Fleming J A, Bourgouin J, Hamilton P
Sleep Disorders Clinic, Shaughnessy Hospital, Vancouver, B.C.
Can J Psychiatry. 1988 Mar;33(2):103-7. doi: 10.1177/070674378803300206.
Six patients between the ages of 25 and 59, with chronic, primary insomnia received the new, non-benzodiazepine, hypnotic zopiclone continuously for 17 weeks after a drug free interval of 12 nights. To qualify for the study, sleep efficiency, determined by a sleep study on two, consecutive, placebo-controlled nights, had to be less than 75%. Patients evaluated their sleep by questionnaire and had sleep studies completed throughout active treatment. Zopiclone (7.5 mg) increased sleep efficiency by decreasing sleep latency, wakefulness after sleep onset and increasing total sleep time. Sleep architecture was minimally affected by zopiclone treatment; no significant changes in delta or REM sleep were observed. The commonest side effect was a bitter or metallic taste. No significant changes in biological functioning were noted throughout the study period. These findings indicate that zopiclone is a safe and effective hypnotic medication which maintains its effectiveness with protracted use.
6名年龄在25至59岁之间的慢性原发性失眠患者,在经历12个无药夜晚的间隔期后,连续17周服用新型非苯二氮䓬类催眠药佐匹克隆。为符合该研究条件,通过连续两个安慰剂对照夜晚的睡眠研究确定的睡眠效率必须低于75%。患者通过问卷评估其睡眠情况,并在整个积极治疗期间完成睡眠研究。佐匹克隆(7.5毫克)通过减少入睡潜伏期、睡眠开始后的清醒时间并增加总睡眠时间来提高睡眠效率。佐匹克隆治疗对睡眠结构的影响极小;未观察到δ波睡眠或快速眼动睡眠有显著变化。最常见的副作用是口苦或金属味。在整个研究期间,未发现生物功能有显著变化。这些发现表明,佐匹克隆是一种安全有效的催眠药物,长期使用仍能保持其有效性。