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Hypothermic Oxygenated Machine Perfusion vs Static Cold Storage: Preliminary Clinical Experience from a Prospective, Multi-Center Randomized Controlled Trial

G. G. Panayotova1, R. Quillin III2, F. Paterno1, K. Lunsford1, M. A. McCarty1, A. Bailey2, G. Dikdan1, J. Rosado1, S. Shah2, J. V. Guarrera1

1Transplant and HPB Surgery, Rutgers NJMS, Newark, NJ, 2Division of Transplantation, University of Cincinnati, Cincinnati, OH

Meeting: 2020 American Transplant Congress

Abstract number: 593

Keywords: Liver grafts, Machine preservation, Perfusion solutions, Preservation

Session Information

Session Name: All Organs: Organ Preservation/Ischemia Reperfusion Injury

Session Type: Oral Abstract Session

Date: Saturday, May 30, 2020

Session Time: 3:15pm-4:45pm

 Presentation Time: 4:03pm-4:15pm

Location: Virtual

*Purpose: Hypothermic oxygenated machine perfusion (HMP-O2) is a novel liver preservation technique currently in clinical trials. It has the potential to mitigate ischemia/reperfusion injury, as well as improve organ function and patient outcomes. Here we present preliminary results from two collaborating centers within the PILOT trial (NCT03484455), a prospective, multi-center randomized controlled trial comparing HMP-O2 vs Static Cold Storage (SCS), using the Lifeport Liver Transporter (LLT) (Organ Recovery Systems, Itasca, IL).

*Methods: Study patients were randomized to SCS or HMP-O2. The HMP perfusate was actively oxygenated using “oxygen pre-charge” (OPC) prior to initiation of perfusion. Liver tissue samples and perfusate were collected. Operative and postoperative care was per institutional protocol, and postoperative parameters were followed. Adverse events (AEs) were tracked; re-operations, hospital re-admissions, and biliary complications were considered severe (SAEs). Statistical analysis was performed using SPSS v26 and GraphPad Prism v8.3.0; p<0.05 was considered significant.

*Results: 26 SCS and 13 HMP-O2 cases were analyzed. Donor and recipient age, match MELD, BMI and anastomotic time were similar between groups. Cold ischemia time (CIT) was greater for HMP-O2 (7 vs 5.1 hrs, p=0.0001). One recipient of a DCD liver in the SCS cohort had PNF and expired on POD1. Early allograft dysfunction (EAD) occurred in 2/13 HMP-O2 and 5/26 SCS cases. The incidence of SAEs, particularly biliary complications (BC), was higher in the SCS arm (p<0.05 and p=0.006, respectively; Figure 1). This was independent of ischemia times and donor/recipient parameters.

*Conclusions: HMP-O2 appears to be a safe and effective preservation method. Early results from two centers in the PILOT trial demonstrate several improved short-term outcomes. Further study is needed to fully characterize the benefits of HMP-O2 in Liver Transplantation.

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To cite this abstract in AMA style:

Panayotova GG, III RQuillin, Paterno F, Lunsford K, McCarty MA, Bailey A, Dikdan G, Rosado J, Shah S, Guarrera JV. Hypothermic Oxygenated Machine Perfusion vs Static Cold Storage: Preliminary Clinical Experience from a Prospective, Multi-Center Randomized Controlled Trial [abstract]. Am J Transplant. 2020; 20 (suppl 3). https://atcmeetingabstracts.com/abstract/hypothermic-oxygenated-machine-perfusion-vs-static-cold-storage-preliminary-clinical-experience-from-a-prospective-multi-center-randomized-controlled-trial/. Accessed May 16, 2025.

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