A totally implantable centrifugal artificial heart has been developed. The
plastic prototype, the Gyro PI 601, passed 2 day hemodynamic tests as a fun
ctional total artificial heart (TAH), 2 week screening tests for anti-throm
bogenecity, and a 1 month system feasibility study. Based upon these result
s, a metallic prototype, the Gyro PI700 series, was subjected to long-term
in vivo left ventricular assist device (LVAD) studies of over 1 month. The
Gyro PI700 series has the same inner dimension and same characteristics of
the Gyro PI 601 such as an eccentric inlet port, a double pivot bearing sys
tem, and a magnet coupling system. The PI metallic pump is also driven with
the Vienna DC brushless motor actuator like the PI 601. The pump-actuator
package was implanted in 3 calves in the preperitoneal space, bypassing fro
m the left ventricular (LV) apex to the descending aorta. Case 1 achieved a
284 day survival. Case 2 was euthanized early at 72 postoperative days as
a result of the functional obstruction of the inlet port due to the excessi
ve growth of the calf. There was no blood clot inside the pumps of either c
ase. Case 3 is on-going (22 days on July 24, 1998). During these periods, a
ll cases showed no physiological abnormalities. In conclusion, the PI700 se
ries pump has excellent results as a long-term implantable LVAD.