ترغب بنشر مسار تعليمي؟ اضغط هنا

A Two-Parameter Model for Ultrasonic Tissue Characterization with Harmonic Imaging

102   0   0.0 ( 0 )
 نشر من قبل Nithin Nagaraj
 تاريخ النشر 2017
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Over the past few decades, researchers have developed several approaches such as the Reference Phantom Method (RPM) to estimate ultrasound attenuation coefficient (AC) and backscatter coefficient (BSC). AC and BSC can help to discriminate pathology from normal tissue during in-vivo imaging. In this paper, we propose a new RPM model to simultaneously compute AC and BSC for harmonic imaging and a normalized score that combines the two parameters as a measure of disease progression. The model utilizes the spectral difference between two regions of interest, the first, a proximal, close to the probe and second, a distal, away from the probe. We have implemented an algorithm based on the model and shown that it provides accurate and stable estimates to within 5% of AC and BSC for simulated received echo from post-focal depths of a homogeneous liver-like medium. For practical applications with time gain and time frequency compensated in-phase and quadrature (IQ) data from ultrasound scanner, the method has been approximated and generalized to estimate AC and BSC for tissue layer underlying a more attenuative subcutaneous layer. The angular spectrum approach for ultrasound propagation in biological tissue is employed as a virtual Reference Phantom (VRP). The VRP is calibrated with a fixed probe and scanning protocol for application to liver tissue. In a feasibility study with 16 subjects, the method is able to separate 9/11 cases of progressive non-alcoholic fatty liver disease from 5 normal. In particular, it is able to separate 4/5 cases of non-alcoholic steato-hepatitis and early fibrosis (F<=2) from normal tissue. More extensive clinical studies are needed to assess the full capability of this model for screening and monitoring disease progression in liver and other tissues.



قيم البحث

اقرأ أيضاً

Self-regulation of living tissue as an example of self-organization phenomena in hierarchical systems of biological, ecological, and social nature is under consideration. The characteristic feature of these systems is the absence of any governing cen ter and, thereby, their self-regulation is based on a cooperative interaction of all the elements. The work develops a mathematical theory of a vascular network response to local effects on scales of individual units of peripheral circulation.
Label-free imaging approaches seek to simplify and augment histopathologic assessment by replacing the current practice of staining by dyes to visualize tissue morphology with quantitative optical measurements. Quantitative phase imaging (QPI) operat es with visible/UV light and thus provides a resolution matched to current practice. Here we introduce and demonstrate confocal QPI for label-free imaging of tissue sections and assess its utility for manual histopathologic inspection. Imaging cancerous and normal adjacent human breast and prostate, we show that tissue structural organization can be resolved with high spatial detail comparable to conventional H&E stains. Our confocal QPI images are found to be free of halo, solving this common problem in QPI. We further describe and apply a virtual imaging system based on Finite-Difference Time-Domain (FDTD) calculations to quantitatively compare confocal with wide-field QPI methods and explore performance limits using numerical tissue phantoms.
Imaging technologies have been developed to assist physicians and dentist in the detection of various diseases. Photoacoustic imaging (PAI) is a new imaging technique that shows great promise to image soft tissues. The prototype of PAI system in this study utilized a non-ionizing 532nm continue-wave diode laser illumination to image oral soft tissue. The aim of this study was to investigate the effect of diode laser intensity modulation to the Photoacoustic image quality. Samples in this study were oral soft tissues from six Sprague Dawley rats imaged by using the PAI system. To determine the optimum duty cycle of laser intensity modulation, the laser exposure for oral soft tissue imaging was set in various duty cycles.
Measurements on embryonic epithelial tissues in a diverse range of organisms have shown that the statistics of cell neighbor numbers are universal in tissues where cell proliferation is the primary cell activity. Highly simplified non-spatial models of proliferation are claimed to accurately reproduce these statistics. Using a systematic critical analysis, we show that non-spatial models are not capable of robustly describing the universal statistics observed in proliferating epithelia, indicating strong spatial correlations between cells. Furthermore we show that spatial simulations using the Subcellular Element Model are able to robustly reproduce the universal histogram. In addition these simulations are able to unify ostensibly divergent experimental data in the literature. We also analyze cell neighbor statistics in early stages of chick embryo development in which cell behaviors other than proliferation are important. We find from experimental observation that cell neighbor statistics in the primitive streak region, where cell motility and ingression are also important, show a much broader distribution. A non-spatial Markov process model provides excellent agreement with this broader histogram indicating that cells in the primitive streak may have significantly weaker spatial correlations. These findings show that cell neighbor statistics provide a potentially useful signature of collective cell behavior.
Characterization of microstructures in live tissues is one of the keys to diagnosing early stages of pathology and understanding disease mechanisms. However, the extraction of reliable information on biomarkers based on microstructure details is stil l a challenge, as the size of features that can be resolved with non-invasive Magnetic Resonance Imaging (MRI) is orders of magnitude larger than the relevant structures. Here we derive from quantum information theory the ultimate precision limits for obtaining such details by MRI probing of water-molecule diffusion. We show that already available MRI pulse sequences can be optimized to attain the ultimate precision limits by choosing control parameters that are uniquely determined by the expected size, the diffusion coefficient and the spin relaxation time $T_{2}$. By attaining the ultimate precision limit per measurement, the number of measurements and the total acquisition time may be drastically reduced compared to the present state of the art. These results will therefore allow MRI to advance towards unravelling a wealth of diagnostic information.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا