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首页> 外文期刊>Journal of child and adolescent psychopharmacology >A meta-analysis of the consistency of atomoxetine treatment effects in pediatric patients with attention-deficit/hyperactivity disorder from 15 clinical trials across four geographic regions
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A meta-analysis of the consistency of atomoxetine treatment effects in pediatric patients with attention-deficit/hyperactivity disorder from 15 clinical trials across four geographic regions

机译:来自四个地理区域的15项临床试验对阿托西汀治疗注意力缺乏/多动障碍患者的疗效一致性的荟萃分析

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Objective: Atomoxetine has been approved as a treatment for children and adolescents with attention-deficit/hyperactivity disorder (ADHD) in the United States, throughout Europe, and in other countries. This meta-analysis was to assess the consistency of the treatment effect of atomoxetine across four global geographic regions. Methods: Data from 15 acute, double-blind, placebo-controlled trials were pooled (2 in Asia, 4 in Europe, 8 in North America, and 1 in Russia), yielding 2569 pediatric patients with ADHD. Improvements during 6-10 weeks of atomoxetine treatment were evaluated using the ADHD Rating Scale-IV or the Swanson, Nolan, and Pelham Scale-Revised. Consistency across regions was assessed by an interaction test and Higgins I2. Consistency of one region versus other regions was assessed by effect sizes of individual regions and pairwise differences. Results: Patient demographics were generally similar across regions. More patients from Asia met diagnostic criteria for ADHD inattentive subtype and fewer for combined subtype compared with patients from Europe, North America, or Russia. Asian patients had a lower mean baseline ADHD total score and mean hyperactivity/impulsivity subscore. Treatment effects showed marginal inconsistency and moderate heterogeneity among the regions (percentage of patients achieving a 40% decrease from baseline ADHD scores, atomoxetine versus placebo: Asia 39.6%, 24.0%; Europe 40.2%, 12.1%; North America 45.3%, 21.7%; Russia 54.2%, 33.3%). Inconsistency was observed primarily in Asia versus the other regions. Completion rates with atomoxetine were higher in Asia and Russia (94.4% and 94.3%, respectively) than in Europe (84.3%) or North America (80.4%). Conclusions: Atomoxetine was demonstrated as an effective treatment for ADHD in 15 clinical trials from four global regions. The current meta-analysis has revealed a degree of heterogeneity in treatment efficacy across regions, most notably in the comparison of Asian patients relative to those from the other regions.
机译:目的:Atomoxetine在美国,整个欧洲和其他国家/地区已被批准用于治疗患有注意力缺陷/多动症(ADHD)的儿童和青少年。这项荟萃分析旨在评估阿托西汀在全球四个地理区域内治疗效果的一致性。方法:汇总了15项急性,双盲,安慰剂对照试验的数据(亚洲2例,欧洲4例,北美8例,俄罗斯1例),共2569名儿童ADHD患者。使用ADHD评分量表IV或Swanson,Nolan和Pelham量表修订版评估了阿托西汀治疗6-10周期间的改善情况。通过互动测试和Higgins I2评估了跨地区的一致性。通过单个区域的效应大小和成对差异评估一个区域与其他区域的一致性。结果:不同地区的患者总体情况相似。与来自欧洲,北美或俄罗斯的患者相比,符合诊断多动症注意力不集中亚型的亚洲患者较多,而合并亚型的诊断患者较少。亚洲患者的平均基线ADHD总得分和平均多动/冲动评分较低。治疗效果显示区域间存在边缘不一致和中等程度的异质性(与基线ADHD得分相比降低40%的患者百分比,阿托莫西汀与安慰剂相比:亚洲39.6%,24.0%;欧洲40.2%,12.1%;北美45.3%,21.7% ;俄罗斯54.2%,33.3%)。主要在亚洲与其他地区发现不一致。亚洲和俄罗斯(分别为94.4%和94.3%)的阿莫西汀完成率高于欧洲(84.3%)或北美(80.4%)。结论:Atomoxetine在全球四个地区的15项临床试验中被证明是ADHD的有效治疗方法。当前的荟萃分析显示,各地区在治疗效果上存在一定程度的异质性,最明显的是将亚裔患者与其他地区的患者进行比较。

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