Preclinical validation of a customized circuit for ex situ uninterrupted cold‐to‐warm prolonged perfusion of the liver

Author:

Scatton Olivier12,Turco Célia23ORCID,Savier Eric12,Pelissié Jérôme4,Legallais Cécile5,Sakka Medhi5,Aoudjehane Lynda26,Wendum Dominique7,Migliazza John8,Spiritelli Sandra8,Conti Filomena29,Goumard Claire12

Affiliation:

1. Department of Hepatobiliary Surgery and Liver Transplantation Sorbonne Université, Hôpital Pitié‐Salpêtrière, Assistance Publique—Hôpitaux de Paris Paris France

2. INSERM UMRS‐938, Centre de Recherche Saint‐Antoine (CRSA) Sorbonne Université Paris France

3. Liver Transplantation Unit, Department of Digestive and Oncologic Surgery University Hospital of Besançon Besançon France

4. Department of Extracorporeal Perfusion and Vascular Surgery Hôpital Pitié‐Salpêtrière, Assistance Publique—Hôpitaux de Paris Paris France

5. Department of Metabolic Biochemistry Sorbonne Université, Hôpital Pitié‐Salpêtrière, Assistance Publique—Hôpitaux de Paris Paris France

6. INSERM, Institute of Cardiometabolism and Nutrition (ICAN) Sorbonne Université Paris France

7. Department of Pathology Saint‐Antoine Hospital (AP‐HP) Paris France

8. Department of Discovery, Research and Development LivaNova PLC London UK

9. Department of Medical Liver Transplantation Assistance Publique—Hôpitaux de Paris (AP‐HP), Pitié‐Salpêtrière Hospital Paris France

Abstract

AbstractContextClinical adoption of ex situ liver perfusion is growing. While hypothermic perfusion protects against ischemia–reperfusion injury in marginal grafts, normothermic perfusion enables organ viability assessment and therefore selection of borderline grafts. The combination of hypothermic and normothermic perfusion, known as “cold‐to‐warm,” may be the optimal sequence for organ preservation, but is difficult to achieve with most commercial perfusion systems. We developed an adaptable customized circuit allowing uninterrupted “cold‐to‐warm” perfusion and conducted preclinical studies on healthy porcine livers and discarded human livers to demonstrate the circuit's efficacy.MethodsIn collaboration with bioengineers, we developed a customized circuit that adapts to extracorporeal circulation consoles used in cardiovascular surgery and includes a proprietary reservoir enabling easy perfusate change without interrupting perfusion. This preclinical study was conducted on porcine and human livers. Perfusion parameters (pressures, flows, oxygenation) and organ viability were monitored.ResultsThe customized circuit was adapted to a LivaNova S5® console, and the perfusions were flow‐driven with real‐time pressure monitoring. Ten porcine liver and 12 discarded human liver perfusions were performed during 14 to 18 h and 7 to 25 h, respectively. No hyperpressure was observed (porcine and human portal pressure 2–6 and 2–8 mm Hg; arterial pressure 10–65 and 20–65 mm Hg, respectively). No severe histological tissue injury was observed (Suzuki score ≤ 3 at the end of perfusion). Seven (70%) porcine livers and five (42%) human livers met the UK viability criteria.ConclusionThe customized circuit and system design enables smooth uninterrupted “cold‐to‐warm” perfusion not present in current commercial perfusion systems.

Publisher

Wiley

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