Sd. Herman et al., COMPARISON OF DOBUTAMINE AND EXERCISE USING TC-99M SESTAMIBI IMAGING FOR THE EVALUATION OF CORONARY-ARTERY DISEASE, The American journal of cardiology, 73(2), 1994, pp. 164-169
Studies using dobutamine thallium-201 myocardial perfusin imaging have
suggested a high sensitivity and specificity for the detection of cor
onary artery disease. However, few data are available comparing dobuta
mine with exercise stress for the detection and localization of perfus
ion defects. This study compared the effects of dobutamine and exercis
e stress using technetium-99m sestamibi single-photon emission compute
d tomographic imaging in the same patients in a prospective crossover
trial. Twenty-four patients with a high likelihood of coronary artery
disease underwent tomographic myocardial imaging at rest, after sympto
m-limited treadmill exercise, and after intravenous dobutamine (maximu
m 30 mug/kg/min). Tomograms of the left ventricle were divided into 20
segments and were interpreted without knowledge of patient identity o
r stress protocol. Dobutamine was well tolerated by all patients. Segm
ent-by-segment concordance between exercise and dobutamine images was
highly significant (kappa = 0.56, p < 0.0001). Global first-order agre
ement (normal vs abnormal) between exercise and dobutamine studies was
96% (kappa = 0.65, p = 0.02); global second-order agreement (normal v
s fixed vs ischemic defect) was 88% (kappa = 0.45, p = 0.02). Regional
first- and second-order agreement were 96 and 93%, respectively (p <
0.001 for both). Twenty patients underwent coronary angiography. compa
risons between exercise and angiography and between dobutamine and ang
iography were similar for both global agreement (95 vs 100%, p = NS) a
nd regional agreement (77 vs 72%, p = NS). In conclusion, technetium-9
9m sestamibi tomograms obtained after exercise and dobutamine stress i
n the same patients with a highly likelihood of coronary artery diseas
e show very similar results with regard to the identification, localiz
ation and reversibility of perfusion defects.