Motion-compensation approach for quantitative digital subtraction angiography and its effect on in-vivo blood
Joseph F Whitehead1, Sarvesh Periyasamy2, Paul F Laeseke2
1University of Wisconsin - Madison, Department of Medical Physics, Madison, Wisconsin, United States.
Purpose:
Quantitative monitoring of flow-altering interventions has been proposed using algorithms that quantify blood velocity from time-resolved two-dimensional angiograms. These algorithms track the movement of contrast oscillations along a vessel centerline. Vessel motion may occur relative to a statically defined vessel centerline, corrupting the blood velocity measurement. We provide a method for motion-compensated blood velocity quantification.
Approach:
The motion-compensation approach utilizes a vessel segmentation algorithm to perform frame-by-frame vessel registration and creates a dynamic vessel centerline that moves with the vasculature. Performance was evaluated in-vivo through comparison with manually annotated centerlines. The method was also compared to a previous uncompensated method using best- and worst-case static centerlines chosen to minimize and maximize centerline placement accuracy. Blood velocities determined through quantitative DSA (qDSA) analysis for each centerline type were compared through linear regression analysis.
Results:
Centerline distance errors were relative to gold standard manual annotations. For the uncompensated approach, the best- and worst-case static centerlines had distance errors of and , respectively. Linear regression analysis found a high -squared between qDSA-derived blood velocities using gold standard centerlines and motion-compensated centerlines () with a slope of 1.15 and a small offset of . The use of static centerlines resulted in low coefficients of determination for the best case () and worst-case () scenarios, with slopes close to zero.
Conclusions:
In-vivo validation of motion-compensated qDSA analysis demonstrated improved velocity quantification accuracy in vessels with motion, addressing an important clinical limitation of the current qDSA algorithm.
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