Novel Dynamic Organ Storage System Enhances Liver Graft Function in a Porcine Donation After Circulatory Death Model

Yutaka Shishido, Kaitlyn M. Tracy, Mark Petrovic, Tioluwanimi Adesanya, Avery K. Fortier, Kimya Raietparvar, Gabriella A. Glomp, Elizabeth Simonds, Timothy R. Harris, Victoria Simon, William D. Tucker, Brandon Petree, Michael Cortelli, Nancy L. Cardwell, Christian Crannell, Jiancong Liang, Alexandria C. Murphy, Blanche L. Fields, Melanie McReynolds, Caitlin T. DemarestRei Ukita, Michael Rizzari, Martin Montenovo, Joseph F. Magliocca, Seth J. Karp, M. Ameen Rauf, Ashish S. Shah, Matthew Bacchetta

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish (US)
Article number10.1097/MAT.0000000000002365
JournalASAIO Journal
DOIs
StateAccepted/In press - 2024

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Bioengineering
  • Biomaterials
  • Biomedical Engineering

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