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Published on: February 23, 2014
Invasive pneumococcal disease in pediatric organ transplant recipients: a high-risk population
Leanne Tran1, Diane Hébert, Anne Dipchand
1Division of Infectious Diseases, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Insights
Pediatric transplant recipients face a higher risk of invasive pneumococcal disease than healthy children. This study found significant missed vaccination opportunities in this vulnerable population.
Area of Science:
- Pediatric Transplant Medicine
- Infectious Diseases
- Vaccinology
Background:
- Invasive pneumococcal disease (IPD) poses a significant risk to pediatric transplant recipients.
- Limited data exists on IPD incidence and outcomes in this specific population.
- The introduction of pneumococcal conjugate vaccines (PCVs) necessitates updated understanding of IPD epidemiology.
Purpose of the Study:
- To determine the incidence and outcomes of invasive pneumococcal disease in pediatric transplant recipients.
- To analyze the timing of IPD occurrence post-transplantation.
- To identify vaccination status and opportunities in this cohort.
Main Methods:
- Retrospective study conducted at a major pediatric transplant center.
- Analysis of IPD cases in pediatric transplant recipients.
- Comparison of IPD incidence rates with healthy pediatric populations.
Main Results:
- IPD occurred at a significantly higher rate (176 episodes/100,000 child-years) compared to healthy children (<5 years).
- Infections occurred at a median of approximately 20 months post-transplantation.
- A notable proportion of patients had missed opportunities for pneumococcal vaccination.
Conclusions:
- Pediatric transplant recipients experience a substantially elevated risk of invasive pneumococcal disease.
- The timing of IPD suggests a potential window for effective vaccination strategies.
- Addressing missed vaccination opportunities is crucial to mitigate IPD risk in this population.
Abstract:
There are few studies on invasive pneumococcal disease in pediatric transplant recipients. Given this fact plus the advent of pneumococcal conjugate vaccines, we conducted a retrospective study at a major pediatric transplant center. The objectives were to determine the incidence and outcomes of invasive pneumococcal diseases in the patient population and to examine the timing of these infections after transplantation. We determined that invasive disease occurred at a rate that was significantly greater than the rate extrapolated from generally healthy children <5 yr of age (176 episodes per 100 000 children per year vs. 35-68.3 per 100 000 children per year). In addition, disease occurred at a median of approximately 20 months after transplantation, thereby theoretically allowing enough time for vaccination with the 7-valent conjugate vaccine. The study also documented significant missed vaccination opportunities.
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