Article ID Journal Published Year Pages File Type
2760649 Journal of Cardiothoracic and Vascular Anesthesia 2009 6 Pages PDF
Abstract

ObjectiveTo describe 6 months of experience in the anesthetic management of percutaneous aortic valve implantation.DesignAn observational, cohort study.SettingA university hospital.ParticipantsEighteen high-risk patients with relative contraindications to surgical valve replacement (78 ± 8.7 years, logistic EuroSCORE 26 ± 19.1).InterventionAn Edwards/Sapien Aortic Bioprosthesis (Edwards Lifesciences LLC, Irvine, CA) was implanted in patients with severe symptomatic aortic stenosis who underwent percutaneous retrograde aortic valve implantation without cardiopulmonary bypass. The procedure was performed using general anesthesia (15 patients) or sedation (3 patients).Measurements and Main ResultsThe valve was successfully implanted in all patients. One patient had prolonged ventricular fibrillation that required advanced cardiopulmonary resuscitation, endotracheal intubation, and placement of an intra-aortic balloon pump. Six patients had vascular access site complications managed either percutaneously or surgically. Five patients were extubated in the catheterization laboratory. All patients were transferred to the intensive care unit for monitoring, and all but one were discharged to an intermediate care unit within 24 hours. Early postoperative complications included acute renal failure (1 patient), arrhythmias (1 atrial fibrillation and 1 transient heart block), and stroke (1 patient). One patient died 58 days after the procedure for noncardiac reasons.ConclusionsTranscatheter aortic valve implantation is possible in selected high-risk patients. Anesthesiologists must be aware of current technology in order to have an active role in patient selection, to develop monitoring and standards of care in the cardiac catheterization laboratory, and to plan postoperative management.

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