Myocardial Viability Mapping by Magnetic Resonance-Based Multiparametric Systolic Strain Analysis
Myocardial Viability Mapping by Magnetic Resonance-Based Multiparametric Systolic Strain Analysis
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DOI:
10.1016/j.athoracsur.2008.06.072
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发表时间:
2008-11-01
影响因子:
4.6
通讯作者:
Pasque, Michael K.
中科院分区:
文献类型:
--
作者:
Cupps, Brian P.;Bree, Douglas R.;Pasque, Michael K.
Background. Regional myocardial contractility can be characterized by three-dimensional left ventricular (LV) multiparametric strain maps generated from sequential magnetic resonance imaging of radiofrequency tissue-tagging grid point displacements.Methods. Normal average and standard deviation values for each of three strain indices at 15,300 LV points were determined from a normal volunteer human strain database ( n = 50) by application of magnetic resonance-based three-dimensional strain analysis. Patient-specific multiparametric strain data from each ischemic cardiomyopathy patient ( n = 20) were then submitted to a point-by-point comparison ( n = 15,300 LV points) to the normal strain database. The resulting 15,300 composite multiparametric Z-score values ( standard deviation from normal average) were color-contour mapped over patient-specific three-dimensional LV geometry to detect the abnormal contractile patterns associated with myocardial infarction and nonviable myocardium.Results. The average multiparametric strain composite Z-score from each LV region ( n = 120) was compared with the respective clinical standard viability testing result and used to construct a receiver-operator characteristic curve. The area under the curve was 0.941 ( p < 0.001; 95% confidence interval: 0.897 to 0.985). A regional average Z-score threshold of 1.525 (> 1.525 being nonviable) resulted in a sensitivity of 90% and a specificity of 90%. Corresponding positive and negative predictive values were 84% and 95%, respectively.Conclusions. The clinical application of magnetic resonance-based multiparametric strain analysis allowed accurate regional characterization and visualization of LV myocardial viability.