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Effectiveness of BNT162b2 and mRNA-1273 COVID-19 vaccines against symptomatic SARS-CoV-2 infection and severe COVID-19 outcomes in Ontario, Canada
Hannah Chung; Siyi He; Sharifa Nasreen; Maria Sundaram; Sarah A Buchan; Sarah E. Wilson; Branson Chen; Andrew Calzavara; Deshayne B Fell; Peter C Austin; Kumanan Wilson; Kevin L Schwartz; Kevin A. Brown; Jonathan Gubbay; Nicole E. Basta; Salaheddin M. Mahmud; Christiaan Righolt; Lawrence W. Svenson; Shannon E MacDonald; Naveed Z. Janjua; Mina Tadrous; Jeffrey C. Kwong.
Afiliación
  • Hannah Chung; ICES, Toronto, ON
  • Siyi He; ICES, Toronto, ON
  • Sharifa Nasreen; ICES, Toronto, ON; University of Toronto
  • Maria Sundaram; ICES, Toronto, ON
  • Sarah A Buchan; Public Health Ontario
  • Sarah E. Wilson; Public Health Ontario
  • Branson Chen; ICES, Toronto, ON
  • Andrew Calzavara; ICES, Toronto, ON
  • Deshayne B Fell; University of Ottawa, ON
  • Peter C Austin; ICES, Toronto, ON; University of Toronto
  • Kumanan Wilson; University of Ottawa, ON
  • Kevin L Schwartz; Public Health Ontario
  • Kevin A. Brown; Public Health Ontario
  • Jonathan Gubbay; Public Health Ontario
  • Nicole E. Basta; McGill University, Montreal, QC
  • Salaheddin M. Mahmud; University of Manitoba, Winnipeg, MB
  • Christiaan Righolt; University of Manitoba
  • Lawrence W. Svenson; University of Alberta, Edmonton, AB
  • Shannon E MacDonald; University of Alberta
  • Naveed Z. Janjua; University of British Columbia, Vancouver, BC
  • Mina Tadrous; ICES, Toronto, ON
  • Jeffrey C. Kwong; ICES, Toronto, ON
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21257744
ABSTRACT
ObjectivesTo estimate the effectiveness of mRNA COVID-19 vaccines against symptomatic infection and severe outcomes. DesignWe applied a test-negative design study to linked laboratory, vaccination, and health administrative databases, and used multivariable logistic regression adjusting for demographic and clinical characteristics associated with SARS-CoV-2 and vaccine receipt to estimate vaccine effectiveness (VE) against symptomatic infection and severe outcomes. SettingOntario, Canada between 14 December 2020 and 19 April 2021. ParticipantsCommunity-dwelling adults aged [≥]16 years who had COVID-19 symptoms and were tested for SARS-CoV-2. InterventionsPfizer-BioNTechs BNT162b2 or Modernas mRNA-1273 vaccine. Main outcome measuresLaboratory-confirmed SARS-CoV-2 by RT-PCR; hospitalization/death associated with SARS-CoV-2 infection. ResultsAmong 324,033 symptomatic individuals, 53,270 (16.4%) were positive for SARS-CoV-2 and 21,272 (6.6%) received [≥]1 vaccine dose. Among test-positive cases, 2,479 (4.7%) had a severe outcome. VE against symptomatic infection [≥]14 days after receiving only 1 dose was 60% (95%CI, 57 to 64%), increasing from 48% (95%CI, 41 to 54%) at 14-20 days after the first dose to 71% (95%CI, 63 to 78%) at 35-41 days. VE [≥]7 days after 2 doses was 91% (95%CI, 89 to 93%). Against severe outcomes, VE [≥]14 days after 1 dose was 70% (95%CI, 60 to 77%), increasing from 62% (95%CI, 44 to 75%) at 14-20 days to 91% (95%CI, 73 to 97%) at [≥]35 days, whereas VE [≥]7 days after 2 doses was 98% (95%CI, 88 to 100%). For adults aged [≥]70 years, VE estimates were lower for intervals shortly after receiving 1 dose, but were comparable to younger adults for all intervals after 28 days. After 2 doses, we observed high VE against E484K-positive variants. ConclusionsTwo doses of mRNA COVID-19 vaccines are highly effective against symptomatic infection and severe outcomes. Single-dose effectiveness is lower, particularly for older adults shortly after the first dose.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Experimental_studies / Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Experimental_studies / Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint