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

机译:通过多次睡眠潜伏期测试(MSLT)评估的精神分裂症患者白天的睡眠倾向会随着氯氮平和奥氮平的增加而增加

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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.
机译:未经治疗的精神分裂症患者白天的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”,但这尚未得到客观化。因此,这项随机,双盲研究纳入了30位精神分裂症患者。使用多重睡眠潜伏期试验(MSLT)评估氯氮平或奥氮平治疗前后2、4和6周的睡眠倾向。在MSLT中,平均白天有5次小睡机会,即20分钟的睡眠潜伏期。另外,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睡眠潜伏期为16.2。 ±。 0.8。基线时的分钟。与基线相比,两种抗精神病药均可引起睡眠倾向的增加,如治疗期间睡眠潜伏期缩短和更多的睡眠发作所表明的。这些影响在早晨最强。四名接受氯氮平治疗的患者和三名接受奥氮平治疗的患者报告主观嗜睡,除一名患者外,其余患者均在治疗的第一周开始,并一直持续到研究结束。尽管这些患者在治疗期间的平均睡眠潜伏期(12.3。±。0.8。min)明显比没有主观嗜睡的患者(14.9。±。0.7。min)短,但短暂的睡眠潜伏不一定与主观嗜睡有关。总之,平均睡眠潜伏期>。未经治疗的精神分裂症患者比以前一致报告的健康受试者长36%(即睡眠倾向较低)。此外,氯氮平和奥氮平可增加精神分裂症患者的睡眠倾向。少数患者报告有主观嗜睡。

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