K. Wei et al., QUANTIFICATION OF MYOCARDIAL BLOOD-FLOW WITH ULTRASOUND-INDUCED DESTRUCTION OF MICROBUBBLES ADMINISTERED AS A CONSTANT VENOUS INFUSION, Circulation, 97(5), 1998, pp. 473-483
Citations number
21
Categorie Soggetti
Peripheal Vascular Diseas",Hematology,"Cardiac & Cardiovascular System
Background-Ultrasound can cause microbubble destruction. If microbubbl
es are administered as a continuous infusion, then their destruction w
ithin the myocardium and measurement of their myocardial reappearance
rate at stead Il state will provide a measure of mean myocardial micro
bubble velocity. Conversely, measurement of their myocardial concentra
tion at steady state will provide an assessment of microvascular cross
-sectional area. Myocardial blood now (MBF) can then be calculated fro
m the product of the two. Methods and Results-Ex vivo and in vitro exp
eriments were performed in which either now was held constant and puls
ing interval (interval between microbubble destruction and replenishme
nt) was altered, or vice versa. In vivo experiments were performed in
21 dogs. In group 1 dogs (n=7), MBF was mechanically altered in a mode
l in which coronary blood volume was constant. In group 2 dogs (n=5),
MBF was altered by direct coronary infusions of vasodilators. In group
3 dogs (n=9), non-now-limiting coronary stenoses were created, and MB
F was measured before and after the venous administration of a coronar
y vasodilator. In all experiments, microbubbles were delivered as a co
nstant infusion, and myocardial contrast echocardiography was performe
d using different pulsing intervals. The myocardial video intensity ve
rsus pulsing interval plots were fitted to an exponential function: ga
mma=A(1-e(-beta t)), where A is the plateau video intensity reflecting
the microvascular cross-sectional area, and beta reflects the rate of
rise of video intensity and, hence, microbubble velocity. Excellent c
orrelations were found between now and beta, as well as now and the pr
oduct of A and beta. Conclusions-MBF can be quantified with myocardial
contrast echocardiography during a venous infusion of microbubbles. T
his novel approach has potential for measuring tissue perfusion in any
organ accessible to ultrasound.