Pharmacotherapy for excessive daytime sleepiness

被引:43
|
作者
Banerjee, D
Vitiello, MV
Grunstein, RR
机构
[1] Royal Prince Alfred Hosp, Woolcock Inst Med Res, Sleep Res Grp, Sydney, NSW 2050, Australia
[2] Univ Sydney, Sydney, NSW 2050, Australia
[3] Birmingham Heartlands Hosp, Dept Resp Med, Sleep & Ventilat Unit, Birmingham B9 5SS, W Midlands, England
[4] Univ Washington, Seattle, WA 98195 USA
关键词
excessive daytime sleepiness; psychostimulants; dexamphetamine;
D O I
10.1016/j.smrv.2004.03.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Excessive daytime sleepiness (EDS) has recognized detrimental consequences such as road traffic accidents, impaired psychological functioning and reduced work performance. EDS can result from multiple causes such as steep deprivation, steep fragmentation, neurological, psychiatric and circadian rhythm disorders. Treating the underlying cause of EDS remains the mainstay of therapy but in those who continue to be excessively sleepy, further treatment may be warranted. Traditionally, the amphetamine derivatives, methylphenidate and pemoline (collectively sympathomimetic) psychostimulants were the commonest form of therapy for EDS, particularly in conditions such as narcolepsy. More recently, the advent of modafinil has broadened the range of therapeutic options. Modafinil has a safer side-effect profile and as a result, interest in this drug for the management of EDS in other disorders, as well as narcolepsy, has increased considerably. There is a growing school of thought that modafinil may have a rote to play in other indications such as obstructive steep apnea/hypopnea syndrome already treated by nasal continuous positive airway pressure but persisting EDS, shift work steep disorders, neurological causes of sleepiness, and healthy adults performing sustained operations, particularly those in the military. However, until adequately powered randomised-controlled trials confirm tong-term efficacy and safety, the recommendation of wakefulness promoters in healthy adults cannot be justified. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:339 / 354
页数:16
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