Percutaneous Cavopulmonary Assist: From Design to 96 Hour Survival in Lethal Cavopulmonary Failure Sheep.
Li LiJingkun WangGuangfeng ZhaoStephen TopazDavid MoralesAjit YoganathanCherry Ballard-CroftJoseph B ZwischenbergerDongfang WangPublished in: ASAIO journal (American Society for Artificial Internal Organs : 1992) (2023)
We are developing a clinically practical percutaneous double lumen cannula (DLC)-based cavopulmonary assist (CPA) system to support failing Fontan patients. In this study, our CPA DLC was redesigned for even blood flow, minimal recirculation, and easy insertion/deployment. After bench testing, this new CPA system was evaluated for 4 hours (n = 10) and 96 hours (n = 5) in our clinically relevant lethal cavopulmonary failure (CPF) sheep model for ease of cannulation/deployment, reversal of CPF hemodynamics/end-organ hypoperfusion, and durability/biocompatibility. Cavopulmonary failure was achieved in all sheep. All DLCs were successfully inserted/deployed into Fontan anatomy. Cavopulmonary assist reversed CPF with normalized central venous pressure and cardiac output. All survival sheep were ambulatory with normal eating/drinking. One sheep was euthanized after 6 hours from cannula kinking, and one sheep died of hypokalemia after 8 hours. Three sheep survived 96 hours with normal hemodynamics. Free hemoglobin was only 3.7 ± 1.2 mg/dl at 96 hours, indicating negligible hemolysis. Creatinine, blood urea nitrogen, and lactate increased from hypoperfusion but normalized by 72 hours CPA. Necropsy showed only a small, immobilized thrombus ring at umbrella attachment to DLC. Our DLC-based system provided total ambulatory CPA in a lethal CPF sheep model with 96 hour survival and complete reversal of hemodynamics and end-organ hypoperfusion.
Keyphrases
- blood pressure
- blood flow
- genome editing
- ultrasound guided
- cognitive impairment
- crispr cas
- weight loss
- physical activity
- left ventricular
- randomized controlled trial
- newly diagnosed
- obstructive sleep apnea
- end stage renal disease
- acute respiratory distress syndrome
- mass spectrometry
- atrial fibrillation
- ejection fraction
- red blood cell
- respiratory failure
- tissue engineering