Flow-controlled ventilation during EVLP improves oxygenation and preserves alveolar recruitment.

Donor management Ex vivo lung perfusion Flow-controlled ventilation Lung transplantation Porcine large animal model Volume-controlled ventilation

Journal

Intensive care medicine experimental
ISSN: 2197-425X
Titre abrégé: Intensive Care Med Exp
Pays: Germany
ID NLM: 101645149

Informations de publication

Date de publication:
25 Nov 2020
Historique:
received: 18 06 2020
accepted: 17 11 2020
entrez: 25 11 2020
pubmed: 26 11 2020
medline: 26 11 2020
Statut: epublish

Résumé

Ex vivo lung perfusion (EVLP) is a widespread accepted platform for preservation and evaluation of donor lungs prior to lung transplantation (LTx). Standard lungs are ventilated using volume-controlled ventilation (VCV). We investigated the effects of flow-controlled ventilation (FCV) in a large animal EVLP model. Fourteen porcine lungs were mounted on EVLP after a warm ischemic interval of 2 h and randomized in two groups (n = 7/group). In VCV, 7 grafts were conventionally ventilated and in FCV, 7 grafts were ventilated by flow-controlled ventilation. EVLP physiologic parameters (compliance, pulmonary vascular resistance and oxygenation) were recorded hourly. After 6 h of EVLP, broncho-alveolar lavage (BAL) was performed and biopsies for wet-to-dry weight (W/D) ratio and histology were taken. The left lung was inflated, frozen in liquid nitrogen vapors and scanned with computed tomography (CT) to assess regional distribution of Hounsfield units (HU). All lungs endured 6 h of EVLP. Oxygenation was better in FCV compared to VCV (p = 0.01) and the decrease in lung compliance was less in FCV (p = 0.03). W/D ratio, pathology and BAL samples did not differ between both groups (p = 0.16, p = 0.55 and p = 0.62). Overall, CT densities tended to be less pronounced in FCV (p = 0.05). Distribution of CT densities revealed a higher proportion of well-aerated lung parts in FCV compared to VCV (p = 0.01). FCV in pulmonary grafts mounted on EVLP is feasible and leads to improved oxygenation and alveolar recruitment. This ventilation strategy might prolong EVLP over time, with less risk for volutrauma and atelectrauma.

Sections du résumé

BACKGROUND BACKGROUND
Ex vivo lung perfusion (EVLP) is a widespread accepted platform for preservation and evaluation of donor lungs prior to lung transplantation (LTx). Standard lungs are ventilated using volume-controlled ventilation (VCV). We investigated the effects of flow-controlled ventilation (FCV) in a large animal EVLP model. Fourteen porcine lungs were mounted on EVLP after a warm ischemic interval of 2 h and randomized in two groups (n = 7/group). In VCV, 7 grafts were conventionally ventilated and in FCV, 7 grafts were ventilated by flow-controlled ventilation. EVLP physiologic parameters (compliance, pulmonary vascular resistance and oxygenation) were recorded hourly. After 6 h of EVLP, broncho-alveolar lavage (BAL) was performed and biopsies for wet-to-dry weight (W/D) ratio and histology were taken. The left lung was inflated, frozen in liquid nitrogen vapors and scanned with computed tomography (CT) to assess regional distribution of Hounsfield units (HU).
RESULTS RESULTS
All lungs endured 6 h of EVLP. Oxygenation was better in FCV compared to VCV (p = 0.01) and the decrease in lung compliance was less in FCV (p = 0.03). W/D ratio, pathology and BAL samples did not differ between both groups (p = 0.16, p = 0.55 and p = 0.62). Overall, CT densities tended to be less pronounced in FCV (p = 0.05). Distribution of CT densities revealed a higher proportion of well-aerated lung parts in FCV compared to VCV (p = 0.01).
CONCLUSIONS CONCLUSIONS
FCV in pulmonary grafts mounted on EVLP is feasible and leads to improved oxygenation and alveolar recruitment. This ventilation strategy might prolong EVLP over time, with less risk for volutrauma and atelectrauma.

Identifiants

pubmed: 33237343
doi: 10.1186/s40635-020-00360-w
pii: 10.1186/s40635-020-00360-w
pmc: PMC7686942
doi:

Types de publication

Journal Article

Langues

eng

Pagination

70

Subventions

Organisme : KULeuven
ID : C24/18/073

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Auteurs

Sofie Ordies (S)

Unit of Anesthesiology and Algology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Anesthesiology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.

Michaela Orlitova (M)

Unit of Anesthesiology and Algology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium.
Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.

Tobias Heigl (T)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Annelore Sacreas (A)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Anke Van Herck (A)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Pneumology, University Hospitals Leuven, Leuven, Belgium.

Janne Kaes (J)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Berta Saez (B)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Pneumology, University Hospitals Leuven, Leuven, Belgium.

Arno Vanstapel (A)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Pathology, University Hospitals Leuven, Leuven, Belgium.

Laurens Ceulemans (L)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Bart M Vanaudenaerde (BM)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Robin Vos (R)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Pneumology, University Hospitals Leuven, Leuven, Belgium.

Johny Verschakelen (J)

Department of Radiology, University Hospitals Leuven, Leuven, Belgium.

Geert M Verleden (GM)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Pneumology, University Hospitals Leuven, Leuven, Belgium.

Stijn E Verleden (SE)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Dirk E Van Raemdonck (DE)

Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium.
Department of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.
Laboratory of Respiratory Diseases and Thoracic Surgery (BREATHE), Department of Chronic Diseases, Metabolism and Ageing (CHROMETA), Katholieke Universiteit Leuven, Leuven, Belgium.

Arne P Neyrinck (AP)

Unit of Anesthesiology and Algology, Department of Cardiovascular Sciences, Katholieke Universiteit Leuven, Leuven, Belgium. arne.neyrinck@uzleuven.be.
Department of Anesthesiology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. arne.neyrinck@uzleuven.be.
Leuven Lung Transplant Group, Katholieke Universiteit Leuven, Leuven, Belgium. arne.neyrinck@uzleuven.be.

Classifications MeSH