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开具短效催眠镇静剂。从安全角度出发的当前建议。

Prescribing short-acting hypnosedatives. Current recommendations from a safety perspective.

作者信息

Wheatley D

机构信息

Department of Psychological Medicine, Royal Masonic Hospital, London, England.

出版信息

Drug Saf. 1992 Mar-Apr;7(2):106-15. doi: 10.2165/00002018-199207020-00003.

Abstract

The duration of action of hypnosedative drugs is mainly determined by their pharmacokinetic properties. The ideal drug should induce sleep within 30 min and maintain a normal pattern of sleep for 6 to 8h, with little or no residual effects the next morning. Clinically, 4 types of insomnia can be distinguished: prolonged latency, 1 to 2 long periods of wakefulness, frequent short awakenings and early morning awakening. An ultra-short-acting drug (2 to 3h), such as triazolam, is useful for prolonged latency. Temazepam, lormetazepam and loprazolam provide more prolonged effects (8 to 10h). These benzodiazepines are not free of daytime adverse effects, particularly drowsiness, dependency potential, rebound insomnia and habituation to the drug effect. Zopiclone and zolpidem are new nonbenzodiazepine hypnotics that are as effective as benzodiazepines but without the problems associated with the latter. They produce a more normal electroencephalogram sleep pattern and so would seem to approach to the ideal hypnosedative for the future. However only further clinical trials and widespread use in practice will determine whether they will live up to this potential.

摘要

催眠镇静药物的作用持续时间主要由其药代动力学特性决定。理想的药物应在30分钟内诱导入睡,并维持6至8小时的正常睡眠模式,次日早晨几乎没有或没有残留效应。临床上,可区分出4种失眠类型:入睡潜伏期延长、1至2次长时间觉醒、频繁短暂觉醒和早醒。超短效药物(2至3小时),如三唑仑,对入睡潜伏期延长有效。替马西泮、氯甲西泮和氯普唑仑的作用持续时间更长(8至10小时)。这些苯二氮䓬类药物并非没有日间不良反应,尤其是嗜睡、潜在依赖性、反弹性失眠和对药物效应的耐受性。佐匹克隆和唑吡坦是新型非苯二氮䓬类催眠药,其效果与苯二氮䓬类药物相同,但没有后者相关的问题。它们产生更正常的脑电图睡眠模式,因此似乎是未来理想的催眠镇静药物。然而,只有进一步的临床试验和在实践中的广泛应用才能确定它们是否能发挥这种潜力。

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