Beaumont Maurice, Batéjat Denise, Piérard Christophe, Van Beers Pascal, Philippe Matthieu, Léger Damien, Savourey Gustave, Jouanin Jean-Claude
Institut de Médecine Aérospatiale du Service de Santé des Armées, Brétigny-sur-Orge, France.
Sleep. 2007 Nov;30(11):1527-33. doi: 10.1093/sleep/30.11.1527.
To assess the effects of zolpidem and zaleplon on nocturnal sleep and breathing patterns at altitude, as well as on daytime attention, fatigue, and sleepiness.
Double-blind, randomized, placebo-controlled, cross-over trial.
3 day and night alpine expedition at 3,613 m altitude.
12 healthy male trekkers.
One week spent at 1,000 m altitude (baseline control), followed by 3 periods of 3 consecutive treatment nights (N1-3) at altitude, to test 10 mg zolpidem, 10 mg zaleplon, and placebo given at 21:45.
Sleep from EEG, actigraphy and sleep logs; overnight arterial saturation in oxygen (SpO2) from infrared oximetry; daytime attention, fatigue and sleepiness from a Digit Symbol Substitution Test, questionnaires, and sleep logs; acute mountain sickness (AMS) from the Lake Louise questionnaire.
Compared to baseline control, sleep at altitude was significantly impaired in placebo subjects as shown by an increase in the amount of Wakefulness After Sleep Onset (WASO) from 17 +/- 8 to 36 +/- 13 min (P<0.05) and in arousals from 5 +/- 3 to 20 +/- 8 (P<0.01). Slow wave sleep (SWS) and stage 4 respectively decreased from 26.7% +/- 5.8% to 20.6% +/- 5.8% of total sleep time (TST) and from 18.2% +/- 5.2% to 12.4% +/- 3.1% TST (P<0.05 and P<0.001, respectively). Subjects also complained from a feeling of poor sleep quality combined with numerous 02 desaturation episodes. Subjective fatigue and AMS score were increased. Compared to placebo control, WASO decreased by approximately 6 min (P<0.05) and the sleep efficiency index increased by 2% (P<0.01) under zaleplon and zolpidem, while SWS and stage 4 respectively increased to 22.5% +/- 5.4% TST (P<0.05) and to 15.0% +/- 3.4% TST (P<0.0001) with zolpidem only; both drugs further improved sleep quality. No adverse effect on nighttime SpO2, daytime attention level, alertness, or mood was observed under either hypnotic. AMS was also found to be reduced under both medications.
Both zolpidem and zaleplon have positive effects on sleep at altitude without adversely affecting respiration, attention, alertness, or mood. Hence, they may be safely used by climbers.
评估唑吡坦和扎来普隆对高原夜间睡眠和呼吸模式的影响,以及对白天注意力、疲劳和嗜睡的影响。
双盲、随机、安慰剂对照、交叉试验。
海拔3613米的高山三日夜探险。
12名健康男性徒步旅行者。
在海拔1000米处度过一周(基线对照),随后在高原进行3个连续治疗夜的3个阶段(N1 - 3),于21:45给予10毫克唑吡坦、10毫克扎来普隆和安慰剂进行测试。
通过脑电图、活动记录仪和睡眠日志评估睡眠;通过红外血氧饱和度仪测量夜间动脉血氧饱和度(SpO2);通过数字符号替换测试、问卷和睡眠日志评估白天注意力、疲劳和嗜睡;通过路易斯湖问卷评估急性高山病(AMS)。
与基线对照相比,安慰剂组受试者在高原的睡眠明显受损,睡眠起始后觉醒时间(WASO)从17±8分钟增加到36±13分钟(P<0.05),觉醒次数从5±3次增加到20±8次(P<0.01)。慢波睡眠(SWS)和4期睡眠分别从总睡眠时间(TST)的26.7%±5.8%降至20.6%±5.8%,以及从18.2%±5.2%降至12.4%±3.1%(分别为P<0.05和P<0.001)。受试者还抱怨睡眠质量差并伴有多次氧饱和度下降发作。主观疲劳和AMS评分增加。与安慰剂对照相比,扎来普隆和唑吡坦治疗下WASO减少约6分钟(P<0.05),睡眠效率指数提高2%(P<0.01),而仅唑吡坦治疗下SWS和4期睡眠分别增加到TST的22.5%±5.4%(P<0.05)和15.0%±3.4%(P<0.0001);两种药物均进一步改善了睡眠质量。两种催眠药物对夜间SpO2、白天注意力水平、警觉性或情绪均未观察到不良影响。两种药物治疗下AMS也有所降低。
唑吡坦和扎来普隆对高原睡眠均有积极影响,且对呼吸、注意力、警觉性或情绪无不良影响。因此,登山者可安全使用。