首页> 美国卫生研究院文献>Journal of Child and Adolescent Psychopharmacology >Weight and Height in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Longitudinal Database Study Assessing the Impact of Guanfacine Stimulants and No Pharmacotherapy
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Weight and Height in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Longitudinal Database Study Assessing the Impact of Guanfacine Stimulants and No Pharmacotherapy

机译:注意缺陷/多动症的儿童和青少年的体重和身高:纵向数据库研究评估胍法辛兴奋剂和无药物治疗的影响

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>Objectives: To assess the impact of long-term pharmacotherapy with guanfacine immediate- or extended-release (GXR), administered alone or as an adjunctive to a stimulant, on weight and height in children and adolescents with attention-deficit/hyperactivity disorder (ADHD).>Methods: Data were extracted from U.S. Department of Defense medical records for patients 4–17 years of age at index date (initiation of any study medication following a year without ADHD medications, or diagnosis if unmedicated) with weight/height measurements for the analysis period (January 2009–June 2013) and the previous year (baseline). Longitudinal weight and height z-scores were analyzed using multivariable regression in three cohorts: guanfacine (initial period of guanfacine exposure), first-line stimulant monotherapy (initial period of exposure), and unmedicated. Guanfacine cohort subgroups were based on previous/concurrent stimulant exposure.>Results: The weight analyses included 47,910 patients (66.8% male) and the height analyses 41,248 (67.2% male). Mean initial exposure in the weight analyses was 237 days (standard deviation [SD] = 258, median = 142) for guanfacine and 257 days (SD = 284, median = 151) for first-line stimulant monotherapy, and was similar in the height analyses. Modeling indicated that guanfacine monotherapy was not associated with clinically meaningful deviations from normal z-score trajectories for weight (first-line, n = 943; nonfirst-line, n = 796) or height (first-line, n = 741; nonfirst-line, n = 644). In patients receiving guanfacine adjunctive to a stimulant, modeled weight (n = 1657) and height (n = 1343) z-scores followed declining trajectories. In this subgroup, mean standardized weight/height had decreased during previous stimulant monotherapy. For first-line stimulant monotherapy, modeled weight (n = 32,999) and height (n = 28,470) z-scores followed declining trajectories during year 1. In the unmedicated cohort, modeled weight (n = 11,515) and height (n = 10,050) z-scores were stable.>Conclusions: Guanfacine monotherapy (first-line or nonfirst-line) was not associated with marked deviations from normal growth in this modeling study of children and adolescents with ADHD. In contrast, growth trajectories followed an initially declining course with stimulants, whether given alone or with adjunctive guanfacine.
机译:>目标:评估长期或单独使用胍法辛或作为兴奋剂的辅助药物与胍法辛立即释放或延长释放(GXR)的药物治疗对儿童和青少年体重和身高的影响缺陷/多动障碍(ADHD)。>方法:数据从美国国防部病历中的4-17岁患者在索引日期提取(在没有ADHD的一年后开始使用任何研究药物)在分析期间(2009年1月至2013年6月)和上一年度(基线)进行体重/身高测量的药物或未诊断的诊断。在三个队列中使用多元回归分析纵向体重和身高Z分数:胍法辛(胍法辛暴露的初始暴露期),一线兴奋剂单药治疗(暴露的初始暴露期)和未药物治疗。 >结果:体重分析包括47,910例患者(男性66.8%),身高分析41,248例(男性67.2%)。体重分析中,胍法辛的平均初始暴露时间为237天(标准差[SD] = 258,中位数= 142),一线刺激单药疗法为257天(SD = 284,中位数= 151),高度相似分析。模型表明,胍法辛单一疗法与体重(第一线,n = 943;非第一线,n = 796)或身高(第一线,n = 741;非第一线)的正常z评分轨线的临床上有意义的偏差无关。行,n = 644)。在接受胍法辛作为兴奋剂的患者中,模型化的体重(n = 1657)和身高(n = 1343)的z评分遵循下降的轨迹。在该亚组中,在先前的兴奋剂单药治疗期间,平均标准体重/身高有所降低。对于一线刺激性单药治疗,模型体重(n = 32,999)和身高(n = 28,470)的z分数在第1年期间遵循下降的轨迹。在非药物队列中,模型体重(n = 11,515)和身高( n = 10,050) z 评分稳定。> 结论: 胍法辛单一疗法(一线或非一线)不相关在儿童多动症儿童青少年模型研究中,与正常生长有明显偏差。相反,无论是单独使用还是与辅助胍法辛一起使用,兴奋剂的生长轨迹最初都在下降。

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