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The Course of Ulcerative Colitis After Pediatric Liver Transplantation for Sclerosing Cholangitis
Marcin Osiecki1, Jarosław Kierkuś1, Joanna Pawłowska1
1Department of Gastroenterology, Hepatology, Feeding Disorders and Paediatrics, The Children's Memorial Health Institute, Warsaw, Poland.
Insights
Liver transplantation for pediatric patients with primary sclerosing cholangitis (PSC) or autoimmune sclerosing cholangitis (ASC) did not worsen ulcerative colitis (UC) outcomes. Ulcerative colitis also did not impact patient or graft survival post-transplant.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Transplant Surgery
Background:
- Primary sclerosing cholangitis (PSC) and autoimmune sclerosing cholangitis (ASC) are frequently associated with ulcerative colitis (UC).
- The impact of PSC/ASC on UC course, especially in pediatric populations, requires further investigation.
- Evidence regarding UC in pediatric patients undergoing liver transplantation for PSC/ASC is limited.
Purpose of the Study:
- To evaluate the clinical course of ulcerative colitis (UC) in pediatric patients who received an orthotopic liver transplantation (OLT) due to primary sclerosing cholangitis (PSC) or autoimmune sclerosing cholangitis (ASC).
- To determine if OLT for PSC/ASC affects UC progression or patient/graft survival.
- To assess UC activity and outcomes in the post-transplant period.
Main Methods:
- Retrospective review of pediatric patients with PSC/ASC and UC who underwent OLT.
- Diagnosis of UC confirmed by clinical presentation, endoscopy, and histology.
- Analysis of UC disease activity, treatment response, and post-transplant outcomes.
Main Results:
- Seventeen pediatric patients (median age 16.8 years) with PSC/ASC and UC underwent OLT.
- UC was diagnosed before OLT in 15 patients; 2 developed UC post-OLT.
- Post-OLT, UC flares occurred in 4 patients, were successfully treated, and patients remained in remission. No colorectal cancer or colectomy was observed during follow-up (median 3.76 years).
Conclusions:
- Orthotopic liver transplantation for PSC/ASC in pediatric patients does not appear to aggravate the course of ulcerative colitis.
- Ulcerative colitis did not adversely affect patient or graft survival following OLT in this cohort.
- Pediatric patients with UC undergoing OLT for PSC/ASC can achieve favorable long-term outcomes.
Background:
Primary sclerosing cholangitis (PSC) and autoimmune sclerosing cholangitis (ASC) are often associated with ulcerative colitis (UC). The impact on the course of UC remains unclear, and up-to-date evidence in pediatric populations is scarce. The aim of the study was to analyze the course of UC in pediatric patients transplanted owing to PSC or ASC.
Material And Methods:
We retrospectively reviewed data from children with PSC/ASC and UC who underwent orthotopic liver transplantation (OLT). In all patients UC diagnosis was based on clinical presentation, endoscopy, and histology.
Results:
Seventeen patients (9 female) with PSC or ASC underwent OLT from deceased donors at a median age of 16.8 years (range = 11.5-18.2 years). In 15 patients, UC was diagnosed before OLT (median age of diagnosis = 10.6 years; range = 6.6-18.0 years), and 2 patients developed UC after OLT. Ten patients (59%) presented with pancolitis on initial endoscopy. Disease activity was severe in 9 patients (53%) and most patients improved after initial treatment with steroids. Before OLT only 2 patients (13%) had severe disease activity. After OLT, 4 patients developed flares of the disease. These patients were successfully treated and remained in remission at the end of the posttransplant follow-up period (median = 3.76 years; range = 0.4-15.5 years). None of the patients developed colorectal cancer or underwent colectomy during 3.7 years of post-OLT follow-up.
Conclusion:
In our experience, the course of UC was not aggravated by OLT for PSC, and UC did not adversely affect patient or graft survival.
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