Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
1.
Multimed Tools Appl ; : 1-23, 2023 Mar 27.
Article in English | MEDLINE | ID: mdl-37362692

ABSTRACT

Corona Virus (COVID-19) could be considered as one of the most devastating pandemics of the twenty-first century. The effective and the rapid screening of infected patients could reduce the mortality and even the contagion rate. Chest X-ray radiology could be designed as one of the effective screening techniques for COVID-19 exploration. In this paper, we propose an advanced approach based on deep learning architecture to automatic and effective screening techniques dedicated to the COVID-19 exploration through chest X-ray (CXR) imaging. Despite the success of state-of-the-art deep learning-based models for COVID-19 detection, they might suffer from several problems such as the huge memory and the computational requirement, the overfitting effect, and the high variance. To alleviate these issues, we investigate the Transfer Learning to the Efficient-Nets models. Next, we fine-tuned the whole network to select the optimal hyperparameters. Furthermore, in the preprocessing step, we consider an intensity-normalization method succeeded by some data augmentation techniques to solve the imbalanced dataset classes' issues. The proposed approach has presented a good performance in detecting patients attained by COVID-19 achieving an accuracy rate of 99.0% and 98% respectively using training and testing datasets. A comparative study over a publicly available dataset with the recently published deep-learning-based architectures could attest the proposed approach's performance.

2.
Med Biol Eng Comput ; 59(1): 85-106, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33231848

ABSTRACT

Compressed Sensing Magnetic Resonance Imaging (CS-MRI) could be considered a challenged task since it could be designed as an efficient technique for fast MRI acquisition which could be highly beneficial for several clinical routines. In fact, it could grant better scan quality by reducing motion artifacts amount as well as the contrast washout effect. It offers also the possibility to reduce the exploration cost and the patient's anxiety. Recently, Deep Learning Neuronal Network (DL) has been suggested in order to reconstruct MRI scans with conserving the structural details and improving parallel imaging-based fast MRI. In this paper, we propose Deep Convolutional Encoder-Decoder architecture for CS-MRI reconstruction. Such architecture bridges the gap between the non-learning techniques, using data from only one image, and approaches using large training data. The proposed approach is based on autoencoder architecture divided into two parts: an encoder and a decoder. The encoder as well as the decoder has essentially three convolutional blocks. The proposed architecture has been evaluated through two databases: Hammersmith dataset (for the normal scans) and MICCAI 2018 (for pathological MRI). Moreover, we extend our model to cope with noisy pathological MRI scans. The normalized mean square error (NMSE), the peak-to-noise ratio (PSNR), and the structural similarity index (SSIM) have been adopted as evaluation metrics in order to evaluate the proposed architecture performance and to make a comparative study with the state-of-the-art reconstruction algorithms. The higher PSNR and SSIM values as well as the lowest NMSE values could attest that the proposed architecture offers better reconstruction and preserves textural image details. Furthermore, the running time is about 0.8 s, which is suitable for real-time processing. Such results could encourage the neurologist to adopt it in their clinical routines. Graphical abstract.


Subject(s)
Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Algorithms , Brain/diagnostic imaging , Humans , Neural Networks, Computer
3.
J Healthc Eng ; 2020: 6092305, 2020.
Article in English | MEDLINE | ID: mdl-32566114

ABSTRACT

The ectopic renal function estimation based on a manual region of interest (ROI) extraction could be considered as time consuming. It could also affect the clinical interpretation and thus deviate the therapeutic attitude. For this purpose, we propose an advanced tool to evaluate such function through the dimercaptosuccinic acid (DMSA) kidney scintigraphy scans. Methods. The proposed study has been performed on one hundred patients (fifty cases with normal kidneys and fifty cases with ectopic kidneys). We present our segmentation problems as several cost functions' optimization, each containing two terms: (i) a distribution matching prior, which evaluates a global similarity between distributions, and (ii) a smoothness prior to avoid the occurrence of small, isolated regions in the solution. Obtained following recent bound-relaxation results, the optima of the cost functions yield each kidney region in near real time. The Dice Metric (DM), the Jaccard Index (JI), and the correlation parameter have been adopted as validation parameters in order to evaluate the segmentation results. The obtained relative function of both kidneys has been then compared with that evaluated in clinical routine (planar projection) and then validated statistically by the Bland-Altman plots and the Interclass Correlation Coefficient (ICC). Results. Compared to the expert's manual kidney segmentation, the obtained results have been judged to be acceptable for clinical use with high Mean Dice Metric (MDM) value and high Jaccard Index (JI). The evaluated relative renal function has been different from those calculated by the projection planar method usually used in clinical routines. Conclusion. The proposed system could efficiently extract the renal region. The relative function estimation could be considered as more accurate. In fact, the background noise correction and the attenuation phenomenon, which could yield an error measure for renal ectopia, have been avoided. Our clinical staff members have validated the results and have suggested using such tool in their clinical routines.


Subject(s)
Kidney Function Tests/methods , Kidney/diagnostic imaging , Succimer , Adult , Algorithms , Female , Humans , Image Processing, Computer-Assisted/methods , Image Processing, Computer-Assisted/statistics & numerical data , Kidney/physiopathology , Male , Middle Aged , Radionuclide Imaging
4.
J Digit Imaging ; 33(4): 903-915, 2020 08.
Article in English | MEDLINE | ID: mdl-32440926

ABSTRACT

Accurate and fully automatic brain tumor grading from volumetric 3D magnetic resonance imaging (MRI) is an essential procedure in the field of medical imaging analysis for full assistance of neuroradiology during clinical diagnosis. We propose, in this paper, an efficient and fully automatic deep multi-scale three-dimensional convolutional neural network (3D CNN) architecture for glioma brain tumor classification into low-grade gliomas (LGG) and high-grade gliomas (HGG) using the whole volumetric T1-Gado MRI sequence. Based on a 3D convolutional layer and a deep network, via small kernels, the proposed architecture has the potential to merge both the local and global contextual information with reduced weights. To overcome the data heterogeneity, we proposed a preprocessing technique based on intensity normalization and adaptive contrast enhancement of MRI data. Furthermore, for an effective training of such a deep 3D network, we used a data augmentation technique. The paper studied the impact of the proposed preprocessing and data augmentation on classification accuracy.Quantitative evaluations, over the well-known benchmark (Brats-2018), attest that the proposed architecture generates the most discriminative feature map to distinguish between LG and HG gliomas compared with 2D CNN variant. The proposed approach offers promising results outperforming the recently supervised and unsupervised state-of-the-art approaches by achieving an overall accuracy of 96.49% using the validation dataset. The obtained experimental results confirm that adequate MRI's preprocessing and data augmentation could lead to an accurate classification when exploiting CNN-based approaches.


Subject(s)
Brain Neoplasms , Glioma , Brain , Brain Neoplasms/diagnostic imaging , Glioma/diagnostic imaging , Humans , Magnetic Resonance Imaging , Neural Networks, Computer
5.
J Med Imaging (Bellingham) ; 6(4): 044002, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31620548

ABSTRACT

We investigate a new preprocessing approach for MRI glioblastoma brain tumors. Based on combined denoising technique (bilateral filter) and contrast-enhancement technique (automatic contrast stretching based on image statistical information), the proposed approach offers competitive results while preserving the tumor region's edges and original image's brightness. In order to evaluate the proposed approach's performance, quantitative evaluation has been realized through the Multimodal Brain Tumor Segmentation (BraTS 2015) dataset. A comparative study between the proposed method and four state-of-the art preprocessing algorithm attests that the proposed approach could yield a competitive performance for magnetic resonance brain glioblastomas tumor preprocessing. In fact, the result of this step of image preprocessing is very crucial for the efficiency of the remaining brain image processing steps: i.e., segmentation, classification, and reconstruction.

6.
J Healthc Eng ; 2018: 1048164, 2018.
Article in English | MEDLINE | ID: mdl-30425818

ABSTRACT

This study investigates a novel classification method for 3D multimodal MRI glioblastomas tumor characterization. We formulate our segmentation problem as a linear mixture model (LMM). Thus, we provide a nonnegative matrix M from every MRI slice in every segmentation process' step. This matrix will be used as an input for the first segmentation process to extract the edema region from T2 and FLAIR modalities. After that, in the rest of segmentation processes, we extract the edema region from T1c modality, generate the matrix M, and segment the necrosis, the enhanced tumor, and the nonenhanced tumor regions. In the segmentation process, we apply a rank-two NMF clustering. We have executed our tumor characterization method on BraTS 2015 challenge dataset. Quantitative and qualitative evaluations over the publicly training and testing dataset from the MICCAI 2015 multimodal brain segmentation challenge (BraTS 2015) attested that the proposed algorithm could yield a competitive performance for brain glioblastomas characterization (necrosis, tumor core, and edema) among several competing methods.


Subject(s)
Brain Neoplasms/diagnostic imaging , Glioblastoma/diagnostic imaging , Image Interpretation, Computer-Assisted/methods , Magnetic Resonance Imaging/methods , Algorithms , Cluster Analysis , Humans
7.
IEEE Trans Nanobioscience ; 14(7): 727-33, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26441424

ABSTRACT

Bridging the gap between mathematical and biological models and clinical applications could be considered as one of the new challenges of medical image analysis over the ten last years. This paper presents an advanced and convivial algorithm for brain glioblastomas tumor growth modelization. The brain glioblastomas tumor region would be extracted using a fast distribution matching developed algorithm based on global pixel wise information. A new model to simulate the tumor growth based on two major elements: cellular automata and fast marching method (CFMM) has been developed and used to estimate the brain tumor evolution during the time. On the basis of this model, experiments were carried out on twenty pathological MRI selected cases that were carefully discussed with the clinical part. The obtained simulated results were validated with ground truth references (real tumor growth measure) using dice metric parameter. As carefully discussed with the clinical partner, experimental results showed that our proposed algorithm for brain glioblastomas tumor growth model proved a good agreement. Our main purpose behind this research was of course to make advances and progress during clinical explorations helping therefore radiologists in their diagnosis. Clinical decisions and guidelines would be hence so more focused with such an advanced tool that could help clinicians and ensuring more accuracy and objectivity.


Subject(s)
Brain Neoplasms/pathology , Glioblastoma/pathology , Image Interpretation, Computer-Assisted/methods , Magnetic Resonance Imaging/methods , Models, Biological , Brain Neoplasms/physiopathology , Cell Proliferation , Computer Simulation , Glioblastoma/physiopathology , Humans , Neoplasm Invasiveness , Prognosis
8.
Comput Med Imaging Graph ; 40: 108-19, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25467804

ABSTRACT

This study investigates a fast distribution-matching, data-driven algorithm for 3D multimodal MRI brain glioma tumor and edema segmentation in different modalities. We learn non-parametric model distributions which characterize the normal regions in the current data. Then, we state our segmentation problems as the optimization of several cost functions of the same form, each containing two terms: (i) a distribution matching prior, which evaluates a global similarity between distributions, and (ii) a smoothness prior to avoid the occurrence of small, isolated regions in the solution. Obtained following recent bound-relaxation results, the optima of the cost functions yield the complement of the tumor region or edema region in nearly real-time. Based on global rather than pixel wise information, the proposed algorithm does not require an external learning from a large, manually-segmented training set, as is the case of the existing methods. Therefore, the ensuing results are independent of the choice of a training set. Quantitative evaluations over the publicly available training and testing data set from the MICCAI multimodal brain tumor segmentation challenge (BraTS 2012) demonstrated that our algorithm yields a highly competitive performance for complete edema and tumor segmentation, among nine existing competing methods, with an interesting computing execution time (less than 0.5s per image).


Subject(s)
Brain Neoplasms/pathology , Edema/pathology , Glioma/pathology , Image Interpretation, Computer-Assisted/methods , Imaging, Three-Dimensional/methods , Magnetic Resonance Imaging/methods , Algorithms , Brain Neoplasms/complications , Edema/etiology , Glioma/complications , Humans , Image Enhancement/methods , Multimodal Imaging/methods , Pattern Recognition, Automated/methods , Sensitivity and Specificity , Statistical Distributions , Subtraction Technique
SELECTION OF CITATIONS
SEARCH DETAIL
...