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Normal Values in Children for Myocardial Ultrasonic Tissue Characterization by Integrated Backscatter
Kazuhiko Shibuya1, Jean-Luc Bigras, Brian W. McCrindle
1The Division of Cardiology, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8.
Echocardiography (Mount Kisco, N.Y.)
|February 15, 2001
Summary
Establishing normal myocardial ultrasonic integrated backscatter values in children is crucial. The left ventricular posterior wall in the long-axis view provides the most reliable data for pediatric ultrasonic tissue characterization.
Area of Science:
- Pediatric Cardiology
- Biomedical Ultrasound
- Cardiac Imaging
Background:
- Adult normal values for ultrasonic tissue characterization by integrated backscatter are established.
- Factors influencing integrated backscatter in pediatric populations remain undefined.
Purpose of the Study:
- To define normal values for myocardial ultrasonic integrated backscatter in a pediatric cohort.
- To identify optimal imaging regions and parameters for pediatric assessment.
Main Methods:
- Studied 72 children with normal cardiac anatomy using an ultrasonic integrated backscatter imaging system.
- Measured parameters at peak, nadir, and end-diastole across eight regions with fixed and variable settings.
- Calculated cyclic variation and its ratios to peak and end-diastolic values.
Main Results:
- Over 90% of data curves from the left ventricular posterior wall (long-axis view) showed normal patterns.
- Abnormal patterns exceeded 50% in other regions.
- No significant differences in cyclic variation were found between posterior wall positions or settings.
- Backscatter variables showed no relation to age, gender, or height, with weak correlation to body surface area.
Conclusions:
- Assessment of integrated backscatter in children is optimal using the left ventricular posterior wall in the long-axis view.
- Relating cyclic variation to peak or end-diastolic values yields more stable estimates.
- These findings establish a basis for normal ultrasonic tissue characterization in pediatric hearts.