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Influence of Sildenafil on Genital Engorgement in Women with Female Sexual Arousal Disorder

机译:西地那非对女性性唤起障碍患者生殖功能的影响

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Introduction. We previously described dynamic, noncontrast magnetic resonance imaging (MRI) of the female genitalia as a reproducible, nonintrusive, objective means of quantifying sexual arousal response in women without sexual difficulties. These studies showed an increase in clitoral engorgement ranging from 50 to 300% in healthy women during sexual arousal. Aim. This study sought to evaluate the genital arousal response in women with female sexual arousal disorder (FSAD) after administration of sildenafil and placebo. We performed a multicenter, double-blind, placebo-controlled, cross-over study to assess the clitoral engorgement response using dynamic MRI in women with FSAD after administering sildenafil and placebo followed by audiovisual sexual stimulation (AVSS). Methods. Nineteen premenopausal women with FSAD underwent two MRI sessions. Subjects were randomized to receive either (i) sildenafil 100mg during the first session followed by placebo during the second session, or (ii) placebo followed by sildenafil. During each session, baseline MR images were obtained while subjects viewed a neutral video. Subjects then ingested sildenafil or placebo. After 30 minutes, a series of MRIs were obtained at 3-minute intervals for 10 time points while subjects viewed AVSS. Main Outcome Measures. A positive sexual arousal response was achieved if clitoral volume increased ≥50% from baseline. Results. Thirteen of 19 (68%) subjects achieved a ≥50% increase in clitoral engorgement from baseline when administered sildenafil or placebo 30 minutes after dose administration. At 60 minutes after administration, 17/19 (89%) subjects receiving sildenafil and 16/19 (84%) subjects receiving placebo had responded (P value 0.3173). Conclusions. Sildenafil did not augment the genital response in women with FSAD. Secondarily, a majority of women in this study did not have impaired clitoral engorgement as measured by MRI, suggesting that FSAD is not predominantly a disorder of genital engorgement.
机译:介绍。我们先前将女性生殖器的动态无造影磁共振成像(MRI)描述为可量化,无干扰的客观方法,用于量化无性障碍女性的性唤起反应。这些研究表明,健康女性在性唤起期间的阴蒂充血增加了50%至300%。目标。这项研究旨在评估服用西地那非和安慰剂后女性性唤起障碍(FSAD)妇女的生殖器唤起反应。我们进行了多中心,双盲,安慰剂对照的交叉研究,在使用昔多芬和安慰剂后进行视听性刺激(AVSS)后,使用动态MRI对FSAD妇女的阴蒂充血反应进行了评估。方法。十九名FSAD绝经前妇女接受了两次MRI检查。受试者被随机分配为(i)在第一个疗程中接受西地那非100mg,然后在第二个疗程中接受安慰剂,或(ii)在接受安慰剂后接受西地那非。在每个阶段中,受试者在观看中性视频时均获得了基线MR图像。然后受试者摄入西地那非或安慰剂。 30分钟后,在受试者观察AVSS的同时,每隔3分钟以10分钟的时间间隔进行一系列MRI检查。主要观察指标。如果阴蒂体积比基线增加≥50%,则将获得积极的性唤起反应。结果。在剂量给药后30分钟给予西地那非或安慰剂时,19名受试者中有13名(68%)的阴蒂充血量较基线增加了50%以上。给药后60分钟,接受西地那非的17/19(89%)受试者和接受安慰剂的16/19(84%)受试者对此有反应(P值0.3173)。结论。西地那非不能增强FSAD女性的生殖器反应。其次,在这项研究中,大多数女性的MRI均未显示阴蒂充血受损,这表明FSAD并不是生殖器充血的主要障碍。

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