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Effectiveness of BNT162b2 COVID-19 Vaccination in Prevention of Hospitalisations and Severe Disease in Adults with Delta (B.1.617.2) and Omicron (B.1.1.529) Variant SARS-CoV-2 Infection: A Prospective Test Negative Case-Control Study

39 Pages Posted: 12 Sep 2022

See all articles by Anastasia Chatzilena

Anastasia Chatzilena

University of Bristol - Department of Engineering Mathematics

Catherine Hyams

University of Bristol - Population Health Sciences

Robert Challen

University of Bristol - Department of Mathematics

Robin Marlow

University of Bristol - Population Health Sciences

Jade King

University Hospitals Bristol & Weston NHS Foundation Trust - Clinical Research and Imaging Centre

David Adegbite

University of Bristol - Population Health Sciences

Jane Kinney

University of Bristol - Department of Population Health Sciences

Madeleine Clout

University of Bristol - Bristol Vaccine Centre

Nick A. Maskell

University of Bristol - Academic Respiratory Unit

Jennifer Oliver

University of Bristol - Bristol Vaccine Centre

Leon Danon

University of Bristol - Engineering Mathematics

Adam Finn

University of Bristol - Bristol Vaccine Centre

More...

Abstract

Background: Whilst other studies have reported the effectiveness of mRNA vaccination against hospitalisation, including emergency department or intensive care admission, few have assessed effectiveness against other more clinically robust indices of COVID-19 severity.

Methods: A prospective single-centre test-negative design case-control study of adults hospitalised with COVID-19 disease or other acute respiratory disease between 1 June 2021 and 20 July 2022. We assessed VE against hospitalisation, length of stay [LOS]>3 days, WHO COVID Score>5 and supplementary oxygen FiO2 >28%, conducting regression analyses controlling for age, gender, index of multiple deprivation, Charlson comorbidity index, time, and community infection prevalence.

Findings: Two-dose BNT162b2 was associated with VE 82∙5% [95% confidence interval 76∙2%-87∙2%] against hospitalisation following Delta infection, 63∙3% [26∙9-81∙8%], 58∙5% [24∙8-77∙3%], and 51∙5% [16∙7-72∙1] against LOS>3 days, WHO COVID Score>5, and requirement for FiO2>28% respectively.Three-dose BNT162b2 protection against hospitalisation with Omicron infection was 30∙9% [5∙9-49∙3%], with sensitivity analyses ranging from 28∙8-72∙6%. Protection against LOS>3 days, WHO COVID Score>5 and requirement for FiO2>28% was 56∙1% [20∙6-76∙5%], 58∙8% [31∙2-75∙8%], and 41∙5% [-0.4-66∙3%], respectively.In the UK, BNT162b2 was prioritised for high-risk individuals and those aged >75 years. In the latter group we found a higher estimate of VE against hospitalisation of 47∙2% [16∙8-66∙6%].

Interpretation: BNT162b2 vaccination results in risk reductions for multiple patient outcomes following Delta and Omicron COVID-19 infection, particularly in older adults. BNT162b2 remains effective against severe SARS-CoV-2 disease.

Funding Information: AvonCAP is an investigator-led project funded under a collaborative agreement by Pfizer.

Declaration of Interests: CH is Principal Investigator of the AvonCAP study which is an investigator-led University of Bristol study funded by Pfizer and has previously received support from the NIHR in an Academic Clinical Fellowship. JO and LD are Co-Investigators on the AvonCAP Study. AF is a member of the Joint Committee on Vaccination and Immunization (JCVI) and chair of the World Health Organization European Technical Advisory Group of Experts on Immunization (ETAGE) committee. In addition to receiving funding from Pfizer as Chief Investigator of this study, he leads another project investigating transmission of respiratory bacteria in families jointly funded by Pfizer and the Gates Foundation. The other authors have no relevant conflicts of interest to declare.

Ethics Approval Statement: The Health Research Authority Research Ethics Committee (East of England, Essex), REC20/EE/0157 approved this study, including use of Section 251 of the 2006 NHS Act under Confidentiality Advisory Group authorisation.

Keywords: COVID-19, SARS-CoV-2, respiratory infection, vaccination

Suggested Citation

Chatzilena, Anastasia and Hyams, Catherine and Challen, Robert and Marlow, Robin and King, Jade and Adegbite, David and Kinney, Jane and Clout, Madeleine and Maskell, Nick A. and Oliver, Jennifer and Danon, Leon and Finn, Adam, Effectiveness of BNT162b2 COVID-19 Vaccination in Prevention of Hospitalisations and Severe Disease in Adults with Delta (B.1.617.2) and Omicron (B.1.1.529) Variant SARS-CoV-2 Infection: A Prospective Test Negative Case-Control Study. Available at SSRN: https://ssrn.com/abstract=4216690 or http://dx.doi.org/10.2139/ssrn.4216690

Anastasia Chatzilena

University of Bristol - Department of Engineering Mathematics ( email )

University of Bristol
Ada Lovelace Building, University Walk
Bristol, BS8 1TW
United Kingdom

Catherine Hyams

University of Bristol - Population Health Sciences

Robert Challen

University of Bristol - Department of Mathematics ( email )

Robin Marlow

University of Bristol - Population Health Sciences

Jade King

University Hospitals Bristol & Weston NHS Foundation Trust - Clinical Research and Imaging Centre ( email )

David Adegbite

University of Bristol - Population Health Sciences

Jane Kinney

University of Bristol - Department of Population Health Sciences ( email )

Madeleine Clout

University of Bristol - Bristol Vaccine Centre ( email )

Nick A. Maskell

University of Bristol - Academic Respiratory Unit ( email )

Jennifer Oliver

University of Bristol - Bristol Vaccine Centre ( email )

Leon Danon

University of Bristol - Engineering Mathematics

Adam Finn (Contact Author)

University of Bristol - Bristol Vaccine Centre ( email )

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