Trends in Cases, Hospitalizations, and Mortality Related to the Omicron BA.4/BA.5 Subvariants in South Africa.
COVID-19
Omicron BA.4
Omicron BA.5
hospital admissions
mortality
Journal
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213
Informations de publication
Date de publication:
17 04 2023
17 04 2023
Historique:
received:
25
08
2022
medline:
19
4
2023
pubmed:
2
12
2022
entrez:
1
12
2022
Statut:
ppublish
Résumé
In this study, we compared admission incidence risk and the risk of mortality in the Omicron BA.4/BA.5 wave to previous waves. Data from South Africa's SARS-CoV-2 case linelist, national COVID-19 hospital surveillance system, and Electronic Vaccine Data System were linked and analyzed. Wave periods were defined when the country passed a weekly incidence of 30 cases/100 000 population. In-hospital case fatality ratios (CFRs) during the Delta, Omicron BA.1/BA.2, and Omicron BA.4/BA.5 waves were compared using post-imputation random effect multivariable logistic regression models. The CFR was 25.9% (N = 37 538 of 144 778), 10.9% (N = 6123 of 56 384), and 8.2% (N = 1212 of 14 879) in the Delta, Omicron BA.1/BA.2, and Omicron BA.4/BA.5 waves, respectively. After adjusting for age, sex, race, comorbidities, health sector, and province, compared with the Omicron BA.4/BA.5 wave, patients had higher risk of mortality in the Omicron BA.1/BA.2 wave (adjusted odds ratio [aOR], 1.3; 95% confidence interval [CI]: 1.2-1.4) and Delta wave (aOR, 3.0; 95% CI: 2.8-3.2). Being partially vaccinated (aOR, 0.9; 95% CI: .9-.9), fully vaccinated (aOR, 0.6; 95% CI: .6-.7), and boosted (aOR, 0.4; 95% CI: .4-.5) and having prior laboratory-confirmed infection (aOR, 0.4; 95% CI: .3-.4) were associated with reduced risks of mortality. Overall, admission incidence risk and in-hospital mortality, which had increased progressively in South Africa's first 3 waves, decreased in the fourth Omicron BA.1/BA.2 wave and declined even further in the fifth Omicron BA.4/BA.5 wave. Mortality risk was lower in those with natural infection and vaccination, declining further as the number of vaccine doses increased.
Sections du résumé
BACKGROUND
In this study, we compared admission incidence risk and the risk of mortality in the Omicron BA.4/BA.5 wave to previous waves.
METHODS
Data from South Africa's SARS-CoV-2 case linelist, national COVID-19 hospital surveillance system, and Electronic Vaccine Data System were linked and analyzed. Wave periods were defined when the country passed a weekly incidence of 30 cases/100 000 population. In-hospital case fatality ratios (CFRs) during the Delta, Omicron BA.1/BA.2, and Omicron BA.4/BA.5 waves were compared using post-imputation random effect multivariable logistic regression models.
RESULTS
The CFR was 25.9% (N = 37 538 of 144 778), 10.9% (N = 6123 of 56 384), and 8.2% (N = 1212 of 14 879) in the Delta, Omicron BA.1/BA.2, and Omicron BA.4/BA.5 waves, respectively. After adjusting for age, sex, race, comorbidities, health sector, and province, compared with the Omicron BA.4/BA.5 wave, patients had higher risk of mortality in the Omicron BA.1/BA.2 wave (adjusted odds ratio [aOR], 1.3; 95% confidence interval [CI]: 1.2-1.4) and Delta wave (aOR, 3.0; 95% CI: 2.8-3.2). Being partially vaccinated (aOR, 0.9; 95% CI: .9-.9), fully vaccinated (aOR, 0.6; 95% CI: .6-.7), and boosted (aOR, 0.4; 95% CI: .4-.5) and having prior laboratory-confirmed infection (aOR, 0.4; 95% CI: .3-.4) were associated with reduced risks of mortality.
CONCLUSIONS
Overall, admission incidence risk and in-hospital mortality, which had increased progressively in South Africa's first 3 waves, decreased in the fourth Omicron BA.1/BA.2 wave and declined even further in the fifth Omicron BA.4/BA.5 wave. Mortality risk was lower in those with natural infection and vaccination, declining further as the number of vaccine doses increased.
Identifiants
pubmed: 36453094
pii: 6855554
doi: 10.1093/cid/ciac921
pmc: PMC10110264
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1468-1475Informations de copyright
© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
Déclaration de conflit d'intérêts
Potential conflicts of interest. S. S. A. K. reports grants or contracts unrelated to this work and paid to institution from the National Institutes of Health, South African Medical Research Council Cooperative Agreement, National Research Foundation/DST, USAID/Right to Care Cooperative agreement, the IQRAA Trust, and EDCTP; an unpaid role as a member of the World Health Organization (WHO) Science Council; a paid role as a member of the Bill and Melinda Gates Foundation (BMGF) Scientific Advisory Committee (meeting honorarium paid to author); and an unpaid role as vice-president of the International Science Council. C. C. reports grants or contracts unrelated to this work and paid to institution from the US Centers for Disease Control and Prevention (CDC), Wellcome Trust, Sanofi Pasteur, PATH, BMGF, and SA-Medical Research Council. A. v. G. reports grants unrelated to this work and paid to institution from the BMGF, Sanofi, CDC, WHO AFRO, Fleming Fund SEQAFRICA, SA MRC, the Solidarity Fund for Innovative Projects, NIH training grant, and ASLM PGI and a role as chair for the National Advisory Group for Immunisation. I. S. reports an institutional grant unrelated to this work from NIH DAIDS–WITS Helen Joseph Hospital CRS. M. J. G. reports grants or contracts unrelated to this work and paid to institution from the South African Medical Research Council and BMGF. N. W. reports grants paid to institution and unrelated to this work from the BMGF, Sanofi, and CDC. R. W. reports shareholding with Adcock Ingram Holdings Ltd, Dischem Pharmacies Ltd, Discovery Ltd, Netcare Ltd, and Aspen Pharmacare Holdings Ltd. S. W. reports grants unrelated to this work and paid to institution from the BMGF, Sanofi, CDC, and Welcome Trust. W. J. reports grants or contracts related to a long coronavirus disease 2019 study, paid to institution, from the BMGF. All remaining authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
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