RESULT OF LIVING DONOR LIVER TRANSPLANTATION TREATMENT BILIARY ATRESIA IN CHILDREN AT THEVIET NAM NATIONAL CHILDREN’S HOSPITAL

Duy Hiền Phạm1,, Phạm Anh Hoa Nguyễn1, Mạnh Hoàn Vũ1, Anh Quỳnh Trần2, Mạnh Tuân Tô2, Lý Thịnh Trường Nguyễn2, Hanh Tiệp Đặng2, Hùng Trần2, Ánh Dương Đặng2, Phan Ninh Trần2, Đình Công Lê2, Tùng Lâm Hoàng 2, Đức Hạnh Nguyễn2, Đức Tâm Trần2, Hồng Long Phan2,3, Thọ Anh Nguyễn2, Xuân Nam Trần2, Công Sơn Nguyễn2, Thị Hồng Quyên Trần2, Ngọc Thạch Hoàng 2, Văn Đô Đỗ2, Thị Hải Yến Phạm2, Thị Ly Na Bạch 2, Thị Vân Anh Hoàng 2, Thị Thủy Trịnh2, Minh Điển Trần2, Văn Thành Lê4
1 Vietnam National Children's Hospital.
2 Vietnam National Children's Hospital
3 University of Medicine and Pharmacy - Hanoi National University
4 Military Central Hospital 108

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Abstract

Background: Biliary atresia is the most common indication for liver transplantation in children. Aims: To evaluate the results of living donor liver transplantation treatment biliary atresia in children at Viet Nam National Children’s Hospital. Materials and Methods: A retrospective review early and mid-term outcome of 22 patients with biliary atresia were peformed living donor transplantation from July 2018 to November 2022. Results: There were 22 living donor liver transplantation cases were performed in National Children Hospital, 10 male (45,5%) and 12 female (54,5%). The median age at operation was 29,5 months (8 months old to 14 years old).  The median body weight was 10,0 kg (7,5kg to 26kg). The left lateral segments were used in 20 cases (91%), right lobe were used in 2 cases (9%). There are 9 cases (40,9%) were performed with ABO blood group incompatibility. No donor complication was encountered. Intra-abdominal bleeding (4 cases, 18,2%), hepatic vein stenosis (4 cases, 18,2%), prolong chylous ascites (5 cases, 22,7%), hepatic artery thrombosis (1 case, 4,5%), intestinal perforation (1 case, 4,5%), 1 case (4,5%) died in post operation day 1 because of coagulation disorders, 1 case (4,5%) died after 3 months because of severe infection progress. Conclusion: Liver transplantation in our center provides encouraging outcomes for pediatric recipients with biliary atresia with the good result 3-years patient survival rate of 88,1%

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References

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