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Updated: Jun 27, 2026

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Published on: August 29, 2025
Audit of eosinophilic oesophagitis in children post-liver transplant
C Noble1, L Francis, G W Withers
1Royal Children's Hospital, Herston, Brisbane, Queensland, Australia.
Insights
Eosinophilic esophagitis (EE) affects 12% of pediatric liver transplant (LT) recipients with upper GI symptoms. Early endoscopic evaluation is crucial for diagnosis and managing this condition post-LT.
Area of Science:
- Gastroenterology
- Pediatric Hepatology
- Transplant Medicine
Background:
- Pediatric liver transplantation (LT) survival rates exceed 70% at 10 years, shifting focus to quality of life.
- Eosinophilic esophagitis (EE) is increasingly recognized in the general population and post-solid organ transplant patients.
- The impact of EE on morbidity in pediatric LT recipients remains unaddressed.
Purpose of the Study:
- To determine the incidence of EE in children undergoing liver transplantation.
- To assess the clinical significance of EE in this patient cohort.
Main Methods:
- Retrospective review of medical records for all pediatric liver transplant recipients over 15.5 years.
- Analysis of esophageal biopsies with mucosal inflammation, using a diagnostic cut-off of 20 eosinophils per high-power field.
- Cross-referencing procedural and electronic laboratory results.
Main Results:
- Four out of 130 surviving pediatric liver transplant recipients (3%) were diagnosed with EE.
- All diagnosed EE cases (12%) were within the 34 patients followed in Queensland.
- The overall incidence is likely underestimated due to patients being followed elsewhere.
Conclusions:
- Eosinophilic esophagitis is a clinically significant condition in pediatric liver transplant recipients.
- Children post-LT presenting with upper GI symptoms warrant endoscopic evaluation and biopsy to rule out EE.
- Further research is needed to fully understand EE's contribution to morbidity in this population.
Abstract:
Pediatric liver transplantation has proven so successful that 10-yr survival post-transplantation is in excess of 70% and following transplantation, emphasis of medical care switches from life saving to promotion of good quality of life. EE is an increasingly recognised phenomenon in the general population. Eosinophilic disorders of the GI tract are increasingly recognised in patient's post-solid organ transplantation but the contribution of EE to morbidity in this population has not been addressed to date. The objective of this study was to identify the incidence of EE in children receiving liver transplantation by the QLTS over the last 15.5 yr. Comprehensive review of medical records of all liver transplant recipients during study period via cross-checking procedural and electronic laboratory results was performed. All oesophageal biopsies reporting mucosal inflammation were reviewed. EE can be diagnosed when oesophageal biopsy reveals > or =5 eosinophils per HPF; however, we used a cut-off of 20 eosinophils per HPF, which is in accordance with current opinion. In the 159 children who received DD OLT, 130 survived and four have been diagnosed with EE (3%). Only 34 are currently followed in Queensland and all four patients diagnosed are in this cohort representing 12% of our follow-up clinic. Many patients are followed elsewhere so occurrence of EE in our total surviving population is an underestimate. EE is clinically important in the post-liver transplant community. Children post-OLT who have upper GI symptoms should be considered for endoscopic evaluation and biopsy to exclude EE.
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