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Efficacy and safety of udenafil for erectile dysfunction: A meta-analysis of randomized controlled trials

机译:乌地那非治疗勃起功能障碍的有效性和安全性:随机对照试验的荟萃分析

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Objective: To systematically review the evidence on the efficacy and safety of udenafil as treatment of erectile dysfunction from randomized controlled trials. Methods: We searched PubMed, Embase, and the Cochrane Library database up to October 2011. The outcome measures assessed were the change from baseline for the International Index of Erectile Function erectile function domain score (primary), the change from baseline for Sexual Encounter Profile questions 2 and 3, the shift to normal rate (erectile function domain <26), the response to the Global Assessment Questionnaire and adverse effects (secondary). Two of us independently assessed the study quality and extracted data. All data were analyzed using Review Manager, version 5.0.2. Results: Five randomized controlled trials totaling 1109 patients were included. At the follow-up endpoints, udenafil was found to be more effective than placebo, and the tolerability was good. The pooled results showed that the udenafil group was significantly greater than the placebo group in the change from baseline for the International Index of Erectile Function erectile function domain score (mean difference 5.65, 95% confidence interval 4.41-6.89, P <.00001). All included studies indicated that most adverse events were mild or moderate in severity, and no serious adverse events were reported during the study period. The most common drug-related adverse events were flushing and headache (udenafil vs placebo, 5.6% vs 1.8% and 3.1% vs 0%, respectively). Conclusion: The results from the current meta-analysis have suggested that udenafil is an effective and well-tolerated therapy for erectile dysfunction. The findings of the present review highlight the need for more efficient performance of higher quality, large-sample, various-race, long-term, randomized controlled trials to verify the efficacy and safety of udenafil.
机译:目的:系统评价随机对照试验中关于乌地那非治疗勃起功能障碍的疗效和安全性的证据。方法:我们搜索截至2011年10月的PubMed,Embase和Cochrane图书馆数据库。评估的结局指标是国际勃起功能勃起功能域评分指数(主要)从基线的变化,性遭遇档案中基线的变化问题2和3,转向正常比率(勃起功能域<26),对《全球评估问卷》的反应和不良影响(次要)。我们两个人独立评估了研究质量并提取了数据。使用Review Manager 5.0.2版分析了所有数据。结果:包括五项随机对照试验,共1109例患者。在随访终点,发现乌地那非比安慰剂更有效,耐受性良好。汇总的结果表明,在国际勃起功能指数勃起功能域评分方面,从基线水平变化,udenafil组显着大于安慰剂组(平均差异5.65,95%置信区间4.41-6.89,P <.00001)。所有纳入的研究表明,大多数不良事件的严重程度为轻度或中度,并且在研究期间未报告严重的不良事件。最常见的与药物相关的不良事件是潮红和头痛(乌地那非vs安慰剂,分别为5.6%vs. 1.8%和3.1%vs 0%)。结论:当前荟萃分析的结果表明,乌地那非是一种有效且耐受良好的勃起功能障碍治疗方法。本综述的结果强调,需要更高效率的高质量,大样本,多种族,长期,随机对照试验来验证乌地那非的疗效和安全性。

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