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Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial

Horby, Peter W.; Emberson, Jonathan R.; Basnyat, Buddha; Campbell, Mark; Peto, Leon; Pessoa-Amorim, Guilherme; Staplin, Natalie; Hamers, Raph L.; Amuasi, John; Nel, Jeremy; Kestelyn, Evelyne; Rawal, Manisha; Kumar Jha, Roshan; Thanh Phong, Nguyen; Sumardi, Uun; Paudel, Damodar; Ngoc Thach, Pham; Nasronudin, Nasronudin; Stratton, Emma; Mew, Louise; Sarkar, Rahuldeb; Baillie, J. Kenneth; Buch, Maya H.; Day, Jeremy; Faust, Saul N.; Jaki, Thomas; Jeffery, Katie; Juszczak, Edmund; Knight, Marian; Shen Lim, Wei; Mafham, Marion; Montgomery, Alan; Mumford, Andrew; Rowan, Kathryn; Thwaites, Guy; Haynes, Richard; Landray, Martin J.; RECOVERY Collaborative Group, RECOVERY Collaborative Group

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Authors

Peter W. Horby

Jonathan R. Emberson

Buddha Basnyat

Mark Campbell

Leon Peto

Guilherme Pessoa-Amorim

Natalie Staplin

Raph L. Hamers

John Amuasi

Jeremy Nel

Evelyne Kestelyn

Manisha Rawal

Roshan Kumar Jha

Nguyen Thanh Phong

Uun Sumardi

Damodar Paudel

Pham Ngoc Thach

Nasronudin Nasronudin

Emma Stratton

Louise Mew

Rahuldeb Sarkar

J. Kenneth Baillie

Maya H. Buch

Jeremy Day

Saul N. Faust

Thomas Jaki

Katie Jeffery

Marian Knight

Wei Shen Lim

Marion Mafham

ALAN MONTGOMERY ALAN.MONTGOMERY@NOTTINGHAM.AC.UK
Director Nottingham Clinical Trials Unit

Andrew Mumford

Kathryn Rowan

Guy Thwaites

Richard Haynes

Martin J. Landray

RECOVERY Collaborative Group RECOVERY Collaborative Group



Abstract

Background: Low-dose corticosteroids have been shown to reduce mortality for patients with COVID-19 requiring oxygen or ventilatory support (non-invasive mechanical ventilation, invasive mechanical ventilation, or extracorporeal membrane oxygenation). We evaluated the use of a higher dose of corticosteroids in this patient group. Methods: This randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]) is assessing multiple possible treatments in patients hospitalised for COVID-19. Eligible and consenting adult patients with clinical evidence of hypoxia (ie, receiving oxygen or with oxygen saturation <92% on room air) were randomly allocated (1:1) to either usual care with higher dose corticosteroids (dexamethasone 20 mg once daily for 5 days followed by 10 mg dexamethasone once daily for 5 days or until discharge if sooner) or usual standard of care alone (which included dexamethasone 6 mg once daily for 10 days or until discharge if sooner). The primary outcome was 28-day mortality among all randomised participants. On May 11, 2022, the independent data monitoring committee recommended stopping recruitment of patients receiving no oxygen or simple oxygen only due to safety concerns. We report the results for these participants only. Recruitment of patients receiving ventilatory support is ongoing. The RECOVERY trial is registered with ISRCTN (50189673) and ClinicalTrials.gov (NCT04381936). Findings: Between May 25, 2021, and May 13, 2022, 1272 patients with COVID-19 and hypoxia receiving no oxygen (eight [1%]) or simple oxygen only (1264 [99%]) were randomly allocated to receive usual care plus higher dose corticosteroids (659 patients) versus usual care alone (613 patients, of whom 87% received low-dose corticosteroids during the follow-up period). Of those randomly assigned, 745 (59%) were in Asia, 512 (40%) in the UK, and 15 (1%) in Africa. 248 (19%) had diabetes and 769 (60%) were male. Overall, 123 (19%) of 659 patients allocated to higher dose corticosteroids versus 75 (12%) of 613 patients allocated to usual care died within 28 days (rate ratio 1·59 [95% CI 1·20–2·10]; p=0·0012). There was also an excess of pneumonia reported to be due to non-COVID infection (64 cases [10%] vs 37 cases [6%]; absolute difference 3·7% [95% CI 0·7–6·6]) and an increase in hyperglycaemia requiring increased insulin dose (142 [22%] vs 87 [14%]; absolute difference 7·4% [95% CI 3·2–11·5]). Interpretation: In patients hospitalised for COVID-19 with clinical hypoxia who required either no oxygen or simple oxygen only, higher dose corticosteroids significantly increased the risk of death compared with usual care, which included low-dose corticosteroids. The RECOVERY trial continues to assess the effects of higher dose corticosteroids in patients hospitalised with COVID-19 who require non-invasive ventilation, invasive mechanical ventilation, or extracorporeal membrane oxygenation. Funding: UK Research and Innovation (Medical Research Council), National Institute of Health and Care Research, and Wellcome Trust.

Citation

Horby, P. W., Emberson, J. R., Basnyat, B., Campbell, M., Peto, L., Pessoa-Amorim, G., …RECOVERY Collaborative Group, R. C. G. (2023). Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial. Lancet, 401(10387), 1499-1507. https://doi.org/10.1016/S0140-6736%2823%2900510-X

Journal Article Type Article
Acceptance Date Feb 19, 2023
Online Publication Date Apr 13, 2023
Publication Date May 6, 2023
Deposit Date Apr 18, 2023
Publicly Available Date Apr 18, 2023
Journal The Lancet
Print ISSN 0140-6736
Electronic ISSN 1474-547X
Peer Reviewed Peer Reviewed
Volume 401
Issue 10387
Pages 1499-1507
DOI https://doi.org/10.1016/S0140-6736%2823%2900510-X
Public URL https://nottingham-repository.worktribe.com/output/19749867
Publisher URL https://www.sciencedirect.com/science/article/pii/S014067362300510X
Additional Information This article is maintained by: Elsevier; Article Title: Higher dose corticosteroids in patients admitted to hospital with COVID-19 who are hypoxic but not requiring ventilatory support (RECOVERY): a randomised, controlled, open-label, platform trial; Journal Title: The Lancet; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/S0140-6736(23)00510-X; CrossRef DOI link to the associated document: https://doi.org/10.1016/S0140-6736(23)00587-1; Content Type: article; Copyright: © 2023 The Author(s). Published by Elsevier Ltd.

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