Fulminant hepatic failure can only be treated successfully by
liver transplantation, which, however, is not always available. To "bridge" the patient with
fulminant hepatic failure until a liver graft is available, various forms of liver support devices had been designed but they were not uniformly successful. To prove the efficacy of a liver support device for
fulminant hepatic failure, testing in an animal model is necessary. We attempted to induce a pig model with
fulminant hepatic failure by administering
galactosamine into pigs and reported the observation. Three pigs were given a dose of 0.5 gm/kg of
galactosamine and five pigs were given 1 gm/kg of
galactosamine. One pig receiving 0.5 gm/kg
galactosamine survived after manifestation of
liver failure, while all the other pigs died. The two pigs receiving 0.5 gm/kg
galactosamine survived longer than the five pigs receiving 1 gm/kg
galactosamine. Before death, a significant elevation of parenchymal liver
enzymes,
lactate dehydrogenase,
bilirubin,
bile acid,
ammonia, tumour
necrosis factor-alpha, activated clotting time, a decrease of platelet concentration,
ketone bodies ratio,
blood glucose and
plasma albumin, and serious impairment of
indocyanine green clearance were indicated. At post-mortem, severe liver
necrosis was observed. The model may be suitable for testing the efficacy of liver support device for
fulminant hepatic failure, preferably 24-48 hours after administration of
galactosamine.