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Efficacy and tolerability of lithium for the treatment of acute mania in children with bipolar disorder: A systematic review

机译:双相障碍儿童治疗急性躁狂症的疗效和耐受性:系统评价

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Objectives To assess the efficacy and tolerability of lithium for the treatment of acute mania in children and adolescent diagnosed with bipolar disorder. Methods A systematic literature search up to August 2017 was conducted for clinical trials that included lithium in males and females up to 18?years of age with a diagnosis of bipolar disorder and experiencing a manic or mixed episode according to standardized diagnostic criteria. The protocol was registered in PROSPERO (CRD42017055675). Results Four independent studies described in seven manuscripts met the inclusion criteria. Overall, 176 patients were treated with lithium either as a monotherapy or adjunct to risperidone. Efficacy results suggest that lithium may be superior to placebo (standardized mean difference [SMD] ?0.42, 95% confidence interval [CI] ?0.88 to 0.04), comparable to sodium divalproex (SMD ?0.07, 95% CI: ?0.31 to 0.18), but significantly less effective than risperidone for treating protracted manic/mixed episodes and comorbid attention‐deficit hyperactivity disorder (ADHD) in prepubertal children (SMD 0.85, 95% CI: 0.54 to 1.15). Lithium was not associated with serious adverse events, and was generally well tolerated with common side effects similar to those reported in adults. Conclusions Limited data suggests that lithium may be an effective and tolerable treatment for some forms of paediatric mania. However, lithium is clearly inferior in efficacy to risperidone in prepubertal patients diagnosed with protracted manic/mixed episodes and comorbid ADHD. There is a lack of data concerning the efficacy and tolerability of lithium as an acute treatment for classical mania in adolescents and important clinical issues remain unaddressed.
机译:目的,评估锂治疗儿童急性躁狂症和青少年诊断的双相障碍的疗效和耐受性。方法对2017年8月的系统文献搜索是针对临床试验的临床试验,其中患有雄性锂和女性,高达18岁的人,诊断双相情感障碍,并根据标准化诊断标准体验躁狂或混合发作。该协议在Prospero注册(CRD42017055675)。结果七种手稿中描述的四项独立研究符合纳入标准。总体而言,176名患者用锂治疗单疗法或辅助Risperidone。功效结果表明,锂可能优于安慰剂(标准化平均差异[SMD]〜0.42,95%置信区间[CI]?0.88至0.04),与DivalProex相当(SMD?0.07,95%CI:?0.31至0.18 ),但明显不如用于治疗Propubertal儿童的长期躁狂/混合发作和合并的关注缺陷多动障碍(SMD 0.85,95%CI:0.54至1.15)的延长躁狂/混合发作和共用缺陷多动障碍(ADHD)。锂与严重不良事件无关,并且通常具有与成人报告的副作用相似的常见副作用。结论有限的数据表明,锂可能是某些形式的儿科躁狂症的有效和耐受的治疗方法。然而,锂在诊断出患有长期躁狂/混合发作和合并症ADHD的Prepubertal患者中对Risperidone的疗效显然劣等。缺乏关于锂的疗效和耐受性,作为青少年古典躁狂症的急性治疗,重要的临床问题仍然没有解决。

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