Effectiveness of Pentavalent Rotavirus Vaccine Under Conditions of Routine Use in Rwanda.
Clin Infect Dis. 2016 May 01; 62 Suppl 2:S208-12.CI

Abstract

BACKGROUND

Rotavirus vaccine efficacy is lower in low-income countries than in high-income countries. Rwanda was one of the first low-income countries in sub-Saharan Africa to introduce rotavirus vaccine into its national immunization program. We sought to evaluate rotavirus vaccine effectiveness (VE) in this setting.

METHODS

VE was assessed using a case-control design. Cases and test-negative controls were children who presented with a diarrheal illness to 1 of 8 sentinel district hospitals and 10 associated health centers and had a stool specimen that tested positive (cases) or negative (controls) for rotavirus by enzyme immunoassay. Due to high vaccine coverage almost immediately after vaccine introduction, the analysis was restricted to children 7-18 weeks of age at time of rotavirus vaccine introduction. VE was calculated as (1 - odds ratio) × 100, where the odds ratio was the adjusted odds ratio for the rotavirus vaccination rate among case-patients compared with controls.

RESULTS

Forty-eight rotavirus-positive and 152 rotavirus-negative children were enrolled. Rotavirus-positive children were significantly less likely to have received rotavirus vaccine (33/44 [73%] unvaccinated) compared with rotavirus-negative children (81/136 [59%] unvaccinated) (P= .002). A full 3-dose series was 75% (95% confidence interval [CI], 31%-91%) effective against rotavirus gastroenteritis requiring hospitalization or a health center visit and was 65% (95% CI, -80% to 93%) in children 6-11 months of age and 81% (95% CI, 25%-95%) in children ≥12 months of age.

CONCLUSIONS

Rotavirus vaccine is effective in preventing rotavirus disease in Rwandan children who began their rotavirus vaccine series from 7 to 18 weeks of age. Protection from vaccination was sustained after the first year of life.

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Authors+Show Affiliations

Tate JE
Centers for Disease Control and Prevention, Atlanta, Georgia.
Ngabo F
Universite Libre de Bruxelles, Ecole de Santé Publique, Brussels, Belgium.
Donnen P
Universite Libre de Bruxelles, Ecole de Santé Publique, Brussels, Belgium.
Gatera M
Rwanda Biomedical Center.
Uwimana J
University Teaching Hospital.
Rugambwa C
World Health Organization, Rwanda Office, Kigali.
Mwenda JM
World Health Organization, Regional Office for Africa, Brazzaville, Republic of Congo.
Parashar UD
Centers for Disease Control and Prevention, Atlanta, Georgia.

MeSH

Africa South of the SaharaCase-Control StudiesDiarrheaFemaleGastroenteritisHumansImmunization ProgramsInfantMaleOdds RatioRotavirusRotavirus InfectionsRotavirus VaccinesRwandaVaccinationVaccine PotencyVaccines, Attenuated

Pub Type(s)

Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

27059358