Evidence map›Paper›PMID 35851597›Full record

ArticleNature communications2022

Duration of protection of CoronaVac plus heterologous BNT162b2 booster in the Omicron period in Brazil.

Thiago Cerqueira-Silva, Vinicius de Araujo Oliveira, Enny S Paixão, Juracy Bertoldo Júnior, Gerson O Penna, Guilherme L Werneck, Neil Pearce, Maurício L Barreto, Viviane S Boaventura, Manoel Barral-Netto

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 7 pooled it
5.1field-weighted citation impact, top 3% of its field
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

32 citing papers in PubMed, 7 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  6. Outcomes of Elderly Patients Hospitalized with the SARS-CoV-2 Omicron B.1.1.529 Variant: A Systematic Review.International journal of environmental research and public health · 2023
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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

10 authors at 4 institutions in 2 countries.

Thiago Cerqueira-SilvaLIB and LEITV Laboratories, Instituto Gonçalo Moniz, Fiocruz, Salvador, Bahia, Brazil.ORCID 0000-0003-4534-2509
Vinicius de Araujo OliveiraUniversidade Federal da Bahia, Salvador, Bahia, Brazil.ORCID 0000-0001-7858-9650
Enny S PaixãoLondon School of Hygiene and Tropical Medicine, London, WC1E 7HT, UK.ORCID 0000-0002-4797-908X
Juracy Bertoldo JúniorUniversidade Federal da Bahia, Salvador, Bahia, Brazil.
Gerson O PennaNúcleo de Medicina Tropical, Universidade de Brasília. Escola Fiocruz de Governo, Fiocruz, DF, Brazil.ORCID 0000-0001-8967-536X
Guilherme L WerneckUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0003-1169-1436
Neil PearceLondon School of Hygiene and Tropical Medicine, London, WC1E 7HT, UK.
Maurício L BarretoUniversidade Federal da Bahia, Salvador, Bahia, Brazil.ORCID 0000-0002-0215-4930
Viviane S BoaventuraLIB and LEITV Laboratories, Instituto Gonçalo Moniz, Fiocruz, Salvador, Bahia, Brazil. viviane.boaventura@fiocruz.br.ORCID 0000-0002-7241-6844
Manoel Barral-NettoLIB and LEITV Laboratories, Instituto Gonçalo Moniz, Fiocruz, Salvador, Bahia, Brazil.
Universidade Federal da Bahia · BRUniversity of London · GBUniversidade de Brasília · BRUniversidade Federal do Rio de Janeiro · BR

Funding

Wellcome TrustWellcome Trust 213589/Z/18/Z
6 · The paper itself

Abstract

To date, no information has been published on the effectiveness of inactivated whole-virus COVID-19 vaccines plus heterologous booster against symptomatic infection and severe outcomes (hospitalization or death) during the dominance of the SARS-CoV-2 Omicron variant period. We evaluated the vaccine effectiveness (VE) of CoronaVac plus BNT162b2 booster during the period of dominance of the Omicron variant in Brazil (January to April 2022). Using a test-negative design, we analysed data for 2,471,576 individuals tested during the Omicron variant's dominant period using a nationally linked database from Brazil. Compared to unvaccinated, vaccinees maintained protection against severe outcomes, with an estimated VE of 84.1% (95% CI:83.2-84.9) at more than 120 days after BNT162b2 booster. Furthermore, while we detected a high level of protection against severe outcomes for individuals up to 79 years old, waning was observed for individuals aged ≥80 years, with VE decreasing from 81.3% (95% CI:77.9-84.2) at 31-60 days to 72.9% (95% CI:70.6-75.1) at 120 days or more after the booster dose. However, no significant protection against symptomatic infection was observed at this time period. In conclusion, except for individuals aged ≥80 years, CoronaVac plus a BNT162b2 booster dose offered high and durable protection against severe outcomes due to Omicron.

Indexed as

COVID-19COVID-19 VaccinesBNT162 VaccineBrazilHumansSARS-CoV-2BNT162 VaccineCOVID-19 Vaccines

Identifiers

PMID35851597
PMCPMC9289933
OpenAlexW4285803421

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.