Effectiveness of CoronaVac in the prevention of COVID-19, a test-negative case-control study in Brazil

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dc.contributorCentro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.authorLuna, Expedito J. A.pt_BR
dc.contributor.authorMoraes, José C.pt_BR
dc.contributor.authorRoediger, Manuela de Almeidapt_BR
dc.contributor.authorde Miranda, Erique Jose Farias Peixotopt_BR
dc.contributor.authorBraga, Patrícia Emíliapt_BR
dc.contributor.authorFrança, João Italo Dias dept_BR
dc.contributor.authorPacheco, Pedro Henrique de Mesquitapt_BR
dc.contributor.authorLima, Marcos Alves dept_BR
dc.contributor.authorRagiotto, Lucaspt_BR
dc.contributor.authorBarros, Eliana Nogueira Castro dept_BR
dc.date.accessioned2024-09-18T12:15:36Z-
dc.date.available2024-09-18T12:15:36Z-
dc.date.issued2024pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/5465-
dc.description.abstractThe 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.extent103856pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofThe Brazilian Journal of Infectious Diseasespt_BR
dc.rightsOpen accesspt_BR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_BR
dc.titleEffectiveness of CoronaVac in the prevention of COVID-19, a test-negative case-control study in Brazilpt_BR
dc.typeArticlept_BR
dc.rights.licenseCC BYpt_BR
dc.identifier.doi10.1016/j.bjid.2024.103856pt_BR
dc.contributor.external(USP) Universidade de São Paulopt_BR
dc.contributor.external(FCMSCSP) Faculdade de Ciências Médicas da Santa Casa de São Paulopt_BR
dc.identifier.citationvolume28pt_BR
dc.identifier.citationissue5pt_BR
dc.subject.keywordSARS-CoV2pt_BR
dc.subject.keywordinactivated vaccinespt_BR
dc.subject.keywordeffectivenesspt_BR
dc.subject.keywordtest-negativept_BR
dc.subject.keywordcase-control studypt_BR
dc.subject.keywordBrazilpt_BR
dc.relation.ispartofabbreviatedBraz J Infect Dispt_BR
dc.identifier.citationabntv. 28, n. 8, 103856, ago. 2024pt_BR
dc.identifier.citationvancouver2024 Aug; 28(5):103856pt_BR
dc.contributor.butantanRoediger, Manuela de Almeida|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantande Miranda, Erique Jose Farias Peixoto|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantanBraga, Patrícia Emília|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantanFrança, João Italo Dias de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantanPacheco, Pedro Henrique de Mesquita|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantanLima, Marcos Alves de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantanRagiotto, Lucas|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.contributor.butantanBarros, Eliana Nogueira Castro de|:Outros|:Centro de Ensaios Clínicos e Farmacovigilânciapt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
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