Strawn Jeffrey R, Welge Jeffrey A, Wehry Anna M, Keeshin Brooks, Rynn Moira A
Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati, College of Medicine, Cincinnati, Ohio; Department of Psychiatry, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Depress Anxiety. 2015 Mar;32(3):149-57. doi: 10.1002/da.22329. Epub 2014 Nov 28.
Randomized controlled trials have demonstrated that antidepressants are efficacious in the treatment of anxiety disorders in youth. However, there are no recent, systematic analyses of the efficacy, safety, or tolerability of these medications in pediatric anxiety disorders.
A systematic review and meta-analysis of prospective, randomized, parallel-group, controlled trials of selective serotonin reuptake inhibitors (SSRIs) and selective serotonin-norepinephrine reuptake inhibitors (SSNRIs) in pediatric patients with non-obsessive compulsive disorder (OCD) anxiety disorders was undertaken using a search of PubMed/Medline (1966-2014). The meta-analysis utilized random-effects models to evaluate change in the Pediatric Anxiety Rating Scale or similar anxiety scale, suicidality, and adverse events. Additionally, pharmacologic variables were explored with regard to effect size, although no correction for multiple comparisons was made with regard to these relationships.
Nine trials involving 1,673 patients and six medications were included. All SSRI/SSNRIs evaluated demonstrated efficacy, and the meta-analytic estimate of effect was of moderate magnitude (Cohen's d = 0.62, confidence interval [CI]: 0.34-0.89, P = .009) and there was evidence of modest heterogeneity (I(2) = 0.29, P = .103). Activation trended toward being more likely with antidepressant treatment (OR: 1.86, CI: 0.98-3.53, P = .054), but no increased risk was observed for nausea/abdominal symptoms (P = .262), discontinuation as a result of an adverse event (P = .132), or suicidality (OR: 1.3, CI: 0.53-3.2, P = .514). Finally, the effect size correlated with the serotonergic specificity of the agent (R = .79, P = .021).
Data for nine SSRI/SSNRIs suggest superiority of antidepressants relative to placebo for the treatment of pediatric anxiety disorders with a moderate effect size.
随机对照试验已证明抗抑郁药在治疗青少年焦虑症方面有效。然而,目前尚无关于这些药物在儿童焦虑症中的疗效、安全性或耐受性的近期系统分析。
使用PubMed/Medline(1966 - 2014年)进行检索,对选择性5-羟色胺再摄取抑制剂(SSRI)和选择性5-羟色胺-去甲肾上腺素再摄取抑制剂(SSNRI)用于非强迫症(OCD)焦虑症儿科患者的前瞻性、随机、平行组对照试验进行系统评价和荟萃分析。荟萃分析采用随机效应模型评估儿童焦虑评定量表或类似焦虑量表的变化、自杀倾向和不良事件。此外,探讨了药物变量与效应大小的关系,尽管未对这些关系进行多重比较校正。
纳入了涉及1673例患者和六种药物的九项试验。所有评估的SSRI/SSNRI均显示出疗效,荟萃分析的效应估计为中等程度(Cohen's d = 0.62,置信区间[CI]:0.34 - 0.89,P = 0.009),且有证据表明存在适度异质性(I(2) = 0.29,P = 0.103)。抗抑郁药治疗时出现激越的趋势更明显(OR:1.86,CI:0.98 - 3.53,P = 0.054),但未观察到恶心/腹部症状风险增加(P = 0.262)、因不良事件停药风险增加(P = 0.132)或自杀倾向风险增加(OR:1.3,CI:0.53 - 3.2,P = 0.514)。最后,效应大小与药物的5-羟色胺能特异性相关(R = 0.79,P = 0.021)。
九种SSRI/SSNRI的数据表明,抗抑郁药在治疗儿童焦虑症方面相对于安慰剂具有优越性,效应大小为中等程度。