TY - JOUR
T1 - Region-Based Endocardium Tracking on Real-Time Three-Dimensional Ultrasound
AU - Duan, Qi
AU - Angelini, Elsa D.
AU - Herz, Susan L.
AU - Ingrassia, Christopher M.
AU - Costa, Kevin D.
AU - Holmes, Jeffrey W.
AU - Homma, Shunichi
AU - Laine, Andrew F.
N1 - Funding Information:
This work was partially funded by the National Science Foundation grant BES-02-01617, the American Heart Association grant #0151250T and #0640005N, Philips Medical Healthcare and the New York State NYSTAR/CAT Technology Program. The authors also would like to thank Dr. Jie Wang (The Skirball Animal Center, Orangeburg, NY) for helping with the animal experiments.
PY - 2009/2
Y1 - 2009/2
N2 - Matrix-phased array transducers for real-time 3-D ultrasound enable fast, noninvasive visualization of cardiac ventricles. Typically, 3-D ultrasound images are semiautomatically segmented to extract the left ventricular endocardial surface at end-diastole and end-systole. Automatic segmentation and propagation of this surface throughout the entire cardiac cycle is a challenging and cumbersome task. If the position of the endocardial surface is provided at one or two time frames during the cardiac cycle, automated tracking of the surface over the remaining time frames could reduce the workload of cardiologists and optimize analysis of 3-D ultrasound data. In this paper, we applied a region-based tracking algorithm to track the endocardial surface between two reference frames that were manually segmented. To evaluate the tracking of the endocardium, the method was applied to 40 open-chest dog datasets with 484 frames in total. Ventricular geometry and volumes derived from region-based endocardial surfaces and manual tracing were quantitatively compared, showing strong correlation between the two approaches. Statistical analysis showed that the errors from tracking were within the range of interobserver variability of manual tracing. Moreover, our algorithm performed well on ischemia datasets, suggesting that the method is robust-to-abnormal wall motion. In conclusion, the proposed optical flow-based surface tracking method is very efficient and accurate, providing dynamic "interpolation" of segmented endocardial surfaces. (E-mail: [email protected]).
AB - Matrix-phased array transducers for real-time 3-D ultrasound enable fast, noninvasive visualization of cardiac ventricles. Typically, 3-D ultrasound images are semiautomatically segmented to extract the left ventricular endocardial surface at end-diastole and end-systole. Automatic segmentation and propagation of this surface throughout the entire cardiac cycle is a challenging and cumbersome task. If the position of the endocardial surface is provided at one or two time frames during the cardiac cycle, automated tracking of the surface over the remaining time frames could reduce the workload of cardiologists and optimize analysis of 3-D ultrasound data. In this paper, we applied a region-based tracking algorithm to track the endocardial surface between two reference frames that were manually segmented. To evaluate the tracking of the endocardium, the method was applied to 40 open-chest dog datasets with 484 frames in total. Ventricular geometry and volumes derived from region-based endocardial surfaces and manual tracing were quantitatively compared, showing strong correlation between the two approaches. Statistical analysis showed that the errors from tracking were within the range of interobserver variability of manual tracing. Moreover, our algorithm performed well on ischemia datasets, suggesting that the method is robust-to-abnormal wall motion. In conclusion, the proposed optical flow-based surface tracking method is very efficient and accurate, providing dynamic "interpolation" of segmented endocardial surfaces. (E-mail: [email protected]).
KW - Endocardium
KW - LV
KW - Open-chest ultrasound
KW - Optical flow
KW - Quantitative evaluation
KW - Real-time 3-D echocardiography
KW - Speckle tracking
UR - https://www.scopus.com/pages/publications/58249141435
U2 - 10.1016/j.ultrasmedbio.2008.08.012
DO - 10.1016/j.ultrasmedbio.2008.08.012
M3 - Article
C2 - 18963396
AN - SCOPUS:58249141435
SN - 0301-5629
VL - 35
SP - 256
EP - 265
JO - Ultrasound in Medicine and Biology
JF - Ultrasound in Medicine and Biology
IS - 2
ER -