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首页|期刊导航|中国临床药理学与治疗学|促觉醒药物用于阻塞性睡眠呼吸暂停残余日间过度思睡的进展

促觉醒药物用于阻塞性睡眠呼吸暂停残余日间过度思睡的进展

欧琼 周若菡 蔡洧丹

中国临床药理学与治疗学2025,Vol.30Issue(12):1625-1631,7.
中国临床药理学与治疗学2025,Vol.30Issue(12):1625-1631,7.DOI:10.12092/j.issn.1009-2501.2025.12.005

促觉醒药物用于阻塞性睡眠呼吸暂停残余日间过度思睡的进展

Advances in wake-promoting agents for residual excessive daytime sleepiness in obstructive sleep apnea

欧琼 1周若菡 1蔡洧丹1

作者信息

  • 1. 广东省老年医学研究所,南方医科大学附属广东省人民医院(广东省医学科学院),广州 510080,广东
  • 折叠

摘要

Abstract

Obstructive sleep apnea(OSA)is a common sleep-related breathing disorder,and ex-cessive daytime sleepiness(EDS)is one of its hall-mark clinical manifestations,impairing quality of life and increasing public-safety risks such as road traf-fic accidents.A considerable proportion of patients continue to experience residual EDS despite ade-quate treatment with continuous positive airway pressure(CPAP).This review summarizes research over the past decade on wake-promoting agents for OSA-related EDS,synthesizing clinical evidence for modafinil,armodafinil,solriamfetol,and pitolisant.Across randomized controlled trials and observa-tional studies,wake-promoting agents improve sub-jective sleepiness(Epworth Sleepiness Scale,ESS)and objective wakefulness(Maintenance of Wake-fulness Test,MWT);recently approved agents agents such as solriamfetol and pitolisant demon-strate overall favorable efficacy and safety profiles compared with traditional options.Subgroup analy-ses indicate that benefits can be observed irrespec-tive of adherence to primary OSA therapy.Impor-tantly,wake-promoting agents are adjunctive,symp-tomatic treatments for EDS and do not replace CPAP or other etiologic therapies;evaluation should ex-clude alternative causes of sleepiness prior to initia-tion,and patients should continue standard OSA management throughout treatment.

关键词

阻塞性睡眠呼吸暂停/日间过度思睡/索安非托/替洛利生/促觉醒药物

Key words

obstructive sleep apnea/excessive daytime sleepiness/solriamfetol/pitolisant/wake-promoting agents

分类

医药卫生

引用本文复制引用

欧琼,周若菡,蔡洧丹..促觉醒药物用于阻塞性睡眠呼吸暂停残余日间过度思睡的进展[J].中国临床药理学与治疗学,2025,30(12):1625-1631,7.

基金项目

国家科技部科技基础资源调查专项(2022FY100803) (2022FY100803)

国家自然科学基金项目(82470083) (82470083)

中国临床药理学与治疗学

OA北大核心

1009-2501

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