4.6 Article

Spatiotemporal Coherence to Quantify Sources of Image Degradation in Ultrasonic Imaging

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TUFFC.2022.3152717

Keywords

Clutter; Acoustics; Thermal noise; Signal to noise ratio; Imaging; Spatial coherence; Coherence; Image quality; image degradation; coherence; clutter; signal-to-noise ratio; signal-to-clutter ratio

Funding

  1. National Science Foundation Graduate Research Fellowship Program [1937963]
  2. National Institute of Biomedical Imaging and Bioengineering under NIH [T32EB021937, R01EB020040]
  3. National Heart, Lung, and Blood Institute [R01HL156034]
  4. National Science Foundation CAREER Award [IIS-1750994]

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Thermal noise and acoustic clutter degrade ultrasonic image quality and cannot be separately measured in vivo. We derived and validated a method to quantify the individual contributions of thermal noise and acoustic clutter to image degradation by leveraging coherence characteristics.
Thermal noise and acoustic clutter signals degrade ultrasonic image quality and contribute to unreliable clinical assessment. When both noise and clutter are prevalent, it is difficult to determine which one is a more significant contributor to image degradation because there is no way to separately measure their contributions in vivo. Efforts to improve image quality often rely on an understanding of the type of image degradation at play. To address this, we derived and validated a method to quantify the individual contributions of thermal noise and acoustic clutter to image degradation by leveraging spatial and temporal coherence characteristics. Using Field II simulations, we validated the assumptions of our method, explored strategies for robust implementation, and investigated its accuracy and dynamic range. We further proposed a novel robust approach for estimating spatial lag-one coherence. Using this robust approach, we determined that our method can estimate the signal-to-thermal noise ratio (SNR) and signal-to-clutter ratio (SCR) with high accuracy between SNR levels of -30 to 40 dB and SCR levels of -20 to 15 dB. We further explored imaging parameter requirements with our Field II simulations and determined that SNR and SCR can be estimated accurately with as few as two frames and sixteen channels. Finally, we demonstrate in vivo feasibility in brain imaging and liver imaging, showing that it is possible to overcome the constraints of in vivo motion using high-frame rate M-Mode imaging.

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