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The Annals of Thoracic Surgery, Vol 55, 276-282, Copyright © 1993 by The Society of Thoracic Surgeons
DJ Farrar and JD Hill
As of October 1991, the Thoratec ventricular assist device (VAD) system has
been used in 154 transplant candidates who were in imminent risk of dying
before donor heart procurement at 39 medical centers in 10 countries. The
VAD system consists of a prosthetic ventricle with a 65- mL pumping chamber
made from Thoratec's BPS-215M polyurethane, cannulas for atrial or
ventricular inflow and arterial outflow connections, and a pneumatic drive
console. The devices can be used for partial or complete support of the
pulmonary, systemic, or both circulations. In all patients (average age, 42
years; range, 11 to 64 years), the pumps were placed in a paracorporeal
position on the anterior abdominal wall and connected to the heart and
great vessels by cannulas crossing the chest wall. Biventricular support
was used in 120 patients (78%) and isolated left VADs were used in 34.
Average flow rate was 5.0 +/- 0.9 L/min for the left VAD and 4.3 +/- 0.8
L/min for the right VAD. The most frequent complications were bleeding (42%
incidence, 7% mortality) and infection (36% incidence, 8% mortality).
Ninety-eight patients (65%) recovered sufficiently to undergo heart
transplantation after 8 hours to 226 days of support (average, 17.5 days),
and 3 are waiting on VADs for transplantation. Eighty-two patients who
received transplants have been discharged. This is an 84% early
post-transplantation survival and a 54% overall survival. The actuarial
survival 1 year after transplantation is 82%, comparable with that of
conventional heart transplantation.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Univentricular and biventricular Thoratec VAD support as a bridge to transplantation
Department of Cardiovascular Surgery, California Pacific Medical Center, San Francisco 94120.
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