Left ventricular assist device (LVAD) implantation has become a mainstay of therapy for advanced heart failure patients who are either ineligible for, or awaiting, cardiac transplantation. Controversy remains over the optimal therapeutic strategy for preexisting aortic valvular dysfunction in these patients at the time of LVAD implant. In patients with moderate to severe aortic regurgitation, surgical approaches are center specific and range from variable leaflet closure techniques to concomitant aortic valve replacement (AVR) with a bioprosthesis. In the present study, we retrospectively analyzed our outcomes in patients who underwent simultaneous AVR and LVAD implantation secondary to antecedent aortic valve pathology. Between January 2004 and June 2010, 144 patients underwent LVAD implantation at a single institution. Of these, 7 patients (4.8%) required concomitant AVR. Five of the 7 patients (71%) survived to hospital discharge and suffered no adverse events in the perioperative period. One-year survival for the discharged patients was 80%, and no prosthetic valve-related adverse events were observed in long-term follow-up. Given our experience, we conclude that bioprosthetic AVR is a plausible alternative for end-stage heart failure patients at the time of LVAD implantation. C ontinuous fl ow pump technology has revolutionized long-term ventricular assist device therapy. Results from the HeartMate II trial show a considerable improvement in both survival and quality of life in recipients of this technology (1, 2). A proportion of these patients have associated aortic regurgitation (AR) that if left untreated may progress and impact the eff ectiveness of the pump by limiting forward fl ow (3). Th ere are several methods of managing AR at the time of left ventricular assist device (LVAD) implantation. Each has its own merits and fl aws. Techniques include patch closure of the outfl ow tract (4), primary aortic cuspal closure with felt strips (5), coaptation stitching of the valve cusps (6), and aortic valve replacement (7). Since our initial experience with the HeartMate II device, we have treated patients with signifi cant AR at the time of HeartMate II implantation by replacing the aortic valve with a bioprosthesis. Th is report describes the outcomes associated with this approach.
METHODSA retrospective review of end-stage heart failure patients who had undergone LVAD implantation with the HeartMate II continuous fl ow pump with concomitant aortic valve replacement at a single institution was conducted. Etiology of heart failure encountered in this study included ischemic and valvular cardiomyopathies. Th e latter was defi ned as end-stage heart failure secondary to untreated aortic or mitral valve disease. Medical records provided demographic and echocardiographic information as well as short-and long-term outcomes. Th is study was conducted with the approval of the institutional review board of the Cleveland Clinic.All procedures were performed through a full median sternotomy. Aortic valve replacements...