254 research outputs found
Computerized Analysis of Magnetic Resonance Images to Study Cerebral Anatomy in Developing Neonates
The study of cerebral anatomy in developing neonates is of great importance for
the understanding of brain development during the early period of life. This
dissertation therefore focuses on three challenges in the modelling of cerebral
anatomy in neonates during brain development. The methods that have been
developed all use Magnetic Resonance Images (MRI) as source data.
To facilitate study of vascular development in the neonatal period, a set of image
analysis algorithms are developed to automatically extract and model cerebral
vessel trees. The whole process consists of cerebral vessel tracking from
automatically placed seed points, vessel tree generation, and vasculature
registration and matching. These algorithms have been tested on clinical Time-of-
Flight (TOF) MR angiographic datasets.
To facilitate study of the neonatal cortex a complete cerebral cortex segmentation
and reconstruction pipeline has been developed. Segmentation of the neonatal
cortex is not effectively done by existing algorithms designed for the adult brain
because the contrast between grey and white matter is reversed. This causes pixels
containing tissue mixtures to be incorrectly labelled by conventional methods. The
neonatal cortical segmentation method that has been developed is based on a novel
expectation-maximization (EM) method with explicit correction for mislabelled
partial volume voxels. Based on the resulting cortical segmentation, an implicit
surface evolution technique is adopted for the reconstruction of the cortex in
neonates. The performance of the method is investigated by performing a detailed
landmark study.
To facilitate study of cortical development, a cortical surface registration algorithm
for aligning the cortical surface is developed. The method first inflates extracted
cortical surfaces and then performs a non-rigid surface registration using free-form
deformations (FFDs) to remove residual alignment. Validation experiments using
data labelled by an expert observer demonstrate that the method can capture local
changes and follow the growth of specific sulcus
A comparative evaluation for liver segmentation from spir images and a novel level set method using signed pressure force function
Thesis (Doctoral)--Izmir Institute of Technology, Electronics and Communication Engineering, Izmir, 2013Includes bibliographical references (leaves: 118-135)Text in English; Abstract: Turkish and Englishxv, 145 leavesDeveloping a robust method for liver segmentation from magnetic resonance images is a challenging task due to similar intensity values between adjacent organs, geometrically complex liver structure and injection of contrast media, which causes all tissues to have different gray level values. Several artifacts of pulsation and motion, and partial volume effects also increase difficulties for automatic liver segmentation from magnetic resonance images. In this thesis, we present an overview about liver segmentation methods in magnetic resonance images and show comparative results of seven different liver segmentation approaches chosen from deterministic (K-means based), probabilistic (Gaussian model based), supervised neural network (multilayer perceptron based) and deformable model based (level set) segmentation methods. The results of qualitative and quantitative analysis using sensitivity, specificity and accuracy metrics show that the multilayer perceptron based approach and a level set based approach which uses a distance regularization term and signed pressure force function are reasonable methods for liver segmentation from spectral pre-saturation inversion recovery images. However, the multilayer perceptron based segmentation method requires a higher computational cost. The distance regularization term based automatic level set method is very sensitive to chosen variance of Gaussian function. Our proposed level set based method that uses a novel signed pressure force function, which can control the direction and velocity of the evolving active contour, is faster and solves several problems of other applied methods such as sensitivity to initial contour or variance parameter of the Gaussian kernel in edge stopping functions without using any regularization term
Cardiac T-2* mapping:Techniques and clinical applications
Cardiac T-2* mapping is a noninvasive MRI method that is used to identify myocardial iron accumulation in several iron storage diseases such as hereditary hemochromatosis, sickle cell disease, and beta-thalassemia major. The method has improved over the years in terms of MR acquisition, focus on relative artifact-free myocardium regions, and T-2* quantification. Several improvement factors involved include blood pool signal suppression, the reproducibility of T-2* measurement as affected by scanner hardware, and acquisition software. Regarding the T-2* quantification, improvement factors include the applied curve-fitting method with or without truncation of the signals acquired at longer echo times and whether or not T-2* measurement focuses on multiple segmental regions or the midventricular septum only. Although already widely applied in clinical practice, data processing still differs between centers, contributing to measurement outcome variations. State of the art T-2* measurement involves pixelwise quantification providing better spatial iron loading information than region of interest-based quantification. Improvements have been proposed, such as on MR acquisition for free-breathing mapping, the generation of fast mapping, noise reduction, automatic myocardial contour delineation, and different T-2* quantification methods. This review deals with the pro and cons of different methods used to quantify T-2* and generate T-2* maps. The purpose is to recommend a combination of MR acquisition and T-2* mapping quantification techniques for reliable outcomes in measuring and follow-up of myocardial iron overload. The clinical application of cardiac T-2* mapping for iron overload's early detection, monitoring, and treatment is addressed. The prospects of T-2* mapping combined with different MR acquisition methods, such as cardiac T-1 mapping, are also described. Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2019
Computational Methods for Segmentation of Multi-Modal Multi-Dimensional Cardiac Images
Segmentation of the heart structures helps compute the cardiac contractile function quantified via the systolic and diastolic volumes, ejection fraction, and myocardial mass, representing a reliable diagnostic value. Similarly, quantification of the myocardial mechanics throughout the cardiac cycle, analysis of the activation patterns in the heart via electrocardiography (ECG) signals, serve as good cardiac diagnosis indicators. Furthermore, high quality anatomical models of the heart can be used in planning and guidance of minimally invasive interventions under the assistance of image guidance.
The most crucial step for the above mentioned applications is to segment the ventricles and myocardium from the acquired cardiac image data. Although the manual delineation of the heart structures is deemed as the gold-standard approach, it requires significant time and effort, and is highly susceptible to inter- and intra-observer variability. These limitations suggest a need for fast, robust, and accurate semi- or fully-automatic segmentation algorithms. However, the complex motion and anatomy of the heart, indistinct borders due to blood flow, the presence of trabeculations, intensity inhomogeneity, and various other imaging artifacts, makes the segmentation task challenging.
In this work, we present and evaluate segmentation algorithms for multi-modal, multi-dimensional cardiac image datasets. Firstly, we segment the left ventricle (LV) blood-pool from a tri-plane 2D+time trans-esophageal (TEE) ultrasound acquisition using local phase based filtering and graph-cut technique, propagate the segmentation throughout the cardiac cycle using non-rigid registration-based motion extraction, and reconstruct the 3D LV geometry. Secondly, we segment the LV blood-pool and myocardium from an open-source 4D cardiac cine Magnetic Resonance Imaging (MRI) dataset by incorporating average atlas based shape constraint into the graph-cut framework and iterative segmentation refinement. The developed fast and robust framework is further extended to perform right ventricle (RV) blood-pool segmentation from a different open-source 4D cardiac cine MRI dataset. Next, we employ convolutional neural network based multi-task learning framework to segment the myocardium and regress its area, simultaneously, and show that segmentation based computation of the myocardial area is significantly better than that regressed directly from the network, while also being more interpretable. Finally, we impose a weak shape constraint via multi-task learning framework in a fully convolutional network and show improved segmentation performance for LV, RV and myocardium across healthy and pathological cases, as well as, in the challenging apical and basal slices in two open-source 4D cardiac cine MRI datasets.
We demonstrate the accuracy and robustness of the proposed segmentation methods by comparing the obtained results against the provided gold-standard manual segmentations, as well as with other competing segmentation methods
An Adaptive Algorithm to Identify Ambiguous Prostate Capsule Boundary Lines for Three-Dimensional Reconstruction and Quantitation
Currently there are few parameters that are used to compare the efficiency of different methods of cancerous prostate surgical removal. An accurate assessment of the percentage and depth of extra-capsular soft tissue removed with the prostate by the various surgical techniques can help surgeons determine the appropriateness of surgical approaches. Additionally, an objective assessment can allow a particular surgeon to compare individual performance against a standard. In order to facilitate 3D reconstruction and objective analysis and thus provide more accurate quantitation results when analyzing specimens, it is essential to automatically identify the capsule line that separates the prostate gland tissue from its extra-capsular tissue. However the prostate capsule is sometimes unrecognizable due to the naturally occurring intrusion of muscle and connective tissue into the prostate gland. At these regions where the capsule disappears, its contour can be arbitrarily reconstructed by drawing a continuing contour line based on the natural shape of the prostate gland. Presented here is a mathematical model that can be used in deciding the missing part of the capsule. This model approximates the missing parts of the capsule where it disappears to a standard shape by using a Generalized Hough Transform (GHT) approach to detect the prostate capsule. We also present an algorithm based on a least squares curve fitting technique that uses a prostate shape equation to merge previously detected capsule parts with the curve equation to produce an approximated curve that represents the prostate capsule. We have tested our algorithms using three shapes on 13 prostate slices that are cut at different locations from the apex and the results are promisin
Analysis of contrast-enhanced medical images.
Early detection of human organ diseases is of great importance for the accurate diagnosis and institution of appropriate therapies. This can potentially prevent progression to end-stage disease by detecting precursors that evaluate organ functionality. In addition, it also assists the clinicians for therapy evaluation, tracking diseases progression, and surgery operations. Advances in functional and contrast-enhanced (CE) medical images enabled accurate noninvasive evaluation of organ functionality due to their ability to provide superior anatomical and functional information about the tissue-of-interest. The main objective of this dissertation is to develop a computer-aided diagnostic (CAD) system for analyzing complex data from CE magnetic resonance imaging (MRI). The developed CAD system has been tested in three case studies: (i) early detection of acute renal transplant rejection, (ii) evaluation of myocardial perfusion in patients with ischemic heart disease after heart attack; and (iii), early detection of prostate cancer. However, developing a noninvasive CAD system for the analysis of CE medical images is subject to multiple challenges, including, but are not limited to, image noise and inhomogeneity, nonlinear signal intensity changes of the images over the time course of data acquisition, appearances and shape changes (deformations) of the organ-of-interest during data acquisition, determination of the best features (indexes) that describe the perfusion of a contrast agent (CA) into the tissue. To address these challenges, this dissertation focuses on building new mathematical models and learning techniques that facilitate accurate analysis of CAs perfusion in living organs and include: (i) accurate mathematical models for the segmentation of the object-of-interest, which integrate object shape and appearance features in terms of pixel/voxel-wise image intensities and their spatial interactions; (ii) motion correction techniques that combine both global and local models, which exploit geometric features, rather than image intensities to avoid problems associated with nonlinear intensity variations of the CE images; (iii) fusion of multiple features using the genetic algorithm. The proposed techniques have been integrated into CAD systems that have been tested in, but not limited to, three clinical studies. First, a noninvasive CAD system is proposed for the early and accurate diagnosis of acute renal transplant rejection using dynamic contrast-enhanced MRI (DCE-MRI). Acute rejectionâthe immunological response of the human immune system to a foreign kidneyâis the most sever cause of renal dysfunction among other diagnostic possibilities, including acute tubular necrosis and immune drug toxicity. In the U.S., approximately 17,736 renal transplants are performed annually, and given the limited number of donors, transplanted kidney salvage is an important medical concern. Thus far, biopsy remains the gold standard for the assessment of renal transplant dysfunction, but only as the last resort because of its invasive nature, high cost, and potential morbidity rates. The diagnostic results of the proposed CAD system, based on the analysis of 50 independent in-vivo cases were 96% with a 95% confidence interval. These results clearly demonstrate the promise of the proposed image-based diagnostic CAD system as a supplement to the current technologies, such as nuclear imaging and ultrasonography, to determine the type of kidney dysfunction. Second, a comprehensive CAD system is developed for the characterization of myocardial perfusion and clinical status in heart failure and novel myoregeneration therapy using cardiac first-pass MRI (FP-MRI). Heart failure is considered the most important cause of morbidity and mortality in cardiovascular disease, which affects approximately 6 million U.S. patients annually. Ischemic heart disease is considered the most common underlying cause of heart failure. Therefore, the detection of the heart failure in its earliest forms is essential to prevent its relentless progression to premature death. While current medical studies focus on detecting pathological tissue and assessing contractile function of the diseased heart, this dissertation address the key issue of the effects of the myoregeneration therapy on the associated blood nutrient supply. Quantitative and qualitative assessment in a cohort of 24 perfusion data sets demonstrated the ability of the proposed framework to reveal regional perfusion improvements with therapy, and transmural perfusion differences across the myocardial wall; thus, it can aid in follow-up on treatment for patients undergoing the myoregeneration therapy. Finally, an image-based CAD system for early detection of prostate cancer using DCE-MRI is introduced. Prostate cancer is the most frequently diagnosed malignancy among men and remains the second leading cause of cancer-related death in the USA with more than 238,000 new cases and a mortality rate of about 30,000 in 2013. Therefore, early diagnosis of prostate cancer can improve the effectiveness of treatment and increase the patientâs chance of survival. Currently, needle biopsy is the gold standard for the diagnosis of prostate cancer. However, it is an invasive procedure with high costs and potential morbidity rates. Additionally, it has a higher possibility of producing false positive diagnosis due to relatively small needle biopsy samples. Application of the proposed CAD yield promising results in a cohort of 30 patients that would, in the near future, represent a supplement of the current technologies to determine prostate cancer type. The developed techniques have been compared to the state-of-the-art methods and demonstrated higher accuracy as shown in this dissertation. The proposed models (higher-order spatial interaction models, shape models, motion correction models, and perfusion analysis models) can be used in many of todayâs CAD applications for early detection of a variety of diseases and medical conditions, and are expected to notably amplify the accuracy of CAD decisions based on the automated analysis of CE images
Coronary Artery Segmentation and Motion Modelling
Conventional coronary artery bypass surgery requires invasive sternotomy and the
use of a cardiopulmonary bypass, which leads to long recovery period and has high
infectious potential. Totally endoscopic coronary artery bypass (TECAB) surgery
based on image guided robotic surgical approaches have been developed to allow the
clinicians to conduct the bypass surgery off-pump with only three pin holes incisions
in the chest cavity, through which two robotic arms and one stereo endoscopic camera
are inserted. However, the restricted field of view of the stereo endoscopic images leads
to possible vessel misidentification and coronary artery mis-localization. This results
in 20-30% conversion rates from TECAB surgery to the conventional approach.
We have constructed patient-specific 3D + time coronary artery and left ventricle
motion models from preoperative 4D Computed Tomography Angiography (CTA)
scans. Through temporally and spatially aligning this model with the intraoperative
endoscopic views of the patient's beating heart, this work assists the surgeon to identify
and locate the correct coronaries during the TECAB precedures. Thus this work has
the prospect of reducing the conversion rate from TECAB to conventional coronary
bypass procedures.
This thesis mainly focus on designing segmentation and motion tracking methods
of the coronary arteries in order to build pre-operative patient-specific motion models.
Various vessel centreline extraction and lumen segmentation algorithms are presented,
including intensity based approaches, geometric model matching method and
morphology-based method. A probabilistic atlas of the coronary arteries is formed
from a group of subjects to facilitate the vascular segmentation and registration procedures.
Non-rigid registration framework based on a free-form deformation model
and multi-level multi-channel large deformation diffeomorphic metric mapping are
proposed to track the coronary motion. The methods are applied to 4D CTA images
acquired from various groups of patients and quantitatively evaluated
Development of registration methods for cardiovascular anatomy and function using advanced 3T MRI, 320-slice CT and PET imaging
Different medical imaging modalities provide complementary anatomical and
functional information. One increasingly important use of such information is in
the clinical management of cardiovascular disease. Multi-modality data is helping
improve diagnosis accuracy, and individualize treatment. The Clinical Research
Imaging Centre at the University of Edinburgh, has been involved in a number
of cardiovascular clinical trials using longitudinal computed tomography (CT) and
multi-parametric magnetic resonance (MR) imaging. The critical image processing
technique that combines the information from all these different datasets is known
as image registration, which is the topic of this thesis. Image registration, especially
multi-modality and multi-parametric registration, remains a challenging field in
medical image analysis. The new registration methods described in this work were
all developed in response to genuine challenges in on-going clinical studies. These
methods have been evaluated using data from these studies.
In order to gain an insight into the building blocks of image registration methods,
the thesis begins with a comprehensive literature review of state-of-the-art algorithms.
This is followed by a description of the first registration method I developed to help
track inflammation in aortic abdominal aneurysms. It registers multi-modality and
multi-parametric images, with new contrast agents. The registration framework uses a
semi-automatically generated region of interest around the aorta. The aorta is aligned
based on a combination of the centres of the regions of interest and intensity matching.
The method achieved sub-voxel accuracy.
The second clinical study involved cardiac data. The first framework failed to
register many of these datasets, because the cardiac data suffers from a common
artefact of magnetic resonance images, namely intensity inhomogeneity. Thus I
developed a new preprocessing technique that is able to correct the artefacts in the
functional data using data from the anatomical scans. The registration framework,
with this preprocessing step and new particle swarm optimizer, achieved significantly
improved registration results on the cardiac data, and was validated quantitatively
using neuro images from a clinical study of neonates. Although on average
the new framework achieved accurate results, when processing data corrupted
by severe artefacts and noise, premature convergence of the optimizer is still a
common problem. To overcome this, I invented a new optimization method, that
achieves more robust convergence by encoding prior knowledge of registration. The
registration results from this new registration-oriented optimizer are more accurate
than other general-purpose particle swarm optimization methods commonly applied
to registration problems.
In summary, this thesis describes a series of novel developments to an image
registration framework, aimed to improve accuracy, robustness and speed. The
resulting registration framework was applied to, and validated by, different types of
images taken from several ongoing clinical trials. In the future, this framework could
be extended to include more diverse transformation models, aided by new machine
learning techniques. It may also be applied to the registration of other types and
modalities of imaging data
Automatic Spatiotemporal Analysis of Cardiac Image Series
RĂSUMĂ
Ă ce jour, les maladies cardiovasculaires demeurent au premier rang des principales causes de
dĂ©cĂšs en AmĂ©rique du Nord. Chez lâadulte et au sein de populations de plus en plus jeunes,
la soi-disant Ă©pidĂ©mie dâobĂ©sitĂ© entraĂźnĂ©e par certaines habitudes de vie tels que la mauvaise
alimentation, le manque dâexercice et le tabagisme est lourde de consĂ©quences pour les personnes
affectées, mais aussi sur le systÚme de santé. La principale cause de morbidité et de
mortalitĂ© chez ces patients est lâathĂ©rosclĂ©rose, une accumulation de plaque Ă lâintĂ©rieur des
vaisseaux sanguins à hautes pressions telles que les artÚres coronaires. Les lésions athérosclérotiques
peuvent entraĂźner lâischĂ©mie en bloquant la circulation sanguine et/ou en provoquant
une thrombose. Cela mĂšne souvent Ă de graves consĂ©quences telles quâun infarctus. Outre les
problÚmes liés à la sténose, les parois artérielles des régions criblées de plaque augmentent la
rigidité des parois vasculaires, ce qui peut aggraver la condition du patient. Dans la population
pédiatrique, la pathologie cardiovasculaire acquise la plus fréquente est la maladie de
Kawasaki. Il sâagit dâune vasculite aigĂŒe pouvant affecter lâintĂ©gritĂ© structurale des parois des
artĂšres coronaires et mener Ă la formation dâanĂ©vrismes. Dans certains cas, ceux-ci entravent
lâhĂ©modynamie artĂ©rielle en engendrant une perfusion myocardique insuffisante et en activant
la formation de thromboses.
Le diagnostic de ces deux maladies coronariennes sont traditionnellement effectuĂ©s Ă lâaide
dâangiographies par fluoroscopie. Pendant ces examens paracliniques, plusieurs centaines de
projections radiographiques sont acquises en sĂ©ries suite Ă lâinfusion artĂ©rielle dâun agent de
contraste. Ces images révÚlent la lumiÚre des vaisseaux sanguins et la présence de lésions
potentiellement pathologiques, sâil y a lieu. Parce que les sĂ©ries acquises contiennent de lâinformation
trĂšs dynamique en termes de mouvement du patient volontaire et involontaire (ex.
battements cardiaques, respiration et dĂ©placement dâorganes), le clinicien base gĂ©nĂ©ralement
son interprĂ©tation sur une seule image angiographique oĂč des mesures gĂ©omĂ©triques sont effectuĂ©es
manuellement ou semi-automatiquement par un technicien en radiologie. Bien que
lâangiographie par fluoroscopie soit frĂ©quemment utilisĂ© partout dans le monde et souvent
considĂ©rĂ© comme lâoutil de diagnostic âgold-standardâ pour de nombreuses maladies vasculaires,
la nature bidimensionnelle de cette modalitĂ© dâimagerie est malheureusement trĂšs
limitante en termes de spécification géométrique des différentes régions pathologiques. En effet,
la structure tridimensionnelle des stĂ©noses et des anĂ©vrismes ne peut pas ĂȘtre pleinement
appréciée en 2D car les caractéristiques observées varient selon la configuration angulaire de
lâimageur. De plus, la prĂ©sence de lĂ©sions affectant les artĂšres coronaires peut ne pas reflĂ©ter
la véritable santé du myocarde, car des mécanismes compensatoires naturels (ex. vaisseaux----------ABSTRACT
Cardiovascular disease continues to be the leading cause of death in North America. In adult
and, alarmingly, ever younger populations, the so-called obesity epidemic largely driven by
lifestyle factors that include poor diet, lack of exercise and smoking, incurs enormous stresses
on the healthcare system. The primary cause of serious morbidity and mortality for these
patients is atherosclerosis, the build up of plaque inside high pressure vessels like the coronary
arteries. These lesions can lead to ischemic disease and may progress to precarious blood
flow blockage or thrombosis, often with infarction or other severe consequences. Besides
the stenosis-related outcomes, the arterial walls of plaque-ridden regions manifest increased
stiffness, which may exacerbate negative patient prognosis. In pediatric populations, the
most prevalent acquired cardiovascular pathology is Kawasaki disease. This acute vasculitis
may affect the structural integrity of coronary artery walls and progress to aneurysmal lesions.
These can hinder the blood flowâs hemodynamics, leading to inadequate downstream
perfusion, and may activate thrombus formation which may lead to precarious prognosis.
Diagnosing these two prominent coronary artery diseases is traditionally performed using
fluoroscopic angiography. Several hundred serial x-ray projections are acquired during selective
arterial infusion of a radiodense contrast agent, which reveals the vesselsâ luminal
area and possible pathological lesions. The acquired series contain highly dynamic information
on voluntary and involuntary patient movement: respiration, organ displacement and
heartbeat, for example. Current clinical analysis is largely limited to a single angiographic
image where geometrical measures will be performed manually or semi-automatically by a
radiological technician. Although widely used around the world and generally considered
the gold-standard diagnosis tool for many vascular diseases, the two-dimensional nature of
this imaging modality is limiting in terms of specifying the geometry of various pathological
regions. Indeed, the 3D structures of stenotic or aneurysmal lesions may not be fully appreciated
in 2D because their observable features are dependent on the angular configuration of
the imaging gantry. Furthermore, the presence of lesions in the coronary arteries may not
reflect the true health of the myocardium, as natural compensatory mechanisms may obviate
the need for further intervention. In light of this, cardiac magnetic resonance perfusion
imaging is increasingly gaining attention and clinical implementation, as it offers a direct
assessment of myocardial tissue viability following infarction or suspected coronary artery
disease. This type of modality is plagued, however, by motion similar to that present in fluoroscopic
imaging. This issue predisposes clinicians to laborious manual intervention in order
to align anatomical structures in sequential perfusion frames, thus hindering automation o
Automatic Spatiotemporal Analysis of Cardiac Image Series
RĂSUMĂ
Ă ce jour, les maladies cardiovasculaires demeurent au premier rang des principales causes de
dĂ©cĂšs en AmĂ©rique du Nord. Chez lâadulte et au sein de populations de plus en plus jeunes,
la soi-disant Ă©pidĂ©mie dâobĂ©sitĂ© entraĂźnĂ©e par certaines habitudes de vie tels que la mauvaise
alimentation, le manque dâexercice et le tabagisme est lourde de consĂ©quences pour les personnes
affectées, mais aussi sur le systÚme de santé. La principale cause de morbidité et de
mortalitĂ© chez ces patients est lâathĂ©rosclĂ©rose, une accumulation de plaque Ă lâintĂ©rieur des
vaisseaux sanguins à hautes pressions telles que les artÚres coronaires. Les lésions athérosclérotiques
peuvent entraĂźner lâischĂ©mie en bloquant la circulation sanguine et/ou en provoquant
une thrombose. Cela mĂšne souvent Ă de graves consĂ©quences telles quâun infarctus. Outre les
problÚmes liés à la sténose, les parois artérielles des régions criblées de plaque augmentent la
rigidité des parois vasculaires, ce qui peut aggraver la condition du patient. Dans la population
pédiatrique, la pathologie cardiovasculaire acquise la plus fréquente est la maladie de
Kawasaki. Il sâagit dâune vasculite aigĂŒe pouvant affecter lâintĂ©gritĂ© structurale des parois des
artĂšres coronaires et mener Ă la formation dâanĂ©vrismes. Dans certains cas, ceux-ci entravent
lâhĂ©modynamie artĂ©rielle en engendrant une perfusion myocardique insuffisante et en activant
la formation de thromboses.
Le diagnostic de ces deux maladies coronariennes sont traditionnellement effectuĂ©s Ă lâaide
dâangiographies par fluoroscopie. Pendant ces examens paracliniques, plusieurs centaines de
projections radiographiques sont acquises en sĂ©ries suite Ă lâinfusion artĂ©rielle dâun agent de
contraste. Ces images révÚlent la lumiÚre des vaisseaux sanguins et la présence de lésions
potentiellement pathologiques, sâil y a lieu. Parce que les sĂ©ries acquises contiennent de lâinformation
trĂšs dynamique en termes de mouvement du patient volontaire et involontaire (ex.
battements cardiaques, respiration et dĂ©placement dâorganes), le clinicien base gĂ©nĂ©ralement
son interprĂ©tation sur une seule image angiographique oĂč des mesures gĂ©omĂ©triques sont effectuĂ©es
manuellement ou semi-automatiquement par un technicien en radiologie. Bien que
lâangiographie par fluoroscopie soit frĂ©quemment utilisĂ© partout dans le monde et souvent
considĂ©rĂ© comme lâoutil de diagnostic âgold-standardâ pour de nombreuses maladies vasculaires,
la nature bidimensionnelle de cette modalitĂ© dâimagerie est malheureusement trĂšs
limitante en termes de spécification géométrique des différentes régions pathologiques. En effet,
la structure tridimensionnelle des stĂ©noses et des anĂ©vrismes ne peut pas ĂȘtre pleinement
appréciée en 2D car les caractéristiques observées varient selon la configuration angulaire de
lâimageur. De plus, la prĂ©sence de lĂ©sions affectant les artĂšres coronaires peut ne pas reflĂ©ter
la véritable santé du myocarde, car des mécanismes compensatoires naturels (ex. vaisseaux----------ABSTRACT
Cardiovascular disease continues to be the leading cause of death in North America. In adult
and, alarmingly, ever younger populations, the so-called obesity epidemic largely driven by
lifestyle factors that include poor diet, lack of exercise and smoking, incurs enormous stresses
on the healthcare system. The primary cause of serious morbidity and mortality for these
patients is atherosclerosis, the build up of plaque inside high pressure vessels like the coronary
arteries. These lesions can lead to ischemic disease and may progress to precarious blood
flow blockage or thrombosis, often with infarction or other severe consequences. Besides
the stenosis-related outcomes, the arterial walls of plaque-ridden regions manifest increased
stiffness, which may exacerbate negative patient prognosis. In pediatric populations, the
most prevalent acquired cardiovascular pathology is Kawasaki disease. This acute vasculitis
may affect the structural integrity of coronary artery walls and progress to aneurysmal lesions.
These can hinder the blood flowâs hemodynamics, leading to inadequate downstream
perfusion, and may activate thrombus formation which may lead to precarious prognosis.
Diagnosing these two prominent coronary artery diseases is traditionally performed using
fluoroscopic angiography. Several hundred serial x-ray projections are acquired during selective
arterial infusion of a radiodense contrast agent, which reveals the vesselsâ luminal
area and possible pathological lesions. The acquired series contain highly dynamic information
on voluntary and involuntary patient movement: respiration, organ displacement and
heartbeat, for example. Current clinical analysis is largely limited to a single angiographic
image where geometrical measures will be performed manually or semi-automatically by a
radiological technician. Although widely used around the world and generally considered
the gold-standard diagnosis tool for many vascular diseases, the two-dimensional nature of
this imaging modality is limiting in terms of specifying the geometry of various pathological
regions. Indeed, the 3D structures of stenotic or aneurysmal lesions may not be fully appreciated
in 2D because their observable features are dependent on the angular configuration of
the imaging gantry. Furthermore, the presence of lesions in the coronary arteries may not
reflect the true health of the myocardium, as natural compensatory mechanisms may obviate
the need for further intervention. In light of this, cardiac magnetic resonance perfusion
imaging is increasingly gaining attention and clinical implementation, as it offers a direct
assessment of myocardial tissue viability following infarction or suspected coronary artery
disease. This type of modality is plagued, however, by motion similar to that present in fluoroscopic
imaging. This issue predisposes clinicians to laborious manual intervention in order
to align anatomical structures in sequential perfusion frames, thus hindering automation o
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