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Estimation of COVID-19 mRNA Vaccine Effectiveness and COVID-19 Illness and Severity by Vaccination Status During Omicron BA.4 and BA.5 Sublineage Periods.
Link-Gelles, Ruth; Levy, Matthew E; Natarajan, Karthik; Reese, Sarah E; Naleway, Allison L; Grannis, Shaun J; Klein, Nicola P; DeSilva, Malini B; Ong, Toan C; Gaglani, Manjusha; Hartmann, Emily; Dickerson, Monica; Stenehjem, Edward; Kharbanda, Anupam B; Han, Jungmi; Spark, Talia L; Irving, Stephanie A; Dixon, Brian E; Zerbo, Ousseny; McEvoy, Charlene E; Rao, Suchitra; Raiyani, Chandni; Sloan-Aagard, Chantel; Patel, Palak; Dascomb, Kristin; Uhlemann, Anne-Catrin; Dunne, Margaret M; Fadel, William F; Lewis, Ned; Barron, Michelle A; Murthy, Kempapura; Nanez, Juan; Griggs, Eric P; Grisel, Nancy; Annavajhala, Medini K; Akinseye, Akintunde; Valvi, Nimish R; Goddard, Kristin; Mamawala, Mufaddal; Arndorfer, Julie; Yang, Duck-Hye; Embí, Peter J; Fireman, Bruce; Ball, Sarah W; Tenforde, Mark W.
  • Link-Gelles R; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
  • Levy ME; Westat, Rockville, Maryland.
  • Natarajan K; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York.
  • Reese SE; New York-Presbyterian Hospital, New York, New York.
  • Naleway AL; Westat, Rockville, Maryland.
  • Grannis SJ; Kaiser Permanente Center for Health Research, Portland, Oregon.
  • Klein NP; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
  • DeSilva MB; School of Medicine, Indiana University, Indianapolis.
  • Ong TC; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
  • Gaglani M; HealthPartners Institute, Minneapolis, Minnesota.
  • Hartmann E; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora.
  • Dickerson M; Baylor Scott and White Health, Temple, Texas.
  • Stenehjem E; Texas A&M University College of Medicine, Temple.
  • Kharbanda AB; Paso del Norte Health Information Exchange, El Paso, Texas.
  • Han J; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
  • Spark TL; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah.
  • Irving SA; Children's Minnesota, Minneapolis.
  • Dixon BE; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York.
  • Zerbo O; Westat, Rockville, Maryland.
  • McEvoy CE; Kaiser Permanente Center for Health Research, Portland, Oregon.
  • Rao S; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
  • Raiyani C; Fairbanks School of Public Health, Indiana University, Indianapolis.
  • Sloan-Aagard C; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
  • Patel P; HealthPartners Institute, Minneapolis, Minnesota.
  • Dascomb K; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora.
  • Uhlemann AC; Baylor Scott and White Health, Temple, Texas.
  • Dunne MM; Paso del Norte Health Information Exchange, El Paso, Texas.
  • Fadel WF; Department of Public Health, Brigham Young University, Provo, Utah.
  • Lewis N; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
  • Barron MA; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah.
  • Murthy K; Department of Internal Medicine, Division of Infectious Disease, Columbia University Irving Medical Center, New York, New York.
  • Nanez J; Westat, Rockville, Maryland.
  • Griggs EP; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
  • Grisel N; Fairbanks School of Public Health, Indiana University, Indianapolis.
  • Annavajhala MK; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
  • Akinseye A; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora.
  • Valvi NR; Baylor Scott and White Health, Temple, Texas.
  • Goddard K; Paso del Norte Health Information Exchange, El Paso, Texas.
  • Mamawala M; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia.
  • Arndorfer J; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah.
  • Yang DH; Department of Internal Medicine, Division of Infectious Disease, Columbia University Irving Medical Center, New York, New York.
  • Embí PJ; Westat, Rockville, Maryland.
  • Fireman B; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana.
  • Ball SW; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland.
  • Tenforde MW; Baylor Scott and White Health, Temple, Texas.
JAMA Netw Open ; 6(3): e232598, 2023 03 01.
Article in English | MEDLINE | ID: covidwho-2269196
ABSTRACT
Importance Recent SARS-CoV-2 Omicron variant sublineages, including BA.4 and BA.5, may be associated with greater immune evasion and less protection against COVID-19 after vaccination.

Objectives:

To evaluate the estimated vaccine effectiveness (VE) of 2, 3, or 4 doses of COVID-19 mRNA vaccination among immunocompetent adults during a period of BA.4 or BA.5 predominant circulation; and to evaluate the relative severity of COVID-19 in hospitalized patients across Omicron BA.1, BA.2 or BA.2.12.1, and BA.4 or BA.5 sublineage periods. Design, Setting, and

Participants:

This test-negative case-control study was conducted in 10 states with data from emergency department (ED) and urgent care (UC) encounters and hospitalizations from December 16, 2021, to August 20, 2022. Participants included adults with COVID-19-like illness and molecular testing for SARS-CoV-2. Data were analyzed from August 2 to September 21, 2022. Exposures mRNA COVID-19 vaccination. Main Outcomes and

Measures:

The outcomes of interest were COVID-19 ED or UC encounters, hospitalizations, and admission to the intensive care unit (ICU) or in-hospital death. VE associated with protection against medically attended COVID-19 was estimated, stratified by care setting and vaccine doses (2, 3, or 4 doses vs 0 doses as the reference group). Among hospitalized patients with COVID-19, demographic and clinical characteristics and in-hospital outcomes were compared across sublineage periods.

Results:

During the BA.4 and BA.5 predominant period, there were 82 229 eligible ED and UC encounters among patients with COVID-19-like illness (median [IQR] age, 51 [33-70] years; 49 682 [60.4%] female patients), and 19 114 patients (23.2%) had test results positive for SARS-CoV-2; among 21 007 hospitalized patients (median [IQR] age, 71 [58-81] years; 11 209 [53.4%] female patients), 3583 (17.1 %) had test results positive for SARS-CoV-2. Estimated VE against hospitalization was 25% (95% CI, 17%-32%) for receipt of 2 vaccine doses at 150 days or more after receipt, 68% (95% CI, 50%-80%) for a third dose 7 to 119 days after receipt, and 36% (95% CI, 29%-42%) for a third dose 120 days or more (median [IQR], 235 [204-262] days) after receipt. Among patients aged 65 years or older who had received a fourth vaccine dose, VE was 66% (95% CI, 53%-75%) at 7 to 59 days after vaccination and 57% (95% CI, 44%-66%) at 60 days or more (median [IQR], 88 [75-105] days) after vaccination. Among hospitalized patients with COVID-19, ICU admission or in-hospital death occurred in 21.4% of patients during the BA.1 period vs 14.7% during the BA.4 and BA.5 period (standardized mean difference 0.17). Conclusions and Relevance In this case-control study of COVID-19 vaccines and illness, VE associated with protection against medically attended COVID-19 illness was lower with increasing time since last dose; estimated VE was higher after receipt of 1 or 2 booster doses compared with a primary series alone.
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 / Female / Humans / Male / Middle aged Language: English Journal: JAMA Netw Open Year: 2023 Document Type: Article Affiliation country: Jamanetworkopen.2023.2598

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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 / Female / Humans / Male / Middle aged Language: English Journal: JAMA Netw Open Year: 2023 Document Type: Article Affiliation country: Jamanetworkopen.2023.2598