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首页> 外文期刊>International Journal of Impotence Research >Retracted: Safety and efficacy of sildenafil citrate in the treatment of Parkinson-emergent erectile dysfunction: a double-blind, placebo-controlled, randomized study
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Retracted: Safety and efficacy of sildenafil citrate in the treatment of Parkinson-emergent erectile dysfunction: a double-blind, placebo-controlled, randomized study

机译:缩回:枸sil酸西地那非治疗帕金森紧急勃起功能障碍的安全性和有效性:一项双盲,安慰剂对照,随机研究

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Parkinson's disease (PD) is one of the most commonly occurring neurodegenerative disorders, with lifetime incidence between 1 and 2% among people older than 65 years. ED is one of the more disabling and poorly addressed aspects of PD. The purpose of this study was to assess the efficacy and safety of sildenafil citrate in Parkinson-emergent ED. Sexual function of participants was assessed using responses to the 15-question International Index of Erectile Function (IIEF), Sexual Encounter Profile (SEP) diary questions 2 and 3, Erectile Dysfunction Inventory of Treatment Satisfaction (EDITS) questionnaire and a Global Efficacy Question ‘Has the treatment you have been taking over the study period improved your erections?’ This randomized, double-blind, placebo-controlled study, comprised a screening period of at least 1 month, a placebo-lead in period of 1 week and treatment period. Two hundred thirty-six patients entered the trial. These patients had mild-to-moderate PD (stages I–III Hoehn–Yahr) and were experiencing Parkinson-emergent neurogenic ED. They were randomized to receive 100?mg sildenafil on demand 1?h before sexual activity (group 1, n=118), or similar regimen of placebo (group 2, n=118). Patients were instructed to use at least 24 doses/attempts at home. At the end of the trial, differences between sildenafil and placebo groups were significant for the IIEF erectile function (EF) score (22.6±4.6 vs 14.8±4.2, P=0.01), for percent Global Efficacy Question ‘Yes’ responses (68.1±4.6 vs 12.2±3.2, P=0.001), for SEP2 ‘Yes’ responses (68.1±4.2 vs 32.5±2.2, P=0.003), for SEP3 ‘Yes’ responses (75.9±5.4 vs 33.5±4.4, P=0.004) and for mean EDITS score (69.8±4.2 vs 13.0±2.7, P=0.004). A normal EF domain score (26) at end point was achieved by 56.9 and 8.7% of the patients in the sildenafil and placebo groups, respectively (P=0.001). Sildenafil can be considered as an effective treatment in patients with Parkinson-emergent ED.
机译:帕金森氏病(PD)是最常见的神经退行性疾病之一,在65岁以上的人群中终生发病率在1-2%之间。 ED是PD的更残障和解决不佳的方面之一。这项研究的目的是评估枸sil酸西地那非在帕金森急症中的疗效和安全性。使用对15个问题的国际勃起功能指数(IIEF),性相遇概况(SEP)日记问题2和3,勃起功能障碍治疗满意度清单(EDITS)问卷和全球疗效问题'您在研究期间接受的治疗是否改善了勃起?'这项随机,双盲,安慰剂对照的研究,包括至少1个月的筛查期,1周的安慰剂引导和治疗期。 236名患者进入了试验。这些患者的PD为轻度至中度(Hoehn-Yahr阶段I–III),并且正在经历帕金森紧急神经源性ED。他们在性活动开始前1小时被随机接受100?mg西地那非(第1组,n = 118)或类似的安慰剂治疗(第2组,n = 118)。指导患者在家中至少使用24剂/次。在试验结束时,西地那非组与安慰剂组之间的差异对于IIEF勃起功能(EF)评分(22.6±4.6对14.8±4.2,P = 0.01),总体有效性问题“是”回答百分率(68.1±对于SEP2``是''响应,分别为4.6 vs 12.2±3.2,P = 0.001)(68.1±4.2对32.5±2.2,P = 0.003),对于SEP3``是''响应(75.9±5.4与33.5±4.4,P = 0.004)平均EDITS评分(69.8±4.2对13.0±2.7,P = 0.004)。西地那非和安慰剂组分别有56.9%和8.7%的患者在终点时获得了正常的EF域评分(26)(P = 0.001)。西地那非可以被认为是帕金森病急诊ED患者的有效治疗方法。

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