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Therapeutic Use of Carbon Monoxide in Ex-Vivo Lung Perfusion in Donor With Prolonged Cold Ischemia.
Kalaf-Mussi, Ricardo; Nakajima, Daisuke; Chen, Manyin; Maahs, Lucas; Coutinho, Rafael; Qaqish, Robert; Liu, Mingyao; Keshavjee, Shaf; Cypel, Marcelo.
Affiliation
  • Kalaf-Mussi R; Department of Thoracic Surgery, Universidade Estadual de Campinas, São Paulo, Brazil.
  • Nakajima D; Department of Thoracic Surgery, Kyoto University, Kyoto, Japan.
  • Chen M; University Health Network, Toronto, Ontario, Canada.
  • Maahs L; University of Illinois College of Medicine at Chicago, Chicago, Illinois.
  • Coutinho R; Hospital da Bahia, Salvador, Salvador, BA, Brazil.
  • Qaqish R; Department of Thoracic Surgery, Erie County Medical Center with UBMD Surgery, Buffalo, New York.
  • Liu M; Toronto General Research Institute, University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Keshavjee S; University of Toronto, University Health Network, Toronto, Ontario, Canada.
  • Cypel M; Latner Thoracic Surgery Research Laboratories, Faculty of Medicine, Toronto General Hospital Research Institute, Department of Surgery, University Health Network, University of Toronto, Toronto, Ontario, Canada. Electronic address: marcelo.cypel@uhn.ca.
J Surg Res ; 301: 315-323, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39013278
ABSTRACT

INTRODUCTION:

Carbon monoxide (CO) has been shown to exert protective effects in multiple organs following ischemic injury, including the lung. The purpose of this study was to examine the effects of CO administration during ex vivo lung perfusion (EVLP) on lung grafts exposed to prolonged cold ischemia.

METHODS:

Ten porcine lungs were subjected to 18 h of cold ischemia followed by 6 h of EVLP. Lungs were randomized to EVLP alone (control, n = 5) or delivery of 500 ppm of CO during the 1st hour of EVLP (treatment, n = 5). Following EVLP, the left lungs were transplanted and reperfused for 4 h.

RESULTS:

At the end of EVLP, pulmonary vascular resistance (P = 0.007) and wet to dry lung weight ratios (P = 0.027) were significantly reduced in CO treated lungs. Posttransplant, lung graft PaO2/FiO2 (P = 0.032) and compliance (P = 0.024) were significantly higher and peak airway pressure (P = 0.032) and wet to dry ratios (P = 0.003) were significantly lower in CO treated lungs. Interleukin-6 was significantly reduced in plasma during reperfusion in the CO treated group (P = 0.040).

CONCLUSIONS:

In this preclinical porcine model, CO application during EVLP resulted in better graft performance and outcomes after reperfusion.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Perfusion / Carbon Monoxide / Lung Transplantation / Cold Ischemia / Lung Limits: Animals Language: En Journal: J Surg Res Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Perfusion / Carbon Monoxide / Lung Transplantation / Cold Ischemia / Lung Limits: Animals Language: En Journal: J Surg Res Year: 2024 Document type: Article Affiliation country: Country of publication: