Evidence map›Paper›PMID 36989570›Full record

Observational studyPublic health2023

COVID-19 vaccines effectiveness against symptomatic disease and severe outcomes, 2021-2022: a test-negative case-control study.

C Brazete, J Brazete, F Alves, A Aguiar, A M Gonçalves, M Cardoso, L Sá, E Gonçalves, M Pinto, R Duarte

Abstract readObservational Study
In one paragraph

Observational study in Public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
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.

C BrazeteUnidade de Saúde Pública Do Alto Minho, Viana Do Castelo, Portugal; EPIUnit - Instituto de Saúde Pública da Universidade Do Porto, Porto, Portugal. Electronic address: catia.brazete@ispup.up.pt.
J BrazeteFaculdade de Medicina da Universidade Do Porto, Porto, Portugal.
F AlvesUnidade de Investigação Clínica da Administração Regional de Saúde Do Norte, Porto, Portugal.
A AguiarEPIUnit - Instituto de Saúde Pública da Universidade Do Porto, Porto, Portugal; Laboratório para a Investigação Integrativa e Translacional (ITR), Porto, Portugal; Instituto de Ciências Biomédicas Abel Salazar, Universidade Do Porto, Porto, Portugal.
A M GonçalvesUnidade de Saúde Pública Do Alto Minho, Viana Do Castelo, Portugal.
M CardosoUnidade de Saúde Pública Do Alto Minho, Viana Do Castelo, Portugal.
L SáUnidade de Saúde Pública Do Alto Minho, Viana Do Castelo, Portugal.
E GonçalvesServiço de Medicina Física e Reabilitação, Centro Hospitalar de Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Portugal.
M PintoFaculdade de Psicologia e Ciências da Educação da Universidade Do Porto, Porto, Portugal.
R DuarteEPIUnit - Instituto de Saúde Pública da Universidade Do Porto, Porto, Portugal; Unidade de Investigação Clínica da Administração Regional de Saúde Do Norte, Porto, Portugal; Laboratório para a Investigação Integrativa e Translacional (ITR), Porto, Portugal; Instituto de Ciências Biomédicas Abel Salazar, Universidade Do Porto, Porto, Portugal; Serviço de Pneumologia, Centro Hospitalar de Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study evaluated the effectiveness of COVID-19 vaccines in preventing symptomatic and severe disease. STUDY

designThis was an observational test-negative case-control study.

methodsStudy participants were adults with at least one symptom included in the World Health Organization COVID-19 definition who sought health care in a public emergency department between 1 November 2021 and 2 March 2022 (corresponding with the fifth pandemic wave in Portugal dominated by the Omicron variant). This study used multivariable logistic regression models to estimate and compare the odds ratio of vaccination between test-positive cases and test-negative controls to calculate the absolute and relative vaccine effectiveness.

resultsThe study included 1059 individuals (522 cases and 537 controls) with a median age of 56 years and 58% were women. Compared with the effectiveness of the primary vaccination scheme that had been completed ≥180 days earlier, the relative effectiveness against symptomatic infection of a booster administered between 14 and 132 days earlier was 71% (95% confidence interval [CI]: 57%, 81%; P < 0.001). The effectiveness of the primary series against symptomatic infection peaked at 85% (95% CI: 56%, 95%) between 14 and 90 days after the last inoculation and decreased to 34% (95% CI: -43%, 50%) after ≥180 days.

conclusionsDespite the known immunological evasion characteristics of the Omicron variant, results from this study show that vaccine effectiveness increases after booster administration. COVID-19 vaccine effectiveness decreases to less than 50% between 3 and 6 months after completion of the primary cycle; therefore, this would be an appropriate time to administer a booster to restore immunity.

Indexed as

COVID-19COVID-19 VaccinesAdultCase-Control StudiesFemaleHumansMaleMiddle AgedSARS-CoV-2COVID-19 VaccinesCase–control studyCOVID-19 vaccineEffectivenessHospitalisationWaning immunity

Identifiers

PMID36989570
PMCPMC9943732

What OpenQuestion holds

Textmetadata
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.