Department of Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
J Clin Psychopharmacol. 2013 Oct;33(5):695-8. doi: 10.1097/JCP.0b013e31829a878b.
Fear of blushing (FB) is a form of social anxiety disorder (SAD) characterized by an intense and obsessive threat of blushing in front of other people. No data are available on the specific efficacy of antidepressants on FB. This open-label pilot study investigated whether the selective serotonin reuptake inhibitor escitalopram specifically improves symptoms of FB in SAD patients. Thirty-nine patients meeting Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria for SAD and presenting a significant FB according to the Salpêtrière Erythrophobia Questionnaire (SEQ) were administered open-label escitalopram (10-30 mg/d) for 12 weeks. A systematic assessment, at baseline and at week 12, included the SEQ, the Liebowitz Social Anxiety Scale, and the Hospital Anxiety and Depression scale. From the 39 patients included, 31 attended the week 4 visit, and 28 the week 12 visit. Significant reductions of FB were observed after 4 weeks of treatment and were more pronounced at the end of the 12-week treatment since patients experienced a 60% decrease in their FB symptoms (P < 0.001). Nineteen subjects (67.8%) reported a 50% decrease or more of their SEQ score, and 14 (50%) met criteria for remission of FB (SEQ score <7). The effect sizes of changes on SEQ, Liebowitz Social Anxiety Scale, and Hospital Anxiety and Depression scale scores were high, with η² ranging between 0.53 and 0.86. Results of this open-label study suggest that escitalopram can be a useful treatment for FB associated with SAD, even if large controlled trials are now needed to further evaluate this result.
对脸红的恐惧(FB)是社交焦虑障碍(SAD)的一种形式,其特征是在其他人面前出现强烈而强烈的脸红威胁。目前尚无关于抗抑郁药对 FB 具体疗效的数据。这项开放标签的初步研究旨在探讨选择性 5-羟色胺再摄取抑制剂依他普仑是否能专门改善 SAD 患者的 FB 症状。39 名符合精神障碍诊断与统计手册,第四版(DSM-IV)SAD 标准且根据萨尔佩特里埃尔红斑恐惧症问卷(SEQ)表现出明显 FB 的患者接受依他普仑(10-30mg/d)开放标签治疗 12 周。基线和第 12 周进行系统评估,包括 SEQ、列博维茨社交焦虑量表和医院焦虑抑郁量表。在纳入的 39 名患者中,有 31 名患者参加了第 4 周的就诊,有 28 名患者参加了第 12 周的就诊。治疗 4 周后观察到 FB 显著减少,在 12 周治疗结束时更为明显,因为患者的 FB 症状减少了 60%(P<0.001)。19 名患者(67.8%)报告说 SEQ 评分降低了 50%或更多,14 名患者(50%)达到了 FB 缓解标准(SEQ 评分<7)。SEQ、列博维茨社交焦虑量表和医院焦虑抑郁量表评分变化的效应大小较高,η² 介于 0.53 和 0.86 之间。这项开放标签研究的结果表明,依他普仑可能是一种治疗与 SAD 相关的 FB 的有效方法,尽管现在需要进行更大规模的对照试验来进一步评估这一结果。