首页> 外文期刊>International Journal of Impotence Research >Comparison of the efficacy and safety of 5-mg once-daily versus 5-mg alternate-day tadalafil in men with erectile dysfunction and lower urinary tract symptoms
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Comparison of the efficacy and safety of 5-mg once-daily versus 5-mg alternate-day tadalafil in men with erectile dysfunction and lower urinary tract symptoms

机译:每日一次5-mg他达拉非与每天5-mg他达拉非治疗勃起功能障碍和下尿路症状的男性的疗效和安全性比较

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The purposeof this study is to investigate and compare the effects of 5-mg once-daily tadalafil versus 5-mg alternate-day tadalafil in men with moderate-to-severe erectile dysfunction (ED) and lower urinary tract symptoms (LUTS). Between January 2012 and June 2013, 144 men presenting with an International Index of Erectile Function-5 (IIEF-5) score of 8 were enrolled to the study. Patients were allocated the simple alternate randomization into Group I (5-mg once-daily tadalafil) and Group II (5-mg alternate-day tadalafil). Changes in IIEF scores, Sexual Encounter Profile Question 3 (SEP Q3) percentage, IPSS, uroflowmetry and post void residual at the first visit (V1), week 4 (V2) and week 12 (V3) were compared. No significant difference was found between the baseline patient characteristics of Group I and Group II. Treatment with 5-mg daily tadalafil demonstrated improvement in IIEF, SEP Q3 percentage and IPSS score between V1 and V2, and that between V1 and V3. Patients receiving 5-mg alternate-day tadalafil also showed a significant improvement in IIEF, SEP Q3 percentage, and IPSS score between V1 and V2, and that between V2 and V3. However, no significant improvements were found in any other parameters. There were no significant differences between Group I and Group II apart from IIEF scores in V2 (19.4 versus 17.9, respectively). The SEP Q3 percentage was also higher at the V2 visit for Group I and Group II (35.6 versus 30.9%). Even with no placebo control and short of LUTS medication control, the use of 5-mg once-daily or alternate-day treatment with tadalafil was well tolerated in patients and effectively improved the IIEF score, IPSS score and SEP Q3 percentage. Management of patients with 5-mg alternate-day tadalafil could be adequate for regular use in patients with ED and LUTS.
机译:这项研究的目的是调查和比较每日一次5 mg他达拉非和5 mg隔日他达拉非对中度至重度勃起功能障碍(ED)和下尿路症状(LUTS)的影响。在2012年1月至2013年6月之间,有144名男性的勃起功能国际指数5(IIEF-5)得分为8。将患者分为第一组(5 mg,每日一次他达拉非)和第二组(5 mg,每日一次他达拉非)。比较了IIEF得分,性接触测验问题3(SEP Q3)百分比,IPSS,尿流测定法和首次就诊(V1),第4周(V2)和第12周(V3)的空洞残留量的变化。第一组和第二组的基线患者特征之间没有发现显着差异。每天服用5 mg他达拉非的治疗证明V1和V2之间以及V1和V3之间的IIEF,SEP Q3百分比和IPSS评分均有改善。接受5 mg隔日他达拉非的患者在V1和V2之间以及V2和V3之间,IIEF,SEP Q3百分比和IPSS评分也显着改善。但是,在任何其他参数上均未发现重大改进。除了V2中的IIEF分数外,第一组和第二组之间没有显着差异(分别为19.4和17.9)。 I组和II组的V2访问时,SEP Q3百分比也更高(35.6对30.9%)。即使没有安慰剂对照并且缺乏LUTS药物控制,患者也可以耐受使用tadalafil每天一次或隔天5 mg的治疗,并有效改善了IIEF评分,IPSS评分和SEP Q3百分比。隔日使用他达拉非5 mg的患者的管理可能足以满足ED和LUTS患者的常规使用。

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