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Rotavirus Vaccine Effectiveness Stratified By National-Level Characteristics: An Introduction to the 24-Country MNSSTER-V Project, 2007-2023

  • on behalf of the Multi-National Subpopulations Study to Evaluate Rotavirus Vaccines (MNSSTER-V) project working group
  • Centers for Disease Control and Prevention
  • Ministerio de Salud
  • JS Consultancy
  • University of Zimbabwe
  • University of the Witwatersrand
  • National Institute of Hygiene and Epidemiology Hanoi
  • Universidad Mayor de San Andrés
  • Ministry of Health of the Republic of Moldova
  • Ministry of Health of the Republic of Armenia
  • Ministry of Health and Social Protection of Population of the Republic of Tajikistan
  • Elderly and Children
  • Centro de investigação de Saúde de Manhiça
  • Centers for Disease Control and Prevention
  • Tashkent State Medical University
  • Lubaga Hospital
  • Université Joseph Ki-Zerbo
  • Tel Aviv University
  • et Prevention
  • Kenya Medical Research Institute
  • University of British Columbia
  • Joseph Ravoahangy Andrianavalona Hospital
  • Universidad del Valle de Guatemala
  • University of Rwanda
  • World Health Organization
  • Pan American Health Organization
  • World Health Organization

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Background Rotavirus vaccines are moderately protective against illness in settings with high compared with low mortality rates. Vaccine effectiveness (VE) evaluations may clarify our understanding of these disparities, but estimates among key subpopulations and against rare outcomes are not available in many analyses due to sample size. We combined 25 data sets from test-negative design case-control evaluations in 24 countries that enrolled children with medically attended diarrhea, laboratory-confirmed rotavirus stool testing, and documented vaccination status. We calculated rotavirus VE stratified by country-level characteristics. Methods Children 3-59 months old with birthdates and surveillance hospital arrival dates were included; other variables were standardized as available. Children were considered vaccinated if they received ≥1 dose of rotavirus vaccine >14 days before arrival. We summarized child- and country-level characteristics, including national <5-year-old mortality rate (U5M). Following the manufacturer recommended dose schedule, complete- and partial-series adjusted VE were estimated using logistic regression models. Results We included 6626 rotavirus-positive children (case patients) and 19 459 rotavirus negative children (controls). Adjusted complete-series VE was significantly higher among children from countries in the low and medium U5M stratum (74% [95% confidence interval, 64%-81%]) compared with all groups within the high U5M stratum (range, 52% [42%-60%]) to 46% [31%-57%]). Partial-series estimates were lower than complete-series estimates. Conclusions These findings are consistent with the published literature, though they suggest heterogeneity in vaccine performance within broad child mortality rate levels. Our findings also highlight the importance of complete-series vaccination.

Original languageEnglish
Pages (from-to)308-315
Number of pages8
JournalJournal of Infectious Diseases
Volume232
Issue number2
DOIs
Publication statusPublished - 15 Aug 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • diarrhea
  • immunization
  • rotavirus
  • rotavirus vaccine
  • vaccine

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