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

被引:51
|
作者
Link-Gelles, Ruth [1 ]
Levy, Matthew E. [2 ]
Natarajan, Karthik [3 ,4 ]
Reese, Sarah E. [2 ]
Naleway, Allison L. [5 ]
Grannis, Shaun J. [6 ,7 ]
Klein, Nicola P. [8 ]
DeSilva, Malini B. [9 ]
Ong, Toan C. [10 ]
Gaglani, Manjusha [11 ,12 ]
Hartmann, Emily [13 ]
Dickerson, Monica [1 ]
Stenehjem, Edward [14 ]
Kharbanda, Anupam B. [15 ]
Han, Jungmi [3 ]
Spark, Talia L. [2 ]
Irving, Stephanie A. [5 ]
Dixon, Brian E. [6 ,16 ]
Zerbo, Ousseny [8 ]
McEvoy, Charlene E. [9 ]
Rao, Suchitra [10 ]
Raiyani, Chandni [11 ]
Sloan-Aagard, Chantel [13 ,17 ]
Patel, Palak [1 ]
Dascomb, Kristin [14 ]
Uhlemann, Anne-Catrin [18 ]
Dunne, Margaret M. [2 ]
Fadel, William F. [6 ,16 ]
Lewis, Ned [8 ]
Barron, Michelle A. [10 ]
Murthy, Kempapura [11 ]
Nanez, Juan [13 ]
Griggs, Eric P. [1 ]
Grisel, Nancy [14 ]
Annavajhala, Medini K. [18 ]
Akinseye, Akintunde [2 ]
Valvi, Nimish R. [6 ]
Goddard, Kristin [8 ]
Mamawala, Mufaddal [11 ]
Arndorfer, Julie [14 ]
Yang, Duck-Hye [2 ]
Embi, Peter J. [6 ,19 ]
Fireman, Bruce [8 ]
Ball, Sarah W. [2 ]
Tenforde, Mark W. [1 ]
机构
[1] Ctr Dis Control & Prevent COVID 19 Response Team, 1600 Clifton Rd,Mailstop H24-5, Atlanta, GA 30329 USA
[2] Westat Corp, Rockville, MD USA
[3] Columbia Univ, Irving Med Ctr, Dept Biomed Informat, New York, NY USA
[4] New York Presbyterian Hosp, New York, NY USA
[5] Kaiser Permanente Ctr Hlth Res, Portland, OR USA
[6] Regenstrief Inst Hlth Care, Ctr Biomed Informat, Indianapolis, IN USA
[7] Indiana Univ, Sch Med, Indianapolis, IN USA
[8] Kaiser Permanente Northern Calif, Kaiser Permanente Vaccine Study Ctr, Div Res, Oakland, CA USA
[9] HealthPartners Inst, Minneapolis, MN USA
[10] Univ Colorado Anschutz Med Campus, Dept Pediat, Aurora, CO USA
[11] Baylor Scott & White Hlth, Temple, TX USA
[12] Texas A&M Univ, Coll Med, Temple, TX 76508 USA
[13] Paso del Norte Hlth Informat Exchange, El Paso, TX USA
[14] Intermountain Healthcare, Div Infect Dis & Clin Epidemiol, Salt Lake City, UT USA
[15] Childrens Minnesota, Minneapolis, MN USA
[16] Indiana Univ, Fairbanks Sch Publ Hlth, Indianapolis, IN 46204 USA
[17] Brigham Young Univ, Dept Publ Hlth, Provo, UT 84602 USA
[18] Columbia Univ, Irving Med Ctr, Div Infect Dis, Dept Internal Med, New York, NY USA
[19] Vanderbilt Univ, Med Ctr, Nashville, TN USA
关键词
UNITED-STATES; HOSPITALIZATIONS; ANTIBODIES; INFECTION; 2-DOSE; ADULTS;
D O I
10.1001/jamanetworkopen.2023.2598
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 82229 eligible ED and UC encounters among patients with COVID-19-like illness (median [IQR] age, 51 [33-70] years; 49682 [60.4%] female patients), and 19114 patients (23.2%) had test results positive for SARS-CoV-2; among 21007 hospitalized patients (median [IQR] age, 71 [58-81] years; 11209 [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.
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