Your browser doesn't support javascript.
loading
Azithromycin in Hospitalised Patients with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
Peter W Horby; Alistair Roddick; Enti Spata; Natalie Staplin; Jonathan R Emberson; Guilherme Pessoa-Amorim; Leon Peto; Mark Campbell; Christopher Brightling; Ben Prudon; David Chadwick; Andrew Ustianowski; Abdul Ashish; Stacy Todd; Bryan Yates; Robert Buttery; Stephen Scott; Diego Maseda; J Kenneth Baillie; Maya H Buch; Lucy C Chappell; Jeremy N Day; Saul N Faust; Thomas Jaki; Katie Jeffery; Edmund Juszczak; Wei Shen Lim; Alan Montgomery; Andrew Mumford; Kathryn Rowan; Guy Thwaites; Marion Mafham; Richard Haynes; Martin J Landray.
Afiliação
  • Peter W Horby; Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
  • Alistair Roddick; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Enti Spata; MRC Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Natalie Staplin; MRC Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Jonathan R Emberson; MRC Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Guilherme Pessoa-Amorim; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Leon Peto; Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
  • Mark Campbell; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Christopher Brightling; Institute for Lung Health, Leicester NIHR Biomedical Research Centre, University of Leicester, Leicester, United Kingdom
  • Ben Prudon; Department of Respiratory Medicine, North Tees & Hartlepool NHS Foundation Trust, Stockton-on-Tees, United Kingdom
  • David Chadwick; Centre for Clinical Infection, James Cook University Hospital, Middlesbrough, United Kingdom
  • Andrew Ustianowski; North Manchester General Hospital & University of Manchester, Manchester, United Kingdom
  • Abdul Ashish; Wrightington Wigan and Leigh NHS Foundation Trust, Wigan, United Kingdom
  • Stacy Todd; Liverpool University Hospitals NHS Foundation Trust, Liverpool, United Kingdom
  • Bryan Yates; Northumbria Healthcare NHS Foundation Trust, North Tyneside, United Kingdom
  • Robert Buttery; North West Anglia NHS Foundation Trust, Peterborough, United Kingdom
  • Stephen Scott; The Countess of Chester Hospital NHS Foundation Trust, Chester, United Kingdom
  • Diego Maseda; Mid Cheshire Hospitals NHS Foundation Trust, Crewe, United Kingdom
  • J Kenneth Baillie; Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom
  • Maya H Buch; Centre for Musculoskeletal Research, University of Manchester, Manchester, United Kingdom
  • Lucy C Chappell; School of Life Sciences, King's College London, London, United Kingdom
  • Jeremy N Day; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam, and Nuffield Department of Medicine, University of Oxford, United Kingdom
  • Saul N Faust; NIHR Southampton Clinical Research Facility and Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust and University of Southampton,
  • Thomas Jaki; Department of Mathematics and Statistics, Lancaster University, Lancaster, United Kingdom; MRC Biostatistics Unit, University of Cambridge, Cambridge, United Ki
  • Katie Jeffery; Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom
  • Edmund Juszczak; School of Medicine, University of Nottingham, Nottingham, United Kingdom
  • Wei Shen Lim; Respiratory Medicine Department, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom
  • Alan Montgomery; School of Medicine, University of Nottingham, Nottingham, United Kingdom
  • Andrew Mumford; School of Cellular and Molecular Medicine, University of Bristol, Bristol, United kingdom
  • Kathryn Rowan; Intensive Care National Audit & Research Centre, London, United Kingdom
  • Guy Thwaites; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam, and Nuffield Department of Medicine, University of Oxford, United Kingdom
  • Marion Mafham; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Richard Haynes; MRC Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Martin J Landray; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-20245944
ABSTRACT
BackgroundAzithromycin has been proposed as a treatment for COVID-19 on the basis of its immunomodulatory actions. We evaluated the efficacy and safety of azithromycin in hospitalised patients with COVID-19. MethodsIn this randomised, controlled, open-label, adaptive platform trial, several possible treatments were compared with usual care in patients hospitalised with COVID-19 in the UK. Eligible and consenting patients were randomly allocated to either usual standard of care alone or usual standard of care plus azithromycin 500 mg once daily by mouth or intravenously for 10 days or until discharge (or one of the other treatment arms). Patients were twice as likely to be randomised to usual care as to any of the active treatment groups. The primary outcome was 28-day mortality. The trial is registered with ISRCTN (50189673) and clinicaltrials.gov (NCT04381936). FindingsBetween 7 April and 27 November 2020, 2582 patients were randomly allocated to receive azithromycin and 5182 patients to receive usual care alone. Overall, 496 (19%) patients allocated to azithromycin and 997 (19%) patients allocated to usual care died within 28 days (rate ratio 1{middle dot}00; 95% confidence interval [CI] 0{middle dot}90-1{middle dot}12; p=0{middle dot}99). Consistent results were seen in all pre-specified subgroups of patients. There was no difference in duration of hospitalisation (median 12 days vs. 13 days) or the proportion of patients discharged from hospital alive within 28 days (60% vs. 59%; rate ratio 1{middle dot}03; 95% CI 0{middle dot}97-1{middle dot}10; p=0{middle dot}29). Among those not on invasive mechanical ventilation at baseline, there was no difference in the proportion meeting the composite endpoint of invasive mechanical ventilation or death (21% vs. 22%; risk ratio 0{middle dot}97; 95% CI 0{middle dot}89-1{middle dot}07; p=0{middle dot}54). InterpretationIn patients hospitalised with COVID-19, azithromycin did not provide any clinical benefit. Azithromycin use in patients hospitalised with COVID-19 should be restricted to patients where there is a clear antimicrobial indication. FundingUK Research and Innovation (Medical Research Council) and National Institute of Health Research (Grant ref MC_PC_19056).
Licença
cc_by
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2020 Tipo de documento: Preprint