Mixed amphetamine salts extended-release in the treatment of adult ADHD: A randomized, controlled trial

被引:127
|
作者
Weisler, Richard H.
Biederman, Joseph
Spencer, Thomas J.
Wilens, Timothy E.
Faraone, Stephen V.
Chrisman, Allan K.
Read, Stephanie C.
Tulloch, Simon J.
机构
[1] Univ N Carolina, Chapel Hill, NC USA
[2] Duke Univ, Durham, NC USA
[3] Massachusetts Gen Hosp, Pediat Psychopharmacol Res Unit, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] MGH, Subst Abuse Serv Pediat Psychopharmacol, Boston, MA USA
[6] SUNY Upstate Med Univ, Syracuse, NY USA
[7] Duke Univ, Med Ctr, Div Child Psychiat, Dept Psychiat & Behav Sci, Durham, NC 27706 USA
[8] Shire Pharmaceut Inc, Globe Med Affairs, Wayne, PA USA
[9] Shire Pharmaceut Inc, CNS Strateg Therapeut Area, Wayne, PA USA
关键词
D O I
10.1017/S1092852900013687
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Attention-deficit/hyperactivity disorder (ADHD) is a serious neurobehavioral disorder of childhood onset that often persists into adolescence and adulthood. Functional impairments, underachievement, and difficult interpersonal relationships illustrate the need for effective treatment of ADHD through adulthood. Method:This prospective, multisite, randomized, double-blind, placebo-controlled, parallel-group, dose-escalation study was conducted to assess the efficacy, safety, and duration of action of mixed amphetamine salts extended-release (MAS XR) in adults with ADHD, combined type. Adults 18 years of age were given placebo or MAS XR 20, 40, or 60 mg/day for 4 weeks. The main outcome measures were the ADHD Rating Scale and Conners' Adult ADHD Rating Scale Short Version Self-Report (CAARS-S-S). Results: Two hundred fifty-five subjects were randomly assigned to treatment with MAS XR or placebo. MAS XR treatment was associated with statistically and clinically significant ADHD symptom reduction at endpoint; mean ADHD Rating Scale scores were 18.5 for the 20-mg group (P=.001), 18.4 for the 40-mg group (P<.001), and 18.5 for the 60-mg group (P<.001). Adults with severe symptoms (ADHD Rating Scale score >= 32 at baseline) had significantly greater symptom reduction with the highest MAS XR dose (60 mg/day), however, this dose-response relationship was determined by post-hoc analysis. The mean MAS XR effect size was 0.8. Statistically significant (P<.05) improvements in CAARS-S-S ADHD index scores occurred at 4- and 12-hours postdose for all MAS XR groups, indicating a 12-hour duration of effect. Symptoms improved within the first treatment week. Most adverse events reported were mild or moderate in intensity, and the most commonly reported adverse events were consistent with the known profile of stimulant medications. Vital signs and electrocardiograms showed no clinically significant cardiovascular changes. Conclusion: These results suggest that MAS XR is safe and effective in adults with ADHD and controlled ADHD symptoms for up to 12 hours.
引用
收藏
页码:625 / 639
页数:17
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