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Effectiveness of mRNA Covid-19 Vaccine among U.S. Health Care Personnel

Background The prioritization of U.S. health care personnel for early receipt of messenger RNA (mRNA) vaccines against severe acute respiratory disease coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (Covid-19), allowed for the evaluation of the effectiveness of these new...

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Published in:New England Journal of Medicine 2021-12
Main Authors: Pilishvili, Tamara, Gierke, Ryan, Fleming-Dutra, Katherine E, Farrar, Jennifer L, Mohr, Nicholas M, Talan, David A, Krishnadasan, Anusha, Harland, Karisa K, Smithline, Howard A, Hou, Peter C, Lee, Lilly C, Lim, Stephen C, Moran, Gregory J, Krebs, Elizabeth, Steele, Mark T, Beiser, David G, Faine, Brett, Haran, John P, Nandi, Utsav, Schrading, Walter A, Chinnock, Brian, Henning, Daniel J, Lovecchio, Frank, Lee, Jane, Barter, Devra, Brackney, Monica, Fridkin, Scott K, Marceaux-Galli, Kaytlynn, Lim, Sarah, Phipps, Erin C, Dumyati, Ghinwa, Pierce, Rebecca, Markus, Tiffanie M, Anderson, Deverick J, Debes, Amanda K, Lin, Michael Y, Mayer, Jeanmarie, Kwon, Jennie H, Safdar, Nasia, Fischer, Marc, Singleton, Rosalyn, Chea, Nora, Magill, Shelley S, Verani, Jennifer R, Schrag, Stephanie J
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container_title New England Journal of Medicine
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creator Pilishvili, Tamara
Gierke, Ryan
Fleming-Dutra, Katherine E
Farrar, Jennifer L
Mohr, Nicholas M
Talan, David A
Krishnadasan, Anusha
Harland, Karisa K
Smithline, Howard A
Hou, Peter C
Lee, Lilly C
Lim, Stephen C
Moran, Gregory J
Krebs, Elizabeth
Steele, Mark T
Beiser, David G
Faine, Brett
Haran, John P
Nandi, Utsav
Schrading, Walter A
Chinnock, Brian
Henning, Daniel J
Lovecchio, Frank
Lee, Jane
Barter, Devra
Brackney, Monica
Fridkin, Scott K
Marceaux-Galli, Kaytlynn
Lim, Sarah
Phipps, Erin C
Dumyati, Ghinwa
Pierce, Rebecca
Markus, Tiffanie M
Anderson, Deverick J
Debes, Amanda K
Lin, Michael Y
Mayer, Jeanmarie
Kwon, Jennie H
Safdar, Nasia
Fischer, Marc
Singleton, Rosalyn
Chea, Nora
Magill, Shelley S
Verani, Jennifer R
Schrag, Stephanie J
description Background The prioritization of U.S. health care personnel for early receipt of messenger RNA (mRNA) vaccines against severe acute respiratory disease coronavirus 2 (SARS-CoV-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 SARS-CoV-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 (
doi_str_mv 10.1056/NEJMoa2106599
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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 SARS-CoV-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 (&lt;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. (Funded by the Centers for Disease Control and Prevention.)</description><identifier>DOI: 10.1056/NEJMoa2106599</identifier><language>eng</language><publisher>Waltham: Massachusetts Medical Society</publisher><subject>COVID-19 vaccines</subject><ispartof>New England Journal of Medicine, 2021-12</ispartof><rights>2021. Not withstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.nejm.org/about-nejm/permissions?query=footer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-e92a0704e12778cbc396ce257db8991353b8ef1adb006c3f051c762092a11af23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2575129460?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>783,787,27939,38530,43909</link.rule.ids><linktorsrc>$$Uhttps://www.proquest.com/docview/2575129460?pq-origsite=primo$$EView_record_in_ProQuest$$FView_record_in_$$GProQuest</linktorsrc></links><search><creatorcontrib>Pilishvili, Tamara</creatorcontrib><creatorcontrib>Gierke, Ryan</creatorcontrib><creatorcontrib>Fleming-Dutra, Katherine E</creatorcontrib><creatorcontrib>Farrar, Jennifer L</creatorcontrib><creatorcontrib>Mohr, Nicholas M</creatorcontrib><creatorcontrib>Talan, David A</creatorcontrib><creatorcontrib>Krishnadasan, Anusha</creatorcontrib><creatorcontrib>Harland, Karisa K</creatorcontrib><creatorcontrib>Smithline, Howard A</creatorcontrib><creatorcontrib>Hou, Peter C</creatorcontrib><creatorcontrib>Lee, Lilly C</creatorcontrib><creatorcontrib>Lim, Stephen C</creatorcontrib><creatorcontrib>Moran, Gregory J</creatorcontrib><creatorcontrib>Krebs, Elizabeth</creatorcontrib><creatorcontrib>Steele, Mark T</creatorcontrib><creatorcontrib>Beiser, David G</creatorcontrib><creatorcontrib>Faine, Brett</creatorcontrib><creatorcontrib>Haran, John P</creatorcontrib><creatorcontrib>Nandi, Utsav</creatorcontrib><creatorcontrib>Schrading, Walter A</creatorcontrib><creatorcontrib>Chinnock, Brian</creatorcontrib><creatorcontrib>Henning, Daniel J</creatorcontrib><creatorcontrib>Lovecchio, Frank</creatorcontrib><creatorcontrib>Lee, Jane</creatorcontrib><creatorcontrib>Barter, Devra</creatorcontrib><creatorcontrib>Brackney, Monica</creatorcontrib><creatorcontrib>Fridkin, Scott K</creatorcontrib><creatorcontrib>Marceaux-Galli, Kaytlynn</creatorcontrib><creatorcontrib>Lim, Sarah</creatorcontrib><creatorcontrib>Phipps, Erin C</creatorcontrib><creatorcontrib>Dumyati, Ghinwa</creatorcontrib><creatorcontrib>Pierce, Rebecca</creatorcontrib><creatorcontrib>Markus, Tiffanie M</creatorcontrib><creatorcontrib>Anderson, Deverick J</creatorcontrib><creatorcontrib>Debes, Amanda K</creatorcontrib><creatorcontrib>Lin, Michael Y</creatorcontrib><creatorcontrib>Mayer, Jeanmarie</creatorcontrib><creatorcontrib>Kwon, Jennie H</creatorcontrib><creatorcontrib>Safdar, Nasia</creatorcontrib><creatorcontrib>Fischer, Marc</creatorcontrib><creatorcontrib>Singleton, Rosalyn</creatorcontrib><creatorcontrib>Chea, Nora</creatorcontrib><creatorcontrib>Magill, Shelley S</creatorcontrib><creatorcontrib>Verani, Jennifer R</creatorcontrib><creatorcontrib>Schrag, Stephanie J</creatorcontrib><title>Effectiveness of mRNA Covid-19 Vaccine among U.S. Health Care Personnel</title><title>New England Journal of Medicine</title><description>Background The prioritization of U.S. health care personnel for early receipt of messenger RNA (mRNA) vaccines against severe acute respiratory disease coronavirus 2 (SARS-CoV-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 SARS-CoV-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 (&lt;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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K</au><au>Lin, Michael Y</au><au>Mayer, Jeanmarie</au><au>Kwon, Jennie H</au><au>Safdar, Nasia</au><au>Fischer, Marc</au><au>Singleton, Rosalyn</au><au>Chea, Nora</au><au>Magill, Shelley S</au><au>Verani, Jennifer R</au><au>Schrag, Stephanie J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effectiveness of mRNA Covid-19 Vaccine among U.S. Health Care Personnel</atitle><jtitle>New England Journal of Medicine</jtitle><date>2021-12-16</date><risdate>2021</risdate><abstract>Background The prioritization of U.S. health care personnel for early receipt of messenger RNA (mRNA) vaccines against severe acute respiratory disease coronavirus 2 (SARS-CoV-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 SARS-CoV-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 (&lt;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. (Funded by the Centers for Disease Control and Prevention.)</abstract><cop>Waltham</cop><pub>Massachusetts Medical Society</pub><doi>10.1056/NEJMoa2106599</doi><oa>free_for_read</oa></addata></record>
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identifier DOI: 10.1056/NEJMoa2106599
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subjects COVID-19 vaccines
title Effectiveness of mRNA Covid-19 Vaccine among U.S. Health Care Personnel
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