Evidence map›Paper›PMID 39305220›Full record

ArticleInternational journal of epidemiology2024

Estimation of vaccine effectiveness against SARS-CoV-2-associated hospitalization using sentinel surveillance in South Africa.

Nicola Chiwandire, Sibongile Walaza, Anne von Gottberg, Nicole Wolter, Mignon Du Plessis, Fahima Moosa, Michelle J Groome, Jeremy Nel, Ebrahim Variava, Halima Dawood and 6 more

Abstract read
In one paragraph

Article in International journal of epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Nicola ChiwandireDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.ORCID 0000-0002-4384-636X
Sibongile WalazaDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.
Anne von GottbergDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.
Nicole WolterDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.ORCID 0000-0002-9526-0133
Mignon Du PlessisDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.
Fahima MoosaDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.
Michelle J GroomeDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.
Jeremy NelDepartment of Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Ebrahim VariavaDepartment of Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Halima DawoodDepartment of Medicine, Greys Hospital, Pietermaritzburg, South Africa.
Mvuyo MakhasiDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.
Leora R FeldsteinCoronavirus and Other Viral Respiratory Diseases Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Perrine MarcenacInfluenza Division, National Center for Immunization and Respiratory Diseases, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.ORCID 0000-0002-6726-6124
Kathryn E LafondInfluenza Division, National Center for Immunization and Respiratory Diseases, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.
Aaron M SamuelsInfluenza Division, National Center for Immunization and Respiratory Diseases, United States Centers for Disease Control and Prevention, Atlanta, GA, USA.
Cheryl CohenDivision of the National Health Laboratory Service, National Institute for Communicable Diseases, Johannesburg, South Africa.

Funding

Wellcome TrustWellcome Trust 221003/Z/20/Z
6 · The paper itself

Abstract

backgroundCOVID-19 vaccine effectiveness (VE) studies leveraging systematic surveillance in sub-Saharan Africa are limited. We assessed the effectiveness of two vaccines (Pfizer BNT162b2 and Johnson & Johnson Ad26.COV2.S) against SARS-CoV-2-associated hospitalization in South African adults aged ≥18 years.

methodsWe conducted a test-negative case-control study using pneumonia surveillance data in South Africa. Inpatients with physician-diagnosed lower respiratory tract infection or suspected COVID-19, testing SARS-CoV-2 positive or negative from June 2021-March 2022, were cases or controls, respectively. Fully vaccinated individuals received one Ad26.COV2.S dose or two BNT162b2 doses ≥14-days before enrollment. VE was estimated using multivariable logistic regression for Delta- and Omicron BA.1/BA.2-predominant periods, stratified by age and HIV status.

resultsThe study included 925 cases and 1890 controls; 38 (4%) cases and 186 (10%) controls were fully vaccinated with BNT162b2, and 30 (3%) cases and 94 (5%) controls with Ad26.COV2.S. The vaccine effectiveness of BNT162b2 against SARS-CoV-2-associated hospitalization over Delta and Omicron BA.1/BA.2 periods was 91% (95% CI: 52%, 98%) and 33% (-16%, 86%), respectively. The vaccine effectiveness of Ad26.COV2.S against hospitalization over Delta and Omicron BA.1/BA.2 periods was 72% (-36% ,94%), and -19% (-130%, 39%), respectively. The vaccine effectiveness of BNT162b2 against hospitalization over the Delta period was 94% (50%, 99%) and 89% (27%, 98%) among adults aged ≥60 years and HIV-uninfected, respectively.

conclusionsThe BNT162b2 vaccine was effective against SARS-CoV-2-associated hospitalization during the Delta period for adults aged ≥18 years, ≥60 years and those HIV-uninfected. VE for Ad26.COV2.S was inconclusive, potentially due to limited sample size or residual confounding. These findings highlight the utility of sentinel surveillance for estimating VE.

Indexed as

COVID-19HospitalizationSARS-CoV-2Sentinel SurveillanceVaccine EfficacyAd26COVS1AdolescentAdultAgedBNT162 VaccineCase-Control StudiesCOVID-19 VaccinesFemaleHumansMaleMiddle AgedAd26COVS1BNT162 VaccineCOVID-19 VaccinesCOVID-19SARS-CoV-2sentinel surveillancetest-negative case controlvaccine effectiveness

Identifiers

PMID39305220
PMCPMC11415825

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.