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西地那非治疗服用 5-羟色胺再摄取抑制剂男性勃起功能障碍的疗效和耐受性。

Efficacy and tolerability of tadalafil for treatment of erectile dysfunction in men taking serotonin reuptake inhibitors.

机构信息

Department of Urology, Adana Numune Education and Research Hospital, Adana, Turkey.

出版信息

Urology. 2011 May;77(5):1137-41. doi: 10.1016/j.urology.2010.12.036. Epub 2011 Feb 12.

Abstract

OBJECTIVES

To evaluate the efficacy and safety of tadalafil in men with treatment-emergent sexual dysfunction due to serotonin reuptake inhibitors.

METHODS

The present prospective, double-blind, 12-week study, randomized in a 1:1 ratio to tadalafil 20 mg or placebo taken on demand, included 50 men. The efficacy measures were the changes in total and domain scores of the International Index of Erectile Function questionnaire, Sexual Encounter Profile diary questions 2-6, and the Global Assessment questions (GAQs) 1 and 2. The safety analyses included the evaluation of adverse events, vital signs, serum chemistry results, and electrocardiography findings.

RESULTS

For the patients who took tadalafil 20 mg, the net median score change from baseline to the endpoint compared with placebo was 26 for the 15-item International Index of Erectile Function; 10, 4, 4, 3, and 3 for the erectile function, intercourse satisfaction, overall satisfaction, orgasmic function, and sexual desire domains; and 3 and 5 points for "yes" responses to the Sexual Encounter Profile 2 and Sexual Encounter Profile 3 questions, respectively. All comparisons between tadalafil and placebo were significant (P < .001). At the endpoint, 92% of the tadalafil group responded affirmatively to both GAQs 1 and 2 compared with 8% of the placebo group (P < .001, for each). In the safety measures, no clinically significant changes attributable to tadalafil use were found.

CONCLUSIONS

Tadalafil 20-mg treatment significantly improved sexual function in patients who were taking serotonin reuptake inhibitors for depression, with mild to moderate, well-tolerable adverse events.

摘要

目的

评估他达拉非治疗因服用 5-羟色胺再摄取抑制剂而出现治疗相关性性功能障碍男性患者的疗效和安全性。

方法

本前瞻性、双盲、12 周研究采用 1:1 随机分组,分别接受按需服用他达拉非 20mg 或安慰剂治疗,共纳入 50 例患者。疗效评估指标包括国际勃起功能指数问卷(IIEF)总评分和各领域评分、性活动体验调查问卷 2-6 问题、总体评估问题 1 和 2 的变化。安全性分析包括不良事件、生命体征、血清化学检查结果和心电图检查结果的评估。

结果

与安慰剂组相比,服用他达拉非 20mg 的患者,从基线到终点的 IIEF 15 项总评分变化的净中位数差值为 26;勃起功能、性生活满意度、总体满意度、性高潮功能和性欲领域分别为 10、4、4、3 和 3;性活动体验调查问卷 2 和性活动体验调查问卷 3 的“是”回答分别为 3 和 5 分。他达拉非与安慰剂之间的所有比较均有统计学意义(P<0.001)。在终点时,92%的他达拉非组患者对总体评估问题 1 和 2 均做出肯定回答,而安慰剂组为 8%(P<0.001,各)。在安全性评估中,未发现与他达拉非使用相关的具有临床意义的变化。

结论

他达拉非 20mg 治疗可显著改善因抑郁而服用 5-羟色胺再摄取抑制剂患者的性功能,且不良反应轻微至中度,患者耐受性良好。

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