Heart disease remains one of the leading causes of death in the western wor
ld. In the 35 years since the first human heart transplants, cardiac transp
lantation has become established as the therapeutic option of choice in the
management of terminal cardiac failure. Since 1981,the introduction of cyc
losporin for immunosuppression has dramatically increased cardiac transplan
tation. However, several obstacles limit further utilization, including lim
ited availability of donor hearts, limited ischemic time tolerated by donor
hearts, and chronic rejection. Research is underway into donor heart prese
rvation and new immunosuppressant drugs in an effort to increase donor orga
n availability. Due to these constraints, alternative therapies are under d
evelopment. More than 2,000 circulatory assist devices have been implanted
with >25% used as a bridge to heart transplantation. The University of Otta
wa Heart Institute began the,first Canadian implantation of circulatory ass
ist devices in 1986 and has implanted 23 total artificial hearts and 23 ven
tricular assist devices. The Heart Institute is also developing a totally i
mplantable electrohydraulic ventricular assist device (EVAD) for long-term
mechanical support outside the hospital. Another alternative being evaluate
d for clinical use is xenotransplantation. The major obstacle for widesprea
d use of clinical xenotransplantation remains graft rejection, and fundamen
tal research is ongoing to address hyperacute and delayed xenograft rejecti
on. While cardiac tranplantation is the most effective treatment of termina
l heart failure, limited donor hearts compel us to rely on alternatives. In
the future, the research underway on xenotransplantation and mechanical ci
rculatory assist devices will provide new options for the clinical treatmen
t of terminal cardiac failure.