The CardioWest total artificial heart is a pneumatically driven device
that totally replaces the failing ventricles. It is currently used as
a bridge to heart transplantation in selected centers in the United S
tates under a study by the Food and Drug Administration. Twenty-seven
patients have undergone placement of the total artificial heart since
1993 with the intention to bridge to transplantation. Inclusion criter
ia included candidacy for heart transplantation, cardiac index (CI) <
2.0 L/ min/m(2), and maximal inotropic support. The population consist
ed of 25 men and 2 women of mean +/- SD age 46.5 +/- 10.3 years, body
surface area 2.01 +/- 0.17 m(2), and duration of implant 52 +/- 42 day
s. Initial diagnosis included ischemic cardiomyopathy (n = 10), idiopa
thic (n = 10), viral (n = 4), valvular (n = 2), and graft failure (n =
1). Infectious complications were defined as systemic (evidence of le
ukocytosis or fever) or local. The population experienced 64 infection
s (range, 0-9 per patient): 45 systemic and 19 local. Three patients d
id not experience any infection. Twenty-five patients reached transpla
ntation, and were discharged home for a survival rate of 92.6%. Two pa
tients died during the bridge, one because of mechanical failure, and
one because of infection (mediastinitis). Therefore, death attributabl
e to infections occurred in 3.7%. Previous reports of the total artifi
cial heart experience in the late 1980s described death rates as high
as 40%. Although infectious complications are common in patients who a
re bridged to heart transplantation with the total artificial heart, m
ortality from infections is 10 times less than previously reported. Th
is may be the result of a better strategy for bridging to transplantat
ion that includes patient selection, mobilization, early central line
removal, and waiting until all possible infections are resolved before
proceeding to transplantation.