Urology and Nephrology Research Centre, Shahid Modarress Hospital, Shahid Beheshti University, Tehran, Iran.
BJU Int. 2010 Sep;106(6):832-9. doi: 10.1111/j.1464-410X.2010.09208.x. Epub 2010 Feb 11.
To compare the efficacy of sustained-release (SR) bupropion to placebo in treating hypoactive sexual desire disorder (HSDD) in ovulating women.
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?').
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).
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.
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。
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。
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)。
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。