H eart failure remains the leading cause of death in the United States and worldwide, and the prevalence of heart failure in the U.S. continues to rise.1 For patients with refractory heart failure, cardiac function deteriorates despite maximal medical therapy, warranting consideration of mechanical circulatory support or heart transplantation. Because of the improvements in overall survival rates and in survival to transplantation imparted by newer, continuous-flow assist devices, the number of patients sustained by mechanical circulatory support as a bridge to transplantation is growing rapidly.2 Malfunction of continuous-flow devices is rare but remains a considerable challenge. Treatment options for patients with device malfunction include sternotomy or thoracotomy with left ventricular assist device (LVAD) exchange, extracorporeal membrane oxygenation, microaxial LVAD placement, intraaortic balloon counterpulsation, or inotropic support alone. The new-generation microaxial LVADs afford full support (generating flow rates of up to 5 L/min) and are inserted endovascularly, without a need to open the chest or to use cardiopulmonary bypass (CPB). Here, we describe the novel and successful use of the Impella ® 5.0 (Abiomed, Inc.; Danvers, Mass) as a bridge to transplantation in a patient with LVAD malfunction.
Case ReportA 54-year-old-man with ischemic cardiomyopathy underwent placement of a HeartMate II ® LVAD (Thoratec Corporation; Pleasanton, Calif ) as a bridge to heart transplantation in December of 2010, 3 years before his presentation at our center. Because of his prolonged time on the transplant list, he was referred to our center for dual listing.While waiting for a suitable donor heart to become available, he developed frequent device malfunction due to malposition of the inflow cannula (Fig. 1). The LVAD malfunctions included intermittent low speeds and transient pump stops. Although poor cannula position is usually apparent early after implantation, our patient might have developed cannula malposition in a delayed manner because of left ventricular (LV) remodeling. We admitted him and listed him for heart transplantation as status 1A. Despite our reductions in pump speed, withholding of diuretics, aggressive fluid administration, and empiric heparinization for possible pump thrombosis, the LVAD alarms persisted. The frequency of alarms increased, and the device was no longer able to generate adequate flows. An echocardiogram showed an LV ejection fraction of 0.15 to 0.25 and no flow in the inflow cannula. The device was turned off to prevent emboli, and the patient was maintained on inotropic support.Despite maximal medical therapy, his cardiac function progressively deteriorated. We considered the risks and benefits of various mechanical circulatory support devices, including repeat sternotomy with LVAD exchange or total artificial heart implan-