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评估阻塞性睡眠呼吸暂停中过度日间嗜睡的药物治疗:全面的网络荟萃分析和系统评价。

Evaluating pharmacological treatments for excessive daytime sleepiness in obstructive sleep apnea: A comprehensive network meta-analysis and systematic review.

机构信息

Department of Epidemiology and Statistics, University of California, San Francisco, CA, USA; Division of Pulmonary, Allergy and Sleep Medicine, Mayo Clinic Jacksonville, Florida, USA.

School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Sleep Med Rev. 2024 Aug;76:101934. doi: 10.1016/j.smrv.2024.101934. Epub 2024 Apr 30.

Abstract

Obstructive sleep apnea (OSA) is associated with excessive daytime sleepiness (EDS). Pharmacotherapy offers a potential treatment approach for EDS in OSA patients. This systematic review and meta-analysis aimed to assess the efficacy and safety of pharmacological interventions for alleviating EDS in patients with OSA. Following PRISMA guidelines, we included randomized controlled trials investigating pharmacological treatments for EDS in adult OSA until August 2023. We conducted meta-analysis, subgroup, and meta-regression analyses using a random effects model. Finally, a network meta-analysis synthesized direct and indirect evidence, followed by a comprehensive safety analysis. We included 32 articles in the meta-analysis (n = 3357). Pharmacotherapy showed a significant improvement in the Epworth Sleepiness Scale (ESS) score (Mean Difference (MD) -2.73, (95 % Confidence Interval (CI) [-3.25, -2.20], p < 0.01) and Maintenance of Wakefulness Test (MWT) score (MD 6.00 (95 % CI [2.66, 9.33] p < 0.01). Solriamfetol, followed by Pitolisant and modafinil, exhibited the greatest ESS reduction, while Danavorexton, followed by Solriamfetol and MK-7288, had the strongest impact on MWT. MK-7288 had the most total adverse events (AEs), followed by Danavorexton and armodafinil. Pharmacological Interventions significantly alleviate EDS in OSA patients but with heterogeneity across medications. Treatment decisions should involve a personalized assessment of patient factors and desired outcomes.

摘要

阻塞性睡眠呼吸暂停(OSA)与日间嗜睡(EDS)有关。药物治疗为 OSA 患者的 EDS 提供了一种潜在的治疗方法。本系统评价和荟萃分析旨在评估药物干预缓解 OSA 患者 EDS 的疗效和安全性。根据 PRISMA 指南,我们纳入了截至 2023 年 8 月,研究药物治疗成人 OSA 患者 EDS 的随机对照试验。我们使用随机效应模型进行荟萃分析、亚组和荟萃回归分析。最后,进行网络荟萃分析综合直接和间接证据,并进行全面的安全性分析。我们纳入了荟萃分析中的 32 篇文章(n=3357)。药物治疗在 Epworth 睡眠量表(ESS)评分(平均差值(MD)-2.73,(95%置信区间(CI)[-3.25,-2.20],p<0.01)和觉醒维持测试(MWT)评分(MD 6.00(95%CI [2.66,9.33],p<0.01)方面均有显著改善。索里昂啡特、随后是吡咯烷酮和莫达非尼表现出最大的 ESS 降低,而丹那瑞克斯、随后是索里昂啡特和 MK-7288 对 MWT 影响最大。MK-7288 发生的总不良事件(AE)最多,其次是丹那瑞克斯和阿莫达非尼。药物干预可显著缓解 OSA 患者的 EDS,但不同药物之间存在异质性。治疗决策应涉及对患者因素和预期结果的个性化评估。

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