Hybrid imaging techniques utilize couplings of physical modalities -they are called hybrid, because, typically, the excitation and measurement quantities belong to different modalities. Recently there has been an enormous research interest in this area because these methods promise very high resolution. In this paper we give a review on hybrid tomography methods for electrical conductivity imaging. The reviewed imaging methods utilize couplings between electric, magnetic and ultrasound modalities. By this it is possible to perform high-resolution electrical impedance imaging and to overcome the low-resolution problem of electric impedance tomography.
The goal of quantitative elastography is to identify biomechanical parameters from interior displacement data, which are provided by other modalities, such as ultrasound or magnetic resonance imaging. In this paper, we analyze the stability of several linearized problems in quantitative elastography. Our method is based on the theory of redundant systems of linear partial differential equations. We analyze the ellipticity properties of the corresponding PDE systems augmented with the interior displacement data; we explicitly characterize the kernel of the forward operators and show injectivity for particular linearizations. Stability criteria can then be deduced. Our results show stability of shear modulus, pressure and density; they indicate that singular strain fields should be avoided, and show how additional measurements can help in ensuring stability.
Elastographic imaging is a widely used technique which can in principle be implemented on top of every imaging modality. In elastography, the specimen is exposed to a force causing local displacements in the probe, and imaging is performed before and during the displacement experiment. From the computed displacements material parameters can be deduced, which in turn can be used for clinical diagnosis. Photoacoustic imaging is an emerging image modality, which exhibits functional and morphological contrast. However, opposed to ultrasound imaging, for instance, it is considered a modality which is not suited for elastography, because it does not reveal speckle patterns. However, this is somehow counter-intuitive, because photoacoustic imaging makes available the whole frequency spectrum as opposed to single frequency standard ultrasound imaging. In this work, we show that in fact artificial speckle patterns can be introduced by using only a band-limited part of the measurement data. We also show that after introduction of artificial speckle patterns, deformation estimation can be implemented more reliably in photoacoustic imaging.
Cardiac motion estimation is an important diagnostic tool for detecting heart diseases and it has been explored with modalities such as MRI and conventional ultrasound (US) sequences. US cardiac motion estimation still presents challenges because of complex motion patterns and the presence of noise. In this work, we propose a novel approach to estimate cardiac motion using ultrafast ultrasound data. Our solution is based on a variational formulation characterized by the L -regularized class. Displacement is represented by a lattice of b-splines and we ensure robustness, in the sense of eliminating outliers, by applying a maximum likelihood type estimator. While this is an important part of our solution, the main object of this work is to combine low-rank data representation with topology preservation. Low-rank data representation (achieved by finding the k-dominant singular values of a Casorati matrix arranged from the data sequence) speeds up the global solution and achieves noise reduction. On the other hand, topology preservation (achieved by monitoring the Jacobian determinant) allows one to radically rule out distortions while carefully controlling the size of allowed expansions and contractions. Our variational approach is carried out on a realistic dataset as well as on a simulated one. We demonstrate how our proposed variational solution deals with complex deformations through careful numerical experiments. The low-rank constraint speeds up the convergence of the optimization problem while topology preservation ensures a more accurate displacement. Beyond cardiac motion estimation, our approach is promising for the analysis of other organs that exhibit motion.
Electropermeabilization is a clinical technique in cancer treatment to locally stimulate the cell metabolism. It is based on electrical fields that change the properties of the cell membrane. With that, cancer treatment can reach the cell more easily. Electropermeabilization occurs only with accurate dosage of the electrical field. For applications, a monitoring for the amount of electropermeabilization is needed. It is a first step to image the macroscopic electrical field during the process. Nevertheless, this is not complete, because electropermeabilization depends on critical individual properties of the cells such as their curvature. From the macroscopic field, one cannot directly infer that microscopic state. In this article, we study effective parameters in a homogenization model as the next step to monitor the microscopic properties in clinical practice. We start from a physiological cell model for electropermeabilization and analyze its well-posedness. For a dynamical homogenization scheme, we prove convergence and then analyze the effective parameters, which can be found by macroscopic imaging methods. We demonstrate numerically the sensitivity of these effective parameters to critical microscopic parameters governing electropermeabilization. This opens the door to solve the inverse problem of rreconstructing these parameters.Mathematics Subject Classification (MSC2000): 35B30, 35R30.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.