Fa. Arabia et al., SUCCESS RATES OF LONG-TERM CIRCULATORY ASSIST DEVICES USED CURRENTLY FOR BRIDGE TO HEART-TRANSPLANTATION, ASAIO journal, 42(5), 1996, pp. 542-546
Circulatory assist devices as bridge to heart transplantation have bec
ome more important as the number of possible recipients has increased
and the number of donors remains stable. The number of patients succes
sfully bridged and discharged home after transplantation was determine
d for the Novacor Left Ventricular Assist System (Baxter Healthcare Co
rp., Oakland, CA) (LVAS), console and wearable; the TCl Left Ventricul
ar Assist Device (Thermo Cardio Systems Inc., Woburn, MA) (LVAD), pneu
matic and electric; the Thoratec LVAD and Biventricular Assist Device
(Thoratec Lab Co., Berkeley, CA) (BIVAD); and the CardioWest total art
ificial heart (CardioWest Tech. Inc., Tuscon, AZ) (TAH). A total of 1,
286 devices (14% Novacor console, 14% Novacor wearable, 35% TCl pneuma
tic, 4% TCl electric, 10% Thoratec LVAD, 19% Thoratec BIVAD, and 4% Ca
rdioWest TAH) were implanted worldwide since 1984. A total of 776 (60%
) patients reached heart transplantation and 687 patients (88.5% of th
ose transplanted) were discharged home. The individual success rate fo
r each device to bridge a patient to heart transplantation and be disc
harged home is as follows: Novacor LVAS console, 90%; Novacor LVAS wea
rable, 92%; TCl LVAD pneumatic, 89%; TCl LVAD electric, 89%; Thoratec
LVAD, 93%; Thoratec BIVAD, 81%; and CardioWest TAH, 92%. The success r
ate with all the available systems to bridge a patient to heart transp
lantation and be discharged home is similar for all devices. The crite
ria used to determine which system to be used should be individualized
for each patient. Some of the factors that should be considered in ma
king a decision on which device to use should include anticoagulation,
univentricular vs biventricular failure, mobility, protocol to discha
rge home, and size of the patient.