TY - JOUR
T1 - Effectiveness of COVID-19 vaccines against hospitalisation in Latin America during three pandemic waves, 2021–2022
T2 - a test-negative case-control design
AU - the REVELAC-i Working Group
AU - Nogareda, Francisco
AU - Regan, Annette K.
AU - Couto, Paula
AU - Fowlkes, Ashley L.
AU - Gharpure, Radhika
AU - Loayza, Sergio
AU - Leite, Juliana Almeida
AU - Rodríguez, Angel
AU - Vicari, Andrea
AU - Azziz-Baumgartner, Eduardo
AU - Salas, Daniel
AU - Olivares Barraza, María Fernanda
AU - Vergara Mallegas, Natalia
AU - Rodríguez Ferrari, Paula
AU - Sotomayor Proschle, Viviana
AU - Fasce Pineda, Rodrigo
AU - Bustos Alister, Patricia
AU - Avendaño, Marcela
AU - Brstilo, Iván
AU - Arroba Tijerino, Roberto
AU - Guzmán Saborío, Guiselle
AU - Brenes Porras, Hebleen
AU - Gobern, Lorena
AU - Paredes, Antonio
AU - Cuyan, Maribel
AU - Estrada, Claudia
AU - Leal, Christa
AU - Parra, Liz
AU - Galindo, Pablo
AU - Santos, Lucas
AU - Pérez Tasigchana, Raúl Francisco
AU - Astudillo Vallejo, Lucía Alexandra
AU - Bruno Caicedo, Alfredo
AU - Whittenbury, Alvaro
AU - Von Horoch, Marta
AU - Battaglia, Silvia
AU - Domínguez, Chavely
AU - Penayo, Elena
AU - Vázquez, Cynthia
AU - Ortega, Maria José
AU - Michel, Fabiana
AU - Nieto, María Emilia
AU - Tritten, Dahiana
AU - Ramas, Viviana
AU - Goñi, Natalia
AU - Chiparelli, Héctor
N1 - © 2023 Published by Elsevier Ltd.
PY - 2023/11
Y1 - 2023/11
N2 - Background: Vaccine effectiveness (VE) is essential to monitor the performance of vaccines and generate strategic information to guide decision making. We pooled data from six Latin American countries to estimate the effectiveness of COVID-19 vaccines in preventing laboratory-confirmed SARS-CoV-2 hospitalisation during three different pandemic waves from February 2021 to September 2022. Methods: We used a test-negative case-control design in hospitalised adults in Chile, Costa Rica, Ecuador, Guatemala, Paraguay, and Uruguay. We estimated adjusted VE by age group (18–64 and ≥65 years), vaccine type and product for primary series vaccination and booster vaccination and by time since last dose during the Omicron variant dominant period. We used mixed effects logistic regression models adjusting for sex, age, week of onset of symptom onset and pre-existing conditions with country fit as a random effect term. Findings: We included 15,241 severe acute respiratory infection (SARI) patients in the analysis. Among adults 18–64 years, VE estimates for primary series vaccination during pre-Delta and Delta periods ranged by product from 66.5% to 95.1% and from 33.5% to 88.2% for older adults. During the Omicron period, VE estimates for primary series were lower and decreased by time since last vaccination, but VE increased to between 26.4% and 57.4% when a booster was administered. Interpretation: mRNA and viral vector vaccines presented higher VE for both primary series and booster. While VE decreased over time, protection against severe COVID-19-associated hospitalisation increased when booster doses were administered. Vaccination with additional doses should be recommended, particularly for persons at increased risk of developing severe COVID-19. Funding: This work was supported by a grant from the U.S. Centers for Disease Control and Prevention (CDC) through cooperative agreements with the Pan American Health Organization/World Health Organization.
AB - Background: Vaccine effectiveness (VE) is essential to monitor the performance of vaccines and generate strategic information to guide decision making. We pooled data from six Latin American countries to estimate the effectiveness of COVID-19 vaccines in preventing laboratory-confirmed SARS-CoV-2 hospitalisation during three different pandemic waves from February 2021 to September 2022. Methods: We used a test-negative case-control design in hospitalised adults in Chile, Costa Rica, Ecuador, Guatemala, Paraguay, and Uruguay. We estimated adjusted VE by age group (18–64 and ≥65 years), vaccine type and product for primary series vaccination and booster vaccination and by time since last dose during the Omicron variant dominant period. We used mixed effects logistic regression models adjusting for sex, age, week of onset of symptom onset and pre-existing conditions with country fit as a random effect term. Findings: We included 15,241 severe acute respiratory infection (SARI) patients in the analysis. Among adults 18–64 years, VE estimates for primary series vaccination during pre-Delta and Delta periods ranged by product from 66.5% to 95.1% and from 33.5% to 88.2% for older adults. During the Omicron period, VE estimates for primary series were lower and decreased by time since last vaccination, but VE increased to between 26.4% and 57.4% when a booster was administered. Interpretation: mRNA and viral vector vaccines presented higher VE for both primary series and booster. While VE decreased over time, protection against severe COVID-19-associated hospitalisation increased when booster doses were administered. Vaccination with additional doses should be recommended, particularly for persons at increased risk of developing severe COVID-19. Funding: This work was supported by a grant from the U.S. Centers for Disease Control and Prevention (CDC) through cooperative agreements with the Pan American Health Organization/World Health Organization.
KW - Adults
KW - COVID-19 vaccine effectiveness
KW - Hospitalisations
KW - Latin America
KW - Older adults
KW - Severe acute respiratory infections
KW - Southern hemisphere
KW - Test-negative case-control design
UR - http://www.scopus.com/inward/record.url?scp=85176440599&partnerID=8YFLogxK
U2 - 10.1016/j.lana.2023.100626
DO - 10.1016/j.lana.2023.100626
M3 - Artículo
C2 - 38035125
AN - SCOPUS:85176440599
SN - 2667-193X
VL - 27
JO - The Lancet Regional Health - Americas
JF - The Lancet Regional Health - Americas
M1 - 100626
ER -