7,640 research outputs found

    Developing Ultrasound-Based Computer-Aided Diagnostic Systems Through Statistical Pattern Recognition

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    Computer-aided diagnosis (CAD) is the use of a computer software to help physicians having a better interpretation of medical images. CAD systems can be viewed as pattern recognition algorithms that identify suspicious signs on a medical image and complement physicians' judgments, by reducing inter-/intra-observer variability and subjectivity. The proposed CAD systems in this thesis have been designed based on the statistical approach to pattern recognition as the most successfully used technique in practice. The main focus of this thesis has been on designing (new) feature extraction and classification algorithms for ultrasound-based CAD purposes. Ultrasound imaging has a broad range of usage in medical applications because it is a safe device which does not use harmful ionizing radiations, it provides clinicians with real-time images, it is portable and relatively cheap. The thesis was concerned with developing new ultrasound-based systems for the diagnosis of prostate cancer (PCa) and myocardial infarction (MI) where these issues have been addressed in two separate parts. In the first part, 1) a new CAD system was designed for prostate cancer biopsy by focusing on handling uncertainties in labels of the ground truth data, 2) the appropriateness of the independent component analysis (ICA) method for learning features from radiofrequency (RF) signals, backscattered from prostate tissues, was examined and, 3) a new ensemble scheme for learning ICA dictionaries from RF signals, backscattered from a tissue mimicking phantom, was proposed. In the second part, 1) principal component analysis (PCA) was used for the statistical modeling of the temporal deformation patterns of the left ventricle (LV) to detect abnormalities in its regional function, 2) a spatio-temporal representation of LV function based on PCA parameters was proposed to detect MI and, 3) a local-to-global statistical shape model based on PCA was presented to detect MI

    Prospects for Theranostics in Neurosurgical Imaging: Empowering Confocal Laser Endomicroscopy Diagnostics via Deep Learning

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    Confocal laser endomicroscopy (CLE) is an advanced optical fluorescence imaging technology that has the potential to increase intraoperative precision, extend resection, and tailor surgery for malignant invasive brain tumors because of its subcellular dimension resolution. Despite its promising diagnostic potential, interpreting the gray tone fluorescence images can be difficult for untrained users. In this review, we provide a detailed description of bioinformatical analysis methodology of CLE images that begins to assist the neurosurgeon and pathologist to rapidly connect on-the-fly intraoperative imaging, pathology, and surgical observation into a conclusionary system within the concept of theranostics. We present an overview and discuss deep learning models for automatic detection of the diagnostic CLE images and discuss various training regimes and ensemble modeling effect on the power of deep learning predictive models. Two major approaches reviewed in this paper include the models that can automatically classify CLE images into diagnostic/nondiagnostic, glioma/nonglioma, tumor/injury/normal categories and models that can localize histological features on the CLE images using weakly supervised methods. We also briefly review advances in the deep learning approaches used for CLE image analysis in other organs. Significant advances in speed and precision of automated diagnostic frame selection would augment the diagnostic potential of CLE, improve operative workflow and integration into brain tumor surgery. Such technology and bioinformatics analytics lend themselves to improved precision, personalization, and theranostics in brain tumor treatment.Comment: See the final version published in Frontiers in Oncology here: https://www.frontiersin.org/articles/10.3389/fonc.2018.00240/ful

    A non-invasive diagnostic system for early assessment of acute renal transplant rejection.

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    Early diagnosis of acute renal transplant rejection (ARTR) is of immense importance for appropriate therapeutic treatment administration. Although the current diagnostic technique is based on renal biopsy, it is not preferred due to its invasiveness, recovery time (1-2 weeks), and potential for complications, e.g., bleeding and/or infection. In this thesis, a computer-aided diagnostic (CAD) system for early detection of ARTR from 4D (3D + b-value) diffusion-weighted (DW) MRI data is developed. The CAD process starts from a 3D B-spline-based data alignment (to handle local deviations due to breathing and heart beat) and kidney tissue segmentation with an evolving geometric (level-set-based) deformable model. The latter is guided by a voxel-wise stochastic speed function, which follows from a joint kidney-background Markov-Gibbs random field model accounting for an adaptive kidney shape prior and for on-going visual kidney-background appearances. A cumulative empirical distribution of apparent diffusion coefficient (ADC) at different b-values of the segmented DW-MRI is considered a discriminatory transplant status feature. Finally, a classifier based on deep learning of a non-negative constrained stacked auto-encoder is employed to distinguish between rejected and non-rejected renal transplants. In the “leave-one-subject-out” experiments on 53 subjects, 98% of the subjects were correctly classified (namely, 36 out of 37 rejected transplants and 16 out of 16 nonrejected ones). Additionally, a four-fold cross-validation experiment was performed, and an average accuracy of 96% was obtained. These experimental results hold promise of the proposed CAD system as a reliable non-invasive diagnostic tool

    Diffusion-weighted magnetic resonance imaging in diagnosing graft dysfunction : a non-invasive alternative to renal biopsy.

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    The thesis is divided into three parts. The first part focuses on background information including how the kidney functions, diseases, and available kidney disease treatment strategies. In addition, the thesis provides information on imaging instruments and how they can be used to diagnose renal graft dysfunction. The second part focuses on elucidating the parameters linked with highly accurate diagnosis of rejection. Four parameters categories were tested: clinical biomarkers alone, individual mean apparent diffusion coefficient (ADC) at 11-different b- values, mean ADCs of certain groups of b-value, and fusion of clinical biomarkers and all b-values. The most accurate model was found to be when the b-value of b=100 s/mm2 and b=700 s/mm2 were fused. The third part of this thesis focuses on a study that uses Diffusion-Weighted MRI to diagnose and differentiate two types of renal rejection. The system was found to correctly differentiate the two types of rejection with a 98% accuracy. The last part of this thesis concludes the work that has been done and states the possible trends and future avenues
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