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dc.contributor.authorCvetkovic-Vega, A.
dc.contributor.authorUrrunaga-Pastor, D.
dc.contributor.authorSoto-Becerra, P.
dc.contributor.authorFigueroa-Montes, L.E.
dc.contributor.authorFernandez-Bolivar, L.
dc.contributor.authorAlvizuri-Pastor, S.
dc.contributor.authorOyanguren-Miranda, M.
dc.contributor.authorNeyra-Vera, I.
dc.contributor.authorCarrillo-Ramos, E.
dc.contributor.authorSagástegui, A.
dc.contributor.authorContreras-Macazana, R.
dc.contributor.authorLecca-Rengifo, D.
dc.contributor.authorGrande-Castro, N.
dc.contributor.authorApolaya-Segura, M.
dc.contributor.authorMaguina, J.L.
dc.date.accessioned2025-10-31T18:41:36Z
dc.date.available2025-10-31T18:41:36Z
dc.date.issued2023
dc.identifier.urihttps://hdl.handle.net/20.500.12805/5903
dc.description.abstractObjective: To estimate the prevalence of post-vaccination seropositivity against SARS-CoV-2 and identify its predictors in Peruvian Social Health Insurance (EsSalud) personnel in 2021. Methods: We conducted a cross-sectional study in a representative simple stratified sample of EsSalud workers. We evaluated IgG anti-SARS-CoV-2 antibodies response (seropositivity) by passive (previous infection) and active immunization (vaccination), and epidemiological and occupational variables obtained by direct interview and a data collection form. Descriptive and inferential statistics were used with correction of sample weights adjusted for non-response rate, and crude and adjusted odds ratio (OR) and geometric mean ratio (GMR) with their respective 95% confidence intervals (95%CI) were estimated. Results: We enrolled 1077 subjects. Seropositivity was 67.4% (95%CI: 63.4–71.1). Predictors of seropositivity were age (negative relation; p < 0.001), previous infection (aOR = 11.7; 95%CI: 7.81–17.5), working in COVID-19 area (aOR = 1.47; 95%CI: 1.02–2.11) and time since the second dose. In relation to antibody levels measured by geometric means, there was an association between male sex (aGMR = 0.77; 95%CI: 0.74–0.80), age (negative relation; p < 0.001), previous infection (aGMR = 13.1; 95%CI:4.99–34.40), non-face-to-face/licensed work modality (aGMR = 0.78; 95%CI: 0.73–0.84), being a nursing technician (aGMR = 1.30; 95%CI: 1.20–1.41), working in administrative areas (aGMR = 1.17; 95%CI: 1.10–1.25), diagnostic support (aGMR = 1.07; 95%CI: 1.01–1.15), critical care (aGMR = 0.85; 95%CI: 0.79–0.93), and in a COVID-19 area (aGMR = 1.30; 95%CI: 1.24–1.36) and time since receiving the second dose (negative relation; p < 0.001). Conclusions: Seropositivity and antibody levels decrease as the time since receiving the second dose increases. Older age and no history of previous infection were associated with lower seropositivity and antibody values. These findings may be useful for sentinel antibody surveillance and the design of booster dose strategies.en_US
dc.description.sponsorshipFunding text 1: This research was carried out with funding from the Peruvian Social Health Insurance - EsSalud.; Funding text 2: The research team would like to thank all the health and non-health personnel who participated in the study. We would also like to thank the EsSalud 107 call team, as well as the teams of the IETSI units and the Flexible Supply Management that provided on-site support in the execution of the research and to the health personnel of the clinical pathology service of the EsSalud Hospital Nivel III Suárez Angamos.
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofurn:issn:1477-8939
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectSDG 3en_US
dc.subjectCOVID-19, Its Impact, and Vaccinationen_US
dc.subjectVaccine Efficacy and Immune Response in COVID-19en_US
dc.titlePost-vaccination seropositivity against SARS-CoV-2 in peruvian health workers vaccinated with BBIBP-CorV (Sinopharm)en_US
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.doihttps://doi.org/10.1016/j.tmaid.2022.102514
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.03.09
dc.type.otherResearch article
dc.identifier.journalTravel Medicine and Infectious Disease
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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