Page 14 - Artificial Intelligence for Computational Modeling of the Heart
P. 14

List of figures xiii





                            displayed in green (mid gray in print version) and the ground-truth
                            in yellow (light gray in print version); and finally, a 3D rendering of
                            the corresponding triangulated surface mesh for the aortic root
                            (both computed using MSDL).                       104
                     Fig. 3.5  Schematic overview of the multi-scale image navigation paradigm
                            based on multi-scale deep reinforcement learning.  107
                     Fig. 3.6  Left: The LV-center (1), the anterior/posterior RV-insertion points
                            (2)/(3) and the RV-extreme point (4) in a short-axis cardiac MR
                            image. Middle: The mitral septal annulus (1) and the mitral lateral
                            annulus points (2) in a cardiac ultrasound image. Right: The center
                            of the aortic root in a frontal slice of a 3D-CT scan.  109
                     Fig. 3.7  Visualization of the considered cardiac and vascular landmarks.  110
                     Fig. 3.8  Segmentation masks for heart isolation computed with a deep
                            neural network.                                   112
                     Fig. 4.1  Overall workflow of the proposed method.        121
                     Fig. 4.2  Three stage approach for generating synthetic coronary
                            geometries: (A) Define coronary tree skeleton, (B) Define healthy
                            coronary anatomy, (C) Define stenoses.             123
                     Fig. 4.3  Multiscale model of the systemic and coronary arterial circulation. 124
                     Fig. 4.4  Deep neural network model employed for computing cFFR ML :
                            fully connected architecture with four hidden layers.  125
                     Fig. 4.5  Features describing a stenosis.                126
                     Fig. 4.6  Examples of hemodynamic interdependence between coronary
                            branches.                                        127
                     Fig. 4.7  Scatterplot of cFFR ML and cFFR CFD (correlation = 0.9994).  129
                     Fig. 4.8  Bland–Altman analysis plot comparing cFFR ML and
                            cFFR CFD : no systematic bias was found (95% limits of
                            agreement, −0.0085 to 0.0067).                    129
                     Fig. 4.9  (A) Scatterplot of cFFR CFD and invasive FFR (correlation =
                            0.725); (B) Scatterplot of cFFR ML and invasive FFR (correlation
                            = 0.729).                                         131
                     Fig. 4.10 Bland–Altman analysis plot comparing cFFR CFD and cFFR ML
                            vs. invasive FFR (cFFR CFD 95% limits of agreement, −0.159 to
                            0.207; cFFR ML 95% limits of agreement, −0.159 to 0.206).  131
                     Fig. 4.11 Receiver operating characteristic (ROC) curves of cFFR CFD
                            and cFFR ML for 125 lesions.                      132
                     Fig. 4.12 Case example of a patient-specific coronary tree with cFFR ML
                            color coded coronary tree: invasive FFR = 0.71 and cFFR ML =
                            0.68.                                             132
                     Fig. 4.13 Diagram of the ionic channels in the CRN atrial cell model
                            (source: CellML, https:/ /
                            models.cellml.org/ exposure/ 0e03bbe01606be5811691f9d5de10b65). 138
                     Fig. 4.14 Left: Action potential of the CRN model with parameters as in
                            [359]; Middle: Current I ion –I Na ; Right: Current I Na .  140
                     Fig. 4.15 Samples with SD=0.3 by different number of parameters.  145
                     Fig. 4.16 Goodness of reconstruction on testing data using PCA and LLE.  146
                     Fig. 4.17 Modes of variation of the action potential profile produced by the
                            CRN model, estimated by PCA components.           147
                     Fig. 4.18 Regression on V peak and V rest : PLSR (1st column), MARS
   9   10   11   12   13   14   15   16   17   18   19