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Covid-19 Rates by Time since Vaccination during Delta Variant Predominance.
Paz-Bailey, Gabriela; Sternberg, Maya; Kugeler, Kiersten; Hoots, Brooke; Amin, Avnika B; Johnson, Amelia G; Barbeau, Bree; Bayoumi, Nagla S; Bertolino, Daniel; Boulton, Rachelle; Brown, Catherine M; Busen, Katherine; Cima, Michael; Drenzek, Cherie; Gent, Ashley; Haney, Gillian; Hicks, Liam; Hook, Sarah; Jara, Amanda; Jones, Amanda; Kamal-Ahmed, Ishrat; Kangas, Sarah; Kanishka, F N U; Khan, Saadiah I; Kirkendall, Samantha K; Kocharian, Anna; Lyons, B Casey; Lauro, Priscilla; McCormick, Donald; McMullen, Chelsea; Milroy, Lauren; Reese, Heather E; Sell, Jessica; Sierocki, Allison; Smith, Elizabeth; Sosin, Daniel; Stanislawski, Emma; Strand, Kyle; Troelstrup, Thomas; Turner, Kathryn A; Vest, Hailey; Warner, Sydni; Wiedeman, Caleb; Silk, Benjamin; Scobie, Heather M.
Affiliation
  • Paz-Bailey G; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Sternberg M; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Kugeler K; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Hoots B; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Amin AB; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Johnson AG; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Barbeau B; Utah Department of Health, Salt Lake City.
  • Bayoumi NS; New Jersey Department of Health, Trenton.
  • Bertolino D; New York City Department of Health and Mental Hygiene, Long Island City.
  • Boulton R; Utah Department of Health, Salt Lake City.
  • Brown CM; Massachusetts Department of Public Health, Boston.
  • Busen K; Michigan Department of Health and Human Services, Lansing.
  • Cima M; Arkansas Department of Health, Little Rock.
  • Drenzek C; Georgia Department of Health, Atlanta.
  • Gent A; Florida Department of Health, Tallahassee.
  • Haney G; Massachusetts Department of Public Health, Boston.
  • Hicks L; Arizona Department of Health Services, Phoenix.
  • Hook S; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Jara A; Georgia Department of Health, Atlanta.
  • Jones A; Center for Surveillance, Epidemiology, and Laboratory Services, Centers for Disease Control and Prevention, Atlanta.
  • Kamal-Ahmed I; Nebraska Department of Health and Human Services, Lincoln.
  • Kangas S; Wisconsin Department of Health Services, Madison.
  • Kanishka FNU; Nebraska Department of Health and Human Services, Lincoln.
  • Khan SI; New Jersey Department of Health, Trenton.
  • Kirkendall SK; Idaho Department of Health and Welfare, Boise.
  • Kocharian A; Wisconsin Department of Health Services, Madison.
  • Lyons BC; Data Analytics and Visualization Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Lauro P; Arizona Department of Health Services, Phoenix.
  • McCormick D; Arkansas Department of Health, Little Rock.
  • McMullen C; New Mexico Department of Health, Santa Fe.
  • Milroy L; Indiana Department of Health, Indianapolis.
  • Reese HE; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Sell J; New York City Department of Health and Mental Hygiene, Long Island City.
  • Sierocki A; Tennessee Department of Health, Nashville.
  • Smith E; Georgia Department of Health, Atlanta.
  • Sosin D; New Mexico Department of Health, Santa Fe.
  • Stanislawski E; New Mexico Department of Health, Santa Fe.
  • Strand K; Nebraska Department of Health and Human Services, Lincoln.
  • Troelstrup T; Florida Department of Health, Tallahassee.
  • Turner KA; Idaho Department of Health and Welfare, Boise.
  • Vest H; Indiana Department of Health, Indianapolis.
  • Warner S; Wisconsin Department of Health Services, Madison.
  • Wiedeman C; Tennessee Department of Health, Nashville.
  • Silk B; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
  • Scobie HM; Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
NEJM Evid ; 1(3)2022 Jan 10.
Article in En | MEDLINE | ID: mdl-37207114
BACKGROUND: With the emergence of the delta variant, the United States experienced a rapid increase in Covid-19 cases in 2021. We estimated the risk of breakthrough infection and death by month of vaccination as a proxy for waning immunity during a period of delta variant predominance. METHODS: Covid-19 case and death data from 15 U.S. jurisdictions during January 3 to September 4, 2021 were used to estimate weekly hazard rates among fully vaccinated persons, stratified by age group and vaccine product. Case and death rates during August 1 to September 4, 2021 were presented across four cohorts defined by month of vaccination. Poisson models were used to estimate adjusted rate ratios comparing the earlier cohorts to July rates. RESULTS: During August 1 to September 4, 2021, case rates per 100,000 person-weeks among all vaccine recipients for the January to February, March to April, May to June, and July cohorts were 168.8 (95% confidence interval [CI], 167.5 to 170.1), 123.5 (95% CI, 122.8 to 124.1), 83.6 (95% CI, 82.9 to 84.3), and 63.1 (95% CI, 61.6 to 64.6), respectively. Similar trends were observed by age group for BNT162b2 (Pfizer-BioNTech) and mRNA-1273 (Moderna) vaccine recipients. Rates for the Ad26.COV2.S (Janssen-Johnson & Johnson) vaccine were higher; however, trends were inconsistent. BNT162b2 vaccine recipients 65 years of age or older had higher death rates among those vaccinated earlier in the year. Protection against death was sustained for the mRNA-1273 vaccine recipients. Across age groups and vaccine types, people who were vaccinated 6 months ago or longer (January-February) were 3.44 (3.36 to 3.53) times more likely to be infected and 1.70 (1.29 to 2.23) times more likely to die from COVID-19 than people vaccinated recently in July 2021. CONCLUSIONS: Our study suggests that protection from SARS-CoV-2 infection among all ages or death among older adults waned with increasing time since vaccination during a period of delta predominance. These results add to the evidence base that supports U.S. booster recommendations, especially for older adults vaccinated with BNT162b2 and recipients of the Ad26.COV2.S vaccine. (Funded by the Centers for Disease Control and Prevention.).

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NEJM Evid Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NEJM Evid Year: 2022 Type: Article