Response/Remission With Guanfacine Extended-Release and Psychostimulants in Children and Adolescents With Attention-Deficit/Hyperactivity Disorder

被引:16
|
作者
Cutler, Andrew J. [1 ,2 ]
Brams, Matthew [3 ]
Bukstein, Oscar [3 ,4 ]
Mattingly, Gregory [5 ]
McBurnett, Keith [6 ]
White, Carla [7 ]
Rubin, Jonathan [8 ]
机构
[1] Florida Clin Res Ctr LLC, Bradenton, FL 34201 USA
[2] Univ Florida, Gainesville, FL USA
[3] Baylor Coll Med, Houston, TX 77030 USA
[4] DePelchin Childrens Ctr, Houston, TX USA
[5] Washington Univ, Sch Med, St Charles, MO USA
[6] Univ Calif San Francisco, San Francisco, CA 94143 USA
[7] Shire Pharmaceut Dev Ltd, Basingstoke, Hants, England
[8] Alcobra Inc, Plymouth Meeting, PA USA
来源
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY | 2014年 / 53卷 / 10期
关键词
alpha(2A)-agonist; guanfacine XR; ADHD; response; remission; DEFICIT-HYPERACTIVITY DISORDER; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; REMISSION; ADHD; ATOMOXETINE; SYMPTOMS; EFFICACY; THERAPY; SAFETY;
D O I
10.1016/j.jaac.2014.08.001
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: In this post hoc analysis, we assessed whether guanfacine extended-release (GXR) adjunctive to a psychostimulant resulted in greater response and remission rates than placebo + psychostimulant in children and adolescents with attention-deficit/hyperactivity disorder (ADHD). Method: In this 9-week, double-blind, placebo-controlled dose-optimization study, participants (N = 461) aged 6 to 17 years with suboptimal response to psychostimulants were randomized to GXR on awakening (AM) + psychostimulant, GXR at bedtime (PM) + psychostimulant, or placebo + psychostimulant. Results: At the final on-treatment assessment, more participants in both GXR + psychostimulant groups versus the placebo + psychostimulant group achieved response as assessed by 2 criteria: reduction from baseline in ADHD Rating Scale IV (ADHD-RS-IV) total score (1) >= 40% (GXR AM + psychostimulant = 69.8%, GXR PM + psychostimulant = 70.3%, versus placebo + psychostimulant = 57.9%; p = .032 and p = .026, respectively), or (2) >= 50% (63.1%, 64.9%, versus 43.4%; p < .001 for both). Results were similar for symptomatic remission (ADHD-RS-IV total score <= 18; 61.1%, 62.2%, versus 46.1%; p = .010 and p = .005, respectively) and syndromal remission (symptomatic remission plus Clinical Global Impressions of Severity of Illness score <= 2). The most common treatment-emergent adverse events in participants receiving GXR + psychostimulant were headache (21.2%) and somnolence (13.6%). Conclusion: GXR + psychostimulant treatment resulted in a greater percentage of participants meeting stringent criteria for response and remission compared with placebo + psychostimulant. The adverse event profile of adjunctive therapy was consistent with known effects of either treatment alone. Clinical trial registration information-Efficacy and Safety of SPD503 in Combination With Psychostimulants; http://clinicaltrials.gov/; NCT00734578.
引用
收藏
页码:1092 / 1101
页数:10
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