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Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada

BACKGROUND: The Canadian coronavirus disease 2019 (COVID-19) immunization strategy deferred second doses and allowed mixed schedules. We compared 2-dose vaccine effectiveness (VE) by vaccine type (mRNA and/or ChAdOx1), interval between doses, and time since second dose in 2 of Canada’s larger provin...

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Autores principales: Skowronski, Danuta M, Febriani, Yossi, Ouakki, Manale, Setayeshgar, Solmaz, El Adam, Shiraz, Zou, Macy, Talbot, Denis, Prystajecky, Natalie, Tyson, John R, Gilca, Rodica, Brousseau, Nicholas, Deceuninck, Geneviève, Galanis, Eleni, Fjell, Chris D, Sbihi, Hind, Fortin, Elise, Barkati, Sapha, Sauvageau, Chantal, Naus, Monika, Patrick, David M, Henry, Bonnie, Hoang, Linda M N, De Wals, Philippe, Garenc, Christophe, Carignan, Alex, Drolet, Mélanie, Jassem, Agatha N, Sadarangani, Manish, Brisson, Marc, Krajden, Mel, De Serres, Gaston
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047203/
https://www.ncbi.nlm.nih.gov/pubmed/35438175
http://dx.doi.org/10.1093/cid/ciac290
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author Skowronski, Danuta M
Febriani, Yossi
Ouakki, Manale
Setayeshgar, Solmaz
El Adam, Shiraz
Zou, Macy
Talbot, Denis
Prystajecky, Natalie
Tyson, John R
Gilca, Rodica
Brousseau, Nicholas
Deceuninck, Geneviève
Galanis, Eleni
Fjell, Chris D
Sbihi, Hind
Fortin, Elise
Barkati, Sapha
Sauvageau, Chantal
Naus, Monika
Patrick, David M
Henry, Bonnie
Hoang, Linda M N
De Wals, Philippe
Garenc, Christophe
Carignan, Alex
Drolet, Mélanie
Jassem, Agatha N
Sadarangani, Manish
Brisson, Marc
Krajden, Mel
De Serres, Gaston
author_facet Skowronski, Danuta M
Febriani, Yossi
Ouakki, Manale
Setayeshgar, Solmaz
El Adam, Shiraz
Zou, Macy
Talbot, Denis
Prystajecky, Natalie
Tyson, John R
Gilca, Rodica
Brousseau, Nicholas
Deceuninck, Geneviève
Galanis, Eleni
Fjell, Chris D
Sbihi, Hind
Fortin, Elise
Barkati, Sapha
Sauvageau, Chantal
Naus, Monika
Patrick, David M
Henry, Bonnie
Hoang, Linda M N
De Wals, Philippe
Garenc, Christophe
Carignan, Alex
Drolet, Mélanie
Jassem, Agatha N
Sadarangani, Manish
Brisson, Marc
Krajden, Mel
De Serres, Gaston
author_sort Skowronski, Danuta M
collection PubMed
description BACKGROUND: The Canadian coronavirus disease 2019 (COVID-19) immunization strategy deferred second doses and allowed mixed schedules. We compared 2-dose vaccine effectiveness (VE) by vaccine type (mRNA and/or ChAdOx1), interval between doses, and time since second dose in 2 of Canada’s larger provinces. METHODS: Two-dose VE against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or hospitalization among adults ≥18 years, including due to Alpha, Gamma, and Delta variants of concern (VOCs), was assessed ≥14 days postvaccination by test-negative design studies separately conducted in British Columbia and Quebec, Canada, between 30 May and 27 November (epi-weeks 22–47) 2021. RESULTS: In both provinces, all homologous or heterologous mRNA and/or ChAdOx1 2-dose schedules were associated with ≥90% reduction in SARS-CoV-2 hospitalization risk for ≥7 months. With slight decline from a peak of >90%, VE against infection was ≥80% for ≥6 months following homologous mRNA vaccination, lower by ∼10% when both doses were ChAdOx1 but comparably high following heterologous ChAdOx1 + mRNA receipt. Findings were similar by age group, sex, and VOC. VE was significantly higher with longer 7–8-week versus manufacturer-specified 3–4-week intervals between mRNA doses. CONCLUSIONS: Two doses of any mRNA and/or ChAdOx1 combination gave substantial and sustained protection against SARS-CoV-2 hospitalization, spanning Delta-dominant circulation. ChAdOx1 VE against infection was improved by heterologous mRNA series completion. A 7–8-week interval between first and second doses improved mRNA VE and may be the optimal schedule outside periods of intense epidemic surge. Findings support interchangeability and extended intervals between SARS-CoV-2 vaccine doses, with potential global implications for low-coverage areas and, going forward, for children.
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spelling pubmed-90472032022-04-28 Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada Skowronski, Danuta M Febriani, Yossi Ouakki, Manale Setayeshgar, Solmaz El Adam, Shiraz Zou, Macy Talbot, Denis Prystajecky, Natalie Tyson, John R Gilca, Rodica Brousseau, Nicholas Deceuninck, Geneviève Galanis, Eleni Fjell, Chris D Sbihi, Hind Fortin, Elise Barkati, Sapha Sauvageau, Chantal Naus, Monika Patrick, David M Henry, Bonnie Hoang, Linda M N De Wals, Philippe Garenc, Christophe Carignan, Alex Drolet, Mélanie Jassem, Agatha N Sadarangani, Manish Brisson, Marc Krajden, Mel De Serres, Gaston Clin Infect Dis Major Article BACKGROUND: The Canadian coronavirus disease 2019 (COVID-19) immunization strategy deferred second doses and allowed mixed schedules. We compared 2-dose vaccine effectiveness (VE) by vaccine type (mRNA and/or ChAdOx1), interval between doses, and time since second dose in 2 of Canada’s larger provinces. METHODS: Two-dose VE against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or hospitalization among adults ≥18 years, including due to Alpha, Gamma, and Delta variants of concern (VOCs), was assessed ≥14 days postvaccination by test-negative design studies separately conducted in British Columbia and Quebec, Canada, between 30 May and 27 November (epi-weeks 22–47) 2021. RESULTS: In both provinces, all homologous or heterologous mRNA and/or ChAdOx1 2-dose schedules were associated with ≥90% reduction in SARS-CoV-2 hospitalization risk for ≥7 months. With slight decline from a peak of >90%, VE against infection was ≥80% for ≥6 months following homologous mRNA vaccination, lower by ∼10% when both doses were ChAdOx1 but comparably high following heterologous ChAdOx1 + mRNA receipt. Findings were similar by age group, sex, and VOC. VE was significantly higher with longer 7–8-week versus manufacturer-specified 3–4-week intervals between mRNA doses. CONCLUSIONS: Two doses of any mRNA and/or ChAdOx1 combination gave substantial and sustained protection against SARS-CoV-2 hospitalization, spanning Delta-dominant circulation. ChAdOx1 VE against infection was improved by heterologous mRNA series completion. A 7–8-week interval between first and second doses improved mRNA VE and may be the optimal schedule outside periods of intense epidemic surge. Findings support interchangeability and extended intervals between SARS-CoV-2 vaccine doses, with potential global implications for low-coverage areas and, going forward, for children. Oxford University Press 2022-04-19 /pmc/articles/PMC9047203/ /pubmed/35438175 http://dx.doi.org/10.1093/cid/ciac290 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Skowronski, Danuta M
Febriani, Yossi
Ouakki, Manale
Setayeshgar, Solmaz
El Adam, Shiraz
Zou, Macy
Talbot, Denis
Prystajecky, Natalie
Tyson, John R
Gilca, Rodica
Brousseau, Nicholas
Deceuninck, Geneviève
Galanis, Eleni
Fjell, Chris D
Sbihi, Hind
Fortin, Elise
Barkati, Sapha
Sauvageau, Chantal
Naus, Monika
Patrick, David M
Henry, Bonnie
Hoang, Linda M N
De Wals, Philippe
Garenc, Christophe
Carignan, Alex
Drolet, Mélanie
Jassem, Agatha N
Sadarangani, Manish
Brisson, Marc
Krajden, Mel
De Serres, Gaston
Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada
title Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada
title_full Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada
title_fullStr Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada
title_full_unstemmed Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada
title_short Two-Dose Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Effectiveness With Mixed Schedules and Extended Dosing Intervals: Test-Negative Design Studies From British Columbia and Quebec, Canada
title_sort two-dose severe acute respiratory syndrome coronavirus 2 vaccine effectiveness with mixed schedules and extended dosing intervals: test-negative design studies from british columbia and quebec, canada
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047203/
https://www.ncbi.nlm.nih.gov/pubmed/35438175
http://dx.doi.org/10.1093/cid/ciac290
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