BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Mass Vaccination Setting
By Noa Dagan, N. Barda, Eldad Kepten, O. Miron, Shay Perchik, M. Katz, Miguel A. Hern'an, Marc Lipsitch, B. Reis, R. Balicer. New England Journal of Medicine, 2021
2,210 citations recorded by the source corpus.
Abstract Background As mass vaccination campaigns against coronavirus disease 2019 (Covid-19) commence worldwide, vaccine effectiveness needs to be assessed for a range of outcomes across diverse populations in a noncontrolled setting. In this study, data from Israel’s largest health care organization were used to evaluate the effectiveness of the BNT162b2 mRNA vaccine. Methods All persons who were newly vaccinated during the period from December 20, 2020, to February 1, 2021, were matched to unvaccinated controls in a 1:1 ratio according to demographic and clinical characteristics. Study outcomes included documented infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), symptomatic Covid-19, Covid-19–related hospitalization, severe illness, and death. We estimated vaccine effectiveness for each outcome as one minus the risk ratio, using the Kaplan–Meier estimator. Results Each study group included 596,618 persons. Estimated vaccine effectiveness for the study outcomes at days 14 through 20 after the first dose and at 7 or more days after the second dose was as follows: for documented infection, 46% (95% confidence interval [CI], 40 to 51) and 92% (95% CI, 88 to 95); for symptomatic Covid-19, 57% (95% CI, 50 to 63) and 94% (95% CI, 87 to 98); for hospitalization, 74% (95% CI, 56 to 86) and 87% (95% CI, 55 to 100); and for severe disease, 62% (95% CI, 39 to 80) and 92% (95% CI, 75 to 100), respectively. Estimated effectiveness in preventing death from Covid-19 was 72% (95% CI, 19 to 100) for days 14 through 20 after the first dose. Estimated effectiveness in specific subpopulations assessed for documented infection and symptomatic Covid-19 was consistent across age groups, with potentially slightly lower effectiveness in persons with multiple coexisting conditions. Conclusions This study in a nationwide mass vaccination setting suggests that the BNT162b2 mRNA vaccine is effective for a wide range of Covid-19–related outcomes, a finding consistent with that of the randomized trial.
Subfields: Health, Immunology, Infectious Diseases
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Citations in the corpus
- Comparing COVID-19 vaccines for their characteristics, efficacy and effectiveness against SARS-CoV-2 and variants of concern: a narrative review (2021, neutral): “3), mRNA vaccine or AZD1222 effectiveness against hospitalization or death was over 87e94% [48,58] when the strain was not sequenced, 89e95% against Alpha [36,38,39], 95% against Beta/Gamma [38], 96% against Alpha/Delta [39], and 80e95% against Delta [59,60].”
- Community transmission and viral load kinetics of the SARS-CoV-2 delta (B.1.617.2) variant in vaccinated and unvaccinated individuals in the UK: a prospective, longitudinal, cohort study (2021, neutral): “Estimates derived from E-gene cycle threshold value data (appendix pp 5, 7, 9, 11) were similar to those for ORF1ab.”
- Safety of the BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Setting (2021, neutral): “60–69 yr 87,236 (10) 87,236 (10) 12,100 (7) 12,100 (7)”
- A global database of COVID-19 vaccinations (2021, background): “Integrating it with 93 other epidemiological data can help researchers evaluate these outcomes.(16,17) Evidence of 94 positive impacts of vaccination on transmission and mortality can also in turn help to 95 strengthen public trust.”
- mRNA Vaccines in the COVID-19 Pandemic and Beyond. (2021, methodology): “These include Alpha (B.1.1.7), first identified in the United Kingdom; Beta (B.1.351), first identified in South Africa; Gamma (P.1), first identified in Brazil; and Delta (B.1.617.2), first identified in India.”