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Article: COVID-19 vaccine effectiveness against the Omicron variant of SARS-CoV-2 in multimorbidity: A territory-wide case-control study

TitleCOVID-19 vaccine effectiveness against the Omicron variant of SARS-CoV-2 in multimorbidity: A territory-wide case-control study
Authors
KeywordsBiological sciences
Health sciences
Public health
Issue Date19-Apr-2024
PublisherCell Press
Citation
iScience, 2024, v. 27, n. 4 How to Cite?
AbstractMultimorbidity entails a higher risk of SARS-CoV-2 infection and COVID-19 complications. We examined vaccine effectiveness (VE) stratified by multimorbidity using a case-control study of territory-wide electronic health records in Hong Kong. Cases of infection (testing positive), hospitalization, and mortality were identified from January to March 2022. Controls were matched by age, sex, outpatient attendance/hospitalization date, and Charlson Comorbidity Index. We demonstrated a consistently good VE among people with increased multimorbidity burden; even more so than among those with minimal such burden. There was also a significantly greater VE after a third dose of BNT162b2 or CoronaVac against infection. The difference in VE between those with multimorbidity and those without was less pronounced for hospitalization, and such difference for COVID-19-related mortality was negligible. In conclusion, VE of both examined vaccines against SARS-CoV-2 infection among people with more complex multimorbidity burden is significant. Further vaccine roll-out should prioritize people with multimorbidity.
Persistent Identifierhttp://hdl.handle.net/10722/346380
ISSN
2023 Impact Factor: 4.6
2023 SCImago Journal Rankings: 1.497

 

DC FieldValueLanguage
dc.contributor.authorLai, Francisco Tsz Tsun-
dc.contributor.authorYan, Vincent Ka Chun-
dc.contributor.authorWan, Eric Yuk Fai-
dc.contributor.authorChan, Cheyenne I.Ying-
dc.contributor.authorWei, Cuiling-
dc.contributor.authorCheng, Franco Wing Tak-
dc.contributor.authorChui, Celine Sze Ling-
dc.contributor.authorLi, Xue-
dc.contributor.authorWong, Carlos King Ho-
dc.contributor.authorCheung, Ching Lung-
dc.contributor.authorWong, Ian Chi Kei-
dc.contributor.authorChan, Esther Wai Yin-
dc.date.accessioned2024-09-16T00:30:32Z-
dc.date.available2024-09-16T00:30:32Z-
dc.date.issued2024-04-19-
dc.identifier.citationiScience, 2024, v. 27, n. 4-
dc.identifier.issn2589-0042-
dc.identifier.urihttp://hdl.handle.net/10722/346380-
dc.description.abstractMultimorbidity entails a higher risk of SARS-CoV-2 infection and COVID-19 complications. We examined vaccine effectiveness (VE) stratified by multimorbidity using a case-control study of territory-wide electronic health records in Hong Kong. Cases of infection (testing positive), hospitalization, and mortality were identified from January to March 2022. Controls were matched by age, sex, outpatient attendance/hospitalization date, and Charlson Comorbidity Index. We demonstrated a consistently good VE among people with increased multimorbidity burden; even more so than among those with minimal such burden. There was also a significantly greater VE after a third dose of BNT162b2 or CoronaVac against infection. The difference in VE between those with multimorbidity and those without was less pronounced for hospitalization, and such difference for COVID-19-related mortality was negligible. In conclusion, VE of both examined vaccines against SARS-CoV-2 infection among people with more complex multimorbidity burden is significant. Further vaccine roll-out should prioritize people with multimorbidity.-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofiScience-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBiological sciences-
dc.subjectHealth sciences-
dc.subjectPublic health-
dc.titleCOVID-19 vaccine effectiveness against the Omicron variant of SARS-CoV-2 in multimorbidity: A territory-wide case-control study-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1016/j.isci.2024.109428-
dc.identifier.scopuseid_2-s2.0-85188077376-
dc.identifier.volume27-
dc.identifier.issue4-
dc.identifier.eissn2589-0042-
dc.identifier.issnl2589-0042-

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