O95* Background: Liver transplantation in infants in the first three months of life, neonates, offers treatment to a patient population in whom life expectancy without hepatic replacement is very limited. Although living-donor liver transplantation (LDLT) has become a well-recognized therapeutic option for children with end-stage liver disease, LDLT in neonates still remains a technically difficult and medically challenging procedure. An analysis of data regarding only LDLT in the first 3 months of life has not performed previously, while several reports about liver transplantation using not only living-donor but also cadaveric graft exist. Therefore, the aim of this retrospective study was to analyze the results of our experience with LDLT in children younger than 3 months of age and to explore strategy to improve survival in the recipients. Patients and Methods: Between June 1990 and December 2003, 600 children (<18 years old) underwent LDLT at our program. Of these, a total of 6 children (3 boys and 3 girls) before the age of 90 days at the time of transplant constitute the study population. Our previous reports have described medical management and surgical techniques. Left lateral segment graft (segments 2 and 3) in 3 cases, reduced-size grafts in 2 cases, and monosegment graft in 1 case were indicated. The arterial anastomosis was made in an end-to-end fashion between one of the hepatic arteries of the recipients and the donor hepatic artery under magnification by surgical microscope. Portal vein was reconstructed in end-to-end manner directly or via venous graft taken from the donor (inferior mesenteric vein). Donor hepatic vein was anastomosed to the stump of the left and the middle hepatic vein. Bile duct was anastomosed to the Roux-en Y loop in an end-to-end fashion. Posttransplant immunosuppression was based on oral FK506 combined with low-dose steroid. Results: The mean age and body weight of the 6 patients was 30 days (range, 27 to 74) and 4.1 kg (range, 3.5 to 4.8), respectively. The age distribution at the time of transplantation included the following: <1 month, 50%; 1–2 months, 33%; and 2–3 months, 17%. Four patients were intensive care unit bound at the time of transplant and 2 patients were hospitalized awaiting transplantation. Liver disease etiology included fluminant hepatic failure (5 cases) and tyrosinemia (1 case). Liver grafts were ABO-identical in 5 patients and ABO-incompatible in the rest. The maximum of the ratio of liver graft weight which was measured at the operation to the recipient body weight (GRWR) was 7.7. Incidence of acute cellular rejection occurred in 2 of 6 patients. Cytomegalovirus or Epstein-Barr virus infection was observed in 4 and 1 cases, respectively. Two patients have been completely withdrawn from immunosuppression for more than three years without any hepatic dysfunction. The patient survival of the neonates was 50%, with follow-up of 1 to 100 months. Three patients died after LDLT. These three deaths were due to sepsis in two cases and vascular occulusion in the other one. Maintenance immunosuppression was FK506-based. Acute rejection episodes occurred in two patients and was managed with intravenous steroid pulse and optimization of FK506. One patient had post-transplant lymphoproliferative disease. Currently, 3 of 6 recipients are alive with good graft function. Conclusions: This is the first report on LDLT in babies younger than 3 months old. From our experience, LDLT offers a promising option for the treatment of severe liver disease in neonates. These neonates should be referred promptly for liver transplantation as reasonable survival can be expected.
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