Key result
Coronary occlusion blunts normal cyclic variation in myocardial integrated backscatter during contraction.
Why the study?
Whether myocardial contraction and relaxation influence quantitative ultrasonic backscatter before and after coronary occlusion was uncertain.
Does myocardial contraction and acute coronary occlusion affect systolic and diastolic integrated ultrasonic backscatter in anesthetized dogs?
Does myocardial contraction and acute coronary occlusion affect systolic and diastolic integrated ultrasonic backscatter in anesthetized dogs?
Normal contracting myocardium exhibits a cyclic decrease in ultrasonic integrated backscatter from end-diastole to end-systole that is blunted during acute ischemia, allowing differentiation of ischemic from normal myocardium at end-systole.
Answers are grounded in this paper and cite their sources.
Supports experimental ischemia detection via backscatter; leaves open human validation before clinical use.
To determine whether contraction and relaxation influence quantitative myocardial ultrasonic backscatter we measured systolic and diastolic integrated backscatter separately in 10 pentobarbital-anesthetized dogs with defined, paced heart rates, before and after coronary occlusion. Data were acquired from intramural sites by coupling a broadband 5-MHz transducer to the left ventricular epicardium. Integrated backscatter was obtained from seven sequential ECG gated intervals throughout the cardiac cycle over the frequencies of 2.5-7.5 MHz and referenced to values obtained with a steel reflector. Before coronary occlusion myocardium in all dogs exhibited a decrease in integrated backscatter from end diastole to end systole (P less than 0.05) in control zones and in zones destined to become ischemic (P less than 0.05). Thirty minutes after occlusion integrated backscatter did not change in control zones but was elevated in ischemic zones with blunting of the diastolic-to-systolic variation. Thus myocardium undergoing contraction exhibits a decrease in integrated backscatter, and measurement of integrated backscatter at end systole differentiates ischemic from normal myocardium.
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Barzilai et al. (1984) studied Myocardial ischemia (n=10). Coronary occlusion and quantitative myocardial ultrasonic backscatter measurement vs. Pre-occlusion myocardium and non-ischemic control myocardial zones was evaluated on Systolic and diastolic integrated ultrasonic backscatter (over 2.5-7.5 MHz) (p=<0.05). Myocardial contraction decreased integrated backscatter from end-diastole to end-systole (P<0.05), a variation blunted 30 minutes after coronary occlusion.
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