Guanfacine extended-release for attention-deficit/hyperactivity disorder (ADHD)

被引:16
作者
Sallee, Floyd R. [1 ]
Eaton, Katherine [1 ]
机构
[1] Univ Cincinnati, Dept Psychiat, Cincinnati, OH 45219 USA
关键词
ADHD; clonidine; guanfacine; non-stimulant; psychostimulant; alpha 2A-adrenoceptor agonist; DEFICIT-HYPERACTIVITY DISORDER; PREFRONTAL CORTICAL ALPHA(2)-ADRENOCEPTORS; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; LONG-TERM; ALPHA-2-ADRENERGIC AGONIST; OPEN-LABEL; CHILDREN; ADOLESCENTS; MONKEYS;
D O I
10.1517/14656566.2010.517523
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Importance of the field: Guanfacine extended-release (GXR) is a non-stimulant approved in the US for treatment of attention deficit/hyperactivity disorder (ADHD). GXR is a 'first in class' alpha(2A)-adrenoceptor agonist reformulated to optimize efficacy. GXR enters a rapidly growing but crowded ADHD market as an alternative not only to psychostimulants but also to atomoxetine. Areas covered in this review: Pharmacodynamics, pharmacokinetics, clinical efficacy and safety of GXR are covered based on a literature review (MEDLINE and EMBASE) from 1980 to 2010. Two large pivotal controlled trials are reviewed along with companion safety studies over 24 months. Collateral studies in ADHD children with oppositional symptoms and combination use of GXR in psychostimulant partial-responders are featured. What the reader will gain: Novel aspects of apparent GXR mechanism of action may complement existing treatments. Study evidence indicates that GXR is a well-tolerated and effective treatment for children and adolescents with ADHD, and appears efficacious to reduce oppositional symptoms in children with these complicating features. The GXR safety database reflects mild and asymptomatic decreases in both blood pressure and heart rate throughout, with most adverse events being somnolence-related and time-limited. Take home message: This review of GXR will allow the reader to determine the place for GXR in the ADHD treatment landscape.
引用
收藏
页码:2549 / 2556
页数:8
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