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Effectiveness of COVID-19 Vaccines at Preventing Emergency Department or Urgent Care Encounters and Hospitalizations Among Immunocompromised Adults: An Observational Study of Real-World Data Across 10 US States from August-December 2021
Peter J. Embi; Matthew E. Levy; Palak Patel; Malini B. DeSilva; Manjusha Gaglani; Kristin Dascomb; Margaret M. Dunne; Nicola P. Klein; Toan C. Ong; Shaun J. Grannis; Karthik Natarajan; Duck-Hye Yang; Edward Stenehjem; Ousseny Zerbo; Charlene McEvoy; Suchitra Rao; Mark G. Thompson; Deepika Konatham; Stephanie A. Irving; Brian E. Dixon; Jungmi Han; Kristin E. Schrader; Nancy Grisel; Ned Lewis; Anupam B. Kharbanda; Michelle A. Barron; Sue Reynolds; I-Chia Liao; William F. Fadel; Elizabeth A. Rowley; Julie Arndorfer; Kristin Goddard; Kempapura Murthy; Nimish R. Valvi; Zachary A. Weber; Bruce Fireman; Sarah E. Reese; Sarah W. Ball; Allison L. Naleway.
Afiliação
  • Peter J. Embi; Regenstrief Institute, Indianapolis, Indiana Vanderbilt University Medical Center, Nashville, Tennessee
  • Matthew E. Levy; Westat, Rockville, Maryland
  • Palak Patel; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia
  • Malini B. DeSilva; HealthPartners Institute, Minneapolis, Minnesota
  • Manjusha Gaglani; Baylor Scott & White Health, Texas A&M University College of Medicine, Temple, Texas
  • Kristin Dascomb; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah
  • Margaret M. Dunne; Westat, Rockville, Maryland
  • Nicola P. Klein; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, California
  • Toan C. Ong; School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado
  • Shaun J. Grannis; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana Indiana University School of Medicine, Indianapolis, Indiana
  • Karthik Natarajan; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York New York Presbyterian Hospital, New York, New York
  • Duck-Hye Yang; Westat, Rockville, Maryland
  • Edward Stenehjem; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah
  • Ousseny Zerbo; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, California
  • Charlene McEvoy; HealthPartners Institute, Minneapolis, Minnesota
  • Suchitra Rao; School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado
  • Mark G. Thompson; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia
  • Deepika Konatham; Baylor Scott & White Health, Temple, Texas
  • Stephanie A. Irving; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon
  • Brian E. Dixon; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana Fairbanks School of Public Health, Indiana University, Indianapolis, Indiana
  • Jungmi Han; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York
  • Kristin E. Schrader; Westat, Rockville, Maryland
  • Nancy Grisel; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah
  • Ned Lewis; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, California
  • Anupam B. Kharbanda; Children's Minnesota, Minneapolis, MN
  • Michelle A. Barron; School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado
  • Sue Reynolds; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia
  • I-Chia Liao; Baylor Scott & White Health, Temple, Texas
  • William F. Fadel; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana Fairbanks School of Public Health, Indiana University, Indianapolis, Indiana
  • Elizabeth A. Rowley; Westat, Rockville, Maryland
  • Julie Arndorfer; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah
  • Kristin Goddard; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, California
  • Kempapura Murthy; Baylor Scott & White Health, Temple, Texas
  • Nimish R. Valvi; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana
  • Zachary A. Weber; Westat, Rockville, Maryland
  • Bruce Fireman; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, California
  • Sarah E. Reese; Westat, Rockville, Maryland
  • Sarah W. Ball; Westat, Rockville, Maryland
  • Allison L. Naleway; Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22281327
ABSTRACT
BackgroundImmunocompromised (IC) persons are at increased risk for severe COVID-19 outcomes and are less protected by 1-2 COVID-19 vaccine doses than are immunocompetent (non-IC) persons. We compared vaccine effectiveness (VE) against medically attended COVID-19 of 2-3 mRNA and 1-2 viral-vector vaccine doses between IC and non-IC adults. MethodsUsing a test-negative design among eight VISION Network sites, VE against laboratory-confirmed COVID-19-associated emergency department (ED) or urgent care (UC) events and hospitalizations from 26 August-25 December 2021 was estimated separately among IC and non-IC adults and among specific IC condition subgroups. Vaccination status was defined using number and timing of doses. VE for each status (versus unvaccinated) was adjusted for age, geography, time, prior positive test result, and local SARS-CoV-2 circulation. ResultsWe analyzed 8,848 ED/UC events and 18,843 hospitalizations among IC patients and 200,071 ED/UC events and 70,882 hospitalizations among non-IC patients. Among IC patients, 3-dose mRNA VE against ED/UC (73% [95% CI 64-80]) and hospitalization (81% [95% CI 76-86]) was lower than that among non-IC patients (ED/UC 94% [95% CI 93-94]; hospitalization 96% [95% CI 95-97]). Similar patterns were observed for viral-vector vaccines. Transplant recipients had lower VE than other IC subgroups. ConclusionsDuring B.1.617.2 (Delta) variant predominance, IC adults received moderate protection against COVID-19-associated medical events from three mRNA doses, or one viral-vector dose plus a second dose of any product. However, protection was lower in IC versus non-IC patients, especially among transplant recipients, underscoring the need for additional protection among IC adults. Key pointsDuring Delta variant predominance, immunocompromised (IC) adults received moderate protection against COVID-19-associated medical events from three mRNA doses, but IC patients, especially transplant recipients, were less protected than non-IC patients, underscoring the need for additional protection beyond the primary series.
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Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Preprint