J. Gorcsan et al., Color-coded tissue Doppler assessment of the effects of acute ischemia on regional left ventricular function: Comparison with sonomicrometry, J AM S ECHO, 14(5), 2001, pp. 335-342
Citations number
33
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY
Echocardiographic assessment of regional left ventricular (LV) function usu
ally consists of subjective visual inspection of endocardial movement and w
all thickening. Color-coded tissue Doppler (TD) is a potential means to qua
ntify: regional LV function more objectively. According, in this study, col
or-coded TD was used to assess the regional effects of acute ischemia in an
open-chest canine model of coronary occlusion, with implanted sonomicromet
ry Length crystals as a standard of reference. Eight dogs were studied duri
ng baseline conditions and during left anterior descending coronary artery
occlusion. Midventricular short-axis images were used to slide the color TD
M-mode cursor through circumflex (septal) and left anterior descending (an
terolateral) perfusion zones. Off-Line conversion of endocardial time-veloc
ity maps was performed. Peak systolic endocardial velocity by TD decreased
from 4.4 +/- 1.4 cm/s to 1.8 +/- 1.5 cm/s with coronary occlusion (P < .05
versus baseline). Similar significant decreases in calculated systolic velo
city by sonomicrometry occurred with ischemia from 11.1 +/- 3.8 mm/s to 8.2
+/- 1.2 mm/s (P < .05 versus baseline). Peak systolic velocity by TD was i
nversely correlated with end-systolic length by sonomicrometry as a measure
of regional function (r = -0.77, P < .001). Time to peak systolic velocity
increased with ischemia from 154 +/- GO ms to 286 +/- 67 ms by TD and 200
+/- 60 ms to 320 +/- 30 ms by sonomicrometry (P < .05 versus baseline). The
delay in time to peak systolic velocity by TD and sonomicrometry were corr
elated (r = 0.75, P < .001). In conclusion, color-coded TD echocardiography
has the potential to quantify regional LV function during coronary ischemi
a.