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MDCT Determination of Volume and Function of the Left Ventricle: Are Short-Axis Image Reformations Necessary?

Kai U. Juergens1, Harald Seifarth1, David Maintz1, Matthias Grude2, Murat Ozgun1, Thomas Wichter2, Walter Heindel1 and Roman Fischbach1

1 Department of Clinical Radiology, University of Muenster, Albert-Schweitzer-Straße 33, D-48149 Muenster, Germany.
2 Department of Cardiology and Angiology, University of Muenster, Muenster, Germany.


Figure 1
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Fig. 1A —Diagrams show anatomic orientation in image reformations from MDCT coronary angiography. SVC = superior vena cava, RA = right atrium, RV = right ventricle, PA = pulmonary artery, LA = left atrium, LV = left ventricle, Aa = ascending aorta, AA = aortic arch. Diagrams show anatomic orientation in axial (A) and short-axis (B) image reformations used for determination of left ventricular volumetric and function parameters from MDCT coronary angiography.

 

Figure 2
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Fig. 1B —Diagrams show anatomic orientation in image reformations from MDCT coronary angiography. SVC = superior vena cava, RA = right atrium, RV = right ventricle, PA = pulmonary artery, LA = left atrium, LV = left ventricle, Aa = ascending aorta, AA = aortic arch. Diagrams show anatomic orientation in axial (A) and short-axis (B) image reformations used for determination of left ventricular volumetric and function parameters from MDCT coronary angiography.

 

Figure 3
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Fig. 2A —Bland-Altman plots show study findings. Bland-Altman plots of left ventricular end-diastolic volumes (LVEDV) (A), left ventricular end-systolic volumes (LVESV) (B), and left ventricular ejection fractions (LVEF) (C) obtained from thick axial images (AX) and short-axis reformations (SA) depict agreement between mean differences (AX - SA) and mean values [(AX + SA) / 2] of both approaches. Mean difference was 24.9 ± 23.9 mL for LVEDV, 19.5 ± 19.3 mL for LVESV, and -0.5% ± 6.7% for LVEF.

 

Figure 4
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Fig. 2B —Bland-Altman plots show study findings. Bland-Altman plots of left ventricular end-diastolic volumes (LVEDV) (A), left ventricular end-systolic volumes (LVESV) (B), and left ventricular ejection fractions (LVEF) (C) obtained from thick axial images (AX) and short-axis reformations (SA) depict agreement between mean differences (AX - SA) and mean values [(AX + SA) / 2] of both approaches. Mean difference was 24.9 ± 23.9 mL for LVEDV, 19.5 ± 19.3 mL for LVESV, and -0.5% ± 6.7% for LVEF.

 

Figure 5
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Fig. 2C —Bland-Altman plots show study findings. Bland-Altman plots of left ventricular end-diastolic volumes (LVEDV) (A), left ventricular end-systolic volumes (LVESV) (B), and left ventricular ejection fractions (LVEF) (C) obtained from thick axial images (AX) and short-axis reformations (SA) depict agreement between mean differences (AX - SA) and mean values [(AX + SA) / 2] of both approaches. Mean difference was 24.9 ± 23.9 mL for LVEDV, 19.5 ± 19.3 mL for LVESV, and -0.5% ± 6.7% for LVEF.

 

Figure 6
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Fig. 3A —53-year-old man with coronary artery disease. Thick-section axial images and short-axis reformations from 16-MDCT show clear delineation of left ventricle (LV) cavity and myocardium in axial (A and D) and short-axis (B, C, E, and F) end-diastolic (A-C) and end-systolic (D-F) image reconstructions. Endocardial contours are outlined (white tracing) using automatic contour detection software (CT MASS [version 6.1], Medis). LV shape is in good agreement with short-axis cine MR images in end-diastolic and end-systolic phases of cardiac cycle.

 

Figure 7
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Fig. 3B —53-year-old man with coronary artery disease. Thick-section axial images and short-axis reformations from 16-MDCT show clear delineation of left ventricle (LV) cavity and myocardium in axial (A and D) and short-axis (B, C, E, and F) end-diastolic (A-C) and end-systolic (D-F) image reconstructions. Endocardial contours are outlined (white tracing) using automatic contour detection software (CT MASS [version 6.1], Medis). LV shape is in good agreement with short-axis cine MR images in end-diastolic and end-systolic phases of cardiac cycle.

 

Figure 8
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Fig. 3C —53-year-old man with coronary artery disease. Thick-section axial images and short-axis reformations from 16-MDCT show clear delineation of left ventricle (LV) cavity and myocardium in axial (A and D) and short-axis (B, C, E, and F) end-diastolic (A-C) and end-systolic (D-F) image reconstructions. Endocardial contours are outlined (white tracing) using automatic contour detection software (CT MASS [version 6.1], Medis). LV shape is in good agreement with short-axis cine MR images in end-diastolic and end-systolic phases of cardiac cycle.

 

Figure 9
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Fig. 3D —53-year-old man with coronary artery disease. Thick-section axial images and short-axis reformations from 16-MDCT show clear delineation of left ventricle (LV) cavity and myocardium in axial (A and D) and short-axis (B, C, E, and F) end-diastolic (A-C) and end-systolic (D-F) image reconstructions. Endocardial contours are outlined (white tracing) using automatic contour detection software (CT MASS [version 6.1], Medis). LV shape is in good agreement with short-axis cine MR images in end-diastolic and end-systolic phases of cardiac cycle.

 

Figure 10
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Fig. 3E —53-year-old man with coronary artery disease. Thick-section axial images and short-axis reformations from 16-MDCT show clear delineation of left ventricle (LV) cavity and myocardium in axial (A and D) and short-axis (B, C, E, and F) end-diastolic (A-C) and end-systolic (D-F) image reconstructions. Endocardial contours are outlined (white tracing) using automatic contour detection software (CT MASS [version 6.1], Medis). LV shape is in good agreement with short-axis cine MR images in end-diastolic and end-systolic phases of cardiac cycle.

 

Figure 11
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Fig. 3F —53-year-old man with coronary artery disease. Thick-section axial images and short-axis reformations from 16-MDCT show clear delineation of left ventricle (LV) cavity and myocardium in axial (A and D) and short-axis (B, C, E, and F) end-diastolic (A-C) and end-systolic (D-F) image reconstructions. Endocardial contours are outlined (white tracing) using automatic contour detection software (CT MASS [version 6.1], Medis). LV shape is in good agreement with short-axis cine MR images in end-diastolic and end-systolic phases of cardiac cycle.

 

Figure 12
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Fig. 4A —72-year-old man with three-vessel coronary artery disease and inferior and inferolateral infarction after bypass surgery. Images obtained from 16-MDCT reformations show reduced wall thickness during diastole and absence of wall thickening during systole for lateral and inferior wall of myocardium of left ventricle (LV). Note thinned inferior papillary muscle on short-axis image from 16-MDCT reformations during diastole (A) and systole (B).

 

Figure 13
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Fig. 4B —72-year-old man with three-vessel coronary artery disease and inferior and inferolateral infarction after bypass surgery. Images obtained from 16-MDCT reformations show reduced wall thickness during diastole and absence of wall thickening during systole for lateral and inferior wall of myocardium of left ventricle (LV). Note thinned inferior papillary muscle on short-axis image from 16-MDCT reformations during diastole (A) and systole (B).

 

Figure 14
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Fig. 4C —72-year-old man with three-vessel coronary artery disease and inferior and inferolateral infarction after bypass surgery. Images obtained from 16-MDCT reformations show reduced wall thickness during diastole and absence of wall thickening during systole for lateral and inferior wall of myocardium of left ventricle (LV). Thinned lateral LV wall is well delineated on axial image from 16-MDCT reformations in basal and midventricular segments during diastole (C) and systole (D).

 

Figure 15
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Fig. 4D —72-year-old man with three-vessel coronary artery disease and inferior and inferolateral infarction after bypass surgery. Images obtained from 16-MDCT reformations show reduced wall thickness during diastole and absence of wall thickening during systole for lateral and inferior wall of myocardium of left ventricle (LV). Thinned lateral LV wall is well delineated on axial image from 16-MDCT reformations in basal and midventricular segments during diastole (C) and systole (D).

 

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