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丁螺环酮对接受选择性5-羟色胺再摄取抑制剂治疗的抑郁症患者性功能障碍的影响。

Effect of buspirone on sexual dysfunction in depressed patients treated with selective serotonin reuptake inhibitors.

作者信息

Landén M, Eriksson E, Agren H, Fahlén T

机构信息

Institute of Clinical Neuroscience, Department of Psychiatry, Göteborg University, Sweden.

出版信息

J Clin Psychopharmacol. 1999 Jun;19(3):268-71. doi: 10.1097/00004714-199906000-00012.

DOI:10.1097/00004714-199906000-00012
PMID:10350034
Abstract

To evaluate the possible influence of buspirone on sexual dysfunction in depressed patients treated with a selective serotonin reuptake inhibitor (SSRI), we analyzed data from a placebo-controlled trial designed to explore the efficacy of buspirone as add-on treatment for patients not responding to an SSRI alone. At baseline, all patients met the criteria for a major depressive episode according to DSM-IV and had received citalopram or paroxetine during a minimum of 4 weeks without responding to the treatment. Buspirone (flexible dosage, 20-60 mg/day) or placebo was added to the SSRI for 4 weeks; the mean daily dose of buspirone at endpoint was 48.5 mg (SD = 1.0). Sexual dysfunction was evaluated using a structured interview. Before starting medication with buspirone or placebo, 40% (47 of 117) reported at least one kind of sexual dysfunction (decreased libido, ejaculatory dysfunction, orgasmic dysfunction). During the 4 weeks of treatment, approximately 58% of subjects treated with buspirone reported an improvement with respect to sexual function; in the placebo group, the response rate was 30%. The difference between placebo and active drug treatment was more pronounced in women than in men. The response was obvious during the first week, with no further improvement during the course of the study. It is suggested that the effect of buspirone on sexual dysfunction is a result of a reversal of SSRI-induced sexual side effects rather than of an antidepressant effect of the drug.

摘要

为评估丁螺环酮对接受选择性5-羟色胺再摄取抑制剂(SSRI)治疗的抑郁症患者性功能障碍的可能影响,我们分析了一项安慰剂对照试验的数据,该试验旨在探究丁螺环酮作为对单独使用SSRI无反应患者的附加治疗的疗效。基线时,所有患者均符合《精神疾病诊断与统计手册》第四版(DSM-IV)中重度抑郁发作的标准,且在至少4周内接受了西酞普兰或帕罗西汀治疗但对治疗无反应。丁螺环酮(灵活剂量,20 - 60毫克/天)或安慰剂添加至SSRI治疗4周;终点时丁螺环酮的平均日剂量为48.5毫克(标准差 = 1.0)。使用结构化访谈评估性功能障碍。在开始使用丁螺环酮或安慰剂治疗前,40%(117例中的47例)报告至少有一种性功能障碍(性欲减退、射精功能障碍、性高潮功能障碍)。在4周治疗期间,接受丁螺环酮治疗的受试者中约58%报告性功能有所改善;在安慰剂组,反应率为30%。安慰剂与活性药物治疗的差异在女性中比在男性中更明显。反应在第一周就很明显,在研究过程中没有进一步改善。提示丁螺环酮对性功能障碍的作用是SSRI引起的性副作用逆转的结果,而非该药物的抗抑郁作用。

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