Risk of mortality in patients infected with SARS-CoV-2 variant of concern 202012/1: matched cohort study.


Journal

BMJ (Clinical research ed.)
ISSN: 1756-1833
Titre abrégé: BMJ
Pays: England
ID NLM: 8900488

Informations de publication

Date de publication:
09 03 2021
Historique:
entrez: 10 3 2021
pubmed: 11 3 2021
medline: 16 3 2021
Statut: epublish

Résumé

To establish whether there is any change in mortality from infection with a new variant of SARS-CoV-2, designated a variant of concern (VOC-202012/1) in December 2020, compared with circulating SARS-CoV-2 variants. Matched cohort study. Community based (pillar 2) covid-19 testing centres in the UK using the TaqPath assay (a proxy measure of VOC-202012/1 infection). 54 906 matched pairs of participants who tested positive for SARS-CoV-2 in pillar 2 between 1 October 2020 and 29 January 2021, followed-up until 12 February 2021. Participants were matched on age, sex, ethnicity, index of multiple deprivation, lower tier local authority region, and sample date of positive specimens, and differed only by detectability of the spike protein gene using the TaqPath assay. Death within 28 days of the first positive SARS-CoV-2 test result. The mortality hazard ratio associated with infection with VOC-202012/1 compared with infection with previously circulating variants was 1.64 (95% confidence interval 1.32 to 2.04) in patients who tested positive for covid-19 in the community. In this comparatively low risk group, this represents an increase in deaths from 2.5 to 4.1 per 1000 detected cases. The probability that the risk of mortality is increased by infection with VOC-202012/01 is high. If this finding is generalisable to other populations, infection with VOC-202012/1 has the potential to cause substantial additional mortality compared with previously circulating variants. Healthcare capacity planning and national and international control policies are all impacted by this finding, with increased mortality lending weight to the argument that further coordinated and stringent measures are justified to reduce deaths from SARS-CoV-2.

Identifiants

pubmed: 33687922
doi: 10.1136/bmj.n579
pmc: PMC7941603
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

n579

Subventions

Organisme : Medical Research Council
ID : MR/S004793/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V009761/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V038613/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19067/2
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19067
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf and declare: support from the Engineering and Physical Sciences Research Council, NHS England, Global Digital Exemplar programme, Alan Turing Institute, Medical Research Council, and National Institute for Health Research Health Protection Research Unit in Behavioural Science and Evaluation, in partnership with Public Health England; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.

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Auteurs

Robert Challen (R)

College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, UK rc538@exeter.ac.uk.
Somerset NHS Foundation Trust, Taunton, UK.
Joint Universities Pandemic and Epidemiological Research (JUNIPER consortium).

Ellen Brooks-Pollock (E)

Joint Universities Pandemic and Epidemiological Research (JUNIPER consortium).
University of Bristol, Bristol Veterinary School, Langford, Bristol, UK.
Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.

Jonathan M Read (JM)

Joint Universities Pandemic and Epidemiological Research (JUNIPER consortium).
Lancaster Medical School, Lancaster University, Bailrigg, Lancaster, UK.

Louise Dyson (L)

Joint Universities Pandemic and Epidemiological Research (JUNIPER consortium).
The Zeeman Institute for Systems Biology and Infectious Disease Epidemiology Research, School of Life Sciences and Mathematics Institute, University of Warwick, Coventry, UK.

Krasimira Tsaneva-Atanasova (K)

College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, UK.
The Alan Turing Institute, British Library, London, UK.

Leon Danon (L)

Joint Universities Pandemic and Epidemiological Research (JUNIPER consortium).
Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
The Alan Turing Institute, British Library, London, UK.
Department of Engineering Mathematics, University of Bristol, Bristol, UK.

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