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首页> 外文期刊>BJU international >A randomized, double-blind, placebo-controlled study of the efficacy and safety of bupropion for treating hypoactive sexual desire disorder in ovulating women.
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A randomized, double-blind, placebo-controlled study of the efficacy and safety of bupropion for treating hypoactive sexual desire disorder in ovulating women.

机译:安非他酮用于治疗排卵期女性性欲减退的有效性和安全性的随机,双盲,安慰剂对照研究。

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摘要

OBJECTIVE: To compare the efficacy of sustained-release (SR) bupropion to placebo in treating hypoactive sexual desire disorder (HSDD) in ovulating women. PATIENTS AND METHODS: After a 1-week, placebo lead-in phase, 232 treatment-seeking women with regular menstrual cycles were randomly assigned to bupropion SR 150 mg/daily (116) or placebo (116) for 12 weeks under double-blind conditions. Efficacy was assessed with the Brief Index of Sexual Functioning for Women (BISF-W), the Personal Distress Scale (PDS), the global efficacy question (GEQ; 'Did the treatment you received during the 12-week improve meaningful your sexual desire?') and overall patient satisfaction question ('Are you satisfied with the efficacy of your treatment?'). RESULTS: The mean (sd) composite score on the BISF-W, increased from 15.8 (2.6) and 15.5 (2.2) at baseline to 33.9 (4.2) and 16.9 (2.6) in the bupropion and placebo groups, respectively (P= 0.001). The odds ratio (95% confidence interval) for response in the bupropion group relative to placebo was 3.2 (2.1-6.3). The thoughts/desire score more than doubled in patients treated with bupropion (P= 0.001). At the 12-week evaluation the reduction in the PDS scale was 29.4% in bupropion and 4.7% in the placebo group (P= 0.01). In response to the GEQ, of patients in the bupropion and placebo groups, 65.3%, and 4.3%, respectively, responded 'Definitely yes' (P= 0.001). Of patients in the bupropion and placebo groups, 71.8%, and 3.7%, respectively, were definitely satisfied with the efficacy of their treatment, (P= 0.001). After 12 weeks of treatment, 82 women (78.1%) in the bupropion and five (4.9%) in the placebo group were willing to continue therapy (P= 0.001). CONCLUSIONS: The results from this study indicate that bupropion SR is an effective and well-tolerated treatment for HSDD in ovulating women. Further controlled trials are warranted.
机译:目的:比较缓释安非他酮和安慰剂在排卵期妇女性欲减退中的功效。患者与方法:在1周安慰剂导入期后,将232名月经周期规律的寻求治疗的妇女随机分配到双盲下安非他酮SR 150 mg /每天(116)或安慰剂(116)12周条件。通过妇女性功能简要指数(BISF-W),个人窘迫量表(PDS),总体疗效问题(GEQ)评估了疗效;“您在12周内接受的治疗是否能使您的性欲有意义? ')和总体患者满意度问题('您是否对治疗效果感到满意?')。结果:BISF-W的平均(sd)综合评分从基线的15.8(2.6)和15.5(2.2)分别提高至安非他酮和安慰剂组的33.9(4.2)和16.9(2.6)(P = 0.001) )。安非他酮组相对于安慰剂的应答比值比(95%置信区间)为3.2(2.1-6.3)。安非他酮治疗的患者的思想/欲望得分翻了一番以上(P = 0.001)。在为期12周的评估中,安非他酮的PDS量表降低为29.4%,安慰剂组为4.7%(P = 0.01)。根据GEQ,在安非他酮和安慰剂组中,分别有65.3%和4.3%的患者回答“肯定是”(P = 0.001)。在安非他酮和安慰剂组中,分别对他们的治疗效果感到满意的患者分别为71.8%和3.7%(P = 0.001)。治疗12周后,安非他酮中的82名女性(78.1%)和安慰剂组中的5名女性(4.9%)愿意继续治疗(P = 0.001)。结论:这项研究的结果表明安非他酮SR是排卵妇女HSDD的有效且耐受良好的治疗方法。有必要进行进一步的对照试验。

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