An extracellular oxygen carrier during prolonged pulmonary preservation improves post-transplant lung function.


Journal

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
ISSN: 1557-3117
Titre abrégé: J Heart Lung Transplant
Pays: United States
ID NLM: 9102703

Informations de publication

Date de publication:
06 2020
Historique:
received: 15 01 2020
revised: 06 03 2020
accepted: 25 03 2020
pubmed: 27 4 2020
medline: 7 7 2021
entrez: 27 4 2020
Statut: ppublish

Résumé

The use of a novel extracellular oxygen carrier (EOC) preservation additive known as HEMO Donor pigs were randomly allocated to either of the following 2 groups (n = 6 per group): (1) 36 hours cold preservation or (2) 36 hours cold preservation with 1 g/liter of EOC. The lungs were evaluated through 12 hours of normothermic ex vivo lung perfusion (EVLP) followed by a left-single lung transplant into a recipient pig. Grafts were reperfused for 4 hours, followed by right pulmonary artery clamping to assess graft oxygenation function. During EVLP assessment, EOC-treated lungs showed improvements in physiologic parameters, whereas the control lungs deteriorated. After a total of 48 hours of preservation (36 hours cold + 12 hours normothermic EVLP), transplanted grafts in the treatment group displayed significantly better oxygenation than in the controls (PaO The use of an EOC during an extended pulmonary preservation period led to significantly superior early post-transplant lung function.

Sections du résumé

BACKGROUND
The use of a novel extracellular oxygen carrier (EOC) preservation additive known as HEMO
METHODS
Donor pigs were randomly allocated to either of the following 2 groups (n = 6 per group): (1) 36 hours cold preservation or (2) 36 hours cold preservation with 1 g/liter of EOC. The lungs were evaluated through 12 hours of normothermic ex vivo lung perfusion (EVLP) followed by a left-single lung transplant into a recipient pig. Grafts were reperfused for 4 hours, followed by right pulmonary artery clamping to assess graft oxygenation function.
RESULTS
During EVLP assessment, EOC-treated lungs showed improvements in physiologic parameters, whereas the control lungs deteriorated. After a total of 48 hours of preservation (36 hours cold + 12 hours normothermic EVLP), transplanted grafts in the treatment group displayed significantly better oxygenation than in the controls (PaO
CONCLUSION
The use of an EOC during an extended pulmonary preservation period led to significantly superior early post-transplant lung function.

Identifiants

pubmed: 32334946
pii: S1053-2498(20)31488-1
doi: 10.1016/j.healun.2020.03.027
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

595-603

Informations de copyright

Copyright © 2020 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

Auteurs

Aadil Ali (A)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Yui Watanabe (Y)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Marcos Galasso (M)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Tatsuaki Watanabe (T)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Manyin Chen (M)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Eddy Fan (E)

Divisions of Respirology and Critical Care Medicine, University Health Network, University of Toronto, Toronto, Ontario, Canada.

Laurent Brochard (L)

Divisions of Respirology and Critical Care Medicine, University Health Network, University of Toronto, Toronto, Ontario, Canada.

Khaled Ramadan (K)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Rafaela Vanin Pinto Ribeiro (RVP)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

William Stansfield (W)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Hemant Gokhale (H)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Anajara Gazzalle (A)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Thomas Waddell (T)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Mingyao Liu (M)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Shaf Keshavjee (S)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Marcelo Cypel (M)

Latner Thoracic Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada. Electronic address: marcelo.cypel@uhn.ca.

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Classifications MeSH