Cross-sectional study evaluating the impact of SARS-CoV-2 variants on Long COVID outcomes in UK hospital survivors.


Journal

BMJ open respiratory research
ISSN: 2052-4439
Titre abrégé: BMJ Open Respir Res
Pays: England
ID NLM: 101638061

Informations de publication

Date de publication:
08 2023
Historique:
received: 14 02 2023
accepted: 22 06 2023
medline: 7 8 2023
pubmed: 4 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

COVID-19 studies report on hospital admission outcomes across SARS-CoV-2 waves of infection but knowledge of the impact of SARS-CoV-2 variants on the development of Long COVID in hospital survivors is limited. We sought to investigate Long COVID outcomes, aiming to compare outcomes in adult hospitalised survivors with known variants of concern during our first and second UK COVID-19 waves, prior to widespread vaccination. Prospective observational cross-sectional study. Secondary care tertiary hospital in the UK. This study investigated Long COVID in 673 adults with laboratory-positive SARS-CoV-2 infection or clinically suspected COVID-19, 6 weeks after hospital discharge. We compared adults with wave 1 (wildtype variant, admitted from February to April 2020) and wave 2 patients (confirmed Alpha variant on viral sequencing (B.1.1.7), admitted from December 2020 to February 2021). Associations of Long COVID presence (one or more of 14 symptoms) and total number of Long COVID symptoms with SARS-CoV-2 variant were analysed using multiple logistic and Poisson regression, respectively. 322/400 (wave 1) and 248/273 (wave 2) patients completed follow-up. Predictors of increased total number of Long COVID symptoms included: pre-existing lung disease (adjusted count ratio (aCR)=1.26, 95% CI 1.07, 1.48) and more COVID-19 admission symptoms (aCR=1.07, 95% CI 1.02, 1.12). Weaker associations included increased length of inpatient stay (aCR=1.02, 95% CI 1.00, 1.03) and later review after discharge (aCR=1.00, 95% CI 1.00, 1.01). SARS-CoV-2 variant was not associated with Long COVID presence (OR=0.99, 95% CI 0.24, 4.20) or total number of symptoms (aCR=1.09, 95% CI 0.82, 1.44). Patients with chronic lung disease or greater COVID-19 admission symptoms have higher Long COVID risk. SARS-CoV-2 variant was not predictive of Long COVID though in wave 2 we identified fewer admission symptoms, improved clinical trajectory and outcomes. Addressing modifiable factors such as length of stay and timepoint of clinical review following discharge may enable clinicians to move from Long COVID risk stratification towards improving its outcome.

Identifiants

pubmed: 37536948
pii: 10/1/e001667
doi: 10.1136/bmjresp-2023-001667
pmc: PMC10401240
pii:
doi:

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: JRH, SM and AS report personal fees, and JRH, SM, AS and AJS report non-financial support from pharmaceutical companies that make medicines and medical devices to treat respiratory disease, outside the submitted work.

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Auteurs

Anita Saigal (A)

UCL Respiratory, University College London, London, UK rmhaa56@ucl.ac.uk.
Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Camila Nagoda Niklewicz (C)

Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Sindhu Bhaarrati Naidu (SB)

Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Heba M Bintalib (HM)

UCL Respiratory, University College London, London, UK.

Amar Jitu Shah (AJ)

UCL Respiratory, University College London, London, UK.
Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

George Seligmann (G)

Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Alan Stewart Hunter (AS)

Department of Infectious Diseases, Royal Free London NHS Foundation Trust, London, UK.

Emmanuel Wey (E)

Department of Infectious Diseases, Royal Free London NHS Foundation Trust, London, UK.
Centre for Clinical Microbiology, Division of Infection and Immunity, University College London, London, UK.

Ibrahim Abubakar (I)

UCL Respiratory, University College London, London, UK.
Faculty of Population Health Sciences, University College London, London, UK.

Tabitha Mahungu (T)

Department of Virology, Royal Free London NHS Foundation Trust, London, UK.

David Miller (D)

Open Health Care, London, UK.

Joseph Barnett (J)

Department of Radiology, Royal Free London NHS Foundation Trust, London, UK.

Neel Gautam Jain (NG)

Department of Radiology, Royal Free London NHS Foundation Trust, London, UK.

Simon Brill (S)

Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

James Goldring (J)

Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Hannah Jarvis (H)

Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Colette Smith (C)

Institute of Global Health, University College London, London, UK.

Chibueze Ogbonnaya (C)

Institute of Child Health, University College London, London, UK.

John R Hurst (JR)

UCL Respiratory, University College London, London, UK.
Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Marc C I Lipman (MCI)

UCL Respiratory, University College London, London, UK.
Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

Swapna Mandal (S)

UCL Respiratory, University College London, London, UK.
Respiratory Medicine, Royal Free London NHS Foundation Trust, London, UK.

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Classifications MeSH