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Effectiveness of two and three mRNA COVID-19 vaccine doses against Omicron- and Delta-Related outpatient illness among adults, October 2021-February 2022.
Kim, Sara S; Chung, Jessie R; Talbot, H Keipp; Grijalva, Carlos G; Wernli, Karen J; Kiniry, Erika; Martin, Emily T; Monto, Arnold S; Belongia, Edward A; McLean, Huong Q; Gaglani, Manjusha; Mamawala, Mufaddal; Nowalk, Mary Patricia; Moehling Geffel, Krissy; Tartof, Sara Y; Florea, Ana; Lee, Justin S; Tenforde, Mark W; Patel, Manish M; Flannery, Brendan; Bentz, Meghan L; Burgin, Alex; Burroughs, Mark; Davis, Morgan L; Howard, Dakota; Lacek, Kristine; Madden, Joseph C; Nobles, Sarah; Padilla, Jasmine; Sheth, Mili.
  • Kim SS; Centers for Disease Control and Prevention Atlanta Georgia USA.
  • Chung JR; Centers for Disease Control and Prevention Atlanta Georgia USA.
  • Talbot HK; Vanderbilt University Medical Center Nashville Tennessee USA.
  • Grijalva CG; Vanderbilt University Medical Center Nashville Tennessee USA.
  • Wernli KJ; Kaiser Permanente Washington Health Research Institute Seattle Washington USA.
  • Kiniry E; Kaiser Permanente Washington Health Research Institute Seattle Washington USA.
  • Martin ET; University of Michigan School of Public Health Ann Arbor Michigan USA.
  • Monto AS; University of Michigan School of Public Health Ann Arbor Michigan USA.
  • Belongia EA; Marshfield Clinic Research Institute Marshfield Wisconsin USA.
  • McLean HQ; Marshfield Clinic Research Institute Marshfield Wisconsin USA.
  • Gaglani M; Baylor Scott and White Health Temple Texas USA.
  • Mamawala M; Texas A&M University College of Medicine Temple Texas USA.
  • Nowalk MP; Baylor Scott and White Health Temple Texas USA.
  • Moehling Geffel K; University of Pittsburgh Schools of Health Sciences Pittsburgh Pennsylvania USA.
  • Tartof SY; University of Pittsburgh Schools of Health Sciences Pittsburgh Pennsylvania USA.
  • Florea A; Kaiser Permanente Southern California Pasadena California USA.
  • Lee JS; Kaiser Permanente Southern California Pasadena California USA.
  • Tenforde MW; Centers for Disease Control and Prevention Atlanta Georgia USA.
  • Patel MM; Centers for Disease Control and Prevention Atlanta Georgia USA.
  • Flannery B; Centers for Disease Control and Prevention Atlanta Georgia USA.
  • Burgin A; Centers for Disease Control and Prevention Atlanta Georgia USA.
  • Burroughs M; Vanderbilt University Medical Center Nashville Tennessee USA.
  • Davis ML; Kaiser Permanente Washington Health Research Institute Seattle Washington USA.
  • Howard D; University of Michigan School of Public Health Ann Arbor Michigan USA.
  • Lacek K; Marshfield Clinic Research Institute Marshfield Wisconsin USA.
  • Madden JC; Baylor Scott and White Health Temple Texas USA.
  • Nobles S; Texas A&M University College of Medicine Temple Texas USA.
  • Padilla J; University of Pittsburgh Schools of Health Sciences Pittsburgh Pennsylvania USA.
  • Sheth M; Kaiser Permanente Southern California Pasadena California USA.
Influenza Other Respir Viruses ; 16(6): 975-985, 2022 11.
Article in English | MEDLINE | ID: covidwho-1968142
ABSTRACT

Background:

We estimated SARS-CoV-2 Delta- and Omicron-specific effectiveness of two and three mRNA COVID-19 vaccine doses in adults against symptomatic illness in US outpatient settings.

Methods:

Between October 1, 2021, and February 12, 2022, research staff consented and enrolled eligible participants who had fever, cough, or loss of taste or smell and sought outpatient medical care or clinical SARS-CoV-2 testing within 10 days of illness onset. Using the test-negative design, we compared the odds of receiving two or three mRNA COVID-19 vaccine doses among SARS-CoV-2 cases versus controls using logistic regression. Regression models were adjusted for study site, age, onset week, and prior SARS-CoV-2 infection. Vaccine effectiveness (VE) was calculated as (1 - adjusted odds ratio) × 100%.

Results:

Among 3847 participants included for analysis, 574 (32%) of 1775 tested positive for SARS-CoV-2 during the Delta predominant period and 1006 (56%) of 1794 participants tested positive during the Omicron predominant period. When Delta predominated, VE against symptomatic illness in outpatient settings was 63% (95% CI 51% to 72%) among mRNA two-dose recipients and 96% (95% CI 93% to 98%) for three-dose recipients. When Omicron predominated, VE was 21% (95% CI -6% to 41%) among two-dose recipients and 62% (95% CI 48% to 72%) among three-dose recipients.

Conclusions:

In this adult population, three mRNA COVID-19 vaccine doses provided substantial protection against symptomatic illness in outpatient settings when the Omicron variant became the predominant cause of COVID-19 in the United States. These findings support the recommendation for a third mRNA COVID-19 vaccine dose.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Outpatients / COVID-19 Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Humans Language: English Journal: Influenza Other Respir Viruses Journal subject: Virology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Outpatients / COVID-19 Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Humans Language: English Journal: Influenza Other Respir Viruses Journal subject: Virology Year: 2022 Document Type: Article