Kliniken Maria Hilf GmbH, Mönchengladbach, Germany.
J Sex Med. 2011 Jan;8(1):261-71. doi: 10.1111/j.1743-6109.2010.02005.x. Epub 2010 Aug 30.
Men with erectile dysfunction (ED) are typically older and have one or more underlying cardiovascular conditions.
To determine the efficacy and safety of a new orodispersible tablet (ODT) formulation of vardenafil for the treatment of ED, and whether age, or the presence of underlying conditions affects treatment outcomes.
This is an integrated analysis of data from two phase III, double-blind, multicenter, randomized, parallel-group, placebo-controlled studies that compared 10 mg on-demand vardenafil ODT with placebo in a general population of men with ED, stratified so that approximately 50% of patients were aged ≥ 65 years. Results were reported by age (<6 5 vs. ≥ 65 years) and presence/absence of diabetes, dyslipidemia, or hypertension.
Primary measures were the erectile function domain of the International Index of Erectile Function (IIEF-EF) and Sexual Encounter Profile questions 2 (SEP2) and 3 (SEP3).
Of the 701 men randomized (51% aged ≥ 65 years), 686 were included in the intent-to-treat population (placebo, n = 334; vardenafil ODT, n = 352). Vardenafil ODT was significantly superior to placebo for all primary efficacy measures, regardless of age, baseline ED severity, or underlying condition (P < 0.0001 for vardenafil vs. placebo for each endpoint). IIEF-EF scores and SEP2/3 success rates in older patients and men with underlying conditions were not significantly different to those of younger patients or men without underlying conditions. Adverse events (AEs) were mostly mild to moderate in severity, occurring with higher incidence in the vardenafil vs. placebo group. The most frequently reported drug-related AEs in the vardenafil group were headache, flushing, nasal congestion, dizziness, and dyspepsia, consistent with the known safety profile of phosphodiesterase type 5 inhibitors.
Vardenafil ODT significantly improves erectile function in men with ED regardless of age, baseline ED severity, or underlying condition.
患有勃起功能障碍(ED)的男性通常年龄较大,且存在一种或多种潜在的心血管疾病。
评估新型口腔崩解片(ODT)制剂伐地那非治疗 ED 的疗效和安全性,以及年龄和潜在疾病是否会影响治疗结果。
这是两项 III 期、双盲、多中心、随机、平行组、安慰剂对照研究数据的综合分析,这些研究将按需服用 10 毫克伐地那非 ODT 与安慰剂在 ED 一般人群中进行了比较,分层后约 50%的患者年龄≥65 岁。结果按年龄(<65 岁与≥65 岁)和是否存在糖尿病、血脂异常或高血压进行了报告。
主要观察指标为国际勃起功能指数(IIEF-EF)的勃起功能域和性经历问卷 2(SEP2)和 3(SEP3)。
701 名随机患者(51%年龄≥65 岁)中,686 名纳入意向治疗人群(安慰剂组 n=334;伐地那非 ODT 组 n=352)。伐地那非 ODT 在所有主要疗效指标上均显著优于安慰剂,无论年龄、基线 ED 严重程度或潜在疾病(每个终点伐地那非与安慰剂相比 P<0.0001)。老年患者和存在潜在疾病的患者的 IIEF-EF 评分和 SEP2/3 成功率与年轻患者和无潜在疾病的患者无显著差异。不良事件(AE)大多为轻度至中度,伐地那非组的发生率高于安慰剂组。伐地那非组报告最多的药物相关 AE 为头痛、潮红、鼻塞、头晕和消化不良,与磷酸二酯酶 5 抑制剂的已知安全性一致。
伐地那非 ODT 可显著改善 ED 男性的勃起功能,无论年龄、基线 ED 严重程度或潜在疾病如何。