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在对 SSRI 或 SNRI 治疗部分反应的广泛性焦虑障碍患者中,加用普瑞巴林辅助治疗。

Adjunctive therapy with pregabalin in generalized anxiety disorder patients with partial response to SSRI or SNRI treatment.

机构信息

Department of Psychiatry, Mood and Anxiety Disorders Section, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

出版信息

Int Clin Psychopharmacol. 2012 May;27(3):142-50. doi: 10.1097/YIC.0b013e328350b133.

Abstract

This study evaluated the efficacy of adjunctive pregabalin versus placebo for treatment of patients with generalized anxiety disorder (GAD) who had not optimally responded to previous or prospective monotherapies. This was a phase 3, randomized, double-blind, placebo-controlled study. Patients diagnosed with GAD who had a historical and current lack of response to pharmacotherapy [Hamilton Anxiety Rating Scale (HAM-A) of ≥ 22 at screening] were randomized to adjunctive treatment with either pregabalin (150-600 mg/day) or placebo. The primary outcome measure was the change in HAM-A total scores after 8 weeks of combination treatment. Adverse events were regularly monitored. Randomized patients (N=356) were treated with pregabalin (n=180) or placebo (n=176). Mean baseline HAM-A scores were 20.7 and 21.4, respectively. After treatment, the mean change in HAM-A was significantly greater for pregabalin compared with placebo (-7.6 vs. -6.4, respectively; P<0.05). HAM-A responder rates (≥ 50% reduction) were significantly higher for pregabalin (47.5%) versus placebo (35.2%; P=0.0145). The time-to-sustained response favored pregabalin over placebo (P=0.014). Adverse events were consistent with previous studies and discontinuations were infrequent for pregabalin (4.4%) and placebo (2.3%). The study was discontinued early after an interim analysis. The results indicate that adjunctive pregabalin is an efficacious therapy for patients with GAD who experience an inadequate response to established treatments.

摘要

这项研究评估了辅助普瑞巴林与安慰剂治疗对先前或预期单一疗法治疗反应不佳的广泛性焦虑症 (GAD) 患者的疗效。这是一项 3 期、随机、双盲、安慰剂对照研究。诊断为 GAD 的患者,既往和当前对药物治疗无反应[筛选时汉密尔顿焦虑量表(HAM-A)≥22],随机分为辅助治疗,分别给予普瑞巴林(150-600mg/天)或安慰剂。主要结局指标是联合治疗 8 周后 HAM-A 总分的变化。定期监测不良事件。随机分组的患者(N=356)接受普瑞巴林(n=180)或安慰剂(n=176)治疗。基线 HAM-A 评分分别为 20.7 和 21.4。治疗后,普瑞巴林组 HAM-A 的平均变化明显大于安慰剂组(分别为-7.6 对-6.4,P<0.05)。普瑞巴林的 HAM-A 应答率(≥50%缓解)明显高于安慰剂(分别为 47.5%和 35.2%;P=0.0145)。持续应答时间有利于普瑞巴林优于安慰剂(P=0.014)。不良事件与既往研究一致,普瑞巴林(4.4%)和安慰剂(2.3%)的停药率较低。中期分析后提前终止了该研究。结果表明,对于对既定治疗反应不足的 GAD 患者,辅助普瑞巴林是一种有效的治疗方法。

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