老年失眠症患者氯甲安定的睡眠实验室研究。

G W Vogel
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引用次数: 6

摘要

洛美他泮是一种新型苯二氮卓类催眠药。先前的研究表明,氯美西泮的消除半衰期为中至短,即在5-15小时的范围内。因此,在老年患者中,该药应该是安全的,并且在剂量等于或小于年轻人推荐剂量时具有催眠作用。本研究验证了这一假设。我们研究了10名55岁及以上的健康受试者,有主观和客观失眠症。主观性失眠症是指每晚至少需要45分钟才能入睡,睡眠时间少于6.5小时。每种抱怨至少在50%的夜晚出现,持续至少三个月。目的:用多导睡眠描记仪测量失眠症,在安慰剂基线连续4晚的最后3晚中至少有2晚出现失眠症。该研究采用双盲方式进行治疗。每个受试者在睡眠实验室里连续研究了14个晚上。该药物连续七个晚上服用,在此之前是安慰剂基线,随后是安慰剂期的药物停药。在每个实验夜,受试者通过连续的、通宵的常规EEG/EOG/EMG记录进行监测。每个实验室早晨的受试者都要完成一份调查问卷,对他们前一晚的六个睡眠特征进行评分。在研究开始时和研究结束时,每个受试者都由委员会内科医生进行身体检查和临床实验室检查。每个实验室早晚受试者进行筛查体检,并填写11项催眠药物副作用问卷和56项医疗系统评价问卷。与中位基线夜相比,中位用药夜lormetazepam 0.5 mg显著增加总睡眠时间约25分钟。药物对睡眠潜伏期的减少是显著的。此外,0.5 mg氯甲氧基安定可显著降低苏醒次数。没有客观证据表明对0.5 mg氯美西泮的催眠效果产生耐受性或反弹性失眠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep laboratory study of lormetazepam in older insomniacs.

Lormetazepam is a new benzodiazepine hypnotic. Previous work has indicated that lormetazepam has an intermediate to short elimination half-life, i.e. in the range of 5-15 h. Hence, in older patients, the drug should be safe and hypnotically active in doses equal to or less than the doses recommended for young adults. The present study tested this hypothesis. We studied ten healthy subjects, aged 55 and older, with both subjective and objective insomnia. Subjective insomnia was the complaint of requiring at least 45 min to fall asleep and sleeping less than six and a half hours per night. Each complaint was present on at least 50% of the nights for at least three months. Objective insomnia was measured polysomnographically and was present on at least two of the last three nights of four consecutive nights of placebo baseline. The study involved a design in which treatment was administered in a double-blind fashion. Each subject was studied for 14 consecutive nights in the sleep laboratory. The drug was administered for seven consecutive nights which were preceded by a placebo baseline and followed by a placebo period of drug withdrawal. On each laboratory night subjects were monitored by continuous, all-night conventional EEG/EOG/EMG recordings. Each laboratory morning subjects completed a questionnaire on which they rated six characteristics of their sleep on the previous night. At study entry and again at study end, each subject had a physical examination by a Board internist and clinical laboratory tests. Each laboratory morning and evening subjects had a screening physical exam and completed an 11-item hypnotic drug side-effect questionnaire and a 56-item review of medical systems questionnaire. Compared with the median baseline night, on the median drug night lormetazepam 0.5 mg significantly increased total sleep time by about 25 min. The drug's reductions of sleep latency were substantial. In addition, lormetazepam 0.5 mg significantly decreased number of awakenings. No objective evidence was found of either tolerance developing to the hypnotic efficacy of lormetazepam 0.5 mg or of rebound insomnia.

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