Spencer T, Biederman J, Wilens T, Faraone S, Prince J, Gerard K, Doyle R, Parekh A, Kagan J, Bearman S K
Pediatric Psychopharmacology Unit (ACC-725), Massachusetts General Hospital, Fruit Street, Boston, MA 02114, USA.
Arch Gen Psychiatry. 2001 Aug;58(8):775-82. doi: 10.1001/archpsyc.58.8.775.
We report on a controlled trial of a mixed amphetamine salts compound (Adderall, dextroamphetamine sulfate, dextro-, levoamphetamine sulfate, dextroamphetamine aspartate, levoamphetamine aspartate, and dextroamphetamine saccharate) in the treatment of adult attention-deficit/hyperactivity disorder (ADHD).
This was a 7-week, randomized, double-blind, placebo-controlled, crossover study of Adderall in 27 well-characterized adults satisfying full DSM-IV criteria for ADHD of childhood onset and persistent symptoms into adulthood. Medication was titrated up to 30 mg twice a day. Outcome measures included the ADHD Rating Scale and the Clinical Global Impression Score. Comorbid psychiatric disorders were assessed to test for potential effects on treatment outcome.
Treatment with Adderall at an average oral dose of 54 mg (administered in 2 daily doses) was effective and well tolerated. Drug-specific improvement in ADHD symptoms was highly significant overall (42% decrease on the ADHD Rating Scale, P<.001), and sufficiently robust to be detectable in a parallel groups comparison restricted to the first 3 weeks of the protocol (P<.001). The percentage of subjects who improved (reduction in the ADHD rating scale of > or =30%) was significantly higher with Adderall treatment than with a placebo (70% vs 7%; P =.001).
Adderall was effective and well tolerated in the short-term treatment of adults with ADHD. More work is needed to evaluate the long-term effects of Adderall, or other amphetamine compounds, in the treatment of adults with ADHD.
我们报告了一项关于混合苯丙胺盐化合物(阿得拉,硫酸右旋苯丙胺、右旋-、左旋硫酸苯丙胺、右旋苯丙胺天冬氨酸盐、左旋苯丙胺天冬氨酸盐和右旋苯丙胺糖酸盐)治疗成人注意力缺陷/多动障碍(ADHD)的对照试验。
这是一项为期7周的随机、双盲、安慰剂对照、交叉研究,研究对象为27名符合儿童期起病且持续至成年的ADHD完整DSM-IV标准的特征明确的成年人。药物剂量滴定至每日两次,每次30毫克。结果测量包括ADHD评定量表和临床总体印象评分。评估共病精神障碍以测试其对治疗结果的潜在影响。
平均口服剂量为54毫克(分两次每日给药)的阿得拉治疗有效且耐受性良好。总体而言,ADHD症状的药物特异性改善非常显著(ADHD评定量表上降低42%,P<.001),并且在仅限于方案前3周的平行组比较中也具有足够的显著性(P<.001)。接受阿得拉治疗的改善受试者百分比(ADHD评定量表降低≥30%)显著高于接受安慰剂治疗的受试者(70%对7%;P =.001)。
阿得拉在成人ADHD的短期治疗中有效且耐受性良好。需要更多的研究来评估阿得拉或其他苯丙胺化合物在成人ADHD治疗中的长期效果。