137 research outputs found
Image based approach for early assessment of heart failure.
In diagnosing heart diseases, the estimation of cardiac performance indices requires accurate segmentation of the left ventricle (LV) wall from cine cardiac magnetic resonance (CMR) images. MR imaging is noninvasive and generates clear images; however, it is impractical to manually process the huge number of images generated to calculate the performance indices. In this dissertation, we introduce a novel, fast, robust, bi-directional coupled parametric deformable models that are capable of segmenting the LV wall borders using first- and second-order visual appearance features. These features are embedded in a new stochastic external force that preserves the topology of the LV wall to track the evolution of the parametric deformable models control points. We tested the proposed segmentation approach on 15 data sets in 6 infarction patients using the Dice similarity coefficient (DSC) and the average distance (AD) between the ground truth and automated segmentation contours. Our approach achieves a mean DSC value of 0.926±0.022 and mean AD value of 2.16±0.60 mm compared to two other level set methods that achieve mean DSC values of 0.904±0.033 and 0.885±0.02; and mean AD values of 2.86±1.35 mm and 5.72±4.70 mm, respectively. Also, a novel framework for assessing both 3D functional strain and wall thickening from 4D cine cardiac magnetic resonance imaging (CCMR) is introduced. The introduced approach is primarily based on using geometrical features to track the LV wall during the cardiac cycle. The 4D tracking approach consists of the following two main steps: (i) Initially, the surface points on the LV wall are tracked by solving a 3D Laplace equation between two subsequent LV surfaces; and (ii) Secondly, the locations of the tracked LV surface points are iteratively adjusted through an energy minimization cost function using a generalized Gauss-Markov random field (GGMRF) image model in order to remove inconsistencies and preserve the anatomy of the heart wall during the tracking process. Then the circumferential strains are straight forward calculated from the location of the tracked LV surface points. In addition, myocardial wall thickening is estimated by co-allocation of the corresponding points, or matches between the endocardium and epicardium surfaces of the LV wall using the solution of the 3D laplace equation. Experimental results on in vivo data confirm the accuracy and robustness of our method. Moreover, the comparison results demonstrate that our approach outperforms 2D wall thickening estimation approaches
Physics-Informed Computer Vision: A Review and Perspectives
Incorporation of physical information in machine learning frameworks are
opening and transforming many application domains. Here the learning process is
augmented through the induction of fundamental knowledge and governing physical
laws. In this work we explore their utility for computer vision tasks in
interpreting and understanding visual data. We present a systematic literature
review of formulation and approaches to computer vision tasks guided by
physical laws. We begin by decomposing the popular computer vision pipeline
into a taxonomy of stages and investigate approaches to incorporate governing
physical equations in each stage. Existing approaches in each task are analyzed
with regard to what governing physical processes are modeled, formulated and
how they are incorporated, i.e. modify data (observation bias), modify networks
(inductive bias), and modify losses (learning bias). The taxonomy offers a
unified view of the application of the physics-informed capability,
highlighting where physics-informed learning has been conducted and where the
gaps and opportunities are. Finally, we highlight open problems and challenges
to inform future research. While still in its early days, the study of
physics-informed computer vision has the promise to develop better computer
vision models that can improve physical plausibility, accuracy, data efficiency
and generalization in increasingly realistic applications
Estimation of smooth growth trajectories with controlled acceleration from time series shape data
pre-printLongitudinal shape analysis often relies on the estimation of a realistic continuous growth scenario from data sparsely distributed in time. In this paper, we propose a new type of growth model para-meterized by acceleration, whereas standard methods typically control the velocity. This mimics the behavior of biological tissue as a mechanical system driven by external forces. The growth trajectories are estimated as smooth flows of deformations, which are twice differentiable. This differs from piecewise geodesic regression, for which the velocity may be discontinuous. We evaluate our approach on a set of anatomical structures of the same subject, scanned 16 times between 4 and 8 years of age. We show our acceleration based method estimates smooth growth, demonstrating improved regularity compared to piecewise geodesic regression. Leave-several-out experiments show that our method is robust to missing observations, as well as being less sensitive to noise, and is therefore more likely to capture the underlying biological growth
3D + t Morphological Processing: Applications to Embryogenesis Image Analysis
We propose to directly process 3D + t image sequences with mathematical morphology operators, using a new classi?cation of the 3D+t structuring elements. Several methods (?ltering, tracking, segmentation) dedicated to the analysis of 3D + t datasets of zebra?sh embryogenesis are introduced and validated through a synthetic dataset. Then, we illustrate the application of these methods to the analysis of datasets of zebra?sh early development acquired with various microscopy techniques. This processing paradigm produces spatio-temporal coherent results as it bene?ts from the intrinsic redundancy of the temporal dimension, and minimizes the needs for human intervention in semi-automatic algorithms
Foetal echocardiographic segmentation
Congenital heart disease affects just under one percentage of all live births [1].
Those defects that manifest themselves as changes to the cardiac chamber volumes
are the motivation for the research presented in this thesis.
Blood volume measurements in vivo require delineation of the cardiac chambers and
manual tracing of foetal cardiac chambers is very time consuming and operator
dependent. This thesis presents a multi region based level set snake deformable
model applied in both 2D and 3D which can automatically adapt to some extent
towards ultrasound noise such as attenuation, speckle and partial occlusion artefacts.
The algorithm presented is named Mumford Shah Sarti Collision Detection (MSSCD).
The level set methods presented in this thesis have an optional shape prior term for
constraining the segmentation by a template registered to the image in the presence
of shadowing and heavy noise.
When applied to real data in the absence of the template the MSSCD algorithm is
initialised from seed primitives placed at the centre of each cardiac chamber. The
voxel statistics inside the chamber is determined before evolution. The MSSCD stops
at open boundaries between two chambers as the two approaching level set fronts
meet. This has significance when determining volumes for all cardiac compartments
since cardiac indices assume that each chamber is treated in isolation. Comparison
of the segmentation results from the implemented snakes including a previous level
set method in the foetal cardiac literature show that in both 2D and 3D on both real
and synthetic data, the MSSCD formulation is better suited to these types of data.
All the algorithms tested in this thesis are within 2mm error to manually traced
segmentation of the foetal cardiac datasets. This corresponds to less than 10% of
the length of a foetal heart. In addition to comparison with manual tracings all the
amorphous deformable model segmentations in this thesis are validated using a
physical phantom. The volume estimation of the phantom by the MSSCD
segmentation is to within 13% of the physically determined volume
Computational Anatomy for Multi-Organ Analysis in Medical Imaging: A Review
The medical image analysis field has traditionally been focused on the
development of organ-, and disease-specific methods. Recently, the interest in
the development of more 20 comprehensive computational anatomical models has
grown, leading to the creation of multi-organ models. Multi-organ approaches,
unlike traditional organ-specific strategies, incorporate inter-organ relations
into the model, thus leading to a more accurate representation of the complex
human anatomy. Inter-organ relations are not only spatial, but also functional
and physiological. Over the years, the strategies 25 proposed to efficiently
model multi-organ structures have evolved from the simple global modeling, to
more sophisticated approaches such as sequential, hierarchical, or machine
learning-based models. In this paper, we present a review of the state of the
art on multi-organ analysis and associated computation anatomy methodology. The
manuscript follows a methodology-based classification of the different
techniques 30 available for the analysis of multi-organs and multi-anatomical
structures, from techniques using point distribution models to the most recent
deep learning-based approaches. With more than 300 papers included in this
review, we reflect on the trends and challenges of the field of computational
anatomy, the particularities of each anatomical region, and the potential of
multi-organ analysis to increase the impact of 35 medical imaging applications
on the future of healthcare.Comment: Paper under revie
Developing advanced mathematical models for detecting abnormalities in 2D/3D medical structures.
Detecting abnormalities in two-dimensional (2D) and three-dimensional (3D) medical structures is among the most interesting and challenging research areas in the medical imaging field. Obtaining the desired accurate automated quantification of abnormalities in medical structures is still very challenging. This is due to a large and constantly growing number of different objects of interest and associated abnormalities, large variations of their appearances and shapes in images, different medical imaging modalities, and associated changes of signal homogeneity and noise for each object. The main objective of this dissertation is to address these problems and to provide proper mathematical models and techniques that are capable of analyzing low and high resolution medical data and providing an accurate, automated analysis of the abnormalities in medical structures in terms of their area/volume, shape, and associated abnormal functionality. This dissertation presents different preliminary mathematical models and techniques that are applied in three case studies: (i) detecting abnormal tissue in the left ventricle (LV) wall of the heart from delayed contrast-enhanced cardiac magnetic resonance images (MRI), (ii) detecting local cardiac diseases based on estimating the functional strain metric from cardiac cine MRI, and (iii) identifying the abnormalities in the corpus callosum (CC) brain structure—the largest fiber bundle that connects the two hemispheres in the brain—for subjects that suffer from developmental brain disorders. For detecting the abnormal tissue in the heart, a graph-cut mathematical optimization model with a cost function that accounts for the object’s visual appearance and shape is used to segment the the inner cavity. The model is further integrated with a geometric model (i.e., a fast marching level set model) to segment the outer border of the myocardial wall (the LV). Then the abnormal tissue in the myocardium wall (also called dead tissue, pathological tissue, or infarct area) is identified based on a joint Markov-Gibbs random field (MGRF) model of the image and its region (segmentation) map that accounts for the pixel intensities and the spatial interactions between the pixels. Experiments with real in-vivo data and comparative results with ground truth (identified by a radiologist) and other approaches showed that the proposed framework can accurately detect the pathological tissue and can provide useful metrics for radiologists and clinicians. To estimate the strain from cardiac cine MRI, a novel method based on tracking the LV wall geometry is proposed. To achieve this goal, a partial differential equation (PDE) method is applied to track the LV wall points by solving the Laplace equation between the LV contours of each two successive image frames over the cardiac cycle. The main advantage of the proposed tracking method over traditional texture-based methods is its ability to track the movement and rotation of the LV wall based on tracking the geometric features of the inner, mid-, and outer walls of the LV. This overcomes noise sources that come from scanner and heart motion. To identify the abnormalities in the CC from brain MRI, the CCs are aligned using a rigid registration model and are segmented using a shape-appearance model. Then, they are mapped to a simple unified space for analysis. This work introduces a novel cylindrical mapping model, which is conformal (i.e., one to one transformation and bijective), that enables accurate 3D shape analysis of the CC in the cylindrical domain. The framework can detect abnormalities in all divisions of the CC (i.e., splenium, rostrum, genu and body). In addition, it offers a whole 3D analysis of the CC abnormalities instead of only area-based analysis as done by previous groups. The initial classification results based on the centerline length and CC thickness suggest that the proposed CC shape analysis is a promising supplement to the current techniques for diagnosing dyslexia. The proposed techniques in this dissertation have been successfully tested on complex synthetic and MR images and can be used to advantage in many of today’s clinical applications of computer-assisted medical diagnostics and intervention
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