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Monovalent Rotavirus Vaccine Effectiveness Against Rotavirus Hospitalizations Among Children in Zimbabwe
Hilda A Mujuru1,2, Eleanor Burnett3, Kusum J Nathoo1,2
1Harare Central Hospital, University of Zimbabwe, Harare.
Insights
The monovalent rotavirus vaccine effectively prevents severe rotavirus diarrhea hospitalizations in Zimbabwean infants. This study provides crucial evidence for rotavirus vaccine effectiveness in high-child-mortality regions.
Area of Science:
- Pediatric infectious diseases
- Vaccinology
- Public health
Background:
- Rotavirus is a significant cause of mortality in children under five globally.
- Zimbabwe introduced a monovalent rotavirus vaccine in May 2014.
- Evaluating vaccine effectiveness (VE) in real-world conditions is crucial for public health strategies.
Purpose of the Study:
- To assess the effectiveness of the monovalent rotavirus vaccine in preventing rotavirus-related hospitalizations in young children in Harare, Zimbabwe.
- To provide evidence on rotavirus vaccine performance in a high-child-mortality setting.
Main Methods:
- A test-negative case-control study design was employed.
- Children under five hospitalized or treated for acute watery diarrhea were enrolled.
- Vaccination status was verified, and VE was calculated using odds ratios.
Main Results:
- The study included 903 rotavirus-positive cases and 2685 rotavirus-negative controls.
- Adjusted 2-dose VE against rotavirus hospitalization was 61% in children aged 6-11 months.
- Effectiveness varied by nutritional status, with higher VE in non-stunted infants (71%) compared to stunted infants (45%).
Conclusions:
- The monovalent rotavirus vaccine demonstrates significant effectiveness in preventing severe rotavirus diarrhea hospitalizations among infants in Zimbabwe.
- These findings support the use of oral rotavirus vaccines in high-mortality settings and inform global vaccination policies.
Background:
Rotavirus is a leading cause of mortality among children <5 years old. We evaluated monovalent rotavirus vaccine effectiveness (VE) under conditions of routine use at 2 surveillance sites in Harare, Zimbabwe, after vaccine introduction in May 2014.
Methods:
Children aged <5 years hospitalized or treated in the accident and emergency department (A&E) for acute watery diarrhea were enrolled for routine surveillance. Copies of vaccination cards were collected to document vaccination status. Among children age-eligible to receive rotavirus vaccine, we estimated VE, calculated as 1 - odds ratio, using a test-negative case-control design.
Results:
We included 903 rotavirus-positive cases and 2685 rotavirus-negative controls in the analysis; 99% had verified vaccination status. Rotavirus-positive children had more severe diarrhea than rotavirus-negative children; 61% of cases and 46% of controls had a Vesikari score ≥11 (P < .01). Among cases and controls, 31% and 37%, respectively, were stunted for their age (P < .01). Among children 6-11 months old, adjusted 2-dose VE against hospitalization or treatment in A&E due to rotavirus of any severity was 61% (95% confidence interval [CI], 21%-81%) and 68% (95% CI, 13%-88%) against severe rotavirus disease. Stratified by nutritional status, adjusted VE was 45% (95% CI, -148% to 88%) among stunted infants and 71% (95% CI, 29%-88%) among infants with a normal height for age.
Conclusions:
Monovalent rotavirus vaccine is effective in preventing hospitalizations due to severe rotavirus diarrhea among infants in Zimbabwe, providing additional evidence for countries considering rotavirus vaccine introduction that live, oral rotavirus vaccines are effective in high-child-mortality settings.
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