Donner Richard, Michaels M Alex, Ambrosini Paul J
Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Biol Psychiatry. 2007 Mar 1;61(5):706-12. doi: 10.1016/j.biopsych.2006.05.002. Epub 2006 Aug 8.
The cardiovascular safety of mixed amphetamine salts extended release (MAS XR) was evaluated in 2968 children 6-12 years of age with attention-deficit/hyperactivity disorder (ADHD).
In this prospective, open-label, noncomparative, community-based study, subjects whose symptoms of ADHD were well controlled with stimulant medication maintained their established treatment regimens for 2 weeks before enrollment into the current study. Subjects' regimens were then converted to an approximately equivalent once-daily dose of MAS XR 10, 20, or 30 mg/d according to a medication-conversion algorithm, which could be adjusted to 40 mg/d for optimal efficacy and tolerability. Systolic blood pressure (SBP), diastolic BP (DBP), and pulse were measured at each study visit. Twelve-lead electrocardiography was performed at screening and at the end of the extension phase or early termination.
No clinically significant changes in BP or pulse were observed. Although one subject experienced a QT-prolongation interval > 25%, no clinically significant prolongation in the mean QT interval was seen. Approximately 2.5% of subjects demonstrated two consecutive SBP or DBP values > 95th percentile for age, sex, and height, and 3.6% of subjects' pulse increased by > or = 25 to > or = 110 beats per minute. No serious cardiovascular adverse events or deaths occurred.
In addition to demonstrated efficacy and safety, the cardiovascular profile of MAS XR showed generally small divergences from age-specific population norms that pose very limited risk in this patient population.
在2968名6至12岁患有注意力缺陷多动障碍(ADHD)的儿童中评估了混合安非他命盐缓释剂(MAS XR)的心血管安全性。
在这项前瞻性、开放标签、非对照、基于社区的研究中,ADHD症状通过兴奋剂药物得到良好控制的受试者在进入本研究之前维持其既定治疗方案2周。然后根据药物转换算法将受试者的治疗方案转换为每日一次的约等效剂量的MAS XR 10、20或30 mg/d,可根据最佳疗效和耐受性调整至40 mg/d。在每次研究访视时测量收缩压(SBP)、舒张压(DBP)和脉搏。在筛查时以及延长期结束或提前终止时进行12导联心电图检查。
未观察到血压或脉搏有临床显著变化。尽管有一名受试者的QT间期延长>25%,但平均QT间期未见临床显著延长。约2.5%的受试者连续两次SBP或DBP值高于年龄、性别和身高的第95百分位数,3.6%的受试者脉搏增加>或=25次/分钟至>或=110次/分钟。未发生严重心血管不良事件或死亡。
除了已证实的疗效和安全性外,MAS XR的心血管特征显示与特定年龄人群规范的差异总体较小,在该患者群体中风险非常有限。