In this study, a method to determine the existence of prosthetic heart
valve cavitation in vivo is presented. Pennsylvania State University
Left Ventricular Assist Devices (LVADs) were implanted in two separate
calves for this study. Bjork-Shiley Monostrut (Irvine, CA) 27 mm and
25 mm valves with Delrin occluders were used in the mitral and aortic
positions, respectively. A high fidelity, piezoelectric pressure trans
ducer was mounted approximately 1.25 cm proximal to the mitral valve a
nd measured the high frequency pressure fluctuations caused by cavitat
ion bubble formation and collapse after valve closure. The root mean s
quare (RMS) value of the mitral pressure signal during a 5 ms interval
after valve closure was used as a measure of cavitation intensity. Th
e pressure signals observed in vivo were similar to ones observed in v
itro with the same type of pressure transducer and were associated wit
h the visually observed cavitation. The percentage of beats with cavit
ation increased from 20.3% to 67.7% when pump filling was decreased by
increasing beat rate. A blood test conducted during post-operative da
ys 1-3 showed a significant increase in plasma hemoglobin during the l
ow filling condition. However, blood tests conducted later (post-opera
tive days 7-44) did not show a significant change in plasma hemoglobin
during low filling conditions.