TY - JOUR
T1 - Novel Dynamic Organ Storage System Enhances Liver Graft Function in a Porcine Donation After Circulatory Death Model
AU - Shishido, Yutaka
AU - Tracy, Kaitlyn M.
AU - Petrovic, Mark
AU - Adesanya, Tioluwanimi
AU - Fortier, Avery K.
AU - Raietparvar, Kimya
AU - Glomp, Gabriella A.
AU - Simonds, Elizabeth
AU - Harris, Timothy R.
AU - Simon, Victoria
AU - Tucker, William D.
AU - Petree, Brandon
AU - Cortelli, Michael
AU - Cardwell, Nancy L.
AU - Crannell, Christian
AU - Liang, Jiancong
AU - Murphy, Alexandria C.
AU - Fields, Blanche L.
AU - McReynolds, Melanie
AU - Demarest, Caitlin T.
AU - Ukita, Rei
AU - Rizzari, Michael
AU - Montenovo, Martin
AU - Magliocca, Joseph F.
AU - Karp, Seth J.
AU - Ameen Rauf, M.
AU - Shah, Ashish S.
AU - Bacchetta, Matthew
N1 - Publisher Copyright:
Copyright © ASAIO 2024.
PY - 2024
Y1 - 2024
N2 - Donation after circulatory death (DCD) livers face increased risks of critical complications when preserved with static cold storage (SCS). Although machine perfusion (MP) may mitigate these risks, its cost and logistical complexity limit widespread application. We developed the Dynamic Organ Storage System (DOSS), which delivers oxygenated perfusate at 10°C with minimal electrical power requirement and allows real-time effluent sampling in a portable cooler. In a porcine DCD model, livers were preserved using DOSS or SCS for 10 hours and evaluated with 4 hours of normothermic MP, with n = 5 per group. After 4 hours of normothermic MP, the DOSS group demonstrated significantly lower perfusate lactate (p = 0.023), increased perfusate fibrinogen (p = 0.005), higher oxygen consumption (p = 0.018), greater bile production (p = 0.013), higher bile bicarbonate levels (p = 0.035) and bile/perfusate sodium ratio (p = 0.002), and lower hepatic arterial resistance after phenylephrine administration (p = 0.018). Histological analysis showed lower apoptotic markers in DOSS-preserved livers, with fewer cleaved caspase-3 (p = 0.039) and terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL; p = 0.009) positive cells. These findings suggest that DOSS can enhance DCD allograft function during transport, offering potential clinical benefits and contributing to the expansion of the donor pool.
AB - Donation after circulatory death (DCD) livers face increased risks of critical complications when preserved with static cold storage (SCS). Although machine perfusion (MP) may mitigate these risks, its cost and logistical complexity limit widespread application. We developed the Dynamic Organ Storage System (DOSS), which delivers oxygenated perfusate at 10°C with minimal electrical power requirement and allows real-time effluent sampling in a portable cooler. In a porcine DCD model, livers were preserved using DOSS or SCS for 10 hours and evaluated with 4 hours of normothermic MP, with n = 5 per group. After 4 hours of normothermic MP, the DOSS group demonstrated significantly lower perfusate lactate (p = 0.023), increased perfusate fibrinogen (p = 0.005), higher oxygen consumption (p = 0.018), greater bile production (p = 0.013), higher bile bicarbonate levels (p = 0.035) and bile/perfusate sodium ratio (p = 0.002), and lower hepatic arterial resistance after phenylephrine administration (p = 0.018). Histological analysis showed lower apoptotic markers in DOSS-preserved livers, with fewer cleaved caspase-3 (p = 0.039) and terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL; p = 0.009) positive cells. These findings suggest that DOSS can enhance DCD allograft function during transport, offering potential clinical benefits and contributing to the expansion of the donor pool.
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U2 - 10.1097/MAT.0000000000002365
DO - 10.1097/MAT.0000000000002365
M3 - Article
C2 - 39693205
AN - SCOPUS:85213016140
SN - 1058-2916
JO - ASAIO Journal
JF - ASAIO Journal
M1 - 10.1097/MAT.0000000000002365
ER -