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SARS-CoV-2 Viral load at presentation to hospital is independently associated with the risk of death

SARS-CoV-2 Viral load at presentation to hospital is independently associated with the risk of death
SARS-CoV-2 Viral load at presentation to hospital is independently associated with the risk of death

Objectives Previous studies have suggested that SARS-CoV-2 viral load, measured on upper respiratory tract samples at presentation to hospital using PCR Cycle threshold (Ct) value, has prognostic utility. However, these studies have not comprehensively adjusted for factors known to be intimately related to viral load. We aimed to evaluate the association between Ct value at admission and patient outcome whilst adjusting carefully for covariates. Methods We evaluated the association between Ct value at presentation and the outcomes of ICU admission and death, in patients hospitalised during the first wave of the pandemic in Southampton, UK. We adjusted for covariates including age, duration of illness and antibody sero-status, measured by neutralisation assay. Results 185 patients were analysed, with a median [IQR] Ct value of 27.9 [22.6–32.1]. On univariate analysis the Ct value at presentation was associated with the risk of both ICU admission and death. In addition, Ct value significantly differed according to age, the duration of illness at presentation and antibody sero-status. On multivariate analysis, Ct value was independently associated with risk of death (aOR 0.84, 95% CI 0.72–0.96; p = 0.011) but not ICU admission (aOR 1.04, 95% CI 0.93–1.16; p = 0.507). Neutralising antibody status at presentation was not associated with mortality or ICU admission (aOR 10.62, 95% CI 0.47–889; p = 0.199 and aOR 0.46, 95% CI 0.10–2.00; p = 0.302, respectively). Conclusions SARS-CoV-2 Ct value on admission to hospital was independently associated with mortality, when comprehensively adjusting for other factors and could be used for risk stratification.

Antibodies, COVID-19, Prognosis, SARS-CoV-2, Viral load
0163-4453
458-466
Tanner, Alex
cac6d816-602b-4dcf-961e-22f2cbdc501d
Phan, Hang Thi Thu
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Brendish, Nathan
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Borca, Florina
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Beard, Kate
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Poole, Stephen
440d7904-ab72-469c-892b-c910cd1cb19b
Clark, Tristan
712ec18e-613c-45df-a013-c8a22834e14f
Tanner, Alex
cac6d816-602b-4dcf-961e-22f2cbdc501d
Phan, Hang Thi Thu
2811b94c-62b7-459d-9cc1-c88057008e3b
Brendish, Nathan
a8a4189e-01eb-4ab3-933e-a24cd188a4d7
Borca, Florina
31fc3965-6bcf-4fd6-85bc-8b0f99f62473
Beard, Kate
85604fec-3541-48cb-9abf-a76c2a32c3f1
Poole, Stephen
440d7904-ab72-469c-892b-c910cd1cb19b
Clark, Tristan
712ec18e-613c-45df-a013-c8a22834e14f

Tanner, Alex, Phan, Hang Thi Thu, Brendish, Nathan, Borca, Florina, Beard, Kate, Poole, Stephen and Clark, Tristan (2021) SARS-CoV-2 Viral load at presentation to hospital is independently associated with the risk of death. Journal of Infection, 83 (4), 458-466. (doi:10.1016/j.jinf.2021.08.003).

Record type: Article

Abstract

Objectives Previous studies have suggested that SARS-CoV-2 viral load, measured on upper respiratory tract samples at presentation to hospital using PCR Cycle threshold (Ct) value, has prognostic utility. However, these studies have not comprehensively adjusted for factors known to be intimately related to viral load. We aimed to evaluate the association between Ct value at admission and patient outcome whilst adjusting carefully for covariates. Methods We evaluated the association between Ct value at presentation and the outcomes of ICU admission and death, in patients hospitalised during the first wave of the pandemic in Southampton, UK. We adjusted for covariates including age, duration of illness and antibody sero-status, measured by neutralisation assay. Results 185 patients were analysed, with a median [IQR] Ct value of 27.9 [22.6–32.1]. On univariate analysis the Ct value at presentation was associated with the risk of both ICU admission and death. In addition, Ct value significantly differed according to age, the duration of illness at presentation and antibody sero-status. On multivariate analysis, Ct value was independently associated with risk of death (aOR 0.84, 95% CI 0.72–0.96; p = 0.011) but not ICU admission (aOR 1.04, 95% CI 0.93–1.16; p = 0.507). Neutralising antibody status at presentation was not associated with mortality or ICU admission (aOR 10.62, 95% CI 0.47–889; p = 0.199 and aOR 0.46, 95% CI 0.10–2.00; p = 0.302, respectively). Conclusions SARS-CoV-2 Ct value on admission to hospital was independently associated with mortality, when comprehensively adjusting for other factors and could be used for risk stratification.

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Ct Value Paper R2 Clean - Accepted Manuscript
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Accepted/In Press date: 1 August 2021
e-pub ahead of print date: 5 August 2021
Published date: October 2021
Additional Information: Acknowledgements We would like to acknowledge and gives thanks to all the pa- tients who kindly participated in this study and to all the clini- cal staff at University Hospital Southampton who cared for them. We would also like to acknowledge the NIHR Southampton Clinical Research Facility (CRF) laboratory, project and nursing teams; the UHSFT research nursing team; and the NIHR Southampton Biomed- ical Research Centre staff and project teams for their support in the set-up of this study. We thank Dr Ashley Banyard, Animal and Plant Health Agency (APHA), Weybridge, Surrey, for his teams work on the serological antibody measurement. This report is independent research supported by the National Institute for Health Research (NIHR Post Doctorial Fellowship, Dr Tristan Clark, PDF 2016–09–061). The views expressed in this pub- lication are those of the author(s) and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health.
Keywords: Antibodies, COVID-19, Prognosis, SARS-CoV-2, Viral load

Identifiers

Local EPrints ID: 450869
URI: http://eprints.soton.ac.uk/id/eprint/450869
ISSN: 0163-4453
PURE UUID: f9368c27-b399-4301-a672-9e804f2785d5
ORCID for Nathan Brendish: ORCID iD orcid.org/0000-0002-9589-4937
ORCID for Tristan Clark: ORCID iD orcid.org/0000-0001-6026-5295

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Date deposited: 17 Aug 2021 16:32
Last modified: 25 Apr 2024 17:44

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Contributors

Author: Alex Tanner
Author: Hang Thi Thu Phan
Author: Nathan Brendish ORCID iD
Author: Florina Borca
Author: Kate Beard
Author: Stephen Poole
Author: Tristan Clark ORCID iD

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