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Evaluation of immunization rates and safety among children with inborn errors of metabolism
Nicola P Klein1, Laurie Aukes, Janelle Lee
1Kaiser Permanente Vaccine Study Center, 1 Kaiser Plaza, 16th Floor, Oakland, CA 94612, USA. nicola.klein@kp.org
Insights
Children with inborn errors of metabolism (IEM) receive routine vaccines on schedule and without increased risk of adverse events. This study provides reassurance for vaccinating this vulnerable pediatric population against preventable diseases.
Area of Science:
- Pediatric immunology
- Metabolic disorders
- Vaccinology
Background:
- Children with inherited metabolic disorders (IMDs) are at higher risk for vaccine-preventable diseases.
- Limited data exist on immunization rates and vaccine safety in children with IMDs.
Purpose of the Study:
- To assess immunization rates in infants with inborn errors of metabolism (IEM).
- To evaluate vaccine safety in children with IEM.
Main Methods:
- Retrospective electronic health record review of children with IEM (1990-2007) at Northern California Kaiser Permanente.
- Comparison of immunization status and age at vaccination with matched healthy controls.
- Assessment of post-vaccination adverse events (emergency department visits, hospitalizations) within 30 days.
Main Results:
- Infants with IEM had similar vaccination rates by age 2 and no delay in vaccine receipt compared to controls.
- Vaccination was not associated with increased emergency department visits or hospitalizations within 30 days post-vaccination.
- A potential increase in hospitalizations was noted within 2 weeks for the sickest children aged 1-4 years.
Conclusions:
- Children with IEM follow the same immunization schedule as healthy children.
- Routine vaccination of children with IEM is safe and not associated with increased serious adverse events.
- Findings offer reassurance for the vaccination of children with IEM against preventable diseases.
Background:
Children with inherited metabolic disorders are a potential high-risk group for vaccine-preventable diseases, yet information regarding immunization rates and vaccine safety within this population is limited.
Methods:
Using Northern California Kaiser Permanente's electronic medical record, we identified children with inborn errors of metabolism from 1990 to 2007. We assessed immunization rates among infants with inborn errors of metabolism born at Northern California Kaiser Permanente matched to healthy infants (1 to 20), comparing both vaccines received by 2 years of age and age at vaccination. We assessed postvaccination adverse events among children up to 18 years old with inborn errors of metabolism, separately comparing emergency-department visits and hospitalizations during postvaccine days 0 to 30 (primary) and days 0 to 14 (secondary).
Results:
Comparing infants with inborn errors of metabolism (n = 77) versus matched control subjects (n = 1540), similar proportions were up to date for vaccines at 2 years of age, and there was no evidence of delay in receipt of recommended vaccines during the first year. Vaccination of children with inborn errors of metabolism (n = 271) was not associated with any significant increase in emergency-department visits or hospitalizations during the 30 days after vaccination. Secondary analyses suggested that there may be increased rates of hospitalizations 2 weeks after vaccination for the sickest 1- to 4-year-old children.
Conclusions:
Children with inborn errors of metabolism at Northern California Kaiser Permanente received vaccines on the same immunization schedule as healthy infants. Immunization was not associated with increased risk for serious adverse events during the month after vaccination, providing overall reassurance that routine vaccination of children with inborn errors of metabolism does not result in adverse effects.
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