A Placebo-Controlled, Fixed-Dose Study of Aripiprazole in Children and Adolescents With Irritability Associated With Autistic Disorder

被引:369
作者
Marcus, Ronald N. [1 ]
Owen, Randall [1 ]
Kamen, Lisa [1 ]
Manos, George [1 ]
McQuade, Robert D.
Carson, William H.
Aman, Michael G. [2 ]
机构
[1] Bristol Myers Squibb Co, Wallingford, CT 06492 USA
[2] Ohio State Univ, Columbus, OH 43210 USA
关键词
aripiprazole; autistic disorder; pediatric; PERVASIVE DEVELOPMENTAL DISORDERS; SPECTRUM DISORDERS; BIPOLAR DISORDER; YOUNG-PEOPLE; OPEN-LABEL; PREVALENCE; RELIABILITY; RISPERIDONE; VALIDITY; BEHAVIOR;
D O I
10.1097/CHI.0b013e3181b76658
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Objective: To evaluate the short-term efficacy and safety of aripiprazole in the treatment of irritability in children and adolescents with autistic disorder. Method: Two hundred eighteen children and adolescents (aged 6-17 years) with a diagnosis of autistic disorder, and with behaviors such as tantrums, aggression, self-injurious behavior, or a combination of these symptoms, were randomized 1:1:1:1 to aripiprazole (5, 10, or 15 mg/day) or placebo in this 8-week double-blind, randomized, placebo-controlled, parallel-group study. Efficacy was evaluated using the caregiver-rated Aberrant Behavior Checklist Irritability subscale (primary efficacy measure) and the clinician-rated Clinical Global Impressions-improvement score. Safety and tolerability were also assessed. Results: At week 8, all aripiprazole doses produced significantly greater improvement than placebo in mean Aberrant Behavior Checklist Irritability subscale scores (5 mg/day, -12.4; 10 mg/day, -13.2; 15 mg/day, -14.4; versus placebo, -8.4; all p < .05). All aripiprazole doses demonstrated significantly greater improvements in mean Clinical Global Impressions-Improvement score than placebo at week 8. Discontinuation rates due to adverse events were as follows: placebo 7.7%, aripiprazole 5 mg/day 9.4%, 10 mg/day 13.6%, and 15 mg/day 7.4%. The most common adverse event leading to discontinuation was sedation. There were two serious adverse events: presyncope (5 mg/day) and aggression (10 mg/day). At week 8, mean weight change (last observation carded forward) was as follows: placebo +0.3 kg, aripiprazole 5 mg/day +1.3 kg, 10 mg/day +1.3 kg, and 15 mg/day +1.5 kg; all p < .05 versus placebo. Conclusions: Aripiprazole was efficacious and generally safe and well tolerated in the treatment of children and adolescents with irritability associated with autistic disorder. J. Am. Acad. Child Adolesc. Psychiatry, 2009;48(11):1110-1119.
引用
收藏
页码:1110 / 1119
页数:10
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