Matsumura Takuma, Terada Jiro, Yoshimura Chikara, Koshikawa Ken, Kinoshita Taku, Yahaba Misuzu, Nagashima Kengo, Sakao Seiichiro, Tatsumi Koichiro
Department of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan,
Department of Respiratory and Sleep Medicine, Fukuoka University School of Medicine, Fukuoka, Japan.
Drug Des Devel Ther. 2019 Feb 28;13:809-816. doi: 10.2147/DDDT.S197237. eCollection 2019.
Although patients with suspected obstructive sleep apnea (OSA) might suffer difficulty in falling asleep during overnight polysomnography (PSG), standard hypnotics to obtain sleep during PSG have not been established. The aim of this study was to investigate the safety and efficacy of a new hypnotic agent, suvorexant, a dual orexin receptor antagonist, for insomnia in suspected OSA patients during in-laboratory PSG.
An observational study was conducted during PSG for 149 patients with suspected OSA who had no insomnia at home. Patients with difficulty in falling asleep during PSG were optionally permitted to take single-use suvorexant. Patients with residual severe insomnia (>1 hour) after taking suvorexant were permitted to take an add-on use zolpidem. Clinical data and sleep questionnaire results were analyzed between a no insomnia group (without hypnotics) and an insomnia group (treated with suvorexant).
Among 84 patients who experienced insomnia during PSG and required hypnotics (the insomnia group; treated with suvorexant), 44 (52.4%) achieved sufficient subjective sleep with single-use of suvorexant, while the other 40 (47.6%) required suvorexant plus zolpidem. An apnea hypopnea index (AHI) of ≥5 was observed in 144 out of 149 patients with predominantly obstructive respiratory events. Among those patients, 70.8% in the no insomnia group and 63.1% in the insomnia group had severe OSA. Regarding both subjective sleep time and morning mood, significant differences between the no insomnia group and the insomnia group were not observed. No patient taking suvorexant had an adverse event, such as delirium or falling.
Single-use suvorexant seems to be a safe and effective (but mild) hypnotic agent for suspected OSA patients with insomnia during in-laboratory PSG.
尽管疑似阻塞性睡眠呼吸暂停(OSA)的患者在夜间多导睡眠图(PSG)检查期间可能难以入睡,但尚未确立用于PSG检查期间助眠的标准催眠药物。本研究的目的是调查一种新型催眠药物——双食欲素受体拮抗剂苏沃雷生,用于实验室PSG检查期间疑似OSA患者失眠治疗的安全性和有效性。
对149例在家中无失眠症状的疑似OSA患者进行PSG检查期间的观察性研究。PSG检查期间难以入睡的患者可选择服用单次剂量的苏沃雷生。服用苏沃雷生后仍有严重失眠(>1小时)的患者可加用唑吡坦。对无失眠组(未使用催眠药物)和失眠组(使用苏沃雷生治疗)的临床数据和睡眠问卷结果进行分析。
在PSG检查期间出现失眠且需要催眠药物的84例患者(失眠组;使用苏沃雷生治疗)中,44例(52.4%)单次服用苏沃雷生后获得了足够的主观睡眠,而另外40例(47.6%)需要苏沃雷生加唑吡坦。149例主要为阻塞性呼吸事件的患者中,144例观察到呼吸暂停低通气指数(AHI)≥5。在这些患者中,无失眠组70.8%、失眠组63.1%患有重度OSA。在主观睡眠时间和早晨情绪方面,未观察到无失眠组和失眠组之间存在显著差异。服用苏沃雷生的患者均未出现谵妄或跌倒等不良事件。
对于实验室PSG检查期间患有失眠的疑似OSA患者,单次使用苏沃雷生似乎是一种安全有效的(但作用较弱的)催眠药物。