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Register a new userFinding New Diagnostic Information for Detecting Glaucoma using Neural Networks
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We describe a new approach to automated Glaucoma detection in 3D Spectral Domain Optical Coherence Tomography (OCT) optic nerve scans. First, we gathered a unique and diverse multi-ethnic dataset of OCT scans consisting of glaucoma and non-glaucomatous cases obtained from four tertiary care eye hospitals located in four different countries. Using this longitudinal data, we achieved state-of-the-art results for automatically detecting Glaucoma from a single raw OCT using a 3D Deep Learning system. These results are close to human doctors in a variety of settings across heterogeneous datasets and scanning environments. To verify correctness and interpretability of the automated categorization, we used saliency maps to find areas of focus for the model. Matching human doctor behavior, the model predictions indeed correlated with the conventional diagnostic parameters in the OCT printouts, such as the retinal nerve fiber layer. We further used our model to find new areas in the 3D data that are presently not being identified as a diagnostic parameter to detect glaucoma by human doctors. Namely, we found that the Lamina Cribrosa (LC) region can be a valuable source of helpful diagnostic information previously unavailable to doctors during routine clinical care because it lacks a quantitative printout. Our model provides such volumetric quantification of this region. We found that even when a majority of the RNFL is removed, the LC region can distinguish glaucoma. This is clinically relevant in high myopes, when the RNFL is already reduced, and thus the LC region may help differentiate glaucoma in this confounding situation. We further generalize this approach to create a new algorithm called DiagFind that provides a recipe for finding new diagnostic information in medical imagery that may have been previously unusable by doctors.
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A supervised diagnosis system for digital mammogram is developed. The diagnosis processes are done by transforming the data of the images into a feature vector using wavelets multilevel decomposition. This vector is used as the feature tailored toward separating different mammogram classes. The suggested model consists of artificial neural networks designed for classifying mammograms according to tumor type and risk level. Results are enhanced from our previous study by extracting feature vectors using multilevel decompositions instead of one level of decomposition. Radiologist-labeled images were used to evaluate the diagnosis system. Results are very promising and show possible guide for future work.
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For several skin conditions such as vitiligo, accurate segmentation of lesions from skin images is the primary measure of disease progression and severity. Existing methods for vitiligo lesion segmentation require manual intervention. Unfortunately, manual segmentation is time and labor-intensive, as well as irreproducible between physicians. We introduce a convolutional neural network (CNN) that quickly and robustly performs vitiligo skin lesion segmentation. Our CNN has a U-Net architecture with a modified contracting path. We use the CNN to generate an initial segmentation of the lesion, then refine it by running the watershed algorithm on high-confidence pixels. We train the network on 247 images with a variety of lesion sizes, complexity, and anatomical sites. The network with our modifications noticeably outperforms the state-of-the-art U-Net, with a Jaccard Index (JI) score of 73.6% (compared to 36.7%). Moreover, our method requires only a few seconds for segmentation, in contrast with the previously proposed semi-autonomous watershed approach, which requires 2-29 minutes per image.
A cascaded multi-planar scheme with a modified residual U-Net architecture was used to segment thalamic nuclei on conventional and white-matter-nulled (WMn) magnetization prepared rapid gradient echo (MPRAGE) data. A single network was optimized to work with images from healthy controls and patients with multiple sclerosis (MS) and essential tremor (ET), acquired at both 3T and 7T field strengths. Dice similarity coefficient and volume similarity index (VSI) were used to evaluate performance. Clinical utility was demonstrated by applying this method to study the effect of MS on thalamic nuclei atrophy. Segmentation of each thalamus into twelve nuclei was achieved in under a minute. For 7T WMn-MPRAGE, the proposed method outperforms current state-of-the-art on patients with ET with statistically significant improvements in Dice for five nuclei (increase in the range of 0.05-0.18) and VSI for four nuclei (increase in the range of 0.05-0.19), while performing comparably for healthy and MS subjects. Dice and VSI achieved using 7T WMn-MPRAGE data are comparable to those using 3T WMn-MPRAGE data. For conventional MPRAGE, the proposed method shows a statistically significant Dice improvement in the range of 0.14-0.63 over FreeSurfer for all nuclei and disease types. Effect of noise on network performance shows robustness to images with SNR as low as half the baseline SNR. Atrophy of four thalamic nuclei and whole thalamus was observed for MS patients compared to healthy control subjects, after controlling for the effect of parallel imaging, intracranial volume, gender, and age (p<0.004). The proposed segmentation method is fast, accurate, performs well across disease types and field strengths, and shows great potential for improving our understanding of thalamic nuclei involvement in neurological diseases.
Quantitative ultrasound (QUS) can reveal crucial information on tissue properties such as scatterer density. If the scatterer density per resolution cell is above or below 10, the tissue is considered as fully developed speckle (FDS) or low-density scatterers (LDS), respectively. Conventionally, the scatterer density has been classified using estimated statistical parameters of the amplitude of backscattered echoes. However, if the patch size is small, the estimation is not accurate. These parameters are also highly dependent on imaging settings. In this paper, we propose a convolutional neural network (CNN) architecture for QUS, and train it using simulation data. We further improve the network performance by utilizing patch statistics as additional input channels. We evaluate the network using simulation data, experimental phantoms and in vivo data. We also compare our proposed network with different classic and deep learning models, and demonstrate its superior performance in classification of tissues with different scatterer density values. The results also show that the proposed network is able to work with different imaging parameters with no need for a reference phantom. This work demonstrates the potential of CNNs in classifying scatterer density in ultrasound images.
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