Modified in vivo lung perfusion allows for prolonged perfusion without acute lung injury

J Thorac Cardiovasc Surg. 2014 Feb;147(2):774-81: discussion 781-2. doi: 10.1016/j.jtcvs.2013.10.009. Epub 2013 Nov 27.

Abstract

Objectives: In vivo lung perfusion (IVLP) is an emergent strategy to treat lung metastases because it allows localized delivery of chemotherapy with minimal systemic exposure. Previously, short-term (± 30 minutes) IVLP resulted in variable efficacy and significant lung toxicity. We hypothesize that a modified IVLP strategy derived from an ex vivo lung perfusion technique could minimize lung injury. Our objective was to demonstrate the feasibility and safety of a modified prolonged (4 hours) IVLP.

Methods: Six Yorkshire pigs were used for the experiments. A thoracotomy was performed, the left pulmonary artery and pulmonary veins were cannulated, and the left lung was isolated in situ. IVLP was performed at normothermia for 4 hours using Steen Solution (XVIVO Perfusion, Göteburg, Sweden) as perfusate. The flow rate was 16% of estimated cardiac output and left atrial pressure was maintained between 3 and 5 mm Hg. Perfusate was deoxygenated and supplied with CO2 to physiologic levels before entering the lungs. A protective mode of ventilation was used. After IVLP, the left lung was allowed to reperfuse for additional 4 hours. Airway dynamics, gas exchange, and pulmonary vascular resistance were used to assess left lung physiology. Histologic signs of lung injury were assessed before and after IVLP, and 4 hours after reperfusion.

Results: Lung function parameters were stable throughout the 4-hour IVLP and during reperfusion. No significant histologic evidence of acute lung injury was observed.

Conclusions: Four hours of IVLP is feasible without adding significant lung injury. Prolonged perfusion time and a protective protocol might provide safer and more efficacious treatment of pulmonary metastases.

Keywords: 10; 10.4; 11.4; 9; EVLP; IVLP; LA; PA; PVR; PawP; ex vivo lung perfusion; in vivo lung perfusion; left atrium; peak airway pressure; pulmonary artery; pulmonary vascular resistance.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / etiology
  • Acute Lung Injury / pathology
  • Acute Lung Injury / physiopathology
  • Acute Lung Injury / prevention & control*
  • Animals
  • Atrial Function, Left
  • Atrial Pressure
  • Cardiac Output
  • Feasibility Studies
  • Lung / blood supply*
  • Lung / pathology
  • Lung / physiopathology
  • Lung Neoplasms / secondary
  • Lung Neoplasms / therapy
  • Models, Animal
  • Perfusion / adverse effects
  • Perfusion / methods*
  • Pulmonary Circulation*
  • Pulmonary Gas Exchange
  • Respiration, Artificial
  • Respiratory Function Tests
  • Respiratory Mechanics
  • Swine
  • Time Factors
  • Vascular Resistance