Abstract
Background - Both intermittent triggered and real-time myocardial contrast echocardiography (MCE) have been proposed to detect impaired myocardial perfusion. We compared the ability of these 2 methods to quantify altered myocardial blood flow (MBF) and transmural distribution of MBF produced by graded coronary stenoses. Methods and Results - In 8 open-chest dogs, we created 4 graded left anterior descending coronary artery (LAD) stenoses: 3 levels of reduced adenosine hyperemia (non-flow-limiting at rest) and 1 grade of flow-limiting at rest. Real-time MCE was performed with SonoVue infusion using low-energy power pulse inversion (ATL) imaging, whereas ECG-gated intermittent triggered imaging used high energy at pulsing intervals from 1:1 to 1:10. LAD signal intensity (SI) was plotted versus time by real-time MCE and versus pulsing intervals by triggered MCE and was fitted to a 1-exponential function to obtain plateau SI (A) and the rate of SI rise (b). Visual detection of decreased opacification was equivalent by triggered and real-time MCE. Fluorescent microsphere-derived MBF ratio in LAD/left circumflex artery beds demonstrated close correlation with both real-time imaging (b, r=0.79; A×b, r=0.81) and triggered imaging (b, r=0.78; A×b, r=0.80). The endocardial/epicardial ratio of MBF in the LAD bed demonstrated closer correlation with the endocardial/epicardial ratios of b (r=0.71) and A×b (r=0.67) obtained by real-time than triggered imaging (b, r=0.42; A×b, r=0.52). Conclusions - Real-time and triggered MCE are equivalent in their ability to identify coronary stenosis and quantify altered MBF.
Author supplied keywords
Cite
CITATION STYLE
Masugata, H., Lafitte, S., Peters, B., Strachan, G. M., & DeMaria, A. N. (2001). Comparison of real-time and intermittent triggered myocardial contrast echocardiography for quantification of coronary stenosis severity and transmural perfusion gradient. Circulation, 104(13), 1550–1556. https://doi.org/10.1161/hc3801.095694
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.