TY - GEN
T1 - Quantification of Spinal Cord Microvascular Perfusion utilizing Ultrasound
AU - Leadingham, Kelley M.Kempski
AU - Routkevitch, Denis
AU - Hersh, Andrew M.
AU - Kerensky, Max
AU - Abramson, Haley G.
AU - Weber-Levine, Carly
AU - Robinson, Kayla
AU - Jiang, Kelly
AU - Judy, Brendan
AU - Perdomo-Pantoja, Alexander
AU - Theodore, Nicholas
AU - Manbachi, Amir
N1 - Publisher Copyright:
© 2023 IEEE.
PY - 2023
Y1 - 2023
N2 - Approximately 900,000 spinal cord injuries (SCI) occur each year. Understanding the severity and progression of the injury can help tailor the treatment plan to optimize a patient's prognosis. One way to determine the progression of a neurological injury is to monitor the blood flow. While software exists for quantifying renal tissue perfusion with Doppler ultrasound, we developed an algorithm optimized to quantify perfusion in spinal cord microvasculature with multiple ultrasound imaging modalities. The objective of this study was to demonstrate spinal cord microvascular quantification methods using non-contrast ultrasound images. Following a T4-T6 laminectomy, ultrasound videos were captured of in vivo porcine spinal cords using color Doppler (CDI), advanced dynamic flow (ADF), and superb microvascular imaging (SMI) modalities. A MATLAB algorithm was developed to import ultrasound videos, extract the velocity map, and quantify the microvasculature blood flow as a function of time by averaging the velocity map in a region of interest. Using the velocity-time curve (VTC), local stroke volume (LSV) and local vascular output (LVO) were calculated. Our algorithm detected slow-flow (< 0.3 cm/s) changes indicative of cardiac cycles in each ultrasound modality for sub-millimeter diameter vessels. Each cardiac cycle from the VTC was extracted to calculate LSV and LVO. The mean ± 1 standard deviation LVO for CDI, ADF, and SMI were 0.23±0.008 mL/min, 0.28±0.003 mL/min, and 0.18±0.004 mL/min, respectively. Calculating these local perfusion metrics and tracking local perfusion after SCI may supplement current treatment by reducing the dependence on global measures of blood flow (e.g., mean arterial pressure).
AB - Approximately 900,000 spinal cord injuries (SCI) occur each year. Understanding the severity and progression of the injury can help tailor the treatment plan to optimize a patient's prognosis. One way to determine the progression of a neurological injury is to monitor the blood flow. While software exists for quantifying renal tissue perfusion with Doppler ultrasound, we developed an algorithm optimized to quantify perfusion in spinal cord microvasculature with multiple ultrasound imaging modalities. The objective of this study was to demonstrate spinal cord microvascular quantification methods using non-contrast ultrasound images. Following a T4-T6 laminectomy, ultrasound videos were captured of in vivo porcine spinal cords using color Doppler (CDI), advanced dynamic flow (ADF), and superb microvascular imaging (SMI) modalities. A MATLAB algorithm was developed to import ultrasound videos, extract the velocity map, and quantify the microvasculature blood flow as a function of time by averaging the velocity map in a region of interest. Using the velocity-time curve (VTC), local stroke volume (LSV) and local vascular output (LVO) were calculated. Our algorithm detected slow-flow (< 0.3 cm/s) changes indicative of cardiac cycles in each ultrasound modality for sub-millimeter diameter vessels. Each cardiac cycle from the VTC was extracted to calculate LSV and LVO. The mean ± 1 standard deviation LVO for CDI, ADF, and SMI were 0.23±0.008 mL/min, 0.28±0.003 mL/min, and 0.18±0.004 mL/min, respectively. Calculating these local perfusion metrics and tracking local perfusion after SCI may supplement current treatment by reducing the dependence on global measures of blood flow (e.g., mean arterial pressure).
KW - microvascular imaging
KW - perfusion
KW - spinal cord injury
KW - ultrasound
UR - https://www.scopus.com/pages/publications/85178576027
UR - https://www.scopus.com/pages/publications/85178576027#tab=citedBy
U2 - 10.1109/IUS51837.2023.10307979
DO - 10.1109/IUS51837.2023.10307979
M3 - Conference contribution
AN - SCOPUS:85178576027
T3 - IEEE International Ultrasonics Symposium, IUS
BT - IUS 2023 - IEEE International Ultrasonics Symposium, Proceedings
PB - IEEE Computer Society
T2 - 2023 IEEE International Ultrasonics Symposium, IUS 2023
Y2 - 3 September 2023 through 8 September 2023
ER -