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Translational Research at Penn: Redefining Endstage Heart Failure

September/October 2008

The translation of research into practice at Penn is perhaps nowhere more striking than in the approach to endstage heart failure.

Endstage heart failure is being redefined at Penn Medicine as an interim in the progress of the disease—a respite, rather than a conclusion—for patients who are ineligible for heart transplant surgery. This is possible because Penn cardiologists, surgeons and researchers have aggressively pursued partnerships with scientists and engineers to translate fundamental research in cardiovascular mechanics and dynamics into instruments that support or replace heart functions. These life-sustaining ventricular assist devices, or VADs, have dramatically altered the prospects for patients in endstage heart failure.

Between 2006 and 2007, the number of Heart Transplant Patients who received VADs as Bridge to Transplant increased by 28%

The Heart Failure and Transplantation Program is the region’s leading advocate for the use of VADs for patients in endstage heart failure and for those patients awaiting heart transplantation. At Penn, VADs are used to bridge the interim between endstage heart failure and transplant, and increasingly, as destination therapy, the permanent implantation of a device to support or replace the failing heart.

In 2007, 24 heart transplant patients at Penn received a VAD as a bridge to transplant, a 28 percent increase over 2006. The advantages of the latest generation of VADs include a greatly decreased risk of infection, greater reliability and durability, and smaller sizes to enhance their suitability for smaller adults and children. An overview of the devices currently available at Penn offers an inventory of the world’s most sophisticated VADS, and a glimpse of what the future may hold for patients with endstage heart failure, as well as heart transplantation patients.

Thoratec® Heart Mate® II
Penn was the first center in the region to implant the Thoratec HeartMate II left ventricular assist device (LVAD) for destination therapy. Light, small and powerful, the HeartMate II has a single moving part that augments the left ventricle by propelling up to 10 liters of blood per minute in a continuous stream from the heart. Penn is currently participating in a study of the HeartMate II for bridge to transplant therapy.

VentrAssist® Left Ventricular Assist Device
The VentrAssist® Left Ventricular Assist Device (LVAD) is designed to be a permanent alternative to heart transplants for patients suffering from heart failure, or as a temporary bridge to transplant. At Penn, the VentrAssist has been studied for destination therapy and as a bridge to heart transplantation.

Thoratec® CentriMag Blood Pumping System
A temporary VAD (up to 14 days), the Thoratec® CentriMag Blood Pumping System is a continuous-flow, centrifugal-type rotary blood pump that is placed extracorporeally. The CentriMag is used at Penn for bridge to transplant therapy. The advantages of the CentriMag include rapid implantation and—because the pump has no bearings or seals—limited potential for hemolysis and thrombus formation.

Temporary total artificial heart (TAH-t) implantation
The Hospital of the University of Pennsylvania became the first heart transplant center in the region to be certified for temporary total artificial heart (TAH-t) implantation. The TAH-t replaces the heart completely, and is considered the gold standard for bridge-to-transplantation for patients awaiting a donor heart or at imminent risk of death. Patients receiving the TAH-t are almost twice as likely to survive to transplant as are patients who received biventricular mechanical support in the past.

Ventricular Assist Device (VAD) Certification
In 2007, the destination therapy program at the Hospital of the University of Pennsylvania received a certification of distinction from the Joint Commission, an independent, not-for-profit organization that accredits and certifies more than 15,000 health care organizations and programs in the United States. A hospital must provide destination therapy to an adult population and place 10 VADs within the previous 36 months to receive VAD certification.

 


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