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COVID-19 住院患者中富马酸二甲酯的随机、对照、开放标签、平台试验(RECOVERY)

Dimethyl fumarate in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.

机构信息

Pandemic Sciences Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

International Severe Acute Respiratory and Emerging Infections Consortium (ISARIC), University of Oxford, Oxford, UK.

出版信息

Nat Commun. 2024 Jan 31;15(1):924. doi: 10.1038/s41467-023-43644-x.

Abstract

Dimethyl fumarate (DMF) inhibits inflammasome-mediated inflammation and has been proposed as a treatment for patients hospitalised with COVID-19. This randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing multiple treatments in patients hospitalised for COVID-19 (NCT04381936, ISRCTN50189673). In this assessment of DMF performed at 27 UK hospitals, adults were randomly allocated (1:1) to either usual standard of care alone or usual standard of care plus DMF. The primary outcome was clinical status on day 5 measured on a seven-point ordinal scale. Secondary outcomes were time to sustained improvement in clinical status, time to discharge, day 5 peripheral blood oxygenation, day 5 C-reactive protein, and improvement in day 10 clinical status. Between 2 March 2021 and 18 November 2021, 713 patients were enroled in the DMF evaluation, of whom 356 were randomly allocated to receive usual care plus DMF, and 357 to usual care alone. 95% of patients received corticosteroids as part of routine care. There was no evidence of a beneficial effect of DMF on clinical status at day 5 (common odds ratio of unfavourable outcome 1.12; 95% CI 0.86-1.47; p = 0.40). There was no significant effect of DMF on any secondary outcome.

摘要

富马酸二甲酯(DMF)可抑制炎症小体介导的炎症,被提议用于治疗因 COVID-19 住院的患者。这项随机、对照、开放性平台试验(RECOVERY,COVID-19 治疗的随机评估)正在评估 COVID-19 住院患者的多种治疗方法(NCT04381936,ISRCTN50189673)。在这项在英国 27 家医院进行的 DMF 评估中,成年人以 1:1 的比例随机分配(随机分配)接受常规标准治疗或常规标准治疗加 DMF。主要结局是第 5 天采用 7 分序贯量表评估的临床状态。次要结局是临床状态持续改善的时间、出院时间、第 5 天外周血氧、第 5 天 C 反应蛋白以及第 10 天临床状态的改善。2021 年 3 月 2 日至 2021 年 11 月 18 日,713 名患者参加了 DMF 评估,其中 356 名患者被随机分配接受常规治疗加 DMF,357 名患者接受常规治疗。95%的患者在常规治疗中接受了皮质类固醇。DMF 对第 5 天临床状态没有明显的有益作用(不良结局的常见比值比为 1.12;95%CI 0.86-1.47;p=0.40)。DMF 对任何次要结局均无显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0025/10831058/1662ffb44dc9/41467_2023_43644_Fig1_HTML.jpg

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