Vaccine effectiveness against COVID-19 hospitalisation in adults (≥ 20 years) during Alpha- and Delta-dominant circulation: I-MOVE-COVID-19 and VEBIS SARI VE networks, Europe, 2021
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu časopisecké články
PubMed
37997666
PubMed Central
PMC10668259
DOI
10.2807/1560-7917.es.2023.28.47.2300186
Knihovny.cz E-zdroje
- Klíčová slova
- Alpha, Delta, Europe, SARS-CoV-2, hospital, vaccine effectiveness,
- MeSH
- COVID-19 * epidemiologie prevence a kontrola MeSH
- dospělí MeSH
- hospitalizace MeSH
- lidé MeSH
- RNA virová MeSH
- SARS-CoV-2 MeSH
- účinnost vakcíny MeSH
- vakcína BNT162 MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Evropa epidemiologie MeSH
- Názvy látek
- RNA virová MeSH
- vakcína BNT162 MeSH
IntroductionTwo large multicentre European hospital networks have estimated vaccine effectiveness (VE) against COVID-19 since 2021.AimWe aimed to measure VE against PCR-confirmed SARS-CoV-2 in hospitalised severe acute respiratory illness (SARI) patients ≥ 20 years, combining data from these networks during Alpha (March-June)- and Delta (June-December)-dominant periods, 2021.MethodsForty-six participating hospitals across 14 countries follow a similar generic protocol using the test-negative case-control design. We defined complete primary series vaccination (PSV) as two doses of a two-dose or one of a single-dose vaccine ≥ 14 days before onset.ResultsWe included 1,087 cases (538 controls) and 1,669 cases (1,442 controls) in the Alpha- and Delta-dominant periods, respectively. During the Alpha period, VE against hospitalisation with SARS-CoV2 for complete Comirnaty PSV was 85% (95% CI: 69-92) overall and 75% (95% CI: 42-90) in those aged ≥ 80 years. During the Delta period, among SARI patients ≥ 20 years with symptom onset ≥ 150 days from last PSV dose, VE for complete Comirnaty PSV was 54% (95% CI: 18-74). Among those receiving Comirnaty PSV and mRNA booster (any product) ≥ 150 days after last PSV dose, VE was 91% (95% CI: 57-98). In time-since-vaccination analysis, complete all-product PSV VE was > 90% in those with their last dose < 90 days before onset; ≥ 70% in those 90-179 days before onset.ConclusionsOur results from this EU multi-country hospital setting showed that VE for complete PSV alone was higher in the Alpha- than the Delta-dominant period, and addition of a first booster dose during the latter period increased VE to over 90%.
AP HP Hôpital Cochin Paris France
Cantacuzino National Military Medical Institute for Research Development Bucharest Romania
Carol Davila University of Medicine and Pharmacy Bucharest Romania
Centre Hospitalier de Luxembourg Luxembourg
Consortium for Biomedical Research in Epidemiology and Public Health Madrid Spain
Croatian Institute of Public Health Zagreb Croatia
Dr Victor Babes Clinical Hospital of Infectious and Tropical Diseases Bucharest Romania
European Centre for Disease Prevention and Control Stockholm Sweden
Faculty of Medicine Masaryk University Brno Czechia
Faculty of Medicine University of Paris City Paris France
Grigore T Popa University of Medicine and Pharmacy Iasi Romania
Health Service Executive Health Protection Surveillance Centre Dublin Ireland
IDCU within Health promotion and disease prevention Directorate G'mangia Malta
Inserm CIC Cochin Pasteur Paris France
Instituto de Salud Pública de Navarra IdiSNA Pamplona Spain
Lithuanian University of Health Sciences Kaunas Lithuania
Luxembourg Institute of Health Luxembourg
National Centre for Epidemiology Institute of Health Carlos 3 Madrid Spain
National Centre for Microbiology Institute of Health Carlos 3 Madrid Spain
National Institute of Health Dr Ricardo Jorge Lisbon Portugal
National Public Health Organisation Athens Greece
Robert Koch Institute Berlin Germany
St Parascheva Clinical Hospital of Infectious Diseases Iasi Romania
Teaching Public Health Institute of Split Dalmatia County Split Croatia
Zobrazit více v PubMed
Harder T, Koch J, Vygen-Bonnet S, Külper-Schiek W, Pilic A, Reda S, et al. Efficacy and effectiveness of COVID-19 vaccines against SARS-CoV-2 infection: interim results of a living systematic review, 1 January to 14 May 2021. Euro Surveill. 2021;26(28):2100563. 10.2807/1560-7917.ES.2021.26.28.2100563 PubMed DOI PMC
European Medicines Agency (EMA). COVID-19 medicines. Amsterdam: EMA. [Accessed: 28 Mar 2021]. Available from: https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/treatments-vaccines-covid-19-authorised-medicines
Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine. N Engl J Med. 2021;384(5):403-16. 10.1056/NEJMoa2035389 PubMed DOI PMC
Polack FP, Thomas SJ, Kitchin N, Absalon J, Gurtman A, Lockhart S, et al. Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine. N Engl J Med. 2020;383(27):2603-15. 10.1056/NEJMoa2034577 PubMed DOI PMC
Sadoff J, Gray G, Vandebosch A, Cárdenas V, Shukarev G, Grinsztejn B, et al. Safety and efficacy of single-dose Ad26.COV2.S vaccine against Covid-19. N Engl J Med. 2021;384(23):2187-201. 10.1056/NEJMoa2101544 PubMed DOI PMC
Voysey M, Clemens SAC, Madhi SA, Weckx LY, Folegatti PM, Aley PK, et al. Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK. Lancet. 2021;397(10269):99-111. 10.1016/S0140-6736(20)32661-1 PubMed DOI PMC
World Health Organization WHO). Evaluation of COVID-19 vaccine effectiveness. Geneva: WHO; 2021. Available from: https://www.who.int/publications-detail-redirect/WHO-2019-nCoV-vaccine_effectiveness-measurement-2021.1
Tregoning JS, Flight KE, Higham SL, Wang Z, Pierce BF. Progress of the COVID-19 vaccine effort: viruses, vaccines and variants versus efficacy, effectiveness and escape. Nat Rev Immunol. 2021;21(10):626-36. 10.1038/s41577-021-00592-1 PubMed DOI PMC
Epiconcept. European study of COVID-19 vaccine effectiveness against hospitalised SARI patients laboratory-confirmed with SARS-CoV-2. Draft generic protocol. Paris: Epiconcept; 2021. Available from: https://www.imoveflu.org/wp-content/uploads/2021/03/08feb2021_draft_generic_VE_protocol_hospital-based_COVID-19_v07.pdf
European Centre for Disease Prevention and Control (ECDC). Core protocol for ECDC studies of COVID-19 vaccine effectiveness against hospitalisation with Severe Acute Respiratory Infection laboratory-confirmed with SARS-CoV-2, version 1.0. Stockholm: ECDC; 2021. Available from: https://www.ecdc.europa.eu/en/publications-data/core-protocol-ecdc-studies-covid-19-vaccine-effectiveness-against-hospitalisation
Shu Y, McCauley J. GISAID: Global initiative on sharing all influenza data - from vision to reality. Euro Surveill. 2017;22(13):30494. 10.2807/1560-7917.ES.2017.22.13.30494 PubMed DOI PMC
Jackson ML, Nelson JC. The test-negative design for estimating influenza vaccine effectiveness. Vaccine. 2013;31(17):2165-8. 10.1016/j.vaccine.2013.02.053 PubMed DOI
Peralta-Santos A. Assessment of COVID-19 surveillance case definitions and data reporting in the European Union. Briefing requested by the ENVI committee. Brussels: European Parliament; July 2020. Available from: https://www.europarl.europa.eu/RegData/etudes/BRIE/2020/652725/IPOL_BRI(2020)652725_EN.pdf
Peduzzi P, Concato J, Feinstein AR, Holford TR. Importance of events per independent variable in proportional hazards regression analysis. II. Accuracy and precision of regression estimates. J Clin Epidemiol. 1995;48(12):1503-10. 10.1016/0895-4356(95)00048-8 PubMed DOI
Covenay J. FIRTHLOGIT: Stata module to calculate bias reduction in logistic regression. Boston: Boston College Department of Economics; 2008. [Accessed: 3 Feb 2020]. Available from: https://econpapers.repec.org/software/bocbocode/s456948.htm
World Health Organization (WHO). WHO surveillance case definitions for ILI and SARI. Geneva: WHO; 2014. Available from: https://www.who.int/teams/global-influenza-programme/surveillance-and-monitoring/case-definitions-for-ili-and-sari
Feikin DR, Abu-Raddad LJ, Andrews N, Davies MA, Higdon MM, Orenstein WA, et al. Assessing vaccine effectiveness against severe COVID-19 disease caused by omicron variant. Report from a meeting of the World Health Organization. Vaccine. 2022;40(26):3516-27. 10.1016/j.vaccine.2022.04.069 PubMed DOI PMC
Stowe J, Andrews N, Kirsebom F, Ramsay M, Bernal JL. Effectiveness of COVID-19 vaccines against Omicron and Delta hospitalisation, a test negative case-control study. Nat Commun. 2022;13(1):5736. 10.1038/s41467-022-33378-7 PubMed DOI PMC
European Centre for Disease Prevention and Control (ECDC). Overview of the implementation of COVID-19 vaccination strategies and vaccine deployment plans in the EU/EEA. Stockholm: ECDC; 2021 [Accessed: 28 Mar 2021]. Available from: https://www.ecdc.europa.eu/en/publications-data/overview-implementation-covid-19-vaccination-strategies-and-vaccine-deployment
European Centre for Disease Prevention and Control (ECDC). COVID-19 vaccine tracker. Stockholm: ECDC. [Accessed: 28 Mar 2021]. Available from: https://vaccinetracker.ecdc.europa.eu/public/extensions/COVID-19/vaccine-tracker.html#uptake-tab
Tenforde MW, Patel MM, Ginde AA, Douin DJ, Talbot HK, Casey JD, et al. . Effectiveness of severe acute respiratory syndrome coronavirus 2 messenger rna vaccines for preventing coronavirus disease 2019 hospitalizations in the United States. Clin Infect Dis. 2022;74(9):1515-24. 10.1093/cid/ciab687 PubMed DOI PMC
Liu Q, Qin C, Liu M, Liu J. Effectiveness and safety of SARS-CoV-2 vaccine in real-world studies: a systematic review and meta-analysis. Infect Dis Poverty. 2021;10(1):132. 10.1186/s40249-021-00915-3 PubMed DOI PMC
Chung H, He S, Nasreen S, Sundaram ME, Buchan SA, Wilson SE, et al. Effectiveness of BNT162b2 and mRNA-1273 covid-19 vaccines against symptomatic SARS-CoV-2 infection and severe covid-19 outcomes in Ontario, Canada: test negative design study. BMJ. 2021;374:n1943. 10.1136/bmj.n1943 PubMed DOI PMC
Stowe J, Andrews N, Gower C, Gallagher E, Utsi L, Simmons R, et al. Effectiveness of COVID-19 vaccines against hospital admission with the Delta (B.1.617.2) variant. Public library. London: UK Health Security Agency. [Accessed: 1 Jan 2023]. Preprint. Available from: https://khub.net/web/phe-national/public-library/-/document_library/v2WsRK3ZlEig/view_file/479607329?_com_liferay_document_library_web_portlet_DLPortlet_INSTANCE_v2WsRK3ZlEig_redirect=https%3A%2F%2Fkhub.net%3A443%2Fweb%2Fphe-national%2Fpublic-library%2F-%2Fdocument_library%2Fv2WsRK3ZlEig%2Fview%2F479607266
Glatman-Freedman A, Bromberg M, Dichtiar R, Hershkovitz Y, Keinan-Boker L. The BNT162b2 vaccine effectiveness against new COVID-19 cases and complications of breakthrough cases: A nation-wide retrospective longitudinal multiple cohort analysis using individualised data. EBioMedicine. 2021;72:103574. 10.1016/j.ebiom.2021.103574 PubMed DOI PMC
Gram MA, Emborg HD, Schelde AB, Friis NU, Nielsen KF, Moustsen-Helms IR, et al. Vaccine effectiveness against SARS-CoV-2 infection or COVID-19 hospitalization with the Alpha, Delta, or Omicron SARS-CoV-2 variant: A nationwide Danish cohort study. PLoS Med. 2022;19(9):e1003992. 10.1371/journal.pmed.1003992 PubMed DOI PMC
Skowronski DM, Setayeshgar S, Zou M, Prystajecky N, Tyson JR, Galanis E, et al. Single-dose mRNA vaccine effectiveness against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), including Alpha and Gamma variants: a test-negative design in adults 70 years and older in British Columbia, Canada. Clin Infect Dis. 2022;74:(7):1158-65. PubMed PMC
Skowronski DM, Setayeshgar S, Zou M, Prystajecky N, Tyson JR, Sbihi H, et al. Comparative single-dose mRNA and ChAdOx1 vaccine effectiveness against severe acute respiratory syndrome coronavirus 2, including variants of concern: test-negative design, British Columbia, Canada. J Infect Dis. 2022;226(1):485-96. 10.1093/infdis/jiac023 PubMed DOI PMC
Starrfelt J, Danielsen AS, Buanes EA, Juvet LK, Lyngstad TM, Rø GØI, et al. Age and product dependent vaccine effectiveness against SARS-CoV-2 infection and hospitalisation among adults in Norway: a national cohort study, July-November 2021. BMC Med. 2022;20(1):278. 10.1186/s12916-022-02480-4 PubMed DOI PMC
Vokó Z, Kiss Z, Surján G, Surján O, Barcza Z, Wittmann I, et al. Effectiveness and waning of protection with different SARS-CoV-2 primary and booster vaccines during the Delta pandemic wave in 2021 in Hungary (HUN-VE 3 study). Front Immunol. 2022;13:919408. 10.3389/fimmu.2022.919408 PubMed DOI PMC
Puranik A, Lenehan PJ, Silvert E, Niesen MJM, Corchado-Garcia J, O’Horo JC, et al. Comparison of two highly-effective mRNA vaccines for COVID-19 during periods of Alpha and Delta variant prevalence. medRxiv; 2021.08.06.21261707. 10.1101/2021.08.06 DOI
Skowronski DM, Febriani Y, Ouakki M, Setayeshgar S, El Adam S, Zou M, et al. Two-dose severe acute respiratory syndrome coronavirus 2 vaccine effectiveness with mixed schedules and extended dosing intervals: test-negative design studies from British Columbia and Quebec, Canada. Clin Infect Dis. 2022;75(11):1980-92. 10.1093/cid/ciac290 PubMed DOI PMC
Goldberg Y, Mandel M, Bar-On YM, Bodenheimer O, Freedman L, Haas EJ, et al. Waning immunity after the BNT162b2 vaccine in Israel. N Engl J Med. 2021;385(24):e85. 10.1056/NEJMoa2114228 PubMed DOI PMC
Andrews N, Tessier E, Stowe J, Gower C, Kirsebom F, Simmons R, et al. Duration of protection against mild and severe disease by Covid-19 vaccines. N Engl J Med. 2022;386(4):340-50. 10.1056/NEJMoa2115481 PubMed DOI PMC
Feikin DR, Higdon MM, Abu-Raddad LJ, Andrews N, Araos R, Goldberg Y, et al. Duration of effectiveness of vaccines against SARS-CoV-2 infection and COVID-19 disease: results of a systematic review and meta-regression. Lancet. 2022;399(10328):924-44. 10.1016/S0140-6736(22)00152-0 PubMed DOI PMC