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帕罗西汀治疗广泛性社交恐惧症(社交焦虑症):一项随机对照试验。

Paroxetine treatment of generalized social phobia (social anxiety disorder): a randomized controlled trial.

作者信息

Stein M B, Liebowitz M R, Lydiard R B, Pitts C D, Bushnell W, Gergel I

机构信息

Department of Psychiatry, University of California at San Diego, La Jolla 92093-0985, USA.

出版信息

JAMA. 1998 Aug 26;280(8):708-13. doi: 10.1001/jama.280.8.708.

Abstract

CONTEXT

The generalized type of social phobia (social anxiety disorder) is a severe and often disabling form of social anxiety that affects approximately 5% of the general population. Earlier research has shown monoamine oxidase inhibitors or benzodiazepines to be effective in treating this condition, but neither has achieved widespread use.

OBJECTIVE

To compare the efficacy of paroxetine, a selective serotonin reuptake inhibitor, with placebo in adults with generalized social phobia.

DESIGN

Twelve-week, multicenter, randomized, double-blind trial.

SETTING

Thirteen centers across the United States and 1 in Canada.

PARTICIPANTS

Between April 13, 1995, and February 28, 1996, 187 persons meeting Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria for generalized social phobia were randomized (and 183 returned for at least 1 efficacy assessment) to treatment.

INTERVENTION

After a 1-week, single-blind, placebo, run-in period, patients received a double-blind, 11-week course of either paroxetine or matching-image placebo. The initial daily dosage of paroxetine (or placebo) was 20 mg with increases of 10 mg/d weekly (flexible dosing to a maximum of 50 mg/d) permitted after the second week of treatment.

MAIN OUTCOME MEASURES

Number of responders based on the Clinical Global Impression Global Improvement Item ("much improved" or "very much improved"); mean change from baseline on the Liebowitz Social Anxiety Scale total score.

RESULTS

Fifty (55.0%) of 91 persons taking paroxetine and 22 (23.9%) of 92 persons taking placebo were much improved or very much improved at the end of treatment (odds ratio [OR], 3.88; 95% confidence interval [CI], 2.81-5.36). Mean Liebowitz Social Anxiety Scale total scores were reduced by 39.1% (the mean baseline score of 78.0 declined by a mean of 30.5 points at follow-up) in the paroxetine group compared with 17.4% (the mean baseline score of 83.5 declined 14.5 points at follow-up) in the placebo group, a difference of 21.7% (95% CI, 8.7%-34.7%) favoring paroxetine.

CONCLUSIONS

Paroxetine is an effective treatment for patients with generalized social phobia. Short-term (ie, 11-week) treatment results in substantial and clinically meaningful reductions in symptoms and disability. Future research should test whether these may be further reduced by extended treatment or supplementation with specific educational-cognitive-behavioral techniques.

摘要

背景

广泛性社交恐惧症(社交焦虑障碍)是一种严重且常导致功能障碍的社交焦虑形式,影响着约5%的普通人群。早期研究表明,单胺氧化酶抑制剂或苯二氮䓬类药物对治疗这种疾病有效,但两者均未得到广泛应用。

目的

比较选择性5-羟色胺再摄取抑制剂帕罗西汀与安慰剂对成人广泛性社交恐惧症的疗效。

设计

为期12周的多中心随机双盲试验。

地点

美国的13个中心和加拿大的1个中心。

参与者

在1995年4月13日至1996年2月28日期间,187名符合《精神疾病诊断与统计手册》第四版广泛性社交恐惧症标准的患者被随机分组(183人返回进行至少1次疗效评估)接受治疗。

干预措施

经过1周的单盲安慰剂导入期后,患者接受为期11周的双盲治疗,服用帕罗西汀或匹配外观的安慰剂。帕罗西汀(或安慰剂)的初始日剂量为20mg,治疗第二周后允许每周增加10mg/d(灵活给药,最大剂量为50mg/d)。

主要观察指标

基于临床总体印象改善项目(“明显改善”或“非常显著改善”)的有效者数量;利博维茨社交焦虑量表总分相对于基线的平均变化。

结果

治疗结束时,服用帕罗西汀的91人中50人(55.0%)明显改善或非常显著改善,服用安慰剂的92人中22人(23.9%)明显改善或非常显著改善(优势比[OR],3.88;95%置信区间[CI],2.81 - 5.36)。帕罗西汀组利博维茨社交焦虑量表总分平均降低39.1%(平均基线分数78.0分,随访时平均下降30.5分),而安慰剂组为17.4%(平均基线分数83.5分,随访时下降14.5分),两组差异为21.7%(95%CI,8.7% - 34.7%),帕罗西汀组更具优势。

结论

帕罗西汀是治疗广泛性社交恐惧症患者的有效药物。短期(即11周)治疗可使症状和功能障碍大幅减轻且具有临床意义。未来研究应测试延长治疗或辅以特定的教育 - 认知行为技术是否可进一步减轻症状。

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