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Comparative complete scheme and booster effectiveness of COVID-19 vaccines in preventing SARS-CoV-2 infections with SARS-CoV-2 Omicron (BA.1) and Delta (B.1.617.2) variants: A case-case study based on electronic health records.
Kislaya, Irina; Peralta-Santos, André; Borges, Vítor; Vieira, Luís; Sousa, Carlos; Ferreira, Bibiana; Pelerito, Ana; Gomes, João Paulo; Leite, Pedro Pinto; Nunes, Baltazar; Machado, Ausenda; Rodrigues, Ana Paula; Peixoto, Vasco Ricoca; Casaca, Pedro; Fernandes, Eugenia; Rodrigues, Eduardo; Ferreira, Rita; Isidro, Joana; Pinto, Miguel; Duarte, Sílvia; Santos, Daniela; Meneses, Luís; Almeida, José Pedro; Matias, Ana; Freire, Samanta; Grilo, Teresa.
Afiliação
  • Kislaya I; Department of Epidemiology National Institute of Health Doutor Ricardo Jorge Lisbon Portugal.
  • Peralta-Santos A; Public Health Research Centre, NOVA National School of Public Health Universidade NOVA de Lisboa Lisbon Portugal.
  • Borges V; Comprehensive Health Research Centre (CHRC) Universidade NOVA de Lisboa Lisbon Portugal.
  • Vieira L; Public Health Research Centre, NOVA National School of Public Health Universidade NOVA de Lisboa Lisbon Portugal.
  • Sousa C; Comprehensive Health Research Centre (CHRC) Universidade NOVA de Lisboa Lisbon Portugal.
  • Ferreira B; Direção de Serviços de Informação e Análise Direção-Geral da Saúde Lisbon Portugal.
  • Pelerito A; Genomic and Bioinformatics Unit, Department of Infectious Diseases National Institute of Health Doutor Ricardo Jorge Lisbon Portugal.
  • Gomes JP; Departamento de Genética Humana, Instituto Nacional de Saúde Doutor Ricardo Jorge Unidade de Tecnologia e Inovação Lisbon Portugal.
  • Leite PP; Unilabs Porto Portugal.
  • Nunes B; Algarve Biomedical Center Research Institute (ABC-RI) Faro Portugal.
  • Machado A; Portuguese Red Cross Laboratory Lisbon Portugal.
  • Rodrigues AP; Genomic and Bioinformatics Unit, Department of Infectious Diseases National Institute of Health Doutor Ricardo Jorge Lisbon Portugal.
  • Peixoto VR; Direção de Serviços de Informação e Análise Direção-Geral da Saúde Lisbon Portugal.
  • Casaca P; Department of Epidemiology National Institute of Health Doutor Ricardo Jorge Lisbon Portugal.
  • Fernandes E; Public Health Research Centre, NOVA National School of Public Health Universidade NOVA de Lisboa Lisbon Portugal.
  • Rodrigues E; Comprehensive Health Research Centre (CHRC) Universidade NOVA de Lisboa Lisbon Portugal.
  • Isidro J; Department of Epidemiology National Institute of Health Doutor Ricardo Jorge Lisbon Portugal.
  • Pinto M; Public Health Research Centre, NOVA National School of Public Health Universidade NOVA de Lisboa Lisbon Portugal.
  • Duarte S; Comprehensive Health Research Centre (CHRC) Universidade NOVA de Lisboa Lisbon Portugal.
  • Santos D; Direção de Serviços de Informação e Análise Direção-Geral da Saúde Lisbon Portugal.
  • Meneses L; Genomic and Bioinformatics Unit, Department of Infectious Diseases National Institute of Health Doutor Ricardo Jorge Lisbon Portugal.
  • Almeida JP; Departamento de Genética Humana, Instituto Nacional de Saúde Doutor Ricardo Jorge Unidade de Tecnologia e Inovação Lisbon Portugal.
  • Matias A; Unilabs Porto Portugal.
  • Freire S; Algarve Biomedical Center Research Institute (ABC-RI) Faro Portugal.
  • Grilo T; Faculty of Medicine and Biomedical Sciences (FMCB), Campus de Gambelas University of Algarve Faro Portugal.
Influenza Other Respir Viruses ; 17(3): e13121, 2023 03.
Article em En | MEDLINE | ID: mdl-36935845
ABSTRACT

Background:

Information on vaccine effectiveness in a context of novel variants of concern (VOC) emergence is of key importance to inform public health policies. This study aimed to estimate a measure of comparative vaccine effectiveness between Omicron (BA.1) and Delta (B.1.617.2 and sub-lineages) VOC according to vaccination exposure (primary or booster).

Methods:

We developed a case-case study using data on RT-PCR SARS-CoV-2-positive cases notified in Portugal during Weeks 49-51, 2021. To obtain measure of comparative vaccine effectiveness, we compared the odds of vaccination in Omicron cases versus Delta using logistic regression adjusted for age group, sex, region, week of diagnosis, and laboratory of origin.

Results:

Higher odds of vaccination were observed in cases infected by Omicron VOC compared with Delta VOC cases for both complete primary vaccination (odds ratio [OR] = 2.1; 95% confidence interval [CI] 1.8 to 2.4) and booster dose (OR = 5.2; 95% CI 3.1 to 8.8), equivalent to reduction of vaccine effectiveness from 44.7% and 92.8%, observed against infection with Delta, to -6.0% (95% CI 29.2% to 12.7%) and 62.7% (95% CI 35.7% to 77.9%), observed against infection with Omicron, for complete primary vaccination and booster dose, respectively.

Conclusion:

Consistent reduction in vaccine-induced protection against infection with Omicron was observed. Complete primary vaccination may not be protective against SARS-CoV-2 infection in regions where Omicron variant is dominant.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article