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从苏沃雷生转换为雷美尔通药物治疗睡眠障碍的疗效。

Effectiveness of change from suvorexant to lemborexant drug in the treatment of sleep disorders.

机构信息

Mental Care Center, Showa University Northern Yokohama Hospital, Yokohama-shi, Japan.

Department of Neuropsychiatry, Showa University School of Medicine, Shinagawa-ku, Japan.

出版信息

Psychogeriatrics. 2022 Sep;22(5):595-604. doi: 10.1111/psyg.12858. Epub 2022 Jun 10.

Abstract

BACKGROUND

This study aimed to examine the effects of a change in medication from suvorexant to lemborexant among patients with insomnia.

METHODS

Patients with chronic insomnia who had persistent insomnia for 3 months or longer and who had been taking suvorexant for 3 months or longer were selected. The participants were divided into two groups: the 'modified' group and the 'non-modified' group. Four sub-types of insomnia (i.e., difficulty initiating sleep, difficulty maintaining sleep, early-morning awakening, and non-restorative sleep) were investigated. Logistic regression was used to investigate improvements in both the groups after 12 weeks.

RESULTS

Among the 77 participants, 43 and 34 patients were in the modified drug group and the non-modified drug group, respectively. Comparing sleep disorders between the two groups, we found significant improvement after 12 weeks in the modified drug group in terms of difficulty initiating sleep, compared with the non-modified drug group (odds ratio = 0.036, P = 0.008, 95% CI = 0.003-0.415). However, no significant differences were found between the two groups in terms of difficulty maintaining sleep, early-morning awakening, and non-restorative sleep.

CONCLUSIONS

Sleep disorders can be treated by alleviating difficulties in initiating sleep by changing from suvorexant to lemborexant. In addition, it was confirmed that the drug change caused no serious side effects and that it was highly safe and tolerated.

摘要

背景

本研究旨在考察失眠患者将药物从苏沃雷生改为雷美替胺的效果。

方法

选择患有慢性失眠症且持续失眠 3 个月或以上且服用苏沃雷生 3 个月或以上的患者。将参与者分为两组:“改良”组和“非改良”组。研究了四种失眠亚型(即入睡困难、睡眠维持困难、早醒和睡眠质量差)。使用逻辑回归分析了两组在 12 周后的改善情况。

结果

在 77 名参与者中,有 43 名和 34 名患者分别在改良药物组和非改良药物组。比较两组之间的睡眠障碍,我们发现改良药物组在入睡困难方面在 12 周后有显著改善,与非改良药物组相比(比值比=0.036,P=0.008,95%置信区间=0.003-0.415)。然而,两组在睡眠维持困难、早醒和睡眠质量差方面无显著差异。

结论

通过从苏沃雷生改为雷美替胺来缓解入睡困难,可以治疗睡眠障碍。此外,还证实了药物的改变没有引起严重的副作用,而且具有很高的安全性和耐受性。

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