Circulation, Vol 70, 309-317, Copyright © 1984 by American Heart Association
AJ Kemper, JE O'Boyle, CA Cohen, A Taylor and AF Parisi
During sustained coronary occlusion in canine preparations, the extent of
regions that fail to show contrast enhancement when imaged by supra- aortic
hydrogen peroxide contrast echocardiography (SHPCE) has been shown to
correlate well for single cross sections with the extent of malperfused
myocardium "at risk" of infarction. In the present study, SHPCE was
investigated as a means of determining the fraction of total left
ventricular mass at risk during occlusion. Since necrotic tissue has low
blood flow even when reperfused, we also investigated the potential of
quantitating the extent of infarcted myocardium by measuring the extent of
contrast defects seen with SHPCE performed during reperfusion. In 20 dogs
the fraction of the left ventricle showing a contrast defect during
coronary occlusion correlated well with the fraction of the left
ventricular mass "at risk" by an autoradiographic technique
(autoradiography = 0.83 echocardiography + 8.6%; r = .89, SEE = 4.5%).
SHPCE was also performed after 3 hr of reperfusion following occlusions
varying in duration from 60 to 150 min. The fraction of the ventricle
showing a contrast defect during reperfusion predicted the infarcted
portion of the left ventricle as shown by triphenyl tetrazolium chloride
staining (% left ventricle infarcted = 0.81 echocardiography + 3.3%; r =
.84, SEE = 5.3%). Observer variability for the fraction of the ventricle
showing a contrast defect was excellent during both occlusion and
reperfusion. The ratio of the left ventricular extent of contrast-negative
regions during reperfusion and occlusion was used to calculate a
necrosis-to- risk index in vivo that correlated relatively well with the
myocardial necrosis-to-risk ratio determined morphologically (r = .77, SEE
= 16%).(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Hydrogen peroxide contrast echocardiography: quantification in vivo of myocardial risk area during coronary occlusion and of the necrotic area remaining after myocardial reperfusion
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