Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/12364
Title: Extended normothermic extracorporeal perfusion of isolated human liver after warm ischaemia: a preliminary report.
Authors: Bellomo, Rinaldo;Marino, Bruno;Starkey, Graham;Fink, Michael A;Wang, Bao Zhong;Eastwood, Glenn M;Peck, Leah;Young, Helen;Houston, Shane;Skene, Alison;Opdam, Helen Ingrid;Jones, Robert M
Affiliation: Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia. rinaldo.bellomo@austin.org.au.
Perfusion Services, Austin Hospital, Melbourne, VIC, Australia.
Department of Liver Transplantation Surgery, Austin Hospital, Melbourne, VIC, Australia.
Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia.
Department of Anatomical Pathology, Austin Hospital, Melbourne, VIC, Australia.
Donate Life Victoria, Melbourne, VIC, Australia.
Issue Date: 1-Sep-2014
Citation: Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine; 16(3): 197-201
Abstract: Donation after circulatory death (DCD) livers are at markedly increased risk of primary graft dysfunction and biliary tract ischaemia. Normothermic extracorporeal liver perfusion (NELP) may increase the ability to transplant DCD livers and may allow their use for artificial extracorporeal liver support of patients with fulminant liver failure.We conducted two proof-of-concept experiments using human livers after DCD to assess the feasibility and functional efficacy of NELP over an extended period.We applied extracorporeal membrane oxygenation, parenteral nutrition, separate hepatic artery and portal vein perfusion and physiological perfusion pressures to two livers obtained after DCD.We achieved NELP and evidence of liver function (bile production, paracetamol removal and maintenance of normal lactate levels) in both livers; one for 24 hours and the other for 43 hours. Histological examination showed areas of patchy ischaemia but preserved biliary ducts and canaliculi.Our experiments justify further investigations of the feasibility and efficacy of extended DCD liver preservation by ex-vivo perfusion.
Internal ID Number: 25161022
URI: http://ahro.austin.org.au/austinjspui/handle/1/12364
URL: http://www.ncbi.nlm.nih.gov/pubmed/25161022
Type: Journal Article
Subjects: Feasibility Studies
Humans
Ischemia
Liver.blood supply.cytology.physiology
Organ Preservation.methods
Perfusion.methods
Time Factors
Tissue and Organ Procurement
Warm Ischemia
Appears in Collections:Journal articles

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