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首页> 外文期刊>Journal of affective disorders >Treatment of generalized anxiety disorder with escitalopram: pooled results from double-blind, placebo-controlled trials.
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Treatment of generalized anxiety disorder with escitalopram: pooled results from double-blind, placebo-controlled trials.

机译:艾司西酞普兰治疗广泛性焦虑症:来自双盲,安慰剂对照试验的合并结果。

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BACKGROUND: Escitalopram 10 mg/day is an effective and well-tolerated antidepressant. Three randomized controlled trials recently evaluated the safety and efficacy of escitalopram in the treatment of generalized anxiety disorder (GAD). METHODS: The trial designs were virtually identical, allowing data to be pooled across studies. Male and female outpatients, ages 18-80 years, with DSM-IV-defined GAD were randomized to double-blind treatment with escitalopram or placebo for 8 weeks. Escitalopram dose was fixed at 10 mg/day for the first 4 weeks, after which increases to 20 mg/day were permitted. The primary efficacy variable was the mean change from baseline in total Hamilton Anxiety Scale (HAMA) score. RESULTS: Approximately 850 patients were randomized to double-blind treatment. In each individual study, escitalopram was significantly superior to placebo (p<0.05) as measured by change from baseline in HAMA score. By-visit analyses of data pooled across studies revealed significantly greater improvement (p<0.05) in the escitalopram group beginning at week 1 or 2 and continuing through week 8 for all primary and secondary efficacy variables. The mean change in HAMA total score from baseline to endpoint also was significantly greater for patients maintained at escitalopram 10 mg/day than for those receiving placebo. Escitalopram was generally well tolerated. LIMITATIONS: The studies included in this analysis were of short-term duration and excluded patients with significant medical and psychiatric comorbidities, such as major depressive disorder. CONCLUSION: Results from the individual trials and the pooled analysis demonstrate that escitalopram is effective and well tolerated for the treatment of GAD.
机译:背景:依西酞普兰10毫克/天是一种有效且耐受良好的抗抑郁药。最近进行的三项随机对照试验评估了依西酞普兰在治疗广泛性焦虑症(GAD)中的安全性和有效性。方法:试验设计实际上是相同的,从而可以将数据汇总到各个研究中。 DSM-IV定义的GAD年龄在18-80岁之间的男性和女性门诊患者被随机分配接受依西酞普兰或安慰剂双盲治疗8周。在头4周,依西酞普兰的剂量固定为10 mg /天,此后允许增加至20 mg /天。主要功效变量是汉密尔顿焦虑量表(HAMA)总分相对于基线的平均变化。结果:约850例患者被随机分配至双盲治疗。在每个单独的研究中,依西酞普兰均明显优于安慰剂组(p <0.05),这是通过从基线AMAH评分的变化来衡量的。对所有研究汇总的数据进行的就诊分析显示,对于所有主要和次要疗效变量,艾司西酞普兰组的改善显着(p <0.05),从第1周或第2周开始,持续到第8周。维持依西酞普兰10 mg /天的患者从基线到终点的HAMA总分的平均变化也显着大于接受安慰剂的患者。依西酞普兰通常耐受良好。局限性:该分析中的研究为短期研究,排除了具有重大医学和精神病合并症(例如重度抑郁症)的患者。结论:各个试验的结果和汇总分析表明,依他普仑对GAD的治疗有效且耐受性良好。

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