Department of Neuropsychiatry, Fukushima Medical University School of Medicine, Fukushima, Japan.
Department of Neuropsychiatry, Horikoshi Psychosomatic Clinic, Fukushima, Japan.
J Clin Sleep Med. 2023 Oct 1;19(10):1753-1758. doi: 10.5664/jcsm.10668.
We conducted a retrospective study to investigate the efficacy and safety of switching from other hypnotics, including benzodiazepines and Z-drugs, suvorexant, ramelteon, mirtazapine, trazodone, and antipsychotics, to lemborexant, a dual orexin receptor antagonist, for 3 months.
Clinical data obtained from the medical records of 61 patients treated at the Horikoshi Psychosomatic Clinic between December 2020 and February 2022 were analyzed, including the Athens Insomnia Scale, Epworth Sleepiness Scale, and Perceived Deficits Questionnaire-5. The primary outcome was the mean change in Athens Insomnia Scale score after 3 months. Secondary outcomes were the mean changes in the Epworth Sleepiness Scale and Perceived Deficits Questionnaire-5 scores over 3 months. We also compared pre- and post-diazepam equivalents.
The mean Athens Insomnia Scale score decreased over 3 months after switching to lemborexant (1 mo: -2.98 ± 5.19, < .001; 2 mo: -3.20 ± 5.64, < .001; 3 mo: -3.38 ± 5.61, < .001). Mean Epworth Sleepiness Scale score did not change from baseline to 1 month (-0.49 ± 3.41, = 0.27), 2 months (0.082 ± 4.62, = .89), or 3 months (-0.64 ± 4.80, = .30). Mean Perceived Deficits Questionnaire-5 score did improve from baseline to 1 month (-1.17 ± 2.47, = .004), 2 months (-1.05 ± 2.97, = .029), and 3 months (-1.24 ± 3.06, = .013). There was also a reduction in the total diazepam equivalent (baseline vs 3 mo: 14.0 ± 20.2 vs 11.3 ± 20.6, < .001).
Our study showed that, by switching to lemborexant from other hypnotics, the risks associated with benzodiazepines and Z-drugs may be reduced.
Horikoshi S, Miura I, Suzuki Y, et al. Switching to lemborexant for the management of insomnia in mental disorders: the SLIM study. . 2023;19(10):1753-1758.
我们进行了一项回顾性研究,以调查将其他催眠药物(包括苯二氮䓬类药物和 Z 药物、苏沃雷生、雷美尔酮、米氮平、曲唑酮和抗精神病药)转换为双通道食欲素受体拮抗剂仑贝格佐替用于治疗 3 个月的疗效和安全性。
分析了 2020 年 12 月至 2022 年 2 月在堀越心身诊所接受治疗的 61 例患者的病历中的临床数据,包括雅典失眠量表、爱泼沃斯嗜睡量表和感知缺陷问卷-5。主要结局是 3 个月后雅典失眠量表评分的平均变化。次要结局是爱泼沃斯嗜睡量表和感知缺陷问卷-5 评分在 3 个月内的平均变化。我们还比较了治疗前后的地西泮等效剂量。
与转换为仑贝格佐替前相比,在使用仑贝格佐替后 3 个月内,雅典失眠量表评分降低(1 个月:-2.98±5.19, <.001;2 个月:-3.20±5.64, <.001;3 个月:-3.38±5.61, <.001)。爱泼沃斯嗜睡量表评分从基线到 1 个月(-0.49±3.41, = 0.27)、2 个月(0.082±4.62, = 0.89)或 3 个月(-0.64±4.80, = 0.30)均未发生变化。感知缺陷问卷-5 评分从基线到 1 个月(-1.17±2.47, = 0.004)、2 个月(-1.05±2.97, = 0.029)和 3 个月(-1.24±3.06, = 0.013)有所改善。总地西泮等效剂量也有所降低(基线与 3 个月时:14.0±20.2 与 11.3±20.6, <.001)。
我们的研究表明,通过从其他催眠药物转换为仑贝格佐替,可以降低与苯二氮䓬类药物和 Z 药物相关的风险。
堀越 S,三浦 I,铃木 Y,等。为治疗精神障碍的失眠而切换至仑贝格佐替:SLIM 研究。. 2023;19(10):1753-1758.