Challenges faced in establishing a pediatric liver transplant program in a lower‐middle‐income country with free healthcare service

• Published in: Pediatric transplantation Vol. 28; no. 1; pp. e14681 - n/a
• Main Authors: Fernando, Meranthi, Tillakaratne, Suchintha, Gunetilleke, Bhagya, Liyanage, Chamila, Appuhamy, Chinthaka, Weerasuriya, Aruna, Uragoda, Buddhika, Welikala, Nadeeshya, Ranaweera, Liyanage, Ganewatte, Eranga, Dissanayake, Janaki, Mudalige, Anushka, Siriwardana, Rohan
• Format: Journal Article
• Language: English
• Published: Denmark Wiley Subscription Services, Inc 01.02.2024
• Subjects: Biliary atresia; children; Cholestasis; Health care; initial experience; Liver diseases; liver failure; liver transplant; Liver transplantation; Liver transplants; Pediatrics; Sri Lanka; Survival; Wilson's disease; Sri Lanka; initial experience; liver failure; Sri Lanka; children; liver transplant
• ISSN: 1397-3142; 1399-3046
• DOI: 10.1111/petr.14681

Background Liver transplant is the cure for children with liver failure. Sri Lanka is a lower‐middle‐income country with a predominant free, state health system. Pediatric liver transplant program in Sri Lanka is still in the budding state where the initial experience of the program is yet to be documented. Methods A retrospective review was performed including the clinical characteristics of all pediatric liver transplant recipients of Colombo North Centre for Liver Diseases since the inception of the program from June 2020 to May 2023. Results There were 14 PLT performed in 3 years. The median recipient age and weight were 8 years (6 months–15 years) and 23.3 kg (6.4–49.2), respectively. The majority were boys (64%). All were from low‐income backgrounds. Indications for LT were acute liver failure (5/14), decompensated chronic liver disease (5/14), and acute on chronic liver failure (4/14). Underlying liver diseases were Wilson disease (6/14), autoimmune liver disease (3/14), biliary atresia (2/14) and progressive familial intrahepatic cholestasis type 3 (1/14), and unknown etiology (2/14). The majority were living donor liver transplants (86%). Of the living donors, 42% (5/12) were Buddhist priests. There were three immediate deaths and two late deaths. The 3‐month survival was 78%, and overall survival was 64%. Living donor transplants carried a higher success rate (92%) compared to diseased donor transplants (0%; 2/2). Conclusions Initial experience of pediatric liver transplant program of Sri Lanka is promising despite being established in a free healthcare system amidst the crisis circumstances. Initial experience of pediatric liver transplant program of Sri Lanka is promising despite being established in a free healthcare system amidst the crisis circumstances. There were 14 PLT performed in 3 years.