Department of Psychiatry, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, Brazil.
Child Study Center, Yale University School of Medicine, New Haven, Connecticut, USA.
J Child Adolesc Psychopharmacol. 2024 Nov;34(9):373-382. doi: 10.1089/cap.2024.0049. Epub 2024 Sep 24.
To evaluate the comparative efficacy of pharmacological interventions for children and adolescents with a dual diagnosis of persistent tic disorders or Tourette disorder and attention-deficit/hyperactivity disorder (TD + ADHD). We searched CENTRAL, Embase, PubMed, PsycInfo, Web of Sciences, ClinicalTrials.gov, and WHO ICTRP up to September 2023 to identify double-blinded randomized controlled trials (RCTs) assessing pharmacological interventions for children and adolescents with TD + ADHD. Outcomes were change in ADHD symptoms (primary) and tics (secondary) severity. Standardized mean difference (SMD) was calculated and pooled in random-effects network meta-analysis. The Confidence in Network Meta-Analysis framework was adopted to determine certainty of evidence. We included 8 RCTs involving 575 participants. Network meta-analyses demonstrated that α2 agonists (SMD, 95% confidence interval [CI] ADHD: -0.72 [-1.13 to -0.31]; TD: -0.70 [-0.96 to -0.45]) and stimulants + α2 agonists (ADHD: -0.84 [-1.54 to -0.13]; TD: -0.60 [-1.04 to -0.17]) were more efficacious than placebo for ADHD symptoms and tics severity. Stimulants alone were more efficacious than placebo for ADHD symptoms severity only, but they did not worsen tics (ADHD: -0.54 [-1.05 to -0.03]; TD: -0.22 [-0.49 to 0.05]). There were no significant differences between any pairs of medications that were found efficacious against placebo for ADHD symptoms or tics severity. Certainty in the evidence varied from low to very low. Stimulants are efficacious for ADHD symptoms severity and do not increase tics severity in TD + ADHD. α2 agonists are efficacious for both ADHD symptoms and tics severity in TD + ADHD. These findings should inform guidelines and help guide shared decision-making to choose a medication for children with TD + ADHD.
评价药物干预对持续性抽动障碍或图雷特综合征合并注意缺陷多动障碍(TD+ADHD)儿童和青少年的疗效。我们检索了 CENTRAL、Embase、PubMed、PsycInfo、Web of Sciences、ClinicalTrials.gov 和 WHO ICTRP,截至 2023 年 9 月,以确定评估药物干预对 TD+ADHD 儿童和青少年的双盲随机对照试验(RCT)。主要结局为 ADHD 症状(主要结局)和抽动严重程度(次要结局)的变化。采用标准化均数差(SMD)并在随机效应网络荟萃分析中进行汇总。采用置信度网络荟萃分析框架来确定证据的确定性。我们纳入了 8 项 RCT,共涉及 575 名参与者。网络荟萃分析表明,α2 激动剂(SMD,95%置信区间[CI]ADHD:-0.72[-1.13 至-0.31];TD:-0.70[-0.96 至-0.45])和兴奋剂+α2 激动剂(ADHD:-0.84[-1.54 至-0.13];TD:-0.60[-1.04 至-0.17])对 ADHD 症状和抽动严重程度的疗效优于安慰剂。兴奋剂单独治疗对 ADHD 症状严重程度的疗效优于安慰剂,但不会加重抽动(ADHD:-0.54[-1.05 至-0.03];TD:-0.22[-0.49 至 0.05])。在 ADHD 症状或抽动严重程度方面,与安慰剂相比,任何有效药物之间均无显著差异。证据的确定性从低到极低不等。兴奋剂对 ADHD 症状严重程度有效,不会增加 TD+ADHD 患者的抽动严重程度。α2 激动剂对 TD+ADHD 患者的 ADHD 症状和抽动严重程度均有效。这些发现应能为指南提供信息,并有助于指导共同决策,为患有 TD+ADHD 的儿童选择药物。