Percutaneous Venopulmonary Extracorporeal Membrane Oxygenation as Bridge to Lung Transplantation.
Asad Ali UsmanAudrey Elizabeth SpeldeWasim LutfiJacob T GutscheWilliam J VernickOmar ToubatSalim E OliaEdward CantuAndrew CourtrightMaria M CrespoJoshua DiamondMauer BiscottiChristian A BermudezPublished in: ASAIO journal (American Society for Artificial Internal Organs : 1992) (2024)
Mechanical circulatory support (MCS) as a bridge to lung transplant is an infrequent but accepted pathway in patients who have refractory end-stage pulmonary failure. The American Association of Thoracic Surgeons Expert Consensus Guidelines, published in 2023, recommends venovenous (VV) extracorporeal membrane oxygenation (ECMO) as the initial configuration for those patients who have failed conventional medical therapy, including mechanical ventilation, while waiting for lung transplantation and needing MCS. Alternatively, venoarterial (VA) ECMO can be used in patients with acute right ventricular failure, hemodynamic instability, or refractory respiratory failure. With the advancement in percutaneous venopulmonary (VP) ECMO cannulation techniques, this option is becoming an attractive configuration as bridge to lung transplantation. This configuration enhances stability of the right ventricle, prevents recirculation with direct introduction of pulmonary artery oxygenation, and promotes hemodynamic stability during mobility, rehabilitation, and sedation-weaning trials before lung transplantation. Here, we present a case series of eight percutaneous VP ECMO as bridge to lung transplant with all patients mobilized, awake, and successfully transplanted with survival to hospital discharge.
Keyphrases
- extracorporeal membrane oxygenation
- acute respiratory distress syndrome
- respiratory failure
- mechanical ventilation
- end stage renal disease
- pulmonary artery
- ejection fraction
- chronic kidney disease
- pulmonary hypertension
- newly diagnosed
- coronary artery
- minimally invasive
- spinal cord
- peritoneal dialysis
- heart failure
- stem cells
- spinal cord injury
- mouse model
- peripheral blood
- quality improvement
- mitral valve
- left ventricular
- deep brain stimulation