首页> 外文期刊>Open Journal of Urology >A Prospective, Multicenter Study on Efficacy of Long-Acting Testosterone Undecanoate, If Desired in Combination with Vardenafil, in Late Onset Hypogonadal Patients with Erectile Dysfunction
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A Prospective, Multicenter Study on Efficacy of Long-Acting Testosterone Undecanoate, If Desired in Combination with Vardenafil, in Late Onset Hypogonadal Patients with Erectile Dysfunction

机译:多发性勃起功能障碍迟发性性腺功能减退患者的长效十一烷酸酯(如果与伐地那非合用)疗效的前瞻性,多中心研究

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Introduction: There is substantial evidence suggesting the additive effect on erectile function (ED) of testosterone and phosphodiesterase (PDE)-5 inhibitors. But the combination of long-acting testosterone undecanoate (TU), in combination with the PDE5-I vardenafil men with with late-onset hypogonadal patients (LOH) with (ED) has not yet been studied. Aims: To evaluate the effects of TU i.m., and if desired, the PDE5i vardenafil (PDE-5I) in LOH patients with ED measured with the International Index of Erectile Function (IIEF-5). Methods: A prospective study was performed following four administrations of TU in week 0, 6, 18, 30. If no improvement of ED assessed with IIEF-5 or the Global Assessment Questionnaire (GAQ) in week 12, the PDE5 inhibitor vardenafil was added. The final evaluation was in week 46. Main Outcome Measures: Aging Male Symptom (AMS) score, IIEF-5 score, and International Prostate Symptoms Score (IPSS) at each visit were summarized as mean with standard deviation; while GAQ was summarized using frequency and percentage. Scores at each visit were also categorized into different levels of symptom severity. Results: AMS score decreased significantly at week 12, 30 and 46. IIEF-5 score increased but a significant change was found only at week 30 and 46. The GAQ assessment indicated erection and sexual intercourse already improved at the first assessment continuing thereafter. IPSS score decreased from baseline at week 46. Levels of total, free and bioavailable testosterone had increased significantly from baseline at all visits. Hematocrit, hemoglobin and prostate specific antigen increased significantly from baseline. Adverse events were rare with pain at injection site found in one patient. The two events were non-serious in type, mild in their intensity and recovered. Conclusions: Therapy with TU and, and if desired, combined with the PDE5 inhibitor vardenafil improved sexual activity in LOH patients with ED.
机译:简介:有大量证据表明对睾丸激素和磷酸二酯酶(PDE)-5抑制剂的勃起功能(ED)有累加作用。但是,尚未研究长效十一酸睾丸激素(TU)与PDE5-I伐地那非男性与迟发性性腺功能减退患者(LOH)与(ED)的组合。目的:为了评估TU i.m.的效果,并根据需要评估国际勃起功能指数(IIEF-5)对LOH ED患者的PDE5i伐地那非(PDE-5I)。方法:在第0、6、18、30周四次施用TU后进行了一项前瞻性研究。如果在第12周用IIEF-5或全球评估问卷(GAQ)评估的ED没有改善,则添加PDE5抑制剂伐地那非。最终评估在第46周进行。主要观察指标:每次就诊时的男性衰老症状(AMS)评分,IIEF-5评分和国际前列腺症状评分(IPSS)均总结为均值,并带有标准差。而GAQ是使用频率和百分比进行汇总的。每次访视的分数也分为不同级别的症状严重程度。结果:AMS评分在第12、30和46周时显着下降。IIEF-5评分升高,但仅在第30周和46周时才发现显着变化。GAQ评估表明在第一次评估中勃起和性交已经改善,此后一直持续。 IPSS评分在第46周时从基线下降。在所有访问中,总睾丸激素,游离睾丸激素和可生物利用睾丸激素的水平均显着高于基线。血细胞比容,血红蛋白和前列腺特异抗原较基线明显增加。一名患者出现注射部位疼痛的不良事件很少。这两个事件的类型不严重,强度轻,已恢复。结论:TU以及必要时与PDE5抑制剂伐地那非联合治疗可改善LOH ED患者的性活动。

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