ)的回答。使用逻辑回归(根据GEQ得出的应答者百分比)和协方差分析(所有其他结果)确定组间差异。
11项试验以及974名患有DM和ED的男性符合纳入标准,这些男性在选定试验中被随机分配至安慰剂组(n = 482)和西地那非组(n = 492)。对于所有结果,总体而言且无论是否存在其他心血管风险,西地那非组的获益均大于安慰剂组(p≤0.0001),包括回应西地那非治疗改善了勃起功能的男性人数增加了两倍(62%对18%),以及成功性交尝试的平均±标准误百分比增加了一倍多(52.6±5.0对22.4±5.1)。不良事件为轻度至中度,包括(西地那非组对安慰剂组)头痛(5%对2%)、潮红(7%对2%)和消化不良(4%对0%),这与西地那非治疗ED的普通男性人群特征相符。
对汇总数据的这项回顾性分析表明,无论是否存在其他心血管危险因素,西地那非在患有ED和DM的男性中耐受性良好,且能改善勃起功能和性交成功率。