Screening for mitochondrial function before use-routine liver assessment during hypothermic oxygenated perfusion impacts liver utilization.

Donation after circulatory death Flavin mononucleotide Hypothermic oxygenated perfusion Liver utilization

Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
30 Oct 2023
Historique:
received: 20 07 2023
revised: 15 10 2023
accepted: 15 10 2023
medline: 3 11 2023
pubmed: 3 11 2023
entrez: 2 11 2023
Statut: aheadofprint

Résumé

To report on a concept of liver assessment during ex situ hypothermic oxygenated perfusion (HOPE) and its significant impact on liver utilization. An analysis of prospectively collected data on donation after circulatory death (DCD) livers, treated by HOPE at our institution, during a 11-year period between January 2012 and December 2022. Four hundred and fifteen DCD Maastricht III livers were offered during the study period in Switzerland, resulting in 249 liver transplants. Of those, we performed 158 DCD III liver transplants at our institution, with 1-year patient survival and death censored graft survival (death with functioning graft) of 87 and 89%, respectively, thus comparable to benchmark graft survivals of ideal DBD and DCD liver transplants (89% and 86%). Correspondingly, graft loss for primary non-function or cholangiopathy was overall low, i.e., 7/158 (4.4%) and 11/158 (6.9%), despite more than 82% of DCD liver grafts ranked high (6-10 points) or futile risk (>10 points) according to the UK-DCD score. Consistently, death censored graft survival was not different between low-, high-risk or futile DCD III livers. The key behind these achievements was the careful development and implementation of a routine perfusate assessment of mitochondrial biomarkers for injury and function, i.e., release of flavin mononucleotide from complex I, perfusate NADH, and mitochondrial CO HOPE after cold storage is a highly suitable and easy to perform perfusion approach, which allows reliable liver graft assessment, enabling surgeons to make a fact based decision on whether or not to implant the organ. HOPE-treatment should be combined with viability assessment particularly when used for high-risk organs, including DCD livers or organs with relevant steatosis. This study was supported by the Swiss National Foundation (SNF) grant 320030_189055/1 to PD.

Sections du résumé

BACKGROUND BACKGROUND
To report on a concept of liver assessment during ex situ hypothermic oxygenated perfusion (HOPE) and its significant impact on liver utilization.
METHODS METHODS
An analysis of prospectively collected data on donation after circulatory death (DCD) livers, treated by HOPE at our institution, during a 11-year period between January 2012 and December 2022.
FINDINGS RESULTS
Four hundred and fifteen DCD Maastricht III livers were offered during the study period in Switzerland, resulting in 249 liver transplants. Of those, we performed 158 DCD III liver transplants at our institution, with 1-year patient survival and death censored graft survival (death with functioning graft) of 87 and 89%, respectively, thus comparable to benchmark graft survivals of ideal DBD and DCD liver transplants (89% and 86%). Correspondingly, graft loss for primary non-function or cholangiopathy was overall low, i.e., 7/158 (4.4%) and 11/158 (6.9%), despite more than 82% of DCD liver grafts ranked high (6-10 points) or futile risk (>10 points) according to the UK-DCD score. Consistently, death censored graft survival was not different between low-, high-risk or futile DCD III livers. The key behind these achievements was the careful development and implementation of a routine perfusate assessment of mitochondrial biomarkers for injury and function, i.e., release of flavin mononucleotide from complex I, perfusate NADH, and mitochondrial CO
INTERPRETATION CONCLUSIONS
HOPE after cold storage is a highly suitable and easy to perform perfusion approach, which allows reliable liver graft assessment, enabling surgeons to make a fact based decision on whether or not to implant the organ. HOPE-treatment should be combined with viability assessment particularly when used for high-risk organs, including DCD livers or organs with relevant steatosis.
FUNDING BACKGROUND
This study was supported by the Swiss National Foundation (SNF) grant 320030_189055/1 to PD.

Identifiants

pubmed: 37918219
pii: S2352-3964(23)00423-1
doi: 10.1016/j.ebiom.2023.104857
pmc: PMC10641151
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104857

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests A.S. received consultant fees for presentations from Bridge to life LTD, all other authors declare no competing interests.

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Auteurs

Janina Eden (J)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Eva Breuer (E)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Dominique Birrer (D)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Matteo Müller (M)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Matthias Pfister (M)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Hemma Mayr (H)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Keyue Sun (K)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Jeannette Widmer (J)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Florian Huwyler (F)

Department of Mechanical and Process Engineering, ETH Zurich, Zurich, Switzerland.

Udo Ungethüm (U)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Bostjan Humar (B)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Anurag Gupta (A)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Stefanie Schiess (S)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Martin Wendt (M)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland.

Franz Immer (F)

Swisstransplant, The Swiss National Foundation for Organ Donation and Transplantation, Effingerstrasse 1, Bern 3011, Switzerland.

Andreas Elmer (A)

Swisstransplant, The Swiss National Foundation for Organ Donation and Transplantation, Effingerstrasse 1, Bern 3011, Switzerland.

David Meierhofer (D)

Max Planck Institute for Molecular Genetics, Mass Spectrometry Facility, Berlin 14195, Germany.

Andrea Schlegel (A)

Transplantation Center, Digestive Disease and Surgery Institute and Department of Immunology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.

Philipp Dutkowski (P)

Department of Surgery and Transplantation, Swiss HPB Centre, University Hospital Zurich, Switzerland. Electronic address: philipp.dutkowski@usz.ch.

Classifications MeSH