Evaluation of Institut Georges Lopez-1 preservation solution in pig pancreas transplantation: a pilot study

Institut Georges Lopez-1 preservation solution (IGL-1) is an emerging extracellular-type electrolyte solution, low in viscosity, containing polyethylene glycol 35 as a colloid. Although IGL-1 has shown beneficial outcomes in kidney and liver preservation, this pilot study is the first to evaluate th...

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Veröffentlicht in:Transplantation 2014-05, Vol.97 (9), p.901-907
Hauptverfasser: García-Gil, Francisco A, Fuentes-Broto, Lorena, Albendea, Carlos D, Serrano, María Trinidad, Roselló-Catafau, Joan, Lampreave, Fermín, López-Pingarrón, Laura, Escartín, Jorge, Soria, Joaquín, Garcia, Joaquín J, Fernández-Cruz, Laureano
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Sprache:eng
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Zusammenfassung:Institut Georges Lopez-1 preservation solution (IGL-1) is an emerging extracellular-type electrolyte solution, low in viscosity, containing polyethylene glycol 35 as a colloid. Although IGL-1 has shown beneficial outcomes in kidney and liver preservation, this pilot study is the first to evaluate the efficacy of IGL-1 in pancreas transplantation (PT) compared with the University of Wisconsin solution (UW). Sixteen Landrace pigs underwent allogeneic PT with 16 hr of cold ischemia. Grafts were preserved with IGL-1 (n=8) or UW (n=8). No immunosuppression was administered. We analyzed graft function, the acute-phase response, and oxidative stress in the pancreatic graft monitoring membrane fluidity and lipid peroxidation. All eight grafts with IGL-1, but only six with UW, were functioning. Graft failures with UW resulted from graft thrombosis. There were no differences between the two solutions in the number of normoglycemic days (IGL-1: 11.5 ± 6.2 versus UW: 8.5 ± 4.4 days, P=0.1357), nor in lipid peroxidation during 16-hr cold ischemia (P=0.672), or reperfusion (P=0.185), but IGL-1 prevented changes in membrane fluidity after reperfusion when compared with UW (P=0.026). IGL-1 offered the same degree of safety and effectiveness as UW in our model of pig PT with 16 hr of cold ischemia.
ISSN:0041-1337
1534-6080
DOI:10.1097/TP.0000000000000050