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一项评估安非他酮治疗排卵女性低性欲障碍的有效性和安全性的随机、双盲、安慰剂对照研究。

A randomized, double-blind, placebo-controlled study of the efficacy and safety of bupropion for treating hypoactive sexual desire disorder in ovulating women.

机构信息

Urology and Nephrology Research Centre, Shahid Modarress Hospital, Shahid Beheshti University, Tehran, Iran.

出版信息

BJU Int. 2010 Sep;106(6):832-9. doi: 10.1111/j.1464-410X.2010.09208.x. Epub 2010 Feb 11.

Abstract

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.

摘要

目的

比较缓释(SR)安非他酮治疗排卵女性低性欲障碍(HSDD)的疗效与安慰剂。

方法

在为期 1 周的安慰剂导入期后,232 名有治疗需求且月经周期规律的女性随机分为安非他酮 SR 150mg/天组(116 例)或安慰剂组(116 例),接受为期 12 周的双盲治疗。采用女性性功能指数(BISF-W)、个人困扰量表(PDS)、整体疗效问题(GEQ;“您接受的治疗是否显著改善了您的性欲?”)和整体患者满意度问题(“您对治疗效果满意吗?”)评估疗效。

结果

BISF-W 综合评分均值(标准差)由基线时的 15.8(2.6)和 15.5(2.2)分别升高至安非他酮组和安慰剂组的 33.9(4.2)和 16.9(2.6)(P=0.001)。安非他酮组的反应比值比(95%置信区间)相对安慰剂组为 3.2(2.1-6.3)。安非他酮治疗的患者的想法/欲望评分增加了一倍以上(P=0.001)。在 12 周评估时,PDS 量表的降低幅度在安非他酮组为 29.4%,安慰剂组为 4.7%(P=0.01)。在对 GEQ 的回答中,安非他酮组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)。安非他酮组和安慰剂组中分别有 71.8%和 3.7%的患者对治疗效果非常满意(P=0.001)。治疗 12 周后,安非他酮组有 82 名(78.1%)女性和安慰剂组有 5 名(4.9%)女性愿意继续治疗(P=0.001)。

结论

本研究结果表明,安非他酮 SR 是治疗排卵女性 HSDD 的一种有效且耐受良好的治疗方法。需要进一步的对照试验。

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