Dolly F R, Block A J
Am J Med. 1982 Aug;73(2):239-43. doi: 10.1016/0002-9343(82)90185-1.
We assessed the effect of 30 mg of oral flurazepam on sleep-disordered breathing and nocturnal oxygen desaturation by performing a double-blind, placebo-controlled, randomized study. Asymptomatic subjects, 17 men and three women (mean age 49 years, mean weight 79 kg), were monitored for two consecutive nights. Flurazepam was given to 10 subjects on night 1 and to 10 subjects on night 2. Placebo was ingested on the other nights. Polysomnographic determinations included chest wall movement by impedance pneumography, nasal and oral airflow by thermistor probes, and continuous oxygen saturation by ear oximetry. Flurazepam was associated with significant increases in the number of sleep events (p = 0.01), episodes of apnea (p less than 0.01), and total duration of apnea (p less than 0.01). The number of episodes of hypopnea of desaturation did not significantly increase, although the degree of desaturation increased after flurazepam ingestion (p = 0.04). Total sleep time significantly increased (p = 0.04), but could not account for the increased number of events. Sleep stage distribution was minimally altered by ingestion of flurazepam.
我们通过进行一项双盲、安慰剂对照、随机研究,评估了30毫克口服氟西泮对睡眠呼吸紊乱和夜间氧饱和度下降的影响。对17名男性和3名女性(平均年龄49岁,平均体重79千克)无症状受试者连续两晚进行监测。在第一晚给10名受试者服用氟西泮,在第二晚给另外10名受试者服用。在其他晚上服用安慰剂。多导睡眠图测定包括通过阻抗式肺量计测量胸壁运动、通过热敏电阻探头测量鼻和口腔气流以及通过耳部血氧饱和度仪测量连续氧饱和度。氟西泮与睡眠事件数量显著增加(p = 0.01)、呼吸暂停发作次数(p < 0.01)以及呼吸暂停总时长(p < 0.01)相关。尽管服用氟西泮后氧饱和度下降程度增加(p = 0.04),但低氧血症发作次数并未显著增加。总睡眠时间显著增加(p = 0.04),但无法解释事件数量的增加。服用氟西泮对睡眠阶段分布的改变极小。