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- •Contents
- •Preface
- •1.1 Introduction
- •1.5 Free-Hand Scanning with Position Sensing
- •1.5.1 Tracked 3-D US with Articulated Arm Sensing
- •1.5.2 Free-Hand 3-D US with Acoustic Tracking
- •1.5.3 Free-Hand 3-D Scanning with Magnetic Field Sensing
- •1.5.4 3-D US Tracked by Speckle Decorrelation
- •1.6 Free-Hand 3-D US Scanning Without Position Sensing
- •1.7 2-D Array Scanning for Dynamic 3-D Ultrasound (4-D US)
- •1.8 3-D Ultrasound Visualization
- •1.8.1 Multiplanar Reformatting
- •1.8.2 Volume Rendering Techniques
- •1.9 3-D Ultrasound-Guided Prostate Therapy
- •1.2 Disadvantages of 2-D Ultrasound
- •1.3 3-D Ultrasound Scanning Techniques
- •1.4 Mechanical Scanning
- •1.4.1 Linear Mechanical 3-D Scanners
- •1.4.2 Tilt 3-D Mechanical Scanners
- •1.4.3 Endocavity Rotational 3-D Scanners
- •1.9.1 Early-Stage Prostate Cancer Management
- •1.9.2 US-Guided Prostate Brachytherapy
- •1.9.3 3-D TRUS-Guided Brachytherapy System
- •1.9.4 3-D TRUS Imaging System
- •1.9.5 Prostate Segmentation
- •1.9.5.1 Initialization
- •1.9.5.2 Refinement
- •1.9.5.3 Propagation
- •1.9.6 Dosimetry
- •1.9.7 Calibration of the Coordinate Systems
- •1.9.8 Needle Segmentation
- •1.10 Evaluation of 3-D TRUS-Guided Brachytherapy System
- •1.10.1 Methods of Calibration
- •1.10.1.1 Fiducial Localization Error
- •1.10.1.2 Fiducial Registration Error
- •1.10.1.3 Target Registration Error
- •1.10.2 Results of Calibration
- •1.10.3 Accuracy of Needle Placement
- •1.10.4 Accuracy of Needle Angulation
- •1.10.5 Accuracy of Needle Targeting
- •1.10.6 Accuracy of Needle Tracking
- •1.10.7 Accuracy of Seed Implantation
- •1.11 Conclusions
- •Acknowledgments
- •References
- •2.1 Introduction
- •2.2 Despeckle Filtering
- •2.2.1 Local Statistics Filtering
- •2.2.1.1 First-Order Statistics Filtering (lsmv, wiener)
- •2.2.1.2 Homogeneous Mask Area Filtering (lsminsc)
- •2.2.2 Median Filtering (median)
- •2.2.3 Maximum Homogeneity over a Pixel Neighborhood Filtering (homog)
- •2.2.4 Geometric Filtering (gf4d)
- •2.2.5 Homomorphic Filtering (homo)
- •2.2.6 Diffusion Filtering
- •2.2.7 Wavelet Filtering (waveltc)
- •2.3 Methodology
- •2.3.1 Material
- •2.3.2 Recording of Ultrasound Images
- •2.3.3 Despeckle Filtering
- •2.3.4 Texture Analysis
- •2.3.4.1 Statistical Features (SF)
- •2.3.4.2 Spatial Gray-Level Dependence Matrices (SGLDMs)
- •2.3.4.3 Gray Level Difference Statistics (GLDS) [44]
- •2.3.4.4 Neighborhood Gray Tone Difference Matrix (NGTDM) [45]
- •2.3.4.5 Statistical Feature Matrix (SFM) [46]
- •2.3.4.6 Laws Texture Energy Measures (TEM) [46]
- •2.3.4.7 Fractal Dimension Texture Analysis (FDTA) [46]
- •2.3.4.8 Fourier Power Spectrum (FPS) [46]
- •2.3.5 Distance Measures
- •2.3.6 Univariate Statistical Analysis
- •2.3.7 kNN Classifier
- •2.3.8 Image Quality Evaluation Metrics
- •2.3.9 Visual Evaluation by Experts
- •2.4 Results
- •2.4.1 Evaluation of Despeckle Filtering on a Symptomatic Ultrasound Image
- •2.4.2 Texture Analysis: Distance Measures
- •2.4.3 Texture Analysis: Univariate Statistical Analysis
- •2.4.4 Texture Analysis: kNN Classifier
- •2.4.5 Image Quality Evaluation Metrics
- •2.4.6 Visual Evaluation by Experts
- •2.5 Discussion
- •Acknowledgments
- •References
- •3.1 Introduction
- •3.1.1 Limitations of Conventional Carotid Ultrasound Imaging
- •3.2 3-D US Imaging of the Carotid Arteries
- •3.2.1 3-D Carotid Ultrasound Scanning Techniques
- •3.2.1.1 Mechanical Linear 3-D Carotid Ultrasound Imaging
- •3.2.2 Reconstruction of 3-D US Images
- •3.2.3 Viewing of 3-D US Images
- •3.3 Measurement of Plaque Volume
- •3.3.1 Plaque Segmentation by Manual Planimetry
- •3.3.8 Local Distribution and Change of Carotid Wall and Plaque
- •3.3.8.1 Reconstructing Surfaces from Polygonal Slices
- •3.3.8.2 3-D Maps of Average and Standard Deviation Carotid Surfaces
- •3.3.2 Studies of Plaque Volume
- •3.3.3 The Effects of Interslice Distance
- •3.3.4 The Accuracy of Plaque Volume Measurements
- •3.3.5 Variability of Plaque Volume Measurements
- •3.3.6 Automated Segmentation of Plaques from 3-D US Images
- •3.3.7 Plaque Surface Morphology
- •3.3.8.3 Vessel Wall Plus Plaque Thickness Map and Its Standard Deviation
- •3.3.8.4 3-D Maps of Carotid Wall Plus Plaque Thickness Change
- •3.3.9 Example Results
- •3.4 Trends and Future Developments
- •3.4.1 The Need for Improved Free-Hand Scanning
- •3.4.2 The Need for Improved Visualization Tools
- •3.4.3 Reduction in the Variability of Plaque Volume Measurement
- •3.4.4 ECG-Triggered Acquisition of 3-D Carotid US Images
- •Acknowledgments
- •References
- •4.1 Introduction
- •4.2 Methodology
- •4.2.1 Ultrasound Imaging Scanners
- •4.2.2 Material
- •4.2.3 Speckle Reduction
- •4.2.4 Image Normalization
- •4.2.5 Statistical and Texture Analysis
- •4.2.5.2 Spatial Gray-Level Dependence Matrix—Range of Values (SGLDM)
- •4.3 Image Quality and Evaluation Metrics
- •4.3.1 Normalized Mean-Square-Error
- •4.3.2 Normalized Root Mean-Square-Error
- •4.3.3 Normalized Error Summation in the Form of the Minkowski Metric
- •4.3.4 Normalized Geometric Average Error
- •4.3.5 Normalized Signal-to-Noise Ratio
- •4.3.6 Normalized Peak Signal-to-Noise Radio
- •4.3.7 Mathematically Defined Universal Quality Index
- •4.3.8 Structural Similarity Index
- •4.4 Visual Perception Evaluation
- •4.5 Results
- •4.6 Discussion
- •Acknowledgments
- •References
- •5.1 Ultrasound Imaging of the Carotid Wall
- •5.1.1 Carotid Artery Anatomy and Pathology
- •5.1.2 Principles and Validity of Ultrasound Analysis of the Carotid Artery
- •5.1.2.1 Normal Carotid Wall
- •5.1.2.2 Ultrasound Analysis of Plaques
- •5.2.1 Different Approaches for ROI Extraction
- •5.2.2 Approaches to Image Segmentation
- •5.3 Structure of the CULEX Algorithm
- •5.3.1 ROI Extraction
- •5.3.2 Segmentation of the Lumen and Carotid Wall
- •5.3.3 Notes About the CULEX Segmentation Strategy
- •5.4 CULEX Characterization and Image Databases
- •5.4.1 Percent Statistics Algorithm
- •5.4.2 Confidence Interval for the Average Segmentation
- •5.4.3 Segmentation Error
- •5.4.4 Image Database and Ultrasound Equipment
- •5.5 ROI Detection and Robustness to Noise
- •5.6.1 Absolute Segmentation Errors and IMT Measurements
- •5.6.2 Percent Statistics
- •5.6.3 Confidence Interval for the Mean Segmentation
- •5.7 Plaque Imaging
- •5.7.1 Stable Plaques
- •5.7.2 Unstable Plaques (Echolucent Type II)
- •5.8 Discussion and Conclusions
- •References
- •6.1 Introduction
- •6.2 Level Set Segmentation Method
- •6.2.1 Basic Level Set Theory
- •6.2.2 Summary of Level Set Theory
- •6.3 Proposed Architecture for the CAD System
- •6.3.1 Data Acquisition
- •6.3.2 Preprocessing Subsystem Architecture
- •6.3.2.1 Anisotropic Diffusion Filtering
- •6.3.2.2 Image Enhancement Via Sigmoid Mapping
- •6.3.3 Segmentation Subsystem Based on the Level Set Framework
- •6.3.4 Beam Angle Statistics
- •6.3.5 Similarity Between Shapes: A Classification Strategy
- •6.3.5.1 Best-Fit Ellipse Computation
- •6.3.5.2 Similarity Measurement Between a True Lesion and a Fitted Lesion
- •6.4 Experimental Protocol, Data Analysis, and Performance Evaluation
- •6.4.1 Similarity Measure Analysis
- •6.4.2 Performance Evaluation
- •6.5 Discussion
- •6.5.1 Discussion About the Dual Level Set
- •6.5.2 Discussion About the Similarity Measure
- •6.5.3 Discussion About Threshold Selection
- •6.6 Conclusion and Future Works
- •References
- •7.1 Introduction
- •7.2 Review of the 2-D Continuous Strain Imaging System
- •7.3 Proposed Architecture of the 3-D Strain Imaging System
- •7.3.1 Data Acquisition
- •7.3.2 Image Enhancement Via Sigmoid Mapping
- •7.3.3 Segmentation Subsystem Based on the Level Set Framework
- •7.3.3.1 Basic Theory of the Level Set
- •7.3.3.2 3-D Strain Imaging and Segmentation
- •7.3.4.1 Normalized Volume Difference
- •7.3.4.2 Normalized Shape Difference
- •7.3.4.3 Normalized Contour Difference
- •7.3.4.4 Shift Distance
- •7.4 Experimental Protocol, Data Analysis, and Results
- •7.4.1 2-D and 3-D Experimental Protocols
- •7.4.2 Segmentation Results
- •7.4.3 Classification Strategy Using ROC Curves and SVM
- •7.4.4 Figure of Merit for 2-D Versus 3-D: Performance Evaluation
- •7.5 Discussions
- •7.5.1 Discussion About the Level Set Framework
- •7.5.2 Discussion About Strain Features
- •7.5.3 Discussion About 3-D Versus 2-D Strain Methods
- •7.6 Conclusion
- •References
- •8.1 Introduction
- •8.2 Related Works
- •8.2.1 Breast Cancer Diagnosis with Autocorrelation Matrix
- •8.2.2 Solid Breast Nodules with Neural Networks
- •8.3 Theoretical Background
- •8.3.1 Tsallis Entropy
- •8.3.2 The Nonextensive Segmentation Approaches
- •8.3.2.1 Nonextensive Segmentation Algorithm for Image Binarization
- •8.3.2.2 The Nonextensive Segmentation Recursive Algorithm
- •8.3.2.3 The Level Set Formulation
- •8.3.2.4 The Support Vector Machine Theory
- •8.3.3 Morphological Chains: Mathematical Morphology Definitions
- •8.4 The Proposed Five-Step Methodology
- •8.5 Performance Evaluation
- •8.6 Discussion and Conclusions
- •Acknowledgments
- •References
- •9.1 Real-Time 3-D Echocardiography
- •9.2 Anisotropic Diffusion
- •9.3.1 Correlation-Based Optical Flow
- •9.3.2 3-D Ultrasound Datasets
- •9.3.3 Surface Tracing
- •9.3.4 Surface Tracking with Optical Flow
- •9.3.5 Evaluation
- •9.3.6 Results
- •9.3.6.1 Dog Data
- •9.3.6.2 Clinical Data
- •9.4 Dynamic Cardiac Information from Optical Flow
- •9.4.1 Coordinate Systems
- •9.4.2 Dynamic Cardiac Information Measurements
- •9.4.3 Data
- •9.4.4 Results and Discussion
- •9.4.5 Discussion About Estimation of the Myocardial Field
- •9.5 Summary
- •Acknowledgments
- •References
- •10.1 Introduction
- •10.1.1 Left Ventricular Systolic Dysfunction
- •10.1.2 Determinants of LV Systolic Performance
- •10.2 Assessment of Left Ventricular Function—An Overview
- •10.2.1 Ejection Phase Indices
- •10.2.1.1 Ejection Fraction and Fractional Shortening
- •10.2.1.2 Myocardial Performance Index
- •10.2.2 Isovolumetric Indices
- •10.2.3 Pressure-Volume Analysis
- •10.2.3.1 End Systolic Pressure-Volume Relationships (ESPVR)
- •10.2.3.2 Stroke Work
- •10.2.3.3 Preload Recruitable Stroke Work
- •10.2.4 Left Ventricular Stress Strain Relationship
- •10.3 Echocardiographic Examinations
- •10.3.1 Echocardiographic Measurements and Calculations
- •10.3.1.1 Echocardiographic Measurement of Left Ventricular Volume
- •10.3.1.2 Left Ventricular dp/dt
- •10.3.1.3 Left Ventricular End-Systolic Wall Stress
- •10.3.1.4 Left Ventricular Forward Stroke Volume and Cardiac Output
- •10.3.1.5 Mitral Regurgitant Volume
- •10.3.1.6 Wall Motion Index
- •10.3.1.7 Mitral Annulus Motion
- •10.3.2 Real-Time Left Ventricular Volume by Automated Boundary Detection
- •10.4 Left Ventricle Systolic Dysfunction Identification
- •10.4.1 Delineation of Left Ventricle
- •10.4.2 Quantification of Systolic Dysfunction
- •10.4.3 Region of Dysfunction Identification
- •10.4.3.1 Centerline Method
- •10.4.3.2 Color Kinesis Method
- •10.4.3.3 Anatomic M-Mode
- •10.4.3.4 Radial Line Method
- •10.4.3.5 Regional Area Method
- •10.5 Real-Time 3-D Echocardiography
- •10.5.1 Sparse Array Transducer
- •10.5.2 Full Matrix Array
- •10.5.3 Real-Time Volume Rendered 3-D Imaging
- •References
- •11.1 Introduction
- •11.2 Origin of Heart Sounds
- •11.2.1 Auscultatory Areas
- •11.2.2 Rate and Rhythm
- •11.2.3 Normal Heart Sounds
- •11.2.3.1 First Heart Sound (S1)
- •11.2.3.2 Second Heart Sound (S2)
- •11.2.3.3 Third Heart Sound (S3)
- •11.2.3.4 Fourth Heart Sound (S4)
- •11.2.4 Abnormal Heart Sounds
- •11.2.4.1 Abnormal S1
- •11.2.4.2 Abnormal S2
- •11.2.5 Murmur Classifications
- •11.2.5.1 Murmur Mechanisms
- •11.2.7 Gallop Sounds
- •11.2.8 Clicks
- •11.2.9 Opening Snaps
- •11.2.9.1 Tricuspid Valve Opening Snap
- •11.2.9.2 Mitral Valve Opening Snap
- •11.2.9.3 Differential Diagnosis of MVOS Versus S3 Gallop
- •11.2.9.4 Differential Diagnosis of MVOS Versus Splitting of S2
- •11.2.10 Maneuvers
- •11.3 Phonocardiograph
- •11.3.2 Amplifier
- •11.3.1 Instrument Description
- •11.3.1.1 Transducer
- •11.3.3 Filter
- •11.3.4 Analysis
- •11.3.5 Segmentation of S1 and S2
- •11.3.5.1 Blind Source Separation
- •11.3.5.2 Complexity-Based Gating
- •11.3.6 Decomposition of PCG
- •11.3.7 Short-Term Fourier Transform
- •11.3.8 Continuous Wavelet Transform
- •11.3.8.1 Resolution
- •11.3.9 Wigner Distribution
- •11.3.10 The Choi-Williams Distribution
- •11.3.11 Autoregressive Modeling
- •11.3.12 Feature Extraction
- •11.3.13 Classification
- •11.3.13.1 Neural Networks
- •11.3.13.2 Fuzzy Systems
- •11.3.13.3 Wavelet Method
- •References
- •12.1 Level Set Method
- •12.1.1 Front Evolution
- •12.1.2 Boundary Value Formulation
- •12.1.3 Initial Value Formulation
- •12.1.4 Applications of Level Set Method
- •12.2 Active Contours in Level Set Framework
- •12.2.1 Front Evolving Geometric Models of Active Contours
- •12.2.2 Geodesic Active Contour Models
- •12.2.3 Tuning Geometric Active Contour with Regularizers
- •12.2.3.1 Clustering-Based Regularizers
- •12.2.3.2 Bayesian-Based Regularizers
- •12.2.3.3 Shape-Based Regularizers
- •12.2.3.4 Coupling-Surfaces Regularizers
- •12.2.4 Region-Based Active Contour Models
- •12.2.4.1 Mumford-Shah (MS) Function
- •12.2.4.2 The Level Set Approach to Solving the Mumford-Shah Function
- •12.3 Fully Automated 3-D Prostate Segmentation from Transrectal Ultrasound (TRUS) Images
- •12.3.1 3-D Shape Prior Extraction
- •12.3.2 Intensity Prior Extraction
- •12.3.3 Segmentation in Bayesian Interface
- •12.4 Evaluation of the System Performance
- •12.4.1 Transrectal Ultrasound Images
- •12.4.2 Validation Method
- •12.5 Results
- •12.6 Conclusions and Future Work
- •References
- •13.1 Introduction
- •13.2 Recent Developments in HIFU and Therapy Planning
- •13.2.1 HIFU Applications
- •13.2.2 HIFU Therapy Guidance
- •13.2.3 HIFU Transducers and Instrumentation
- •13.2.4 Theoretical and Experimental Study of the HIFU Mechanism
- •13.2.5 HIFU Dosimetry and Therapy Planning
- •13.3 Generalized Strategies for HIFU Therapy Planning
- •13.3.1 Overview of Generalized Strategy
- •13.3.2 Pretreatment Imaging
- •13.3.3 Defining the Target and Surrounding Tissues
- •13.3.4 Simulation of HIFU
- •13.3.5 Integration and Visualization
- •13.3.6 Planning of HIFU Delivery and Control
- •13.3.7 Overall Software Design and Integration of Tools
- •13.3.8 Validation and Clinical Use of the HIFU Therapy Planning System
- •13.4 Challenges and Work Ahead
- •Acknowledgments
- •References
- •14.1 Introduction to HIFU
- •14.2 Ultrasonic System and Various Measurement Systems
- •14.2.1 Attenuation Measurement
- •14.2.2 Ultrasonic System
- •14.2.3 Acoustical Monitoring of Cavitation
- •14.2.4 Software
- •14.2.5 Acoustical Field Measurement
- •14.2.6 In Vitro Experiments
- •14.2.7 In Vivo Experiments
- •14.3 Simulation Model
- •14.3.1 Estimation of Temperature
- •14.3.2 Estimation of Thermal Dose
- •14.3.3 Estimation of Lesion Size
- •14.3.4 Effect of Attenuation
- •14.4 Attenuation Measurement as a Function of Thermal Dose
- •14.4.1 Results of Attenuation Versus Thermal Dose
- •14.4.2 Simulation Results Using Variable Attenuation
- •14.5 Kidney Ablation
- •14.5.1 Results
- •14.6 Kidney Ablation Under MRI Guidance
- •14.6.1 HIFU Parameters
- •14.6.2 MRI Parameters
- •14.6.3 Results
- •14.7 Liver Ablation
- •14.7.1 HIFU Parameters
- •14.7.2 MRI Analysis
- •14.7.3 Results
- •14.8 Effect of Interfaces in HIFU Ablation
- •14.8.1 MRI Analysis
- •14.8.2 Results
- •References
- •15.1 Introduction
- •15.2 Thermal Ablation Mechanisms
- •15.2.1 Hyperthermia and Ablation
- •15.2.2 Cryoablation
- •15.2.3 Chemical Ablation
- •15.3 Therapeutic Modalities for Thermal Ablation
- •15.3.1 RF Ablation
- •15.3.2 Microwave Ablation
- •15.3.3 Laser Thermal Ablation
- •15.3.4 Focused Ultrasound-Based Ablation
- •15.4 Focal Ultrasound Surgery Robots—FUSBOTs
- •15.5 Concluding Remarks
- •References
- •About the Editors
- •List of Contributors
- •Index


PART IV
3-D Cardiac Ultrasound Imaging


CHAPTER 9
Cardiac Motion Analysis Based on Optical
Flow of Real-Time 3-D Ultrasound Data
Qi Duan, Elsa D. Angelini, Olivier Gerard, Kevin D. Costa, Jeffrey W. Holmes,
Shunichi Homma, and Andrew F. Laine
With relatively high frame rates and the ability to acquire volume datasets with a
stationary transducer, 3-D ultrasound systems based on matrix phased-array trans-
ducers provide valuable 3-D information, from which quantitative measures of car-
diac function can be extracted. Such analyses require segmentation and visual
tracking of the myocardial borders. Due to the large size of the volumetric datasets,
manual tracing of the endocardial border is tedious and impractical for clinical
applications. In addition, manual tracing usually requires slicing the 3-D dataset
into 2-D images, resulting in a loss of some of the spatial continuity and making
manual boundary detection more error prone. Therefore, the development of auto-
matic methods for tracking 3-D endocardial motion is essential.
In this study, we evaluate a 4-D optical flow motion tracking algorithm to
determine its ability to follow the left ventricular borders in 3-D ultrasound data
through time. The optical flow method was implemented using a 3-D correlation.
We tested the algorithm on an experimental open-chest dog dataset and a clinical
dataset, both of which were acquired with a Philips iE33 3-D ultrasound machine.
Initialized with left ventricular endocardial data points obtained from manual trac-
ing at end diastole, the algorithm automatically tracked these points frame by frame
through the whole cardiac cycle. A finite element surface was fitted through the data
points obtained by both optical flow tracking and manual tracing from an experi-
enced observer for quantitative comparison of the results. Parameterization of the
finite element surfaces was performed, and maps displaying relative differences
between the manual and semiautomatic methods were compared.
The results showed good consistency between manual tracing and optical flow
estimation on 73% of the entire surface with less than a 10% difference. In addi-
tion, the optical flow motion tracking algorithm greatly reduced the processing time
(about 94% reduction compared to human involvement per cardiac cycle) for ana-
lyzing cardiac function in 3-D ultrasound datasets. A displacement field was com-
puted from the optical flow output, and a framework for computation of dynamic
cardiac information was introduced. The method was applied to a clinical dataset
from a heart transplant patient, and dynamic measurements agreed with physio-
logic knowledge as well as experimental results.
227

9.1 Real-Time 3-D Echocardiography
Developments in 3-D echocardiography started in the late 1980s with the introduc-
tion of off-line 3-D medical ultrasound imaging systems. The evolution of 3-D ultra-
sound acquisition systems can be divided into three generations: free-hand scanning,
mechanical scanning, and matrix phased arrays. Many review articles have been
published during the past decade that assessed the progress and limitations of 3-D
ultrasound technology for clinical screening [1–10].
Development of real-time 3-D (RT 3-D) echocardiography started in the late
1990s by Volumetrics [11] based on matrix phased-array transducers. Recently, a
new generation of RT 3-D transducers was introduced by Philips Medical Systems
(Best, the Netherlands) with the SONOS 7500 transducer followed by the iE33,
which can acquire a fully sampled cardiac volume in four cardiac cycles. This techni-
cal design enabled a dramatic increase in spatial resolutionand image quality, which
makes such 3-D ultrasound techniques increasingly attractive for daily cardiac clini-
cal diagnoses. Because RT 3-D ultrasound acquires volumetric ultrasound
sequences with fairly high temporal resolution and a stationary transducer, it can
capture the complex 3-D cardiac motion very well.
Advantages of using 3-D ultrasound in cardiology include the possibility to dis-
play a 3-D dynamic view of the beating heart, and the ability for the cardiologist to
explore the 3-D anatomy at arbitrary angles to localize abnormal structures and
assess wall motion. During the past decade, this technology has been shown to pro-
vide more accurate and reproduciblescreening forquantification ofcardiac function
for two main reasons: the elimination of assumptions about ventricular geometry
and the improved selection of the visualization planes for performing the ventricular
volume measurements. It was validated through several clinical studies for quantifi-
cation of left ventricle (LV) function as reviewed in [12]. Nevertheless, full exploita-
tion of 3-D ultrasound data for qualitative and quantitative evaluation of cardiac
function remains suboptimal for two reasons: lack of appropriate display and lack
of automatic boundary detection. Manual tracing of myocardial borders is a tedious
task that requires the intervention of an expert cardiologist familiar with the ultra-
sound machine. Also, slicing the 3-D dataset into 2-D images results in a loss of
some of the spatial continuity and makes manual boundary detection more error
prone. For this reason, ventricular volumes are commonly estimated via visual
inspection of 2-D B-scan images or semiautomated segmentation for difficult cases.
Existing commercialized semiautomatic segmentation programs include TomTec
(TomTec, Germany) and QLAB (Philips, the Netherlands).
9.2 Anisotropic Diffusion
The presence of speckle noise patterns makes the interpretation of ultrasound
images, either by a human operator or with a computer-based system, very difficult.
It is highly desirable for certain applications, such as automatic segmentation, to
apply some denoising prior to scan conversion in order to remove speckle noise arti-
facts and improve signal homogeneity within distinct anatomic tissues.
228 Cardiac Motion Analysis Based on Optical Flow of Real-Time 3-D Ultrasound Data

A number of methods have been proposed to denoise and improve the ultra-
sound image quality including temporal averaging, median filtering, maximum
amplitude writing (temporal dilation), adaptive speckle reduction (ASR) (statistical
enhancement) [13–17], adaptive weighted median filter (AWMF) [18], homomor-
phic Wiener filtering, and wavelet shrinkage (WS) [19, 20]. Most of these methods
suffer from insufficient denoising, image quality degradation, or high computa-
tional costs. Furthermore, some of them require raw RF data, available prior to
logarithmic compression [21].
Our group has presented previous work on applying brushlet denoising in
spherical coordinates to RT 3-D cardiac ultrasound [22]. Experiments on phantom
and clinical cardiac datasets have shown excellent performance for the method.
However, the main limitation of this type of denoising remains the computational
costs, which currently prevent its implementation for real-time visualization appli-
cations in clinical practice.
In this context, in [23], we investigated the performance of a more
computationally efficient denoising filter based on anisotropic diffusion for data
represented in spherical coordinates. A similar framework can be found in the work
of Abd-Elmoniem et al. [21, 24] who used 2-D anisotropic filtering in radial coordi-
nates. Anisotropic diffusion methods are very efficient for speckle reduction in
ultrasound and radar images. Yu and Acton [25, 26] applied their speckle reducing
filter to syntheticaperture radar images and compared their performance to Lee and
Kuan filters and to Frost filters. These filters are all derived from anisotropic diffu-
sion. Finally, Montagnat et al. [27] applied a 3-D anisotropic diffusion filter for
rotational cardiac 3-D ultrasound data.
Anisotropic diffusion methods apply the following heat diffusion type of
dynamic equation to the gray levels of a given 3-D image data I(x, y, z, t):
()
()
∂
∂
I
t
cxyzt I=∇div ,,,
(9.1)
where c(x, y, z, t) is the diffusion parameter, div denotes the divergence operator,
and ∇I denotes the gradient of the image intensity. In the original work of Perona
and Malik [28, 29], the concept of anisotropic diffusion was introduced with the
selection of a variable diffusion parameter, as a function ofthe gradientof the data:
()()
()
c xyzt g I xyzt,,, ,,,=∇
(9.2)
We used the diffusionfunction proposed by Weickert[30], defined as follows:
()
(
)
gx
x
ex
x
,
.
λ
λ
=
≤
−>
⎧
⎨
⎪
⎩
⎪
10
10
3315
4
(9.3)
The parameter λ serves as a gradient threshold, defining edge points x
k
as loca-
tions where
∇>I
x
k
λ
. This bell-shaped diffusion function acts as an edge-enhancing
filter, with high diffusion values in smooth areas and low values at edge points. The
9.2 Anisotropic Diffusion 229

structure of the diffusion tensor with separate weights for each dimension enables it
to control the direction ofthe diffusionprocess, with flowsparallel toedge contours.
In the case of ultrasound, as the diffusion process evolves, image data properties
change dramatically, and it is desirable to modify the gradient threshold parameter
value. In their paper, Montagnat et al. [27] reported a decrease in the value of signif-
icant edges as the homogeneous regions in the ultrasound data are filtered. There-
fore, they chose to decrease the threshold gradient in time and proposed values
based on a fraction of the cumulative histograms of the data gradients recomputed
at each iteration of the diffusion process. In our case, we used a linear model in [23]
where:
()
λλtat=+
0
(9.4)
with λ
0
as the initial gradient value, a is a slope parameter, and t is the time iteration
index. Parameters were set empirically for the datasets processed. Specifically, in
[23], we chose an increasing threshold in order to smooth out sampling artifacts and
remove speckle noise.
Filtering performance was assessed in terms of visual quality and for quantita-
tive measurements on a phantom object in [23]. Our quantitative study showed that
very high measurement accuracy could be achieved, but required suitable parameter
settings for the scan conversion method, whereas the visual quality was similar for
all interpolation kernels.
9.3 Tracking of LV Endocardial Surface on Real-Time 3-D Ultrasound
with Optical Flow
Clinical evaluation of 3-D ultrasound data for assessment of cardiac function is per-
formed via interactive inspection of animated data, along selected projection planes.
Facing the difficulty of inspecting a 3-D dataset with 2-D visualization tools, it is
highly desirable to assist the cardiologist with quantitative tools for analysis of 3-D
ventricular function. Complex and abnormal ventricular wall motion, for example,
can be detected,at a high frame rate, via quantitative 4-D analysis of the endocardial
surface and computation of local fractional shortening [31]. Such preliminary stud-
ies showed that RT 3-D ultrasound provides unique and valuable quantitative infor-
mation about cardiac motion, when derived from manually traced endocardial
contours. Recent software tools provide interactive segmentation capabilities for the
endocardium using a 3-D deformable model that alleviates the need for full manual
tracing of the endocardial border. To assist the segmentation process over the entire
cardiac cycle, we evaluated the use of optical flow (OF) tracking between segmented
frames and tried to answer the following questions in [32]: Can OF track the
endocardial surface between end diastole (ED) and end systole (ES) with reliable
positioning accuracy? How does dynamic information derived from OF tracking on
RT 3-D ultrasound compare to the manual tracing method, given the high
intervariability andintravariability of segmentation by experts? Can OF be used as a
dynamic interpolation tool for tracking the endocardial surface?
Cardiac motion analysis from images has been an active research area during
the past decade. However, most research efforts were based on CT and MRI data.
230 Cardiac Motion Analysis Based on Optical Flow of Real-Time 3-D Ultrasound Data

Previous efforts using ultrasound data for motion analysis include intensity-based
OF tracking, strain imaging, and elastography. Intensity-based OF tracking meth-
ods described in [33–38] combine a local intensity correlation with specific regular-
izing constraints (e.g., continuity). For strain imaging or elastography, strain
calculation and motion estimation are typically derived from autocorrelations and
cross-correlations of RF data. The commercialized strain imaging package 2-D
Strain from General Electric [39] uses such a paradigm. Most published papers on
strain imaging or elastography [39–43] are limited to 1-D or 2-D images. Early
studies [44] used simple simulated phantoms, whereas recent research [45] used a
3-D ultrasound data sequence for LV volume estimation. The presence of speckle
noise in ultrasound prevents the use of gradient-based methods, although relatively
large region-matching methods are reasonably robust to the presence of noise. In
this study, we propose a surface tracking technique based on a 4-D correlation-
based OF method on 3-D volumetric ultrasound intensity data.
9.3.1 Correlation-Based Optical Flow
Optical flow tracking refers to the computation of the displacement field of objects
in an image, based on the assumption that the intensity of the object remains con-
stant. In this context, motion of the object is characterized by a flow of pixels with
constant intensity. The assumption of intensity conservation is typically unrealistic
for natural movies and medical imaging applications, motivating the argument that
OF can only provide qualitative estimation of object motions. There are two global
families of OF computation techniques: (1) differential techniques [46–48] that
compute velocity from spatiotemporal derivatives of pixel intensities, and (2)
region-based matching techniques [49, 50], which compute OF via identification of
local displacements that provide optimal homogeneity measurements between two
consecutive image frames. Compared to differential OF approaches, region-based
methods using homogeneity measures are less sensitive to noisy conditions and fast
motion [51] but assume that displacements in small neighborhoods are similar. For
3-D ultrasound, this latter approach appeared more appropriate and was selected
for this study. Given two datasets from consecutive time frames, (I(x, t), I(x, t +Δt)),
the displacement vector Δx for each pixel in a small neighborhood Ω around a pixel
x is estimated via maximization of the cross-correlation coefficient, which is defined
as:
()( )
()
() ( )
r
ItI t t
ItI tt
=
++
++
∈
∈∈
∑
∑∑
xxx
xxx
x
xx
,,
,,
ΔΔ
ΔΔ
Ω
ΩΩ
22
(9.5)
In [32], correlation-based OF was applied to estimate the displacement of
selected voxels between two consecutive ultrasound volumes in the cardiac cycle.
The search window Ω was centered about every (5 × 5 ×5) pixel volume and was set
to size (7 × 7 × 7). To increase the robustness of the estimation, the final estimation
of the displacement for each point is the average within a 6-connected neighbor-
hood (i.e., considering, for each voxel, the elements connected in the 3-D space).
9.3 Tracking of LV Endocardial Surface on Real-Time 3-D Ultrasound with Optical Flow 231

9.3.2 3-D Ultrasound Datasets
The tracking approach was tested on three datasets acquired with the SONOS 7500
3-D ultrasound machine mentioned earlier:
1. Two datasets on an anesthetized open-chest dog were acquired before
(baseline) and 2 minutes after induction of ischemia via occlusion of the
proximal left anterior descending coronary artery. These datasets were
obtained by positioning the transducer directly on the apex of the heart,
providing high image quality and a small field of view. Spatial resolution of
the analyzed data was 0.56 mm
3
, and 16 frames were acquired per cardiac
cycle.
2. One transthoracic clinical dataset was acquired from a heart transplant
patient. Spatial resolution of the analyzed data was 0.8 mm
3
, and 16 frames
were acquired for one cardiac cycle. Because of the smaller field of view used
to acquire the open-chest dog data and the positioning of the transducer
directly on the dog’s heart, image quality was significantly higher in this
dataset, with some fine anatomic structures visible. Cross-sectional views at
ED from the open-chest baseline dataset and the patient dataset are shown in
Figure 9.1.
9.3.3 Surface Tracing
The endocardial surface of the LV was extracted with two methods. (1) An expert
performed manual tracing of all time frames in the datasets, on rotating B-scan
views (long-axis views rotating around the central axis of the ventricle) and C-scan
views (short-axis views at different depths). (2) QLAB software was used to segment
the endocardial surface. Initialization was performed by a human expert, and a
parametric deformable model was fit to the data at each time frame. Segmentation
results were reviewed by the same expert and adjusted manually for final correc-
232 Cardiac Motion Analysis Based on Optical Flow of Real-Time 3-D Ultrasound Data
(a) (b)
(d) (e) (f)
(c)
Figure 9.1 Cross-sectional views at ED for (a–c) open-chest dog data, prior to ischemia, and (d–f)
patient with transplanted heart; (a, d) axial, (b, e) elevation, and (c, f) azimuth views.

tions. We emphasize here that QLAB is used as a semiautomated segmentation tool.
The QLAB software was designed to process human clinical datasets. Because sig-
nificant anatomic differences between canine and human hearts could lead to mis-
behavior of the segmentation software, we decided to apply the software tool only
to clinical datasets.
9.3.4 Surface Tracking with Optical Flow
Tracking of the endocardial surface with OF was applied after initialization using
the manually traced surfaces (for the dog data and clinical data) and the QLAB seg-
mented surfaces (for the clinical data). Starting with a set of endocardial surface
points (about 3,000 points, roughly 1 mm apart for manual tracing, and about 800
points, roughly 3 mm apart for QLAB) defined at ED, the OF algorithm was used to
track the surface in time through the whole cardiac cycle. Because the correlation-
based OF method is very sensitive to speckle noise, all datasets were presmoothed
with edge-preserving anisotropic diffusion as developed in [23] and described in
Section 9.2. We emphasize here that OF was not applied as a segmentation tool but
as a surface tracking tool for a given segmentation method.
9.3.5 Evaluation
We evaluated OF tracking performance via visualization and quantification of
dynamic ventricular geometry compared to segmented surfaces. Usually compari-
son of segmentation results is performed via global measurements such as volume
difference or MSE. To provide local comparisons, we proposed a novel comparison
method in [52] based on a parameterization of the endocardial surface in prolate
spheroidal coordinates [53] and previously used for comparison of ventricular
geometries from two 3-D ultrasound machines in [54].
The endocardial surfaces were registered using three manually selected ana-
tomic landmarks: the center of the mitral orifice, the endocardial apex, and the
equatorial midseptum. The data were fitted in prolate spheroidal coordinates (λ, μ,
θ), projecting the radial coordinate λ to a 64-element surface mesh with bicubic
Hermite interpolation, yielding a realistic 3-D endocardial surface. The fitting pro-
cess (illustrated in Figure 9.2 for a single endocardial surface) was performed using
custom routines written in MATLAB. In this figure, we can observe the initial posi-
tioning of the data points and the surface mesh, and the finite element surface after
fitting with very high agreement between the data and the mesh. The inset provided
for a small region shows the quality of agreement between the fitted surface and the
points resulting from region-based global optimization of radial projections.
The fitted nodal values and spatial derivatives of the radial coordinate, λ, were
then used to map relative differences between two surfaces, ε = (λ
seg
− λ
OF
), using cus-
tom software. Hammer mapping was used to flatten the endocardial surface via an
area-preserving mapping [55]. For each time frame, the RMSE of the difference in λ
summed over all nodes on the endocardial surface, were computed between OF and
individual segmentation methods. Ventricular volumes were also computed from
the segmented and the tracked endocardial surfaces. Finally relative λ difference
maps were generated for ES, providing a direct quantitative comparison of ventricu
-
9.3 Tracking of LV Endocardial Surface on Real-Time 3-D Ultrasound with Optical Flow 233
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