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Effectiveness of CoronaVac in the prevention of COVID-19, a test-negative case-control study in Brazil
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DC Field | Value | Language |
---|---|---|
dc.contributor | Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.author | Luna, Expedito J. A. | pt_BR |
dc.contributor.author | Moraes, José C. | pt_BR |
dc.contributor.author | Roediger, Manuela de Almeida | pt_BR |
dc.contributor.author | de Miranda, Erique Jose Farias Peixoto | pt_BR |
dc.contributor.author | Braga, Patrícia Emília | pt_BR |
dc.contributor.author | França, João Italo Dias de | pt_BR |
dc.contributor.author | Pacheco, Pedro Henrique de Mesquita | pt_BR |
dc.contributor.author | Lima, Marcos Alves de | pt_BR |
dc.contributor.author | Ragiotto, Lucas | pt_BR |
dc.contributor.author | Barros, Eliana Nogueira Castro de | pt_BR |
dc.date.accessioned | 2024-09-18T12:15:36Z | - |
dc.date.available | 2024-09-18T12:15:36Z | - |
dc.date.issued | 2024 | pt_BR |
dc.identifier.uri | https://repositorio.butantan.gov.br/handle/butantan/5465 | - |
dc.description.abstract | The present study aimed to evaluate the effectiveness of two doses of CoronaVac in preventing SARS-CoV-2 symptomatic disease with virological confirmation, as well as in the prevention of COVID-19 moderate and severe cases. A test-negative unmatched case-control design was used, in which cases were patients with suspected COVID-19 (presenting at least two of the following symptoms: fever, chills, sore throat, headache, cough, runny nose, olfactory or taste disorders) with virological confirmation, and controls were those whose SARS-CoV-2 test was negative. As for exposure, participants were classified as unvaccinated, or vaccinated with a complete schedule. Suspected COVID-19 cases were identified from March to November 2021, in two cities located in the State of Sao Paulo, Brazil. All participa ~ nts signed the Informed Consent Form before enrollment. RT-PCR results and vaccination data were obtained from the local surveillance systems. Up to two phone calls were made to obtain information on the outcome of the cases. A total of 2981 potential participants were screened for eligibility, of which 2163 were included, being 493 cases and 1670 controls. Vaccination, age, the reported contact with a COVID-19 suspected or confirmed case in the 14 days before symptoms onset, and the educational level were the variables independently associated with the outcome. The adjusted vaccine effectiveness for symptomatic COVID-19 (AVE) was 39.0 % (95 % CI 6.0−60.0 %). The AVE in the prevention of moderate and severe disease was 91.0 % (95 % CI 76.0−97.0 %). Our results were influenced by the waning of the Gamma variant, in the second trimester of 2021, followed by the increase in vaccination coverage, and a drop in the number of cases in the second half of the year. The study demonstrated the high effectiveness of CoronaVac in preventing moderate/severe COVID-19 cases. | pt_BR |
dc.format.extent | 103856 | pt_BR |
dc.language.iso | English | pt_BR |
dc.relation.ispartof | The Brazilian Journal of Infectious Diseases | pt_BR |
dc.rights | Open access | pt_BR |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | pt_BR |
dc.title | Effectiveness of CoronaVac in the prevention of COVID-19, a test-negative case-control study in Brazil | pt_BR |
dc.type | Article | pt_BR |
dc.rights.license | CC BY | pt_BR |
dc.identifier.doi | 10.1016/j.bjid.2024.103856 | pt_BR |
dc.contributor.external | (USP) Universidade de São Paulo | pt_BR |
dc.contributor.external | (FCMSCSP) Faculdade de Ciências Médicas da Santa Casa de São Paulo | pt_BR |
dc.identifier.citationvolume | 28 | pt_BR |
dc.identifier.citationissue | 5 | pt_BR |
dc.subject.keyword | SARS-CoV2 | pt_BR |
dc.subject.keyword | inactivated vaccines | pt_BR |
dc.subject.keyword | effectiveness | pt_BR |
dc.subject.keyword | test-negative | pt_BR |
dc.subject.keyword | case-control study | pt_BR |
dc.subject.keyword | Brazil | pt_BR |
dc.relation.ispartofabbreviated | Braz J Infect Dis | pt_BR |
dc.identifier.citationabnt | v. 28, n. 8, 103856, ago. 2024 | pt_BR |
dc.identifier.citationvancouver | 2024 Aug; 28(5):103856 | pt_BR |
dc.contributor.butantan | Roediger, Manuela de Almeida|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | de Miranda, Erique Jose Farias Peixoto|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Braga, Patrícia Emília|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | França, João Italo Dias de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Pacheco, Pedro Henrique de Mesquita|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Lima, Marcos Alves de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Ragiotto, Lucas|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.contributor.butantan | Barros, Eliana Nogueira Castro de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilância | pt_BR |
dc.identifier.bvscc | BR78.1 | pt_BR |
dc.identifier.bvsdb | IBProd | pt_BR |
dc.description.dbindexed | Yes | pt_BR |
item.grantfulltext | open | - |
item.languageiso639-1 | English | - |
item.fulltext | Com Texto completo | - |
item.openairetype | Article | - |
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