A prolongation of hepatic vascular exclusion by in situ hypothermic perfusion in dogs
T. Takeuchi, H. Egawa, Y. Yamaoka, Y. Taki, J. Ueda, Y. Konishi, N. Yamamoto, R. Kagawa, M. Washida, R. Okamoto and al. et
Second Department of Surgery, Faculty of Medicine, Kyoto University, Japan.
In situ hypothermic hepatic perfusion was performed in dogs to explore
whether the time limit of hepatic vascular exclusion could be prolonged.
During hepatic vascular exclusion, hepatic hypothermic perfusion was
performed via portal vein using various perfusates under active bypass from
the portal vein and infrahepatic inferior vena cava area to the superior
vena cava system. Dogs receiving hepatic hypothermic perfusion for 1 hour
died when given Ringer's solution but survived more than 7 days when given
Euro-Collins' and University of Wisconsin solutions. Although dogs
tolerated 2 hours of hepatic hypothermic perfusion when give University of
Wisconsin solution, all dogs died by 2 hours of hepatic hypothermic
perfusion when given Euro-Collins' solution. The hepatic energy charge and
arterial ketone body ratio of dogs that died were significantly lower than
for those that survived. This suggests that the regimen of hepatic
hypothermic perfusion with University of Wisconsin solution is able to
maintain the energy metabolism of the liver under hepatic vascular
exclusion for prolonged periods, hence, its possible clinical application.