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Quantitative Analysis of Regional Motion and Thickening by Gated Myocardial Perfusion SPECT: Normal Heterogeneity and Criteria for Abnormality

Tali Sharir, Daniel S. Berman, Parker B. Waechter, Joseph Areeda, Paul B. Kavanagh, Jim Gerlach, Xingping Kang and Guido Germano

Departments of Imaging and Medicine, Cedars-Sinai Medical Center, Los Angeles; CSMC Burns and Allen Research Institute, Los Angeles; and Departments of Medicine and Radiological Sciences, University of California Los Angeles School of Medicine, Los Angeles, California



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FIGURE 1. Schematic representation of 20-segment model of left ventricle.

 


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FIGURE 2. Plot of normal motion and thickening (mean ± SEM) at 4 levels from apex to base.

 


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FIGURE 3. Circumferential variations in normal segmental motion at distal, mid, and basal ventricular levels.

 


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FIGURE 4. Circumferential variations in normal segmental thickening at distal, mid, and basal ventricular levels.

 


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FIGURE 5. Thresholds (number of SDs below reference value) for defining motion (A) and thickening (B) abnormalities.

 


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FIGURE 6. Overall sensitivity (black bars) and specificity (white bars) in detecting segmental motion and thickening abnormalities by quantitative algorithm in validation group.

 


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FIGURE 7. Segment-by-segment sensitivity (black bars) and specificity (white bars) in detecting motion (A) and thickening (B) abnormalities by quantitative algorithm in validation group.

 


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FIGURE 8. Correlation between quantitative versus visual summed motion score (A) and summed thickening score (B). Solid line indicates linear fit and dashed line indicates line of identity.

 





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