752 research outputs found

    Magnetic resonance multitasking for motion-resolved quantitative cardiovascular imaging.

    Get PDF
    Quantitative cardiovascular magnetic resonance (CMR) imaging can be used to characterize fibrosis, oedema, ischaemia, inflammation and other disease conditions. However, the need to reduce artefacts arising from body motion through a combination of electrocardiography (ECG) control, respiration control, and contrast-weighting selection makes CMR exams lengthy. Here, we show that physiological motions and other dynamic processes can be conceptualized as multiple time dimensions that can be resolved via low-rank tensor imaging, allowing for motion-resolved quantitative imaging with up to four time dimensions. This continuous-acquisition approach, which we name cardiovascular MR multitasking, captures - rather than avoids - motion, relaxation and other dynamics to efficiently perform quantitative CMR without the use of ECG triggering or breath holds. We demonstrate that CMR multitasking allows for T1 mapping, T1-T2 mapping and time-resolved T1 mapping of myocardial perfusion without ECG information and/or in free-breathing conditions. CMR multitasking may provide a foundation for the development of setup-free CMR imaging for the quantitative evaluation of cardiovascular health

    Multi-modality cardiac image computing: a survey

    Get PDF
    Multi-modality cardiac imaging plays a key role in the management of patients with cardiovascular diseases. It allows a combination of complementary anatomical, morphological and functional information, increases diagnosis accuracy, and improves the efficacy of cardiovascular interventions and clinical outcomes. Fully-automated processing and quantitative analysis of multi-modality cardiac images could have a direct impact on clinical research and evidence-based patient management. However, these require overcoming significant challenges including inter-modality misalignment and finding optimal methods to integrate information from different modalities. This paper aims to provide a comprehensive review of multi-modality imaging in cardiology, the computing methods, the validation strategies, the related clinical workflows and future perspectives. For the computing methodologies, we have a favored focus on the three tasks, i.e., registration, fusion and segmentation, which generally involve multi-modality imaging data, either combining information from different modalities or transferring information across modalities. The review highlights that multi-modality cardiac imaging data has the potential of wide applicability in the clinic, such as trans-aortic valve implantation guidance, myocardial viability assessment, and catheter ablation therapy and its patient selection. Nevertheless, many challenges remain unsolved, such as missing modality, modality selection, combination of imaging and non-imaging data, and uniform analysis and representation of different modalities. There is also work to do in defining how the well-developed techniques fit in clinical workflows and how much additional and relevant information they introduce. These problems are likely to continue to be an active field of research and the questions to be answered in the future

    Simulating Developmental Cardiac Morphology in Virtual Reality Using a Deformable Image Registration Approach

    Get PDF
    While virtual reality (VR) has potential in enhancing cardiovascular diagnosis and treatment, prerequisite labor-intensive image segmentation remains an obstacle for seamlessly simulating 4-dimensional (4-D, 3-D + time) imaging data in an immersive, physiological VR environment. We applied deformable image registration (DIR) in conjunction with 3-D reconstruction and VR implementation to recapitulate developmental cardiac contractile function from light-sheet fluorescence microscopy (LSFM). This method addressed inconsistencies that would arise from independent segmentations of time-dependent data, thereby enabling the creation of a VR environment that fluently simulates cardiac morphological changes. By analyzing myocardial deformation at high spatiotemporal resolution, we interfaced quantitative computations with 4-D VR. We demonstrated that our LSFM-captured images, followed by DIR, yielded average dice similarity coefficients of 0.92 ± 0.05 (n = 510) and 0.93 ± 0.06 (n = 240) when compared to ground truth images obtained from Otsu thresholding and manual segmentation, respectively. The resulting VR environment simulates a wide-angle zoomed-in view of motion in live embryonic zebrafish hearts, in which the cardiac chambers are undergoing structural deformation throughout the cardiac cycle. Thus, this technique allows for an interactive micro-scale VR visualization of developmental cardiac morphology to enable high resolution simulation for both basic and clinical science

    Accelerated Cardiac Diffusion Tensor Imaging Using Joint Low-Rank and Sparsity Constraints

    Full text link
    Objective: The purpose of this manuscript is to accelerate cardiac diffusion tensor imaging (CDTI) by integrating low-rankness and compressed sensing. Methods: Diffusion-weighted images exhibit both transform sparsity and low-rankness. These properties can jointly be exploited to accelerate CDTI, especially when a phase map is applied to correct for the phase inconsistency across diffusion directions, thereby enhancing low-rankness. The proposed method is evaluated both ex vivo and in vivo, and is compared to methods using either a low-rank or sparsity constraint alone. Results: Compared to using a low-rank or sparsity constraint alone, the proposed method preserves more accurate helix angle features, the transmural continuum across the myocardium wall, and mean diffusivity at higher acceleration, while yielding significantly lower bias and higher intraclass correlation coefficient. Conclusion: Low-rankness and compressed sensing together facilitate acceleration for both ex vivo and in vivo CDTI, improving reconstruction accuracy compared to employing either constraint alone. Significance: Compared to previous methods for accelerating CDTI, the proposed method has the potential to reach higher acceleration while preserving myofiber architecture features which may allow more spatial coverage, higher spatial resolution and shorter temporal footprint in the future.Comment: 11 pages, 16 figures, published on IEEE Transactions on Biomedical Engineerin

    Towards enabling cardiac digital twins of myocardial infarction using deep computational models for inverse inference

    Get PDF
    Cardiac digital twins (CDTs) have the potential to offer individualized evaluation of cardiac function in a non-invasive manner, making them a promising approach for personalized diagnosis and treatment planning of myocardial infarction (MI). The inference of accurate myocardial tissue properties is crucial in creating a reliable CDT of MI. In this work, we investigate the feasibility of inferring myocardial tissue properties from the electrocardiogram (ECG) within a CDT platform. The platform integrates multi-modal data, such as cardiac MRI and ECG, to enhance the accuracy and reliability of the inferred tissue properties. We perform a sensitivity analysis based on computer simulations, systematically exploring the effects of infarct location, size, degree of transmurality, and electrical activity alteration on the simulated QRS complex of ECG, to establish the limits of the approach. We subsequently present a novel deep computational model, comprising a dual-branch variational autoencoder and an inference model, to infer infarct location and distribution from the simulated QRS. The proposed model achieves mean Dice scores of 0.457 ± 0.317 and 0.302 ± 0.273 for the inference of left ventricle scars and border zone, respectively. The sensitivity analysis enhances our understanding of the complex relationship between infarct characteristics and electrophysiological features. The in silico experimental results show that the model can effectively capture the relationship for the inverse inference, with promising potential for clinical application in the future. The code is available at https: //github.com/lileitech/MI_inverse_inference

    Generative Interpretation of Medical Images

    Get PDF

    Review of Journal of Cardiovascular Magnetic Resonance 2014

    Get PDF
    There were 102 articles published in the Journal of Cardiovascular Magnetic Resonance (JCMR) in 2014, which is a 6 % decrease on the 109 articles published in 2013. The quality of the submissions continues to increase. The 2013 JCMR Impact Factor (which is published in June 2014) fell to 4.72 from 5.11 for 2012 (as published in June 2013). The 2013 impact factor means that the JCMR papers that were published in 2011 and 2012 were cited on average 4.72 times in 2013. The impact factor undergoes natural variation according to citation rates of papers in the 2 years following publication, and is significantly influenced by highly cited papers such as official reports. However, the progress of the journal’s impact over the last 5 years has been impressive. Our acceptance rate is <25 % and has been falling because the number of articles being submitted has been increasing. In accordance with Open-Access publishing, the JCMR articles go on-line as they are accepted with no collating of the articles into sections or special thematic issues. For this reason, the Editors have felt that it is useful once per calendar year to summarize the papers for the readership into broad areas of interest or theme, so that areas of interest can be reviewed in a single article in relation to each other and other recent JCMR articles. The papers are presented in broad themes and set in context with related literature and previously published JCMR papers to guide continuity of thought in the journal. We hope that you find the open-access system increases wider reading and citation of your papers, and that you will continue to send your quality papers to JCMR for publication

    Identification of weakly coupled multiphysics problems. Application to the inverse problem of electrocardiography

    Get PDF
    This work addresses the inverse problem of electrocardiography from a new perspective, by combining electrical and mechanical measurements. Our strategy relies on the defini-tion of a model of the electromechanical contraction which is registered on ECG data but also on measured mechanical displacements of the heart tissue typically extracted from medical images. In this respect, we establish in this work the convergence of a sequential estimator which combines for such coupled problems various state of the art sequential data assimilation methods in a unified consistent and efficient framework. Indeed we ag-gregate a Luenberger observer for the mechanical state and a Reduced Order Unscented Kalman Filter applied on the parameters to be identified and a POD projection of the electrical state. Then using synthetic data we show the benefits of our approach for the estimation of the electrical state of the ventricles along the heart beat compared with more classical strategies which only consider an electrophysiological model with ECG measurements. Our numerical results actually show that the mechanical measurements improve the identifiability of the electrical problem allowing to reconstruct the electrical state of the coupled system more precisely. Therefore, this work is intended to be a first proof of concept, with theoretical justifications and numerical investigations, of the ad-vantage of using available multi-modal observations for the estimation and identification of an electromechanical model of the heart

    Steady-state anatomical and quantitative magnetic resonance imaging of the heart using RF-frequencymodulated techniques

    Get PDF
    Cardiovascular disease (CVD) is the leading cause of death in the United States and Europe and generates healthcare costs of hundreds of billions of dollars annually. Conventional methods of diagnosing CVD are often invasive and carry risks for the patient. For example, the gold standard for diagnosing coronary artery disease, a major class of CVD, is x-ray coronary angiography, which has the disadvantages of being invasive, being expensive, using ionizing radiation, and having a ris k of complications. Conversely, coronary MR angiography (MRA) does not use ionizing radiation, can effectively visualize tissues without the need for exogenous contrast agents, and benefits from an adaptable temporal resolution. However, the acquisition time of cardiac MRI is far longer than the temporal scales of cardiac and respiratory motion, necessitating some method of compensating for this motion. The free-running framework is a novel development in our lab, benefitting from advances over the past three decades, that attempts to address disadvantages of previous cardiac MRI approaches: it provides fully self-gated 5D cardiac MRI with a simplified workflow, improved ease-of-use, reduced operator dependence, and automatic patient-specific motion detection. Free-running imaging increases the amount of information available to the clinician and is flexible enough to be translated to different app lications within cardiac MRI. Moreover, the self-gating of the free-running framework decoupled the acquisition from the motion compensation and thereby opened up cardiac MRI to the wider class of steady-state-based techniques utilizing balanced steady-state free precession (bSSFP) sequences, which have the benefits of practical simplicity and high signal-to-noise ratio. The focus of this thesis was therefore on the application of steady- state techniques to cardiac MRI. The first part addressed the long acquisition time of the current free-running framework and focused on anatomical coronary imaging. The published protocol of the free- running framework used an interrupted bSSFP acquisition where CHESS fat saturation modules were inserted to provide blood-fat contrast, as they suppress the signal of fat tissue surrounding the coronary arteries, and were followed by ramp-up pulses to reduce artefacts arising from the return to steady-state. This interrupted acquisition, however, suffered from an interrupted steady-state, reduced time efficiency, and higher specific absorption rate (SAR). Using novel lipid-insensitive binomial off-resonant RF excitation (LIBRE) pulses developed in our lab, the first project showed that LIBRE pulses incorporated into an uninterrupted free-running bSSFP sequence could be successfully used for 5D cardiac MRI at 1.5T. The free-running LIBRE approach reduced the acquisition time and SAR relative to the previous interrupted approach while maintaining image quality and vessel conspicuity. Furthermore, this had been the first successful use of a fat-suppressing RF excitation pulse in an uninterrupted bSSFP sequence for cardiac imaging, demonstrating that uninterrupted bSSFP can be used for cardiac MRI and addressing the problem of clinical sequence availability. Inspired by the feasibility of uninterrupted bSSFP for cardiac MRI, the second part investigated the potential of PLANET, a novel 3D multiparametric mapping technique, for free-running 5D myocardial mapping. PLANET utilizes a phase-cycled bSSFP acquisition and a direct ellipse-fitting algorithm to calculate T1 and T2 relaxation times, which suggested that it could be readily integrated into the free-running framework without interrupting the steady-state. After initially calibrating the acquisition, the possibility of accelerating the static PLANET acquisition was explored prior to applying it to the moving heart. It was shown that PLANET accuracy and precision could be maintained with two-fold acceleration with a 3D Cartesian spiral trajectory, suggesting that PLANET for myocardial mapping with the free-running 5D radial acquisition is feasible. Further work should investigate optimizing the reconstruction scheme, improving the coil sensitivity estimate, and examining the use of the radial trajectory with a view to implementing free-running 5D myocardial T1 and T2 mapping. This thesis presents two approaches utilizing RF-frequency-modulated steady-state techniques for cardiac MRI. The first approach involved the novel application of an uninterrupted bSSFP acquisition with off-resonant RF excitation for anatomical coronary imaging. The second approach investigated the use of phase-cycled bSSFP for free-running 5D myocardial T1 and T2 mapping. Both methods addressed the challenge of clinical availability of sequences in cardiac MRI, by showing that a common and simple sequence like bSSFP can be used for acquisition while the steps of motion compensation and reconstruction can be handled offline, and thus have the potential to improve adoption of cardiac MRI. -- Les maladies cardiovasculaires (MCV) reprĂ©sentent la principale cause de dĂ©cĂšs aux États-Unis et en Europe et gĂ©nĂšrent des coĂ»ts de santĂ© de plusieurs centaines de milliards de dollars par an. Les mĂ©thodes conventionnelles de diagnostic des MCV sont souvent invasives et comportent des risques pour le patient. Par exemple, la mĂ©thode de rĂ©fĂ©rence pour le diagnostic de la maladie coronarienne, une catĂ©gorie majeure de MCV, est la coronarographie par rayons X qui a comme inconvĂ©nients son caractĂšre invasif, son coĂ»t, l’utilisation de rayonnements ionisants et le risque de complications. A l’inverse, l'angiographie coronarienne par rĂ©sonance magnĂ©tique (ARM) n'utilise pas de rayonnements ionisants, permet de visualiser efficacement les tissus sans avoir recours Ă  des agents de contraste exogĂšnes et bĂ©nĂ©ficie d'une rĂ©solution temporelle ajustable. Cependant, le temps d'acquisition en IRM cardiaque est bien plus long que les Ă©chelles temporelles des mouvements cardiaques et respiratoires en jeu, ce qui rend la compensation de ces mouvements indispensable. Le cadre dit de « free -running » est un nouveau dĂ©veloppement de notre laboratoire qui bĂ©nĂ©ficie des progrĂšs rĂ©alisĂ©s au cours des trois derniĂšres dĂ©cennies et tente de remĂ©dier aux inconvĂ©nients des approches prĂ©cĂ©dentes pour l'IRM cardiaque : il fournit une IRM cardiaque en cinq dimensions (5D) complĂštement « self-gated » , c’est-Ă -dire capable de dĂ©tecter les mouvements cardiaques et respiratoires, forte d’une implĂ©mentation simplifiĂ©e, d’une plus grande facilitĂ© d'utilisation, d’une dĂ©pendance rĂ©duite vis-Ă -vis de l'opĂ©rateur et d’une dĂ©tection automatique des mouvements spĂ©cifiques du patient. L'imagerie « free- running » augmente la quantitĂ© d'informations Ă  disposition du clinicien et est suffisamment flexible pour ĂȘtre appliquĂ©e Ă  diffĂ©rents domaines de l'IRM cardiaque. De plus, le « self-gating » du cadre « free-running » a dĂ©couplĂ© l'acquisition de la compensation de mouvement et a ainsi ouvert l'IRM cardiaque Ă  la classe plus large des techniques basĂ©es sur l'Ă©tat stationnaire utilisant des sĂ©quences de prĂ©cession libre Ă©quilibrĂ©e en Ă©tat stationnaire (bSSFP), qui se distinguent par leur simplicitĂ© d’utilisation et leur rapport signal sur bruit Ă©levĂ©. Le thĂšme de cette thĂšse est donc l'application des techniques basĂ©es sur l'Ă©tat stationnaire Ă  l'IRM cardiaque. La premiĂšre partie porte sur le long temps d'acquisition de l'actuel cadre « free-running» et se concentre sur l'imagerie anatomique coronaire. Le protocole publiĂ© utilise une acquisition bSSFP interrompue oĂč des modules de saturation de graisse (CHESS) sont insĂ©rĂ©s de façon Ă  fournir un contraste sang-graisse puisqu’ils suppriment le signal du tissu graisseux entourant les artĂšres coronaires, et sont suivis par des impulsions en rampe pour rĂ©duire les artefacts rĂ©sultant du retour Ă  l'Ă©tat stable. Cette acquisition interrompue souffre cependant d'un Ă©tat d'Ă©quilibre interrompu, d'une efficacitĂ© temporelle rĂ©duite et d'un dĂ©bit d'absorption spĂ©cifique (DAS) plus Ă©levĂ©. En utilisant les nouvelles impulsions d'excitation radiofrĂ©quence (RF) binomiales hors -rĂ©sonance insensibles aux lipides (LIBRE) dĂ©veloppĂ©es dans notre laboratoi re, ce premier projet montre que les impulsions LIBRE incorporĂ©es dans une sĂ©quence bSSFP ininterrompue et « free-running » peuvent ĂȘtre utilisĂ©es avec succĂšs pour l'IRM cardiaque 5D Ă  1,5 T. L'approche « free-running LIBRE » permet de rĂ©duire le temps d'acquisition et le DAS par rapport Ă  l'approche interrompue prĂ©cĂ©dente, tout en maintenant la perceptibilitĂ© des artĂšres coronariennes. En outre, il s'agit de la premiĂšre utilisation rĂ©ussie d'une impulsion d'excitation RF supprimant la graisse dans une sĂ©quence bSSFP ininterrompue pour l'imagerie cardiaque, ce qui dĂ©montre le potentiel d’utilisation de la sĂ©quence bSSFP ininterrompue pour l'IRM cardiaque et rĂ©sout le problĂšme de la disponibilitĂ© de la sĂ©quence en clinique. InspirĂ©e par la faisabilitĂ© d’utilisation de la sĂ©quence bSSFP ininterrompue pour l'IRM cardiaque, la deuxiĂšme partie Ă©tudie le potentiel de PLANET, une nouvelle technique de cartographie 3D multiparamĂ©trique, pour la cartographie 5D du myocarde via l’imagerie « free-running ». PLANET utilise une acquisition bSSFP Ă  cycle de phase et un algorithme d'ajustement d'ellipse direct pour calculer les temps de relaxation T1 et T2, ce qui suggĂšre que cette mĂ©thode pourrait ĂȘtre facilement intĂ©grĂ©e au cadre « free - running » sans interruption de l’état d'Ă©quilibre. AprĂšs calibration de l'acquisition, nous explorons la possibilitĂ© d'accĂ©lĂ©rer l'acquisition statique de PLANET pour l'appliquer au cƓur. Nous dĂ©montrons que l'exactitude et la prĂ©cision de PLANET peuvent ĂȘtre maintenues pour une accĂ©lĂ©ration double avec une trajectoire 3D cartĂ©sienne en spirale, ce qui suggĂšre que PLANET est rĂ©alisable pour la cartographie du myocarde avec une acquisition radiale 5D « free-running ». D'autres travaux devraient porter sur l'optimisation du schĂ©ma de reconstruction, l'amĂ©lioration de l'estimation de la sensibilitĂ© de l’antenne et l'examen de l'utilisation de la trajectoire radiale en vue de la mise en Ɠuvre de la cartographie 5D « free-running » T1 et T2 du myocarde. Cette thĂšse prĂ©sente deux approches utilisant des techniques de modulation de frĂ©quence radio en Ă©tat stationnaire pour l'IRM cardiaque. La premiĂšre approche implique l'application nouvelle d'une acquisition bSSFP ininterrompue avec une excitation RF hors rĂ©sonance pour l'imagerie anatomique coronaire. La seconde approche porte sur l'utilisation d’une sĂ©quence bSSFP Ă  cycle de phase pour la cartographie 5D T1 et T2 du myocarde. Ces deux mĂ©thodes permettent de rĂ©pondre au dĂ©fi posĂ© par la disponibilitĂ© des sĂ©quences en IRM cardiaque en montrant qu'une sĂ©quence commune et simple comme la bSSFP peut ĂȘtre utilisĂ©e pour l'acquisition, tandis que les Ă©tapes de compensation du mouvement et de reconstruction peuvent ĂȘtre traitĂ©es hors ligne. Ainsi, ces mĂ©thodes ont le potentiel de favoriser l'adoption de l'IRM cardiaque
    • 

    corecore