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Published on: November 1, 2011
Duration of protection of pentavalent rotavirus vaccination in Nicaragua
Manish Patel1, Cristina Pedreira, Lucia Helena De Oliveira
1Centers for Disease Control and Prevention, 1600 Clifton Rd, NE, Atlanta GA 30333, USA. aul3@cdc.gov
Insights
The pentavalent rotavirus vaccine (RV5) effectively protects young children against severe rotavirus disease in Nicaragua. However, protection wanes with age, suggesting a need for booster dose evaluation.
Area of Science:
- Vaccinology
- Pediatric Infectious Diseases
- Public Health
Background:
- Rotavirus is a leading cause of severe diarrheal disease and hospitalization in infants globally.
- Developing countries face a significant burden of rotavirus gastroenteritis, necessitating effective vaccination strategies.
- The pentavalent rotavirus vaccine (RV5) has been introduced in several low- and middle-income countries.
Purpose of the Study:
- To assess the duration of protection offered by the pentavalent rotavirus vaccine (RV5) against rotavirus hospitalizations in Nicaragua.
- To evaluate the vaccine's effectiveness in a real-world setting in Central America.
- To inform public health policy regarding rotavirus vaccination schedules.
Main Methods:
- A case-control study was conducted in Nicaragua from 2007 to 2010.
- Inclusion criteria: children aged ≥ 6 months hospitalized with laboratory-confirmed rotavirus diarrhea (cases) or other diarrheal/non-diarrheal conditions (controls).
- Vaccine effectiveness was calculated by comparing vaccination status between cases and controls, with duration assessed by age groups (<1 year vs. ≥1 year).
Main Results:
- RV5 vaccination significantly reduced the risk of rotavirus hospitalization (OR: 0.30-0.55).
- Protection was notably higher in children under one year of age (OR: 0.36) compared to those one year and older (OR: 0.70).
- Test-negative and non-diarrhea controls provided comparable socioeconomic and non-rotavirus vaccination indicators.
Conclusions:
- RV5 provides robust protection against severe rotavirus disease during the first year of life in Nicaragua.
- A decline in RV5 protection was observed in children older than one year.
- Continued surveillance and evaluation of booster doses are recommended to sustain protection throughout early childhood.
Objective:
To evaluate the duration of protection of pentavaent rotavirus vaccine (RV5) against rotavirus hospitalizations in Nicaragua, a developing country in Central America.
Methods:
We conducted a case-control study at 4 hospitals from 2007 through 2010, including 1016 children hospitalized with laboratory-confirmed rotavirus diarrhea, 4930 controls with nonrotavirus diarrhea (ie, "test-negative"), and 5627 controls without diarrhea. All cases and controls were aged ≥ 6 months and born after August 2006. Outcomes included odds of antecedent vaccination between case-patients and controls, and effectiveness of vaccination (1 - adjusted odds ratio [OR] × 100). Duration of protection was assessed by comparing effectiveness among children aged <1 year compared with ≥ 1 year.
Results:
Indicators of socioeconomic conditions and nonrotavirus vaccination (oral polio vaccine and diphtheria/tetanus/pertussis/hepatitis A/hepatitis B) for test-negative controls were more comparable to the rotavirus case-patients than nondiarrhea controls. RV5 vaccination was associated with a significantly lower risk of rotavirus hospitalization by using test-negative controls (OR: 0.55; 95% confidence interval [CI]: 0.41-0.74) and nondiarrhea controls (OR: 0.30; 95% CI: 0.22-0.40). Risk of rotavirus hospitalization was twofold lower among RV5 vaccinated children aged <1 year (OR: 0.36; 95% CI: 0.22-0.57) compared with RV5 vaccinated children aged ≥ 1 year (OR: 0.70; 95% CI: 0.47-1.05).
Conclusions:
RV5 provided good protection against severe rotavirus disease in Nicaragua during the first year of life, when most severe and fatal rotavirus disease in developing countries occurs. However, the decline in protection with age warrants monitoring of disease among older children and consideration of a booster dose evaluation at the end of infancy.
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