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

Author:

Link-Gelles Ruth1,Levy Matthew E.2,Natarajan Karthik34,Reese Sarah E.2,Naleway Allison L.5,Grannis Shaun J.67,Klein Nicola P.8,DeSilva Malini B.9,Ong Toan C.10,Gaglani Manjusha1112,Hartmann Emily13,Dickerson Monica1,Stenehjem Edward14,Kharbanda Anupam B.15,Han Jungmi3,Spark Talia L.2,Irving Stephanie A.5,Dixon Brian E.616,Zerbo Ousseny8,McEvoy Charlene E.9,Rao Suchitra10,Raiyani Chandni11,Sloan-Aagard Chantel1317,Patel Palak1,Dascomb Kristin14,Uhlemann Anne-Catrin18,Dunne Margaret M.2,Fadel William F.616,Lewis Ned8,Barron Michelle A.10,Murthy Kempapura11,Nanez Juan13,Griggs Eric P.1,Grisel Nancy14,Annavajhala Medini K.18,Akinseye Akintunde2,Valvi Nimish R.6,Goddard Kristin8,Mamawala Mufaddal11,Arndorfer Julie14,Yang Duck-Hye2,Embí Peter J.619,Fireman Bruce8,Ball Sarah W.2,Tenforde Mark W.1

Affiliation:

1. Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, Georgia

2. Westat, Rockville, Maryland

3. Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, New York

4. New York–Presbyterian Hospital, New York, New York

5. Kaiser Permanente Center for Health Research, Portland, Oregon

6. Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, Indiana

7. School of Medicine, Indiana University, Indianapolis

8. Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland

9. HealthPartners Institute, Minneapolis, Minnesota

10. Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora

11. Baylor Scott and White Health, Temple, Texas

12. Texas A&M University College of Medicine, Temple

13. Paso del Norte Health Information Exchange, El Paso, Texas

14. Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, Utah

15. Children’s Minnesota, Minneapolis

16. Fairbanks School of Public Health, Indiana University, Indianapolis

17. Department of Public Health, Brigham Young University, Provo, Utah

18. Department of Internal Medicine, Division of Infectious Disease, Columbia University Irving Medical Center, New York, New York

19. Vanderbilt University Medical Center, Nashville, Tennessee

Abstract

ImportanceRecent 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.ObjectivesTo 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 ParticipantsThis 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.ExposuresmRNA COVID-19 vaccination.Main Outcomes and MeasuresThe 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.ResultsDuring 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 RelevanceIn 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.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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