Apical closure device for full‐percutaneous transapical structural and valve procedures with large‐sized introducer sheaths: The final preclinical study

• Published in: Journal of cardiac surgery Vol. 37; no. 7; pp. 1877 - 1884
• Main Authors: Ferrari, Enrico, Pozzoli, Alberto, Maisano, Francesco, Segesser, Ludwig K.
• Format: Journal Article
• Language: English
• Published: United States 01.07.2022
• Subjects: Animals; apical closure device; Cardiac Catheterization - methods; Catheters; Fluoroscopy; Heart Valve Prosthesis Implantation - methods; Heart Ventricles - surgery; Hemodynamics; Hemorrhage - etiology; Humans; large‐sized introducer sheaths; structural heart procedures; Swine; transapical valve implantation; transapical valve implantation; structural heart procedures; apical closure device; large-sized introducer sheaths
• DOI: 10.1111/jocs.16390
• ISSN: 0886-0440

Background Closed‐chest transapical valve implantations (aortic, mitral, and tricuspid) and cardiac structural procedures requiring large‐sized introducer sheaths cannot be safely performed with the available technology. We tested a self‐expanding apical closure device in a closed‐chest animal model, using large‐sized introducer sheaths and human‐sized animals to establish the technique for future tests in humans. Methods Six human‐sized pigs (mean weight: 89.7 ± 3.7 kg) received general anesthesia, intubation, and full heparinization (15,000 IU/animal; expected activated clotting time >200 s). Under fluoroscopy and multimodality imaging guidance with next‐generation fusion imaging prototypes, a 15‐cm long needle and a standard guidewire were percutaneously inserted under the xiphoidal aponeurosis and into the ventricular apex. After the exchange with a stiff guidewire, a 21‐Fr introducer sheath for transapical procedures (outer diameter: 25‐Fr) was placed in the left ventricle through the apex. The self‐expanding closure device was inserted and deployed under fluoroscopic guidance while the 21‐Fr sheath was gently removed. Hemodynamic conditions were monitored for 30 min and then the chest was opened to inspect the closure device and quantify the blood loss in the pericardium. Animals were killed and the hearts were removed and inspected. Results All six apical closure devices were successfully deployed without adverse events. No death, hemodynamic collapse, or cardiac tamponade occurred during the 30‐min observational period (mean systolic and diastolic pressures: 88 ± 11 and 58 ± 13 mmHg, respectively; mean heart rate: 60 ± 11 beats per minutes). Pre‐ and postdeployment (after protamine administration) mean activated clotting time was 541 ± 263 and 217 ± 62 s, respectively. The plugs provided good sealing with a mean of 27.2 ± 13.86 ml of blood lost in the pericardium. Postmortem inspection showed good plug fixation without myocardial damage. Conclusion This self‐expanding apical closure device successfully sealed the percutaneous access sites made with large‐sized introducer sheaths in human‐sized animals. This preclinical study suggests that transapical valve and structural procedures requiring large‐sized introducer sheaths can be performed percutaneously.