Alberta Research Centre for Health Evidence, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
Pediatrics. 2012 Mar;129(3):e771-84. doi: 10.1542/peds.2011-2158. Epub 2012 Feb 20.
Despite increasing on-label and off-label use of antipsychotics, prescribing antipsychotics to children remains controversial due to uncertainty of their relative benefits and safety. We systematically reviewed the effectiveness and safety of first- (FGA) and second-generation antipsychotics (SGA) for patients aged ≤24 years with psychiatric and behavioral conditions.
We searched 10 databases from January 1987 to February 2011, gray literature, trial registries, and reference lists. Two reviewers independently selected studies, assessed methodologic quality, and graded the evidence. One reviewer extracted, and a second verified, data. We summarized findings qualitatively and conducted meta-analyses when appropriate.
Sixty-four trials and 17 cohort studies were included. Most trials had a high risk of bias; cohort studies had moderate quality. All comparisons of FGAs versus SGAs, FGAs versus FGAs, and FGAs versus placebo had low or insufficient strength of evidence. There was moderate strength of evidence for the following comparisons. Olanzapine caused more dyslipidemia and weight gain, but fewer prolactin-related events, than risperidone. Olanzapine caused more weight gain than quetiapine. Compared with placebo, SGAs improved clinical global impressions (schizophrenia, bipolar and disruptive behavior disorders) and diminished positive and negative symptoms (schizophrenia), behavior symptoms (disruptive behavior disorders), and tics (Tourette syndrome).
This is the first comprehensive review comparing the effectiveness and safety across the range of antipsychotics for children and young adults. The evidence on the comparative benefits and harms of antipsychotics is limited. Some SGAs have a better side effect profile than other SGAs. Additional studies using head-to-head comparisons are needed.
尽管越来越多的抗精神病药物被批准用于适应证内和适应证外的治疗,但由于对其相对益处和安全性存在不确定性,儿童抗精神病药物的处方仍存在争议。我们系统地评价了第一代(FGA)和第二代(SGA)抗精神病药物治疗精神和行为障碍的儿童和青少年患者的疗效和安全性。
我们检索了 1987 年 1 月至 2011 年 2 月的 10 个数据库、灰色文献、试验注册处和参考文献列表。两位评审员独立选择研究、评估方法学质量并对证据进行分级。一位评审员提取数据,另一位评审员验证数据。我们对发现进行了定性总结,并在适当的情况下进行了荟萃分析。
共纳入 64 项试验和 17 项队列研究。大多数试验存在较高的偏倚风险;队列研究的质量为中等。FGA 与 SGA、FGA 与 FGA、FGA 与安慰剂的比较均仅有低或不足的证据强度。以下比较具有中等强度的证据。与利培酮相比,奥氮平引起更多的血脂异常和体重增加,但较少的催乳素相关事件。与喹硫平相比,奥氮平引起更多的体重增加。与安慰剂相比,SGA 改善了临床总体印象(精神分裂症、双相和破坏性行为障碍)和阴性及阳性症状(精神分裂症)、行为症状(破坏性行为障碍)和抽动(妥瑞氏症)。
这是第一项全面比较儿童和青少年使用各种抗精神病药物的疗效和安全性的综述。关于抗精神病药物的相对益处和危害的证据有限。一些 SGA 的副作用谱优于其他 SGA。需要进一步开展头对头比较的研究。