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Temperature profiles of different cooling methods in porcine pancreas procurement
Authors:Bradley P. Weegman  Thomas M. Suszynski  William E. Scott III  Joana Ferrer Fábrega  Efstathios S. Avgoustiniatos  Takayuki Anazawa  Timothy D. O'Brien  Michael D. Rizzari  Theodore Karatzas  Tun Jie  David E. R. Sutherland  Bernhard J. Hering  Klearchos K. Papas
Affiliation:1. Department of Surgery, Schulze Diabetes Institute, University of Minnesota, , Minneapolis, MN, USA;2. Department of Surgery, Institute for Cellular Transplantation, University of Arizona, , Tucson, AZ, USA;3. College of Veterinary Medicine, University of Minnesota, , St. Paul, MN, USA;4. Second Department of Propedeutic Surgery, University of Athens, , Athens, Greece
Abstract:
Porcine islet xenotransplantation is a promising alternative to human islet allotransplantation. Porcine pancreas cooling needs to be optimized to reduce the warm ischemia time (WIT) following donation after cardiac death, which is associated with poorer islet isolation outcomes. This study examines the effect of four different cooling Methods on core porcine pancreas temperature (n = 24) and histopathology (n = 16). All Methods involved surface cooling with crushed ice and chilled irrigation. Method A, which is the standard for porcine pancreas procurement, used only surface cooling. Method B involved an intravascular flush with cold solution through the pancreas arterial system. Method C involved an intraductal infusion with cold solution through the major pancreatic duct, and Method D combined all three cooling Methods. Surface cooling alone (Method A) gradually decreased core pancreas temperature to <10 °C after 30 min. Using an intravascular flush (Method B) improved cooling during the entire duration of procurement, but incorporating an intraductal infusion (Method C) rapidly reduced core temperature 15–20 °C within the first 2 min of cooling. Combining all methods (Method D) was the most effective at rapidly reducing temperature and providing sustained cooling throughout the duration of procurement, although the recorded WIT was not different between Methods (P = 0.36). Histological scores were different between the cooling Methods (P = 0.02) and the worst with Method A. There were differences in histological scores between Methods A and C (P = 0.02) and Methods A and D (P = 0.02), but not between Methods C and D (P = 0.95), which may highlight the importance of early cooling using an intraductal infusion. In conclusion, surface cooling alone cannot rapidly cool large (porcine or human) pancreata. Additional cooling with an intravascular flush and intraductal infusion results in improved core porcine pancreas temperature profiles during procurement and histopathology scores. These data may also have implications on human pancreas procurement as use of an intraductal infusion is not common practice.
Keywords:cold preservation  islet xenotransplantation  organ cooling  pancreas procurement
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