Prescrire Int. 1999 Feb;8(39):5-7.
(1) Modafinil, a psychostimulant, has been available in France for the treatment of narcolepsy and idiopathic hypersomnia since 1994. (2) The initial clinical file was inadequate to judge its possible clinical value. (3) In narcolepsy three new short-term clinical trials have compared modafinil with a placebo (nearly 500 patients treated with modafinil). (4) These trials show that the effects of modafinil on daytime drowsiness are only moderate (average reduction of one unwanted sleep episode a day) but are subjectively better than those of a placebo. In all, 84% of patients preferred the modafinil period to the placebo period during a cross-over trial. In contrast, modafinil does not improve cataplexy. (5) No new trials have been done in idiopathic hypersomnia. (6) The effects of modafinil persist for at least four months according to a double-blind placebo-controlled trial. (7) The safety profile of modafinil appears to be similar to that of non amphetamine psychostimulants. (8) There is currently no evidence of dependence leading to withdrawal symptoms after abrupt treatment cessation, or of a risk of abuse.
(1)莫达非尼是一种精神振奋剂,自1994年起在法国可用于治疗发作性睡病和特发性嗜睡症。(2)最初的临床资料不足以判断其可能的临床价值。(3)在发作性睡病方面,三项新的短期临床试验将莫达非尼与安慰剂进行了比较(近500名患者接受了莫达非尼治疗)。(4)这些试验表明,莫达非尼对日间嗜睡的影响仅为中等程度(平均每天减少一次不必要的睡眠发作),但主观上比安慰剂效果更好。在一项交叉试验中,总体上84%的患者在服用莫达非尼期间比服用安慰剂期间感觉更好。相比之下,莫达非尼并不能改善猝倒症状。(5)尚未针对特发性嗜睡症开展新的试验。(6)根据一项双盲安慰剂对照试验,莫达非尼的效果至少持续四个月。(7)莫达非尼的安全性似乎与非苯丙胺类精神振奋剂相似。(8)目前没有证据表明突然停药后会出现导致戒断症状的依赖性,也没有滥用风险。