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Vaccine effectiveness of primary series and booster doses against covid-19 associated hospital admissions in the United States: living test negative design study.
Adams, Katherine; Rhoads, Jillian P; Surie, Diya; Gaglani, Manjusha; Ginde, Adit A; McNeal, Tresa; Talbot, H Keipp; Casey, Jonathan D; Zepeski, Anne; Shapiro, Nathan I; Gibbs, Kevin W; Files, D Clark; Hager, David N; Frosch, Anne E; Exline, Matthew C; Mohamed, Amira; Johnson, Nicholas J; Steingrub, Jay S; Peltan, Ithan D; Brown, Samuel M; Martin, Emily T; Lauring, Adam S; Khan, Akram; Busse, Laurence W; Duggal, Abhijit; Wilson, Jennifer G; Chang, Steven Y; Mallow, Christopher; Kwon, Jennie H; Chappell, James D; Halasa, Natasha; Grijalva, Carlos G; Lindsell, Christopher J; Lester, Sandra N; Thornburg, Natalie J; Park, SoHee; McMorrow, Meredith L; Patel, Manish M; Tenforde, Mark W; Self, Wesley H.
  • Adams K; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • Rhoads JP; Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Surie D; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • Gaglani M; Baylor Scott and White Health, Texas A&M University College of Medicine, Temple, TX, USA.
  • Ginde AA; Department of Emergency Medicine, University of Colorado School of Medicine, Aurora, CO, USA.
  • McNeal T; Baylor Scott and White Health, Texas A&M University College of Medicine, Temple, TX, USA.
  • Talbot HK; Department of Medicine¸ Vanderbilt University Medical Center, Nashville, TN, USA.
  • Casey JD; Department of Health Policy, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Zepeski A; Department of Medicine¸ Vanderbilt University Medical Center, Nashville, TN, USA.
  • Shapiro NI; Department of Emergency Medicine, University of Iowa, Iowa City, IA, USA.
  • Gibbs KW; Department of Emergency Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Files DC; Department of Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Hager DN; Department of Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
  • Frosch AE; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Exline MC; Department of Medicine, Hennepin County Medical Center, Minneapolis, MN, USA.
  • Mohamed A; Department of Medicine, The Ohio State University, Columbus, OH, USA.
  • Johnson NJ; Department of Medicine, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Steingrub JS; Department of Emergency Medicine and Division of Pulmonary, Critical Care and Sleep Medicine, University of Washington, Seattle, WA, USA.
  • Peltan ID; Department of Medicine, Baystate Medical Center, Springfield, MA, USA.
  • Brown SM; Department of Medicine, Intermountain Medical Center, Murray, Utah and University of Utah, Salt Lake City, UT, USA.
  • Martin ET; Department of Medicine, Intermountain Medical Center, Murray, Utah and University of Utah, Salt Lake City, UT, USA.
  • Lauring AS; School of Public Health, University of Michigan, Ann Arbor, MI, USA.
  • Khan A; Departments of Internal Medicine and Microbiology and Immunology, University of Michigan, Ann Arbor, MI, USA.
  • Busse LW; Department of Medicine, Oregon Health and Sciences University, Portland, OR, USA.
  • Duggal A; Department of Medicine, Emory University, Atlanta, GA, USA.
  • Wilson JG; Department of Medicine, Cleveland Clinic, Cleveland, OH, USA.
  • Chang SY; Department of Emergency Medicine, Stanford University School of Medicine, Stanford, CA, USA.
  • Mallow C; Department of Medicine, University of California-Los Angeles, Los Angeles, CA, USA.
  • Kwon JH; Department of Medicine, University of Miami, Miami, FL, USA.
  • Chappell JD; Department of Medicine, Washington University, St Louis, MI, USA.
  • Halasa N; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Grijalva CG; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Lindsell CJ; Department of Health Policy, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Lester SN; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Thornburg NJ; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • Park S; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • McMorrow ML; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • Patel MM; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • Tenforde MW; CDC COVID-19 Response Team, Atlanta, GA, USA.
  • Self WH; CDC COVID-19 Response Team, Atlanta, GA, USA.
BMJ ; 379: e072065, 2022 10 11.
Article in English | MEDLINE | ID: covidwho-2064091
ABSTRACT

OBJECTIVE:

To compare the effectiveness of a primary covid-19 vaccine series plus booster doses with a primary series alone for the prevention of hospital admission with omicron related covid-19 in the United States.

DESIGN:

Multicenter observational case-control study with a test negative design.

SETTING:

Hospitals in 18 US states.

PARTICIPANTS:

4760 adults admitted to one of 21 hospitals with acute respiratory symptoms between 26 December 2021 and 30 June 2022, a period when the omicron variant was dominant. Participants included 2385 (50.1%) patients with laboratory confirmed covid-19 (cases) and 2375 (49.9%) patients who tested negative for SARS-CoV-2 (controls). MAIN OUTCOME

MEASURES:

The main outcome was vaccine effectiveness against hospital admission with covid-19 for a primary series plus booster doses and a primary series alone by comparing the odds of being vaccinated with each of these regimens versus being unvaccinated among cases versus controls. Vaccine effectiveness analyses were stratified by immunosuppression status (immunocompetent, immunocompromised). The primary analysis evaluated all covid-19 vaccine types combined, and secondary analyses evaluated specific vaccine products.

RESULTS:

Overall, median age of participants was 64 years (interquartile range 52-75 years), 994 (20.8%) were immunocompromised, 85 (1.8%) were vaccinated with a primary series plus two boosters, 1367 (28.7%) with a primary series plus one booster, and 1875 (39.3%) with a primary series alone, and 1433 (30.1%) were unvaccinated. Among immunocompetent participants, vaccine effectiveness for prevention of hospital admission with omicron related covid-19 for a primary series plus two boosters was 63% (95% confidence interval 37% to 78%), a primary series plus one booster was 65% (58% to 71%), and for a primary series alone was 37% (25% to 47%) (P<0.001 for the pooled boosted regimens compared with a primary series alone). Vaccine effectiveness was higher for a boosted regimen than for a primary series alone for both mRNA vaccines (BNT162b2 (Pfizer-BioNTech) 73% (44% to 87%) for primary series plus two boosters, 64% (55% to 72%) for primary series plus one booster, and 36% (21% to 48%) for primary series alone (P<0.001); mRNA-1273 (Moderna) 68% (17% to 88%) for primary series plus two boosters, 65% (55% to 73%) for primary series plus one booster, and 41% (25% to 54%) for primary series alone (P=0.001)). Among immunocompromised patients, vaccine effectiveness for a primary series plus one booster was 69% (31% to 86%) and for a primary series alone was 49% (30% to 63%) (P=0.04).

CONCLUSION:

During the first six months of 2022 in the US, booster doses of a covid-19 vaccine provided additional benefit beyond a primary vaccine series alone for preventing hospital admissions with omicron related covid-19. READERS' NOTE This article is a living test negative design study that will be updated to reflect emerging evidence. Updates may occur for up to two years from the date of original publication.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Aged / Humans / Middle aged Country/Region as subject: North America Language: English Journal: BMJ Journal subject: Medicine Year: 2022 Document Type: Article Affiliation country: Bmj-2022-072065

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Aged / Humans / Middle aged Country/Region as subject: North America Language: English Journal: BMJ Journal subject: Medicine Year: 2022 Document Type: Article Affiliation country: Bmj-2022-072065