Normothermic acellular EX vivo liver perfusion reduces liver and bile duct injury of pig livers retrieved after cardiac death

M. U. Boehnert, J. C. Yeung, F. Bazerbachi, J. M. Knaak, N. Selzner, I. D. McGilvray, O. D. Rotstein, O. A. Adeyi, S. M. Kandel, P. Rogalla, P. M. Yip, G. A. Levy, S. Keshavjee, D. R. Grant, M. Selzner

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We compared cold static with acellular normothermic ex vivo liver perfusion (NEVLP) as a novel preservation technique in a pig model of DCD liver injury. DCD livers (60 min warm ischemia) were cold stored for 4 h, or treated with 4 h cold storage plus 8 h NEVLP. First, the livers were reperfused with diluted blood as a model of transplantation. Liver injury was determined by ALT, oxygen extraction, histology, bile content analysis and hepatic artery (HA) angiography. Second, AST levels and bile production were assessed after DCD liver transplantation. Cold stored versus NEVLP grafts had higher ALT levels (350 ± 125 vs. 55 ± 35 U/L; p < 0.0001), decreased oxygen extraction (250 ± 65 mmHg vs. 410 ± 58 mmHg, p < 0.01) and increased hepatocyte necrosis (45% vs. 10%, p = 0.01). Levels of bilirubin, phospholipids and bile salts were fivefold decreased, while LDH was sixfold higher in cold stored versus NEVLP grafts. HA perfusion was decreased (twofold), and bile duct necrosis was increased (100% vs. 5%, p < 0.0001) in cold stored versus NEVLP livers. Following transplantation, mean serum AST level was higher in the cold stored versus NEVLP group (1809 ± 205 U/L vs. 524 ± 187 U/L, p < 0.05), with similar bile production (2.5 ± 1.2 cc/h vs. 2.8 ± 1.4 cc/h; p = 0.2). NEVLP improved HA perfusion and decreased markers of liver duct injury in DCD grafts. Normothermic ex vivo liver perfusion decreases hepatocyte death and bile duct injury of grafts obtained after cardiac death.

Original languageEnglish (US)
Pages (from-to)1441-1449
Number of pages9
JournalAmerican Journal of Transplantation
Issue number6
StatePublished - Jun 1 2013


  • Biliary complication
  • preservation
  • preservation temperature
  • preservation-reperfusion injury


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