A multimodal characterization of cardiopulmonary resuscitation-associated lung edema.


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:
09 Oct 2024
Historique:
received: 16 07 2024
accepted: 02 10 2024
medline: 9 10 2024
pubmed: 9 10 2024
entrez: 9 10 2024
Statut: epublish

Résumé

Cardiopulmonary resuscitation-associated lung edema (CRALE) is a phenomenon that has been recently reported in both experimental and out-of-hospital cardiac arrest patients. We aimed to explore the respiratory and cardiovascular pathophysiology of CRALE in an experimental model of cardiac arrest undergoing prolonged manual and mechanical chest compression (CC). Oxygen delivery achieved during mechanical or manual CC were also investigated as a secondary aim, to describe CRALE evolution under different hemodynamic supports generated during CPR. Ventricular fibrillation (VF) was induced and left untreated for 5 min prior to begin cardiopulmonary resuscitation (CPR), including CC, ventilation with oxygen, epinephrine administration and defibrillation. Continuous mechanical and manual CC was performed alternating one of the two strategies every 5 min for a total of 25 min. Unsynchronized mechanical ventilation was resumed simultaneously to CC. A lung computed tomography (CT) was performed at baseline and 1 h after return of spontaneous circulation (ROSC) in surviving animals. Partitioned respiratory mechanics, gas exchange, hemodynamics, and oxygen delivery were evaluated during the experimental study at different timepoints. Lung histopathology was performed. After 25 min of CPR, a marked decrease of the respiratory system compliance with reduced oxygenation and CO In this porcine model of cardiac arrest followed by a 25-min interval of CPR with mechanical and manual CC, CRALE was consistently present and was characterized by lung inhomogeneity with alveolar tissue and hemorrhage replacing alveolar airspace. Despite mechanical CPR is associated with a more severe CRALE, the higher cardiac output generated by the mechanical compression ultimately accounted for a greater oxygen delivery. Whether specific ventilation strategies might prevent CRALE while preserving hemodynamics remains to be proved.

Sections du résumé

BACKGROUND BACKGROUND
Cardiopulmonary resuscitation-associated lung edema (CRALE) is a phenomenon that has been recently reported in both experimental and out-of-hospital cardiac arrest patients. We aimed to explore the respiratory and cardiovascular pathophysiology of CRALE in an experimental model of cardiac arrest undergoing prolonged manual and mechanical chest compression (CC). Oxygen delivery achieved during mechanical or manual CC were also investigated as a secondary aim, to describe CRALE evolution under different hemodynamic supports generated during CPR.
METHODS METHODS
Ventricular fibrillation (VF) was induced and left untreated for 5 min prior to begin cardiopulmonary resuscitation (CPR), including CC, ventilation with oxygen, epinephrine administration and defibrillation. Continuous mechanical and manual CC was performed alternating one of the two strategies every 5 min for a total of 25 min. Unsynchronized mechanical ventilation was resumed simultaneously to CC. A lung computed tomography (CT) was performed at baseline and 1 h after return of spontaneous circulation (ROSC) in surviving animals. Partitioned respiratory mechanics, gas exchange, hemodynamics, and oxygen delivery were evaluated during the experimental study at different timepoints. Lung histopathology was performed.
RESULTS RESULTS
After 25 min of CPR, a marked decrease of the respiratory system compliance with reduced oxygenation and CO
CONCLUSIONS CONCLUSIONS
In this porcine model of cardiac arrest followed by a 25-min interval of CPR with mechanical and manual CC, CRALE was consistently present and was characterized by lung inhomogeneity with alveolar tissue and hemorrhage replacing alveolar airspace. Despite mechanical CPR is associated with a more severe CRALE, the higher cardiac output generated by the mechanical compression ultimately accounted for a greater oxygen delivery. Whether specific ventilation strategies might prevent CRALE while preserving hemodynamics remains to be proved.

Identifiants

pubmed: 39382715
doi: 10.1186/s40635-024-00680-1
pii: 10.1186/s40635-024-00680-1
doi:

Types de publication

Journal Article

Langues

eng

Pagination

91

Subventions

Organisme : University of Milan
ID : Re-Starting Grant 2023

Informations de copyright

© 2024. The Author(s).

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Auteurs

Aurora Magliocca (A)

Department of Pathophysiology and Transplants, University of Milan, Milan, Italy.

Davide Zani (D)

Department of Veterinary Medicine and Animal Sciences, University of Milan, Milan, Italy.

Donatella De Zani (D)

Department of Veterinary Medicine and Animal Sciences, University of Milan, Milan, Italy.

Valentina Castagna (V)

Department of Pathophysiology and Transplants, University of Milan, Milan, Italy.

Giulia Merigo (G)

Department of Biomedical Sciences for Health, University of Milan, Milan, Italy.

Daria De Giorgio (D)

Department of Acute Brain and Cardiovascular Injury, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Francesca Fumagalli (F)

Department of Acute Brain and Cardiovascular Injury, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.

Vanessa Zambelli (V)

School of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.

Antonio Boccardo (A)

Department of Veterinary Medicine and Animal Sciences, University of Milan, Milan, Italy.

Davide Pravettoni (D)

Department of Veterinary Medicine and Animal Sciences, University of Milan, Milan, Italy.

Giacomo Bellani (G)

CISMed - Centre for Medical Sciences, University of Trento, Trento, Italy.
Anesthesia and Intensive Care, Santa Chiara Hospital, Trento, Italy.

Jean Christophe Richard (JC)

Ventilation Laboratory (Vent'Lab), Medical Intensive Care Unit (ICU), Angers University Hospital, Angers, France.
Med(2)Lab, Air Liquide Medical Systems, Antony, France.
Medical Intensive Care Unit (ICU), Angers University Hospital, Angers, France.

Giacomo Grasselli (G)

Department of Pathophysiology and Transplants, University of Milan, Milan, Italy.
Department of Anesthesia, Critical Care and Emergency, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Della Commenda, 16, 20122, Milan, Italy.

Emanuele Rezoagli (E)

School of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.
Department of Emergency and Intensive Care, Fondazione IRCCS San Gerardo dei Tintori Hospital, Monza, Italy.

Giuseppe Ristagno (G)

Department of Pathophysiology and Transplants, University of Milan, Milan, Italy. Giuseppe.ristagno@unimi.it.
Department of Anesthesia, Critical Care and Emergency, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Della Commenda, 16, 20122, Milan, Italy. Giuseppe.ristagno@unimi.it.

Classifications MeSH