Evidence map›Paper›PMID 37716830›Full record

ArticleVaccine2023

COVID-19 vaccine effectiveness against hospitalizations in Paraguay, May 2021-April 2022: A test-negative design.

Sandra Irala, Sarah Hamid, Elena Penayo, Fabiana Michel, Paula Couto, Cynthia Vazquez, María José Ortega, Chavely Domínguez, Silvia Battaglia, Marta Von Horoch and 3 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2023. 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
0.2field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Trial
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

13 authors at 6 institutions in 3 countries.

Sandra IralaDirectorate General for Health Surveillance, Ministry of Public Health and Social Welfare, Paraguay.
Sarah HamidNational Center for Immunization and Respiratory Diseases, US Centers for Disease Control and Prevention, Atlanta, GA, USA; Epidemic Intelligence Service, US Centers for Disease Control and Prevention, Atlanta, GA, USA. Electronic address: tsl4@cdc.gov.
Elena PenayoDirectorate General for Health Surveillance, Ministry of Public Health and Social Welfare, Paraguay. Electronic address: umedgvspy@gmail.com.
Fabiana MichelPan American Health Organization, Asunción, Paraguay.
Paula CoutoPan American Health Organization, Washington, DC, USA.
Cynthia VazquezDepartment of Virology, Central Laboratory for Public Health, Asunción, Paraguay.
María José OrtegaDepartment of Virology, Central Laboratory for Public Health, Asunción, Paraguay.
Chavely DomínguezDirectorate General for Health Surveillance, Ministry of Public Health and Social Welfare, Paraguay.
Silvia BattagliaNational Program for Vaccine Preventable Diseases and Expanded Program on Immunization, Asunción, Paraguay.
Marta Von HorochNational Program for Vaccine Preventable Diseases and Expanded Program on Immunization, Asunción, Paraguay.
Romeo MontoyaPan American Health Organization, Asunción, Paraguay.
Guillermo SequeraDirectorate General for Health Surveillance, Ministry of Public Health and Social Welfare, Paraguay.
Francisco NogaredaPan American Health Organization, Washington, DC, USA.
Ministerio de Salud Pública y Bienestar Social · PYGuyra Paraguay · PYIPS Central · PYWorld Health Organization Regional Office for the Americas · USCenters for Disease Control and Prevention · USDirectorate of Health · IS

Funding

Intramural CDC HHS CC999999NCIRD CDC HHS H23 IP000940
6 · The paper itself

Abstract

backgroundVaccine effectiveness (VE) estimates vary by population characteristics and circulating variants. North America and Europe have generated many COVID-19 VE estimates but relied heavily on mRNA vaccines. Fewer estimates are available for non-mRNA vaccines and from Latin America. We aimed to estimate the effectiveness of several COVID-19 vaccines in preventing SARS-CoV-2-associated severe acute respiratory infection (SARI) in Paraguay from May 2021 to April 2022.

methodsUsing sentinel surveillance data from four hospitals in Paraguay, we conducted a test-negative case-control study to estimate COVID-19 vaccine effectiveness against SARI by vaccine type/brand and period of SARS-CoV-2 variant predominance (Gamma, Delta, Omicron). We used multivariable logistic regression adjusting for month of symptom onset, age group, and presence of ≥1 comorbidity to estimate the odds of COVID-19 vaccination in SARS-CoV-2 test-positive SARI case-patients compared to SARS-CoV-2 test-negative SARI control-patients.

resultsOf 4,229 SARI patients, 2,381 (56%) were SARS-CoV-2-positive case-patients and 1,848 (44%) were SARS-CoV-2-negative control-patients. A greater proportion of case-patients (73%; 95% CI: 71-75) than of control-patients (40%; 95% CI: 38-42) were unvaccinated. During the Gamma variant-predominant period, VE estimates for partial vaccination with mRNA vaccines and Oxford/AstraZeneca Vaxzevria were 90.4% (95% CI: 66.4-97.6) and 52.2% (95% CI: 25.0-69.0), respectively. During the Delta variant-predominant period, VE estimates for complete vaccination with mRNA vaccines, Oxford/AstraZeneca Vaxzevria, or Gamaleya Sputnik V were 90.4% (95% CI: 74.3-97.3), 83.2% (95% CI: 67.8-91.9), and 82.9% (95% CI: 53.0-95.2), respectively. The effectiveness of all vaccines declined substantially during the Omicron variant-predominant period.

conclusionsThis study contributes to our understanding of COVID-19 VE in Latin America and to global understanding of vaccines that have not been widely used in North America and Europe. VE estimates from Paraguay can parameterize models to estimate the impact of the national COVID-19 vaccination campaign in Paraguay and similar settings.

Indexed as

COVID-19COVID-19 VaccinesHospitalizationSARS-CoV-2Vaccine EfficacyAdolescentAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedParaguaySentinel SurveillanceYoung AdultCOVID-19 VaccinesCOVID-19ParaguayVaccinationVaccine effectiveness

Identifiers

PMID37716830
PMCPMC11556362
OpenAlexW4386787449

What OpenQuestion holds

Textmetadata
LicenceTDM
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.