Maneeton Narong, Maneeton Benchalak, Woottiluk Pakapan, Suttajit Sirijit, Likhitsathian Surinporn, Charnsil Chawanun, Srisurapanont Manit
Department of Psychiatry, Faculty of Medicine, Faculty of Nursing, Chiang Mai University, Chiang Mai, Thailand.
Division of Psychiatric Nursing, Faculty of Nursing, Chiang Mai University, Chiang Mai, Thailand.
Neuropsychiatr Dis Treat. 2015 Nov 25;11:2943-52. doi: 10.2147/NDT.S91765. eCollection 2015.
The efficacy of dexmethylphenidate (d-MPH) has been proven in the treatment of children and adolescents with attention-deficit hyperactivity disorder (ADHD).
The aim of this systematic review is to determine the efficacy, acceptability, and tolerability of d-MPH in child and adolescent ADHD.
The searches of SCOPUS, MEDLINE, CINAHL, and Cochrane Controlled Trials Register were performed in February 2015. All randomized controlled trials of d-MPH versus placebo that were performed in children and adolescents with ADHD up to 18 years of age were included in the study. The efficacy was measured by using the pooled mean-endpoint or mean-changed scores of ADHD rating scales and the response rate. Acceptability and tolerability were measured by using the pooled rates of overall discontinuation and discontinuation due to adverse events, respectively.
A total of 1,124 children and adolescents diagnosed as having ADHD were included in this review. In a laboratory school setting, the pooled mean-change and mean-endpoint scores in the d-MPH-treated group were significantly greater than those of the placebo-treated group with standardized mean difference (95% confidence interval [CI]) of -1.20 (-1.73, -0.67), I (2)=95%. Additionally, the pooled mean-changed scores of the ADHD rating scales for teachers and parents in the d-MPH-treated group were significantly greater than that of the placebo-treated group with weighted mean difference (95% CI) of -13.01 (-15.97, -10.05), I (2)=0% and (95% CI) of -12.99 (-15.57, -10.42), I (2)=0%, respectively. The pooled response rate in the d-MPH-treated groups had a significance higher than that of the placebo-treated group. The rates of pooled overall discontinuation and discontinuation due to adverse events between the two groups were not significantly different.
Based on the findings in this review, it can be concluded that d-MPH medication is efficacious and tolerable in child and adolescent ADHD. However, the acceptability of d-MPH is no greater than that of the placebo. Further systematic studies may confirm these findings.
右哌甲酯(d-MPH)治疗儿童和青少年注意力缺陷多动障碍(ADHD)的疗效已得到证实。
本系统评价旨在确定d-MPH治疗儿童和青少年ADHD的疗效、可接受性和耐受性。
于2015年2月检索了SCOPUS、MEDLINE、CINAHL和Cochrane对照试验注册库。纳入所有在18岁及以下ADHD儿童和青少年中进行的d-MPH与安慰剂对比的随机对照试验。疗效通过ADHD评定量表的合并平均终点或平均变化分数以及缓解率来衡量。可接受性和耐受性分别通过总体停药合并率和因不良事件停药合并率来衡量。
本评价共纳入1124例诊断为ADHD的儿童和青少年。在实验室学校环境中,d-MPH治疗组的合并平均变化和平均终点分数显著高于安慰剂治疗组,标准化平均差(95%置信区间[CI])为-1.20(-1.73,-0.67),I² = 95%。此外,d-MPH治疗组教师和家长ADHD评定量表中的合并平均变化分数显著高于安慰剂治疗组,加权平均差(95%CI)分别为-13.01(-15.97,-10.05),I² = 0%和(95%CI)为-12.99(-15.57,-10.42),I² = 0%。d-MPH治疗组的合并缓解率显著高于安慰剂治疗组。两组间总体停药合并率和因不良事件停药合并率无显著差异。
基于本评价结果,可得出结论:d-MPH药物治疗儿童和青少年ADHD有效且耐受性良好。然而,d-MPH的可接受性不高于安慰剂。进一步的系统研究可能会证实这些发现。