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首页> 外文期刊>Journal of child and adolescent psychopharmacology >Parent-reported executive function behaviors and clinician ratings of attention-deficit/hyperactivity disorder symptoms in children treated with lisdexamfetamine dimesylate
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Parent-reported executive function behaviors and clinician ratings of attention-deficit/hyperactivity disorder symptoms in children treated with lisdexamfetamine dimesylate

机译:来德沙胺丁苯二甲酸酯治疗儿童的父母报告的执行功能行为和注意缺陷/多动障碍症状的临床医生评分

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摘要

Objective: The purpose of this article was to describe the relationships between parent-rated executive function (EF) and clinician-rated attention-deficit/hyperactivity disorder (ADHD) symptoms before and after lisdexamfetamine dimesylate (LDX) treatment in children with and without EF deficit. Methods: In post-hoc analyses of children with ADHD who participated in a 7 week open-label, dose-optimized (LDX 20-70 mg/day) trial, ADHD Rating Scale-IV (ADHD-RS-IV) change scores were compared (using two-sample t tests) between youth with and without clinically significant EF impairment at baseline. Clinically significant impairment was defined as parent-rated Behavior Rating Inventory of EF (BRIEF) Global Executive Composite (GEC) t scores ??65. Relationships between baseline and endpoint BRIEF and ADHD-RS-IV scores were examined using Pearson correlations and generalized effect linear model. Safety assessment included treatment-emergent adverse events (TEAEs). Results: At baseline, 265/315 participants (84.1%) had a clinically significant BRIEF score. Their mean (SD) ADHD-RS-IV total score at baseline was 42.1 (6.64) for those with, and 36.5 (6.67) for those without, clinically significant BRIEF. At endpoint, ADHD-RS-IV total and subscale scores were significantly improved (p0.0001) for both those with and those without clinically significant baseline BRIEF scores. Moderately strong, positive Pearson correlations were observed between BRIEF and ADHD-RS-IV total and subscale scores. In the generalized effect linear model, ADHD-RS-IV change scores were significantly correlated with endpoint BRIEF scores (r2=0.35, ??=0.73, p0.0001). In the subgroup without clinically significant BRIEF t scores at endpoint, parents and clinicians rated 90% and 95%, respectively, as improved. In the subgroup with clinically significant BRIEF t scores at endpoint, parents and clinicians rated 69% and 78%, respectively, as improved. TEAEs were experienced by 269/318 (84.9%) participants; most (82.7%) experienced events mild to moderate in intensity. A total of 12/318 (4.1%) participants discontinued because of TEAEs. Conclusion: Clinically significant impairment of EF behaviors in children with ADHD was associated with more severe ADHD symptoms. LDX therapy improved ADHD symptom severity, and at endpoint, fewer participants displayed impairment of EF behaviors (versus baseline). The parent-rated BRIEF may describe clinically important EF behaviors not assessed by the 18-item ADHD-RS-IV. ? Mary Ann Liebert, Inc.
机译:目的:本文旨在描述在接受和未接受EF的儿童中,来德沙胺丁二酸二甲磺酸酯(LDX)治疗前后父母评估的执行功能(EF)与临床医师评估的注意缺陷/多动障碍(ADHD)症状之间的关系。赤字。方法:在参加为期7周的开放标签,剂量优化(LDX 20-70 mg /天)试验的ADHD儿童的事后分析中,ADHD评分量表IV(ADHD-RS-IV)的变化得分为在基线时有无临床上显着EF损伤的青年之间进行比较(使用两次样本t检验)。临床上显着的损伤定义为EF(BRIEF)的全球父母行为评估父母评分(GEC)t评分≥65。使用Pearson相关性和广义效应线性模型检查基线和终点BRIEF和ADHD-RS-IV评分之间的关​​系。安全性评估包括治疗紧急不良事件(TEAE)。结果:基线时,有265/315名参与者(84.1%)具有临床上显着的Brief评分。基线时,他们的平均(SD)ADHD-RS-IV总得分对于有临床意义的简报的患者为42.1(6.64),对于没有临床意义的Brief为36.5(6.67)。在终点,有和没有临床显着基线BRIEF评分者的ADHD-RS-IV总评分和子量表评分均得到显着改善(p <0.0001)。在BRIEF和ADHD-RS-IV总分和分量表得分之间观察到中等程度强的Pearson正相关。在广义效应线性模型中,ADHD-RS-IV变化评分与终点BRIEF评分显着相关(r2 = 0.35,Δε= 0.73,p <0.0001)。在终点没有临床显着的Bief t评分的亚组中,父母和临床医生的改善程度分别为90%和95%。在终点具有临床上显着的BRIEF t分值的亚组中,父母和临床医生的改善程度分别为69%和78%。 269/318(84.9%)位参与者体验了TEAE;大多数(82.7%)经历的事件的强度为轻度到中度。共有12/318(4.1%)位参与者因TEAE停赛。结论:ADHD患儿EF行为的临床显着损害与更严重的ADHD症状有关。 LDX疗法改善了ADHD症状的严重程度,并且在终点时,较少的参与者表现出EF行为的损害(相对于基线)。父母评价的“摘要”可能描述了18个项目ADHD-RS-IV未评估的临床上重要的EF行为。 ?玛丽·安·利伯特公司

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