Taylor F B, Russo J
Rainier Associates, Tacoma, Washington 98467, USA.
J Child Adolesc Psychopharmacol. 2000 Winter;10(4):311-20. doi: 10.1089/cap.2000.10.311.
Our objective was to compare the efficacy of the new wake-promoting drug modafinil to that of dextroamphetamine for the treatment of attention deficit hyperactivity disorder (ADHD) in adults. Twenty-two adults who met DSM-IV criteria for ADHD participated in a randomized, double-blind, placebo-controlled, three-phase crossover study comparing placebo, modafinil, and dextroamphetamine for the treatment of ADHD. The twice-daily study medications were titrated to doses of optimum efficacy over 4-7 days and then held constant during the rest of each 2-week treatment phase. Measures of improvement included the DSM-IV ADHD Behavior Checklist for Adults, the Controlled Oral Word Association Test (COWAT, using the letters C, F, and L version), Stroop, and Digit Span (Wechsler Adult Intelligence Scale version). For the 21 (96%) completers, the mean (+/- SD) optimum doses of modafinil and dextroamphetamine were 206.8 mg/day +/- 84.9 and 21.8 mg/day +/- 8.9, respectively. Scores on the DSM-IV ADHD Checklist (p < 0.001) were significantly improved over the placebo condition following treatment with both active medications. Performance on the COWAT (p < 0.05) reached trend levels of significance. Both medications were generally well tolerated. This preliminary study suggests that modafinil may be a viable alternative to conventional stimulants for the treatment of adults with ADHD.
我们的目标是比较新型促醒药物莫达非尼与右旋苯丙胺治疗成人注意力缺陷多动障碍(ADHD)的疗效。22名符合ADHD的DSM-IV标准的成年人参与了一项随机、双盲、安慰剂对照、三阶段交叉研究,比较安慰剂、莫达非尼和右旋苯丙胺治疗ADHD的效果。每日两次的研究药物在4 - 7天内滴定至最佳疗效剂量,然后在每个2周治疗阶段的剩余时间保持不变。改善指标包括成人DSM-IV ADHD行为检查表、受控口语词汇联想测验(COWAT,使用字母C、F和L版本)、斯特鲁普测验和数字广度测验(韦氏成人智力量表版本)。对于21名(96%)完成研究的患者,莫达非尼和右旋苯丙胺的平均(±标准差)最佳剂量分别为206.8毫克/天±84.9和21.8毫克/天±8.9。两种活性药物治疗后,DSM-IV ADHD检查表上的得分(p < 0.001)相对于安慰剂组有显著改善。COWAT测验的表现(p < 0.05)达到了趋势性显著水平。两种药物总体耐受性良好。这项初步研究表明,莫达非尼可能是治疗成人ADHD的传统兴奋剂的一种可行替代药物。