Post Hoc Analysis: Early Changes in ADHD-RS Items Predict Longer Term Response to Atomoxetine in Pediatric Patients

被引:11
作者
Block, Stan L. [2 ]
Williams, David [3 ]
Donnelly, Craig L. [4 ]
Dunn, David W. [5 ]
Saylor, Keith E. [6 ]
Ruberg, Stephen J. [1 ]
机构
[1] Eli Lilly & Co, Adv Anal, Global Stat Sci, Indianapolis, IN 46285 USA
[2] Kentucky Pediat Res, Bardstown, KY USA
[3] Lilly USA LLC, Indianapolis, IN USA
[4] Darthmouth Hitchcock Med Ctr, Lebanon, NH USA
[5] Indiana Univ, Indianapolis, IN 46204 USA
[6] NeuroScience Inc, Herndon, VA USA
基金
美国国家卫生研究院;
关键词
prediction; treatment response; ADHD-RS; CART; DEFICIT-HYPERACTIVITY DISORDER; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; ONCE-DAILY ATOMOXETINE; PANIC DISORDER; CHILDREN; ANTECEDENTS;
D O I
10.1177/0009922810368134
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Data from 5 atomoxetine trials in pediatric outpatients with attention-deficit/hyperactivity disorder (ADHD) were divided into training and validation data sets to develop models predicting atomoxetine treatment response, using changes in individual ADHD Rating Scale (ADHD-RS) items early in treatment. Treatment response was predicted after 1 week by a >= 1-point score decrease in ADHD-RS item 15 ("easily distracted;" positive predictive values [PPVs]: 84.9%, 74.3%, and 73.3%; negative predictive values [NPVs]: 52.6%, 50.5%, and 46.3%; training and 2 validation data sets, respectively); after 2 to 3 weeks, by a >= 1-point score decrease in ADHD-RS item 1 ("fails to give close attention or makes careless mistakes;" PPV = 77.7% and 77.9%) and by the absence of a >= 1-point score decrease on ADHD-RS items 1 and 10 ("on the go;" NPV = 72.2% and 77.5%), or by the combination of items 1 and 10 (PPVs: 75.1% and 75.4%; NPVs: 72.2% and 77.5%; training and validation data sets, respectively).
引用
收藏
页码:768 / 776
页数:9
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