Rynn Moira A, Riddle Mark A, Yeung Paul P, Kunz Nadia R
New York State Psychiatric Institute, 1051 Riverside Drive, Unit 74, New York, NY 10032, USA.
Am J Psychiatry. 2007 Feb;164(2):290-300. doi: 10.1176/ajp.2007.164.2.290.
The authors evaluated the efficacy, safety, and tolerability of extended-release venlafaxine in the treatment of pediatric generalized anxiety disorder.
Two randomized, double-blind, placebo-controlled trials were conducted at 59 sites in 2000 and 2001. Participants 6 to 17 years of age who met DSM-IV criteria for generalized anxiety disorder received a flexible dosage of extended-release venlafaxine (N=157) or placebo (N=163) for 8 weeks. The primary outcome measure was the composite score for nine delineated items from the generalized anxiety disorder section of a modified version of the Schedule for Affective Disorders and Schizophrenia for School-Age Children, and the primary efficacy variable was the baseline-to-endpoint change in this composite score. Secondary outcome measures were overall score on the nine delineated items, Pediatric Anxiety Rating Scale, Hamilton Anxiety Rating Scale, Screen for Child Anxiety Related Emotional Disorders, and the severity of illness and improvement scores from the Clinical Global Impression scale (CGI).
The extended-release venlafaxine group showed statistically significant improvements in the primary and secondary outcome measures in study 1 and significant improvements in some secondary outcome measures but not the primary outcome measure in study 2. In a pooled analysis, the extended-release venlafaxine group showed a significantly greater mean decrease in the primary outcome measure compared with the placebo group (-17.4 versus -12.7). The response rate as indicated by a CGI improvement score <3 was significantly greater with extended-release venlafaxine than placebo (69% versus 48%). Common adverse events were asthenia, anorexia, pain, and somnolence. Statistically significant changes in height, weight, blood pressure, pulse, and cholesterol levels were observed in the extended-release venlafaxine group.
Extended-release venlafaxine may be an effective, well-tolerated short-term treatment for pediatric generalized anxiety disorder.
作者评估了缓释文拉法辛治疗儿童广泛性焦虑症的疗效、安全性和耐受性。
2000年和2001年在59个地点进行了两项随机、双盲、安慰剂对照试验。符合DSM-IV广泛性焦虑症标准的6至17岁参与者接受了8周的灵活剂量缓释文拉法辛(N = 157)或安慰剂(N = 163)治疗。主要结局指标是学龄儿童情感障碍和精神分裂症量表修订版中广泛性焦虑症部分九个划定项目的综合评分,主要疗效变量是该综合评分从基线到终点的变化。次要结局指标是九个划定项目的总分、儿童焦虑评定量表、汉密尔顿焦虑评定量表、儿童焦虑相关情绪障碍筛查量表,以及临床总体印象量表(CGI)的疾病严重程度和改善评分。
在研究1中,缓释文拉法辛组在主要和次要结局指标上有统计学意义的改善,在研究2中,缓释文拉法辛组在一些次要结局指标上有显著改善,但在主要结局指标上没有改善。在汇总分析中,与安慰剂组相比,缓释文拉法辛组在主要结局指标上的平均下降幅度显著更大(-17.4对-12.7)。CGI改善评分<3所表明的缓解率,缓释文拉法辛组显著高于安慰剂组(69%对48%)。常见不良事件有乏力、厌食、疼痛和嗜睡。在缓释文拉法辛组观察到身高、体重、血压、脉搏和胆固醇水平有统计学意义的变化。
缓释文拉法辛可能是治疗儿童广泛性焦虑症的一种有效且耐受性良好的短期疗法。