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Impact of Hepatoblastoma on Infectious Complications Following Pediatric Liver Transplantation
Ashton D Hall1, Hope A Hendricks2, Katherine A Bowers3
1Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.
Insights
Pediatric liver transplant recipients frequently experience infections, particularly those with hepatoblastoma (HB). Underlying disease impacts infection type and timing, guiding targeted management post-transplant.
Area of Science:
- Pediatric Hepatology
- Transplant Infectious Diseases
- Pediatric Oncology
Background:
- Pediatric liver transplantation (pLT) is crucial for end-stage liver disease and hepatoblastoma (HB).
- Biliary atresia (BA) is the primary indication for pLT, while HB is the most common pediatric liver cancer.
- Post-transplant infections complicate pLT despite advances in surgery and immunosuppression.
Purpose of the Study:
- To assess the impact of underlying diseases on post-transplant infectious events in pediatric liver transplant recipients.
- To compare infectious event profiles between biliary atresia (BA) and hepatoblastoma (HB) cohorts.
Main Methods:
- Retrospective review of pediatric liver transplant recipients at Cincinnati Children's Hospital Medical Center.
- Patients stratified by underlying disease: biliary atresia (BA), hepatoblastoma (HB), and other conditions.
- Analysis of infectious events (IE) in the year following pLT.
Main Results:
- 93% of pLT recipients experienced at least one infectious event within a year.
- Hepatoblastoma (HB) patients, youngest at transplant, had the highest mean number of IE (5.5/patient).
- HB patients showed increased fever/neutropenia and EBV infections, with earlier onset of C. difficile and fever/neutropenia.
Conclusions:
- Infectious events are frequent in HB patients post-pLT, potentially linked to chemotherapy and neutropenia.
- Underlying disease, such as HB, influences the type and timing of infections after pLT.
- Tailoring infection management strategies based on the underlying disease is recommended for pediatric liver transplant recipients.
Background:
Liver transplantation is the standard therapy for end-stage liver disease in pediatric patients with biliary atresia (BA), congenital and metabolic conditions, and for an unresectable malignant tumor like hepatoblastoma (HB). BA is the leading indication for pediatric liver transplantation, while HB is the most common childhood liver cancer. Despite improved outcomes through advanced surgical techniques and novel immunosuppression, pediatric liver transplantation (pLT) is complicated by post-transplant infections.
Methods:
A retrospective review was performed of pLT recipients at Cincinnati Children's Hospital Medical Center (CCHMC) and stratified patients by underlying disease to assess impact on post-transplant infectious events.
Results:
BA patients were youngest at pLT (12.5 months; p < 0.001) compared to other disease cohorts (HB 30.8, other 43.7). All HB patients received organs from deceased donors. In the year following pLT, 93% of the patients experienced at least one infectious event (IE). HB patients had the highest mean number of IE across disease groups (5.5 IE/patient vs. BA 4.5, other 4.0; p = 0.055), with significantly more patients with fever and neutropenia (p < 0.001) and EBV infections (p = 0.012). HB patients were more likely to develop IE earlier after pLT than non-HB groups (p = 0.013), especially Clostridioides difficile (p < 0.01) and fever and neutropenia (p < 0.01). Despite having variable IE experiences, 1-and-5-year survival across disease groups were similar.
Conclusions:
IE were frequently observed in HB patients after pLT, possibly related to pre-and-postoperative chemotherapy and associated neutropenia. Underlying disease may help inform targeted infection-related patient management following pLT.
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