Newer surgical techniques and immunosuppressive therapies have resulted in
paediatric liver transplantation being available for most children with end
-stage liver disease and has resulted in a greater than 80% 5-year survival
rate. The most common indications for paediatric liver transplantation are
biliary atresia (43%), metabolic disease (13%) and acute hepatic necrosis
(11%). For approximately 75% of children with acute hepatic failure, the ca
use is unknown. Timing of liver transplantation not only affects survival r
ate, but may influence neurodevelopmental outcome. Fortunately, numerous ty
pes of donors, such as reduced-sized, living related or unrelated and blood
-type mismatched, have reduced the mortality of children who are waiting fo
r liver transplantation. However, the, mortality and morbidity before and a
fter liver transplantation remain high for children who have fulminant hepa
tic failure or are less than 5 months of age at the time of transplantation
. The principle medical complications after liver transplantation are rejec
tion and infection. Although use of newer immunosuppressive regimens has re
duced the rate of rejection, Epstein-Barr virus infection with associated l
ymphoproliferative disorder remains the principle cause for morbidity and m
ortality after the initial 3 months post-liver transplant.