TY - JOUR
T1 - Effectiveness of mRNA covid-19 vaccine among U.S. Health care personnel
AU - The Vaccine Effectiveness among Healthcare Personnel Study Team
AU - Pilishvili, Tamara
AU - Gierke, Ryan
AU - Fleming-Dutra, Katherine E.
AU - Farrar, Jennifer L.
AU - Mohr, Nicholas M.
AU - Talan, David A.
AU - Krishnadasan, Anusha
AU - Harland, Karisa K.
AU - Smithline, Howard A.
AU - Hou, Peter C.
AU - Lee, Lilly C.
AU - Lim, Stephen C.
AU - Moran, Gregory J.
AU - Krebs, Elizabeth
AU - Steele, Mark T.
AU - Beiser, David G.
AU - Faine, Brett
AU - Haran, John P.
AU - Nandi, Utsav
AU - Schrading, Walter A.
AU - Chinnock, Brian
AU - Henning, Daniel J.
AU - Lovecchio, Frank
AU - Lee, Jane
AU - Barter, Devra
AU - Brackney, Monica
AU - Fridkin, Scott K.
AU - Marceaux-Galli, Kaytlynn
AU - Lim, Sarah
AU - Phipps, Erin C.
AU - Dumyati, Ghinwa
AU - Pierce, Rebecca
AU - Markus, Tiffanie M.
AU - Anderson, Deverick J.
AU - Debes, Amanda K.
AU - Lin, Michael Y.
AU - Mayer, Jeanmarie
AU - Kwon, Jennie H.
AU - Safdar, Nasia
AU - Fischer, Marc
AU - Singleton, Rosalyn
AU - Chea, Nora
AU - Magill, Shelley S.
AU - Verani, Jennifer R.
AU - Schrag, Stephanie J.
N1 - Funding Information:
Supported by the CDC through agreements or contracts with the following partners: a cooperative agreement with the Emerging Infections Program (www.cdc.gov/ncezid/dpei/eip/ index.html), a cooperative agreement (Project PREVENT) with EMERGEncy ID NET (www.emergencyidnet.org), an interagency agreement with the Denali Commission, and contracts with SHEPheRD (www.cdc.gov/hai/research/safehealthcare.html).
Publisher Copyright:
© 2021 Massachusetts Medical Society.
PY - 2021/12/16
Y1 - 2021/12/16
N2 - BACKGROUND The prioritization of U.S. health care personnel for early receipt of messenger RNA (mRNA) vaccines against severe acute respiratory syndrome coronavirus 2 (SARSCoV-2), the virus that causes coronavirus disease 2019 (Covid-19), allowed for the evaluation of the effectiveness of these new vaccines in a real-world setting. METHODS We conducted a test-negative case-control study involving health care personnel across 25 U.S. states. Cases were defined on the basis of a positive polymerase-chain-reaction (PCR) or antigen-based test for SARS-CoV-2 and at least one Covid-19-like symptom. Controls were defined on the basis of a negative PCR test for SARSCoV-2, regardless of symptoms, and were matched to cases according to the week of the test date and site. Using conditional logistic regression with adjustment for age, race and ethnic group, underlying conditions, and exposures to persons with Covid-19, we estimated vaccine effectiveness for partial vaccination (assessed 14 days after receipt of the first dose through 6 days after receipt of the second dose) and complete vaccination (assessed ≥7 days after receipt of the second dose). RESULTS The study included 1482 case participants and 3449 control participants. Vaccine effectiveness for partial vaccination was 77.6% (95% confidence interval [CI], 70.9 to 82.7) with the BNT162b2 vaccine (Pfizer-BioNTech) and 88.9% (95% CI, 78.7 to 94.2) with the mRNA-1273 vaccine (Moderna); for complete vaccination, vaccine effectiveness was 88.8% (95% CI, 84.6 to 91.8) and 96.3% (95% CI, 91.3 to 98.4), respectively. Vaccine effectiveness was similar in subgroups defined according to age (<50 years or ≥50 years), race and ethnic group, presence of underlying conditions, and level of patient contact. Estimates of vaccine effectiveness were lower during weeks 9 through 14 than during weeks 3 through 8 after receipt of the second dose, but confidence intervals overlapped widely. CONCLUSIONS The BNT162b2 and mRNA-1273 vaccines were highly effective under real-world conditions in preventing symptomatic Covid-19 in health care personnel, including those at risk for severe Covid-19 and those in racial and ethnic groups that have been disproportionately affected by the pandemic.
AB - BACKGROUND The prioritization of U.S. health care personnel for early receipt of messenger RNA (mRNA) vaccines against severe acute respiratory syndrome coronavirus 2 (SARSCoV-2), the virus that causes coronavirus disease 2019 (Covid-19), allowed for the evaluation of the effectiveness of these new vaccines in a real-world setting. METHODS We conducted a test-negative case-control study involving health care personnel across 25 U.S. states. Cases were defined on the basis of a positive polymerase-chain-reaction (PCR) or antigen-based test for SARS-CoV-2 and at least one Covid-19-like symptom. Controls were defined on the basis of a negative PCR test for SARSCoV-2, regardless of symptoms, and were matched to cases according to the week of the test date and site. Using conditional logistic regression with adjustment for age, race and ethnic group, underlying conditions, and exposures to persons with Covid-19, we estimated vaccine effectiveness for partial vaccination (assessed 14 days after receipt of the first dose through 6 days after receipt of the second dose) and complete vaccination (assessed ≥7 days after receipt of the second dose). RESULTS The study included 1482 case participants and 3449 control participants. Vaccine effectiveness for partial vaccination was 77.6% (95% confidence interval [CI], 70.9 to 82.7) with the BNT162b2 vaccine (Pfizer-BioNTech) and 88.9% (95% CI, 78.7 to 94.2) with the mRNA-1273 vaccine (Moderna); for complete vaccination, vaccine effectiveness was 88.8% (95% CI, 84.6 to 91.8) and 96.3% (95% CI, 91.3 to 98.4), respectively. Vaccine effectiveness was similar in subgroups defined according to age (<50 years or ≥50 years), race and ethnic group, presence of underlying conditions, and level of patient contact. Estimates of vaccine effectiveness were lower during weeks 9 through 14 than during weeks 3 through 8 after receipt of the second dose, but confidence intervals overlapped widely. CONCLUSIONS The BNT162b2 and mRNA-1273 vaccines were highly effective under real-world conditions in preventing symptomatic Covid-19 in health care personnel, including those at risk for severe Covid-19 and those in racial and ethnic groups that have been disproportionately affected by the pandemic.
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U2 - 10.1056/NEJMoa2106599
DO - 10.1056/NEJMoa2106599
M3 - Article
C2 - 34551224
AN - SCOPUS:85119107504
SN - 0028-4793
VL - 385
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 25
M1 - e90
ER -