Liver transplantation is a major life-saving procedure, and donation after
cardiac death (
DCD) has increased the pool of potential liver donors. However,
DCD livers are at increased risk of
primary graft dysfunction and biliary tract ischaemia. Normothermic extracorporeal liver perfusion (NELP) may increase the ability to protect, evaluate and, in future, transplant
DCD livers. We conducted proof-of-concept experiments using a
DCD model in the pig to assess the short-term (4 hours) feasibility and functional efficacy of NELP. Using
extracorporeal membrane oxygenation,
parenteral nutrition, separate hepatic artery and portal vein perfusion, and physiological perfusion pressures, we achieved NELP and evidence of function (bile production,
paracetamol removal, maintenance of normal
ammonia and
lactate levels) for 4 hours in pig livers subjected to 15 and 30 minutes of
cardiac arrest before explantation. Our experiments justify further investigations of the feasibility and efficacy of human
DCD liver preservation by ex-vivo perfusion.