TY - JOUR
T1 - Rotavirus Vaccine Effectiveness Stratified By National-Level Characteristics
T2 - An Introduction to the 24-Country MNSSTER-V Project, 2007-2023
AU - on behalf of the Multi-National Subpopulations Study to Evaluate Rotavirus Vaccines (MNSSTER-V) project working group
AU - Burnett, Eleanor
AU - Umana, Jazmina
AU - Anwari, Palwasha
AU - Mujuru, Hilda A.
AU - Groome, Michelle J.
AU - Van Trang, Nguyen
AU - Iniguez, Volga
AU - Gheorghita, Stela
AU - Sahakyan, Gayane
AU - Nazurdinov, Anvar
AU - Michael, Fausta
AU - Mandomando, Inacio
AU - Desormeaux, Anne Marie
AU - Eraliev, Umid
AU - Enweronu-Laryea, Christabel
AU - Nalunkuma, Cissy
AU - Bonkoungou, Isidore
AU - Muhsen, Khitam
AU - Luhata Lungayo, Christophe
AU - Omore, Richard
AU - Goldfarb, David M.
AU - Robinson, Annick Lalaina
AU - McCracken, John
AU - Uwimana, Jeannine
AU - N'Zue, Kofi
AU - Rey-Benito, Gloria
AU - Weldegebriel, Goitom
AU - Mwenda, Jason M.
AU - Parashar, Umesh D.
AU - Tate, Jacqueline E.
N1 - Publisher Copyright:
© 2024 Published by Oxford University Press on behalf of Infectious Diseases Society of America.
PY - 2025/8/15
Y1 - 2025/8/15
N2 - 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.
AB - 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.
KW - diarrhea
KW - immunization
KW - rotavirus
KW - rotavirus vaccine
KW - vaccine
UR - https://www.scopus.com/pages/publications/105013310940
U2 - 10.1093/infdis/jiae597
DO - 10.1093/infdis/jiae597
M3 - Article
C2 - 39607893
AN - SCOPUS:105013310940
SN - 0022-1899
VL - 232
SP - 308
EP - 315
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 2
ER -