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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.
Embi, Peter J; Levy, Matthew E; Patel, Palak; DeSilva, Malini B; Gaglani, Manjusha; Dascomb, Kristin; Dunne, Margaret M; Klein, Nicola P; Ong, Toan C; Grannis, Shaun J; Natarajan, Karthik; Yang, Duck-Hye; Stenehjem, Edward; Zerbo, Ousseny; McEvoy, Charlene; Rao, Suchitra; Thompson, Mark G; Konatham, Deepika; Irving, Stephanie A; Dixon, Brian E; Han, Jungmi; Schrader, Kristin E; Grisel, Nancy; Lewis, Ned; Kharbanda, Anupam B; Barron, Michelle A; Reynolds, Sue; Liao, I-Chia; Fadel, William F; Rowley, Elizabeth A; Arndorfer, Julie; Goddard, Kristin; Murthy, Kempapura; Valvi, Nimish R; Weber, Zachary A; Fireman, Bruce; Reese, Sarah E; Ball, Sarah W; Naleway, Allison L.
Affiliation
  • Embi PJ; Vanderbilt University Medical Center, Nashville, TN, USA; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA. Electronic address: peter.embi@vumc.org.
  • Levy ME; Westat, Rockville, MD, USA.
  • Patel P; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • DeSilva MB; HealthPartners Institute, Minneapolis, MN, USA.
  • Gaglani M; Baylor Scott & White Health, Texas A&M College of Medicine, Temple, TX, USA; Texas A&M University College of Medicine, Temple, Texas, USA.
  • Dascomb K; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Dunne MM; Westat, Rockville, MD, USA.
  • Klein NP; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Ong TC; School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Grannis SJ; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA; Indiana University School of Medicine, Indianapolis, IN, USA.
  • Natarajan K; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA; New York Presbyterian Hospital, New York, NY, USA.
  • Yang DH; Westat, Rockville, MD, USA.
  • Stenehjem E; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Zerbo O; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • McEvoy C; HealthPartners Institute, Minneapolis, MN, USA.
  • Rao S; School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Thompson MG; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Konatham D; Baylor Scott & White Health, Texas A&M College of Medicine, Temple, TX, USA.
  • Irving SA; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Dixon BE; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA; Fairbanks School of Public Health, Indiana University, Indianapolis, IN, USA.
  • Han J; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
  • Schrader KE; Westat, Rockville, MD, USA.
  • Grisel N; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Lewis N; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Kharbanda AB; Children's Minnesota, Minneapolis, MN, USA.
  • Barron MA; School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Reynolds S; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Liao IC; Baylor Scott & White Health, Texas A&M College of Medicine, Temple, TX, USA.
  • Fadel WF; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA; Fairbanks School of Public Health, Indiana University, Indianapolis, IN, USA.
  • Rowley EA; Westat, Rockville, MD, USA.
  • Arndorfer J; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Goddard K; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Murthy K; Baylor Scott & White Health, Texas A&M College of Medicine, Temple, TX, USA.
  • Valvi NR; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA.
  • Weber ZA; Westat, Rockville, MD, USA.
  • Fireman B; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Reese SE; Westat, Rockville, MD, USA.
  • Ball SW; Westat, Rockville, MD, USA.
  • Naleway AL; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
Vaccine ; 41(37): 5424-5434, 2023 08 23.
Article in En | MEDLINE | ID: mdl-37479609
BACKGROUND: Immunocompromised (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. METHODS: Using 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. RESULTS: We 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. CONCLUSIONS: During 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.
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Full text: 1 Collection: 01-internacional Health context: 1_ASSA2030 / 2_ODS3 / 4_TD Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Type of study: Observational_studies Limits: Adult / Humans Language: En Journal: Vaccine Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 1_ASSA2030 / 2_ODS3 / 4_TD Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Type of study: Observational_studies Limits: Adult / Humans Language: En Journal: Vaccine Year: 2023 Document type: Article