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Published on: December 10, 2013
Hospitalizations for Respiratory Syncytial Virus and Vaccine Preventable Infections following Pediatric Heart
Emily A Hayes1, Stephen A Hart1, Charitha Gowda2
1The Heart Center, Nationwide Children's Hospital, Columbus, OH.
Insights
Pediatric heart transplant recipients frequently experience respiratory syncytial virus (RSV) and vaccine-preventable infections (R/VPI), leading to significant hospitalizations and costs. Risk factors include pre-transplant support and younger age post-transplant.
Area of Science:
- Pediatric Cardiology
- Infectious Diseases
- Transplant Immunology
Background:
- Pediatric heart transplant recipients are vulnerable to respiratory infections.
- Respiratory syncytial virus (RSV) and vaccine-preventable infections (R/VPI) pose significant risks.
- Understanding risk factors is crucial for improving outcomes.
Purpose of the Study:
- To identify risk factors for R/VPI acquisition in pediatric heart transplant recipients.
- To assess the associated morbidity and hospital resource utilization.
- To inform strategies for infection prevention.
Main Methods:
- Retrospective analysis of pediatric heart transplant recipients (<18 years) from 2003-2018.
- Utilized the Pediatric Health Information System database.
- Negative binomial regression models adjusted for confounders.
Main Results:
- 17.9% of 3815 recipients had R/VPI hospitalizations.
- RSV, influenza, and pneumococcus were common causes.
- Increased risk associated with pre-transplant mechanical support, multiple immunosuppressants, and age <2 years in the first year post-transplant.
Conclusions:
- R/VPI hospitalizations are frequent and costly post-pediatric heart transplant.
- Strategies include optimizing vaccine schedules and palivizumab use.
- Immunogenicity monitoring and re-vaccination are recommended.
Objective:
To determine the risk factors for acquiring a respiratory syncytial virus (RSV) and vaccine-preventable infections (R/VPI) in pediatric heart transplant recipients and the associated morbidity and hospital resource use.
Study Design:
Patients <18 years who underwent heart transplantation from September 2003 to December 2018 at hospitals using the Pediatric Health Information System database were identified. Their transplant hospitalization and subsequent hospitalizations for R/VPI through December 2018 were analyzed. Risk factors for R/VPI hospitalizations were evaluated using negative regression binomial models adjusted for demographic and clinical confounders. Total hospital costs were adjusted for 2018 US$.
Results:
Of 3815 transplant recipients, 681 (17.9%) had an R/VPI hospitalization during 23 746 available person-years of follow-up. There were 984 R/VPIs diagnosed during 951 hospitalizations, and 440 (44.7%) occurred the first year after transplantation. The most common causes were RSV (n = 380; 38.6%), influenza (n = 265; 26.9%), and pneumococcus (n = 105; 10.7%). In adjusted analyses, there was an increased risk of R/VPI hospitalization in patients requiring mechanical circulatory support before transplantation, patients receiving induction with ≥2 immunosuppressive agents, and patients <2 years in the first year after transplantation. The median length of stay for an R/VPI hospitalization was 4 days (IQR, 2-8 days) with a median total cost of $11 081 (IQR, $6215-$24 322).
Conclusions:
Hospitalization for R/VPIs occurred frequently after heart transplantation and were associated with significant costs. Potential strategies to minimize R/VPI include expanding vaccine use through accelerated immunization schedules, further studies of use of palivizumab beyond 2 years of age, and immunogenicity monitoring after vaccination with re-immunization based on guidelines.
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