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精神分裂症患者日间睡眠倾向(通过多次睡眠潜伏期试验评估)随氯氮平及奥氮平增加而增加。

Sleep propensity at daytime as assessed by Multiple Sleep Latency Tests (MSLT) in patients with schizophrenia increases with clozapine and olanzapine.

机构信息

Department of Psychiatry and Psychotherapy, University of Leipzig, Leipzig, Germany.

出版信息

Schizophr Res. 2012 Mar;135(1-3):123-7. doi: 10.1016/j.schres.2011.12.017. Epub 2012 Jan 16.

Abstract

Sleep propensity at daytime has not been investigated in untreated patients with schizophrenia. Furthermore, while the antipsychotics clozapine and olanzapine are considered to frequently cause 'sleepiness' or 'sedation', this has not been objectified yet. Therefore, 30 patients with schizophrenia were included in this randomized, double-blind study. Sleep propensity was assessed before and after 2, 4 and 6 weeks of treatment with either clozapine or olanzapine using a Multiple Sleep Latency Test (MSLT); in the MSLT, sleep latencies of 5 nap opportunities of 20 min during daytime are averaged. In addition, the number of sleep onsets was recorded. Mean sleep latency in untreated schizophrenic patients was 16.2 ± 0.8 min at baseline. Both antipsychotics induced an increase of sleep propensity as indicated by a shortened sleep latency and more sleep onsets during the treatment period as compared to baseline. These effects were strongest in the morning. Four patients receiving clozapine and 3 patients receiving olanzapine reported subjective sleepiness, in all but one commencing in the first treatment week and persisting until study end. While the mean sleep latency during treatment was significantly shorter in these patients (12.3 ± 0.8 min) than in those without subjective sleepiness (14.9 ± 0.7 min), a short sleep latency was not necessarily associated with subjective sleepiness. In conclusion, mean sleep latency was >36% longer (i.e. sleep propensity was lower) in untreated patients with schizophrenia than in healthy subjects previously consistently reported. Furthermore, clozapine and olanzapine increased sleep propensity in schizophrenic patients. A minority of patients reported subjective sleepiness.

摘要

未治疗的精神分裂症患者的日间睡眠倾向尚未得到研究。此外,虽然抗精神病药氯氮平和奥氮平被认为经常引起“嗜睡”或“镇静”,但这尚未得到客观证实。因此,这项随机、双盲研究纳入了 30 名精神分裂症患者。使用多睡眠潜伏期测试(MSLT)在接受氯氮平或奥氮平治疗 2、4 和 6 周前后评估睡眠倾向;在 MSLT 中,日间 5 次 20 分钟小睡的睡眠潜伏期平均。此外,还记录了睡眠发作的次数。未经治疗的精神分裂症患者的平均基础睡眠潜伏期为 16.2 ± 0.8 分钟。与基线相比,两种抗精神病药在治疗期间均导致睡眠倾向增加,表现为睡眠潜伏期缩短和更多的睡眠发作。这些影响在早晨最强。4 名接受氯氮平治疗的患者和 3 名接受奥氮平治疗的患者报告出现主观嗜睡,除 1 例外,均在第 1 周开始治疗并持续到研究结束。虽然这些患者(12.3 ± 0.8 分钟)在治疗期间的平均睡眠潜伏期明显短于无主观嗜睡的患者(14.9 ± 0.7 分钟),但短的睡眠潜伏期不一定与主观嗜睡相关。总之,未经治疗的精神分裂症患者的平均睡眠潜伏期比以前一致报道的健康受试者长 >36%(即睡眠倾向较低)。此外,氯氮平和奥氮平增加了精神分裂症患者的睡眠倾向。少数患者报告出现主观嗜睡。

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