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Hospital-based surveillance of intussusception among infants
Eder Gatti Fernandes1, Eyal Leshem2, Manish Patel3
1Field Epidemiology Training Program/São Paulo State (EPISUS-SP), Secretaria de Estado da Saúde de São Paulo, São Paulo, SP, Brazil.
Insights
Surveillance for intussusception after rotavirus vaccine (RV1) introduction showed no increase in cases. Further epidemiologic methods are needed to assess the rare adverse event link.
Area of Science:
- Pediatric Gastroenterology
- Vaccine Safety Epidemiology
- Public Health Surveillance
Background:
- Intussusception is a serious gastrointestinal condition in infants.
- The introduction of rotavirus vaccines necessitates monitoring for potential adverse events.
- Understanding intussusception epidemiology is crucial for public health.
Purpose of the Study:
- To assess the epidemiology of intussusception.
- To compare intussusception case counts before and after the introduction of the live attenuated monovalent rotavirus vaccine (RV1).
Main Methods:
- Utilized a prospective enhanced passive surveillance system in sentinel hospitals (March 2006-January 2008).
- Conducted a retrospective review of medical records for cases from January 2001 to February 2006.
- Analyzed 331 intussusception cases identified between 2001 and 2008.
Main Results:
- Peak intussusception incidence was observed in infants aged 18-24 weeks.
- Vomiting, bloody stool, and abdominal distention were common symptoms.
- No significant increase in intussusception events was detected in 2007-2008 compared to the 2001-2005 baseline.
Conclusions:
- The study did not find an increased risk of intussusception following RV1 introduction.
- Specialized epidemiologic methods are essential for evaluating rare potential vaccine-related adverse events.
- Continued surveillance is important for vaccine safety monitoring.
Objective:
Intussusception surveillance was initiated after the nationwide introduction of live attenuated monovalent rotavirus vaccine (RV1). The objective is to assess the epidemiology of intussusception and compare the number of cases before and after the introduction of rotavirus vaccine.
Methods:
Cases of intussusception occurring between March 2006 and January 2008 were identified through a prospective enhanced passive surveillance system established in sentinel state hospitals. Retrospective review of medical records was used to identify cases, which occurred in sentinel hospitals between January 2001 and February 2006.
Results:
From 2001 to 2008, 331 intussusception cases were identified, 59.5% were male, with peak incidence among those 18-24 weeks of age. Overall <10% of cases were among infants 6-14 weeks of age (when the first dose of RV1 is administered). The most frequently observed signs or symptoms of intussusception included vomiting (89.4%), bloody stool (75.5%), and abdominal distention (71.8%). A majority (92.1%) of the case-patients required surgery for treatment; 31.8% of those who underwent surgery required bowel resection, and 13 (3.9%) died. Among the 21 hospitals that reported cases throughout the entire surveillance period (2001-2008), the number of intussusception events during 2007 (n=26) and 2008 (n=19) was not greater than the average annual number (n=31, range 24-42) during baseline years 2001-2005.
Conclusions:
Although this analysis did not identify an increase in intussusception cases during the two years after RV1 introduction, these results support the need for special epidemiologic methods to assess the potential link between rotavirus vaccine and this very rare adverse event.
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