Atomoxetine for the treatment of attention-deficit/hyperactivity disorder and oppositional defiant disorder

被引:56
作者
Bangs, Mark E. [1 ]
Hazell, Philip [2 ]
Danckaerts, Marina [3 ]
Hoare, Peter [4 ]
Coghill, David R. [5 ]
Wehmeier, Peter M. [6 ]
Williams, David W. [1 ]
Moore, Rodney J. [1 ]
Levine, Louise [1 ]
机构
[1] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
[2] Univ Newcastle, Child & Adolescent Mental Hlth Serv, Newcastle, NSW 2308, Australia
[3] Univ Ziekenhuis Gasthuisberg Leuven, Div Psychiat, Louvain, Belgium
[4] Univ Edinburgh, Child & Family Hlth Serv, Edinburgh, Midlothian, Scotland
[5] Univ Dundee, Div Pathol & Neurosci, Sect Psychiat, Dundee, Scotland
[6] Lilly Deutschland, Bad Homburg, Germany
关键词
ADHD; adolescents; atomoxetine;
D O I
10.1542/peds.2006-1880
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVE. In this study we examined the effectiveness of atomoxetine for the treatment of oppositional defiant disorder comorbid with attention-deficit/hyperactivity disorder. METHODS. Patients were aged 6 to 12 years and met Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, diagnostic criteria for attention-deficit/hyperactivity disorder with a Swanson, Nolan, and Pelham Rating Scale-Revised attention-deficit/hyperactivity disorder subscale score above age and gender norms; Clinical Global Impressions-Severity Scale score of >= 4; and Swanson, Nolan, and Pelham Rating Scale-Revised oppositional defiant disorder subscale score of >= 15. Patients were randomly assigned in a 2: 1 ratio to receive 1.2 mg/kg per day of atomoxetine (n = 156) or placebo (n = 70) for 8 weeks. Treatment effect on oppositional defiant disorder and attention-deficit/hyperactivity disorder symptoms was measured by using the investigator-rated Swanson, Nolan, and Pelham Rating Scale-Revised. RESULTS. Repeated-measures analysis demonstrated a statistically significant difference favoring atomoxetine over placebo in the reduction of Swanson, Nolan, and Pelham Rating Scale-Revised oppositional defiant disorder total scores. There were significant pairwise treatment differences at weeks 2 and 5 but not at week 8 postbaseline. A last-observation-carried-forward analysis showed Swanson, Nolan, and Pelham Rating Scale-Revised scores at endpoint for the atomoxetine and placebo groups were significantly different for attention-deficit/hyperactivity disorder symptoms but not for oppositional defiant disorder symptoms. Atomoxetine was superior to placebo in a last-observation-carried-forward analysis of Clinical Global Impression-Improvement and Clinical Global Impression-Severity scores. CONCLUSIONS. This study confirms previous findings that patients with attention-deficit/hyperactivity disorder and comorbid oppositional defiant disorder show statistically and clinically significant improvement in attention-deficit/hyperactivity disorder symptoms and global clinical functioning when treated with atomoxetine. It remains uncertain, however, whether atomoxetine exerts a specific and enduring effect on oppositional defiant disorder symptoms.
引用
收藏
页码:E314 / E320
页数:7
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