TY - JOUR
T1 - Comparison of dipyridamole-Doppler echocardiography to thallium-201 imaging and quantitative coronary arteriography in the assessment of coronary artery disease
AU - Grayburn, Paul A.
AU - Popma, Jeffrey J.
AU - Pryor, Susan L.
AU - Walker, Brandy S.
AU - Simon, Theodore R.
AU - Smitherman, Thomas C.
PY - 1989/6/1
Y1 - 1989/6/1
N2 - This study was undertaken to determine whether Doppler measurements of systolic aortic and diastolic mitral blood flow velocities could reliably detect the presence of reversible myocardial perfusion defects during intravenous dipyridamole-thallium-201 imaging. In addition, the ability of dipyridamole-Doppler echocardiography to predict the presence of significant coronary artery disease (CAD) was evaluated. Baseline and post-dipyridamole Doppler studies were performed in 10 normal control subjects and 23 patients with CAD. Aortic peak velocity and acceleration increased from baseline to post-dipyridamole in normal subjects by 0.07 ± 0.07 m/s (p = 0.016) and 2.1 ± 2.0 m/s2 (p = 0.009), respectively. The ratio of early to late peak transmitral velocities decreased slightly in normal subjects, by 0.18 ± 0.72 (difference not significant), whereas the ratio of early to late transmitral velocity-time integrals increased by 0.07 ± 0.93 (difference not significant). The response of aortic velocity and acceleration to intravenous dipyridamole was not significantly different between normal subjects, patients without reversible thallium-201 perfusion defects and patients with reversible thallium-201 perfusion defects. Furthermore, only 3 of 14 subjects with reversible thallium-201 perfusion defects had abnormal (>2 standard deviations from the mean) responses of aortic velocity or acceleration to intravenous dipyridamole. No patient had an abnormal response of the early to late mitral peak velocity ratio. In addition, the response of Doppler aortic and mitral indexes to intravenous dipyridamole was not able to identify the presence of significant CAD as assessed by quantitative coronary arteriography. Thus, Doppler indexes of aortic and mitral blood flow after intravenous dipyridamole are insensitive in detecting either the presence of reversible perfusion thallium-201 defects or significant CAD.
AB - This study was undertaken to determine whether Doppler measurements of systolic aortic and diastolic mitral blood flow velocities could reliably detect the presence of reversible myocardial perfusion defects during intravenous dipyridamole-thallium-201 imaging. In addition, the ability of dipyridamole-Doppler echocardiography to predict the presence of significant coronary artery disease (CAD) was evaluated. Baseline and post-dipyridamole Doppler studies were performed in 10 normal control subjects and 23 patients with CAD. Aortic peak velocity and acceleration increased from baseline to post-dipyridamole in normal subjects by 0.07 ± 0.07 m/s (p = 0.016) and 2.1 ± 2.0 m/s2 (p = 0.009), respectively. The ratio of early to late peak transmitral velocities decreased slightly in normal subjects, by 0.18 ± 0.72 (difference not significant), whereas the ratio of early to late transmitral velocity-time integrals increased by 0.07 ± 0.93 (difference not significant). The response of aortic velocity and acceleration to intravenous dipyridamole was not significantly different between normal subjects, patients without reversible thallium-201 perfusion defects and patients with reversible thallium-201 perfusion defects. Furthermore, only 3 of 14 subjects with reversible thallium-201 perfusion defects had abnormal (>2 standard deviations from the mean) responses of aortic velocity or acceleration to intravenous dipyridamole. No patient had an abnormal response of the early to late mitral peak velocity ratio. In addition, the response of Doppler aortic and mitral indexes to intravenous dipyridamole was not able to identify the presence of significant CAD as assessed by quantitative coronary arteriography. Thus, Doppler indexes of aortic and mitral blood flow after intravenous dipyridamole are insensitive in detecting either the presence of reversible perfusion thallium-201 defects or significant CAD.
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U2 - 10.1016/0002-9149(89)91041-2
DO - 10.1016/0002-9149(89)91041-2
M3 - Article
C2 - 2729104
AN - SCOPUS:0024389365
SN - 0002-9149
VL - 63
SP - 1315
EP - 1320
JO - The American journal of cardiology
JF - The American journal of cardiology
IS - 18
ER -