COVID-19 infection, admission and death and the impact of corticosteroids among people with rare autoimmune rheumatic disease during the second wave of COVID-19 in England: results from the RECORDER Project.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
01 12 2023
Historique:
received: 30 01 2023
accepted: 20 03 2023
medline: 4 12 2023
pubmed: 6 4 2023
entrez: 5 4 2023
Statut: ppublish

Résumé

To calculate the rates of COVID-19 infection and COVID-19-related death among people with rare autoimmune rheumatic diseases (RAIRD) during the second wave of the COVID-19 pandemic in England, and describe the impact of corticosteroids on outcomes. Hospital Episode Statistics data were used to identify people alive on 1 August 2020 with ICD-10 codes for RAIRD from the whole population of England. Linked national health records were used to calculate rates and rate ratios of COVID-19 infection and death up to 30 April 2021. Primary definition of COVID-19-related death was mention of COVID-19 on the death certificate. NHS Digital and Office for National Statistics general population data were used for comparison. The association between 30-day corticosteroid usage and COVID-19-related death, COVID-19-related hospital admissions and all-cause deaths was also described. Of 168 330 people with RAIRD, 9961 (5.92%) had a positive COVID-19 PCR test. The age-standardized infection rate ratio between RAIRD and the general population was 0.99 (95% CI: 0.97, 1.00). 1342 (0.80%) people with RAIRD died with COVID-19 on their death certificate and the age-sex-standardized mortality rate for COVID-19-related death was 2.76 (95% CI: 2.63, 2.89) times higher than in the general population. There was a dose-dependent relationship between 30-day corticosteroid usage and COVID-19-related death. There was no increase in deaths due to other causes. During the second wave of COVID-19 in England, people with RAIRD had the same risk of COVID-19 infection but a 2.76-fold increased risk of COVID-19-related death compared with the general population, with corticosteroids associated with increased risk.

Identifiants

pubmed: 37018139
pii: 7108765
doi: 10.1093/rheumatology/kead150
pmc: PMC10691923
doi:

Substances chimiques

Adrenal Cortex Hormones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3828-3837

Subventions

Organisme : Versus Arthritis Clinical Research
ID : 22727
Organisme : NIHR
ID : NIHR300863
Organisme : Lupus UK
Organisme : Scleroderma and Raynaud's UK

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

Megan Rutter (M)

Department of Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, UK.
Department of Rheumatology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.

Peter C Lanyon (PC)

Department of Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, UK.
Department of Rheumatology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.
National Institute for Health Research (NIHR), Nottingham Biomedical Research Centre, Nottingham, UK.

Matthew J Grainge (MJ)

Department of Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, UK.

Richard Hubbard (R)

Department of Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, UK.
National Institute for Health Research (NIHR), Nottingham Biomedical Research Centre, Nottingham, UK.

Mary Bythell (M)

National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.

Peter Stilwell (P)

National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.

Jeanette Aston (J)

National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.

Sean McPhail (S)

National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.

Sarah Stevens (S)

National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.

Fiona A Pearce (FA)

Department of Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, UK.
Department of Rheumatology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.
National Institute for Health Research (NIHR), Nottingham Biomedical Research Centre, Nottingham, UK.

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