Your browser doesn't support javascript.
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
1.
Comput Biol Med ; 154: 106567, 2023 03.
Article in English | MEDLINE | ID: covidwho-2177840

ABSTRACT

BACKGROUND: The coronavirus disease 2019 (COVID-19) and community-acquired pneumonia (CAP) present a high degree of similarity in chest computed tomography (CT) images. Therefore, a procedure for accurately and automatically distinguishing between them is crucial. METHODS: A deep learning method for distinguishing COVID-19 from CAP is developed using maximum intensity projection (MIP) images from CT scans. LinkNet is employed for lung segmentation of chest CT images. MIP images are produced by superposing the maximum gray of intrapulmonary CT values. The MIP images are input into a capsule network for patient-level pred iction and diagnosis of COVID-19. The network is trained using 333 CT scans (168 COVID-19/165 CAP) and validated on three external datasets containing 3581 CT scans (2110 COVID-19/1471 CAP). RESULTS: LinkNet achieves the highest Dice coefficient of 0.983 for lung segmentation. For the classification of COVID-19 and CAP, the capsule network with the DenseNet-121 feature extractor outperforms ResNet-50 and Inception-V3, achieving an accuracy of 0.970 on the training dataset. Without MIP or the capsule network, the accuracy decreases to 0.857 and 0.818, respectively. Accuracy scores of 0.961, 0.997, and 0.949 are achieved on the external validation datasets. The proposed method has higher or comparable sensitivity compared with ten state-of-the-art methods. CONCLUSIONS: The proposed method illustrates the feasibility of applying MIP images from CT scans to distinguish COVID-19 from CAP using capsule networks. MIP images provide conspicuous benefits when exploiting deep learning to detect COVID-19 lesions from CT scans and the capsule network improves COVID-19 diagnosis.


Subject(s)
COVID-19 , Deep Learning , Pneumonia , Humans , COVID-19/diagnostic imaging , COVID-19 Testing , SARS-CoV-2 , Pneumonia/diagnostic imaging , Tomography, X-Ray Computed/methods
2.
Comput Biol Med ; 141: 105182, 2022 02.
Article in English | MEDLINE | ID: covidwho-1588025

ABSTRACT

BACKGROUND: Chest computed tomography (CT) is crucial in the diagnosis of coronavirus disease 2019 (COVID-19). However, the persistent pandemic and similar CT manifestations between COVID-19 and community-acquired pneumonia (CAP) raise methodological requirements. METHODS: A fully automatic pipeline of deep learning is proposed for distinguishing COVID-19 from CAP using CT images. Inspired by the diagnostic process of radiologists, the pipeline comprises four connected modules for lung segmentation, selection of slices with lesions, slice-level prediction, and patient-level prediction. The roles of the first and second modules and the effectiveness of the capsule network for slice-level prediction were investigated. A dataset of 326 CT scans was collected to train and test the pipeline. Another public dataset of 110 patients was used to evaluate the generalization capability. RESULTS: LinkNet exhibited the largest intersection over union (0.967) and Dice coefficient (0.983) for lung segmentation. For the selection of slices with lesions, the capsule network with the ResNet50 block achieved an accuracy of 92.5% and an area under the curve (AUC) of 0.933. The capsule network using the DenseNet121 block demonstrated better performance for slice-level prediction, with an accuracy of 97.1% and AUC of 0.992. For both datasets, the prediction accuracy of our pipeline was 100% at the patient level. CONCLUSIONS: The proposed fully automatic deep learning pipeline of deep learning can distinguish COVID-19 from CAP via CT images rapidly and accurately, thereby accelerating diagnosis and augmenting the performance of radiologists. This pipeline is convenient for use by radiologists and provides explainable predictions.


Subject(s)
COVID-19 , Deep Learning , Pneumonia , Humans , Neural Networks, Computer , Pneumonia/diagnostic imaging , SARS-CoV-2 , Tomography, X-Ray Computed
3.
Comput Methods Programs Biomed ; 211: 106406, 2021 Nov.
Article in English | MEDLINE | ID: covidwho-1401346

ABSTRACT

BACKGROUND AND OBJECTIVE: Given that the novel coronavirus disease 2019 (COVID-19) has become a pandemic, a method to accurately distinguish COVID-19 from community-acquired pneumonia (CAP) is urgently needed. However, the spatial uncertainty and morphological diversity of COVID-19 lesions in the lungs, and subtle differences with respect to CAP, make differential diagnosis non-trivial. METHODS: We propose a deep represented multiple instance learning (DR-MIL) method to fulfill this task. A 3D volumetric CT scan of one patient is treated as one bag and ten CT slices are selected as the initial instances. For each instance, deep features are extracted from the pre-trained ResNet-50 with fine-tuning and represented as one deep represented instance score (DRIS). Each bag with a DRIS for each initial instance is then input into a citation k-nearest neighbor search to generate the final prediction. A total of 141 COVID-19 and 100 CAP CT scans were used. The performance of DR-MIL is compared with other potential strategies and state-of-the-art models. RESULTS: DR-MIL displayed an accuracy of 95% and an area under curve of 0.943, which were superior to those observed for comparable methods. COVID-19 and CAP exhibited significant differences in both the DRIS and the spatial pattern of lesions (p<0.001). As a means of content-based image retrieval, DR-MIL can identify images used as key instances, references, and citers for visual interpretation. CONCLUSIONS: DR-MIL can effectively represent the deep characteristics of COVID-19 lesions in CT images and accurately distinguish COVID-19 from CAP in a weakly supervised manner. The resulting DRIS is a useful supplement to visual interpretation of the spatial pattern of lesions when screening for COVID-19.


Subject(s)
COVID-19 , Deep Learning , Pneumonia , Humans , Lysergic Acid Diethylamide/analogs & derivatives , Pneumonia/diagnostic imaging , SARS-CoV-2 , Tomography, X-Ray Computed
4.
J Xray Sci Technol ; 28(5): 821-839, 2020.
Article in English | MEDLINE | ID: covidwho-709463

ABSTRACT

BACKGROUND: The novel coronavirus disease 2019 (COVID-19) constitutes a public health emergency globally. The number of infected people and deaths are proliferating every day, which is putting tremendous pressure on our social and healthcare system. Rapid detection of COVID-19 cases is a significant step to fight against this virus as well as release pressure off the healthcare system. OBJECTIVE: One of the critical factors behind the rapid spread of COVID-19 pandemic is a lengthy clinical testing time. The imaging tool, such as Chest X-ray (CXR), can speed up the identification process. Therefore, our objective is to develop an automated CAD system for the detection of COVID-19 samples from healthy and pneumonia cases using CXR images. METHODS: Due to the scarcity of the COVID-19 benchmark dataset, we have employed deep transfer learning techniques, where we examined 15 different pre-trained CNN models to find the most suitable one for this task. RESULTS: A total of 860 images (260 COVID-19 cases, 300 healthy and 300 pneumonia cases) have been employed to investigate the performance of the proposed algorithm, where 70% images of each class are accepted for training, 15% is used for validation, and rest is for testing. It is observed that the VGG19 obtains the highest classification accuracy of 89.3% with an average precision, recall, and F1 score of 0.90, 0.89, 0.90, respectively. CONCLUSION: This study demonstrates the effectiveness of deep transfer learning techniques for the identification of COVID-19 cases using CXR images.


Subject(s)
Coronavirus Infections/diagnostic imaging , Deep Learning , Pneumonia, Viral/diagnostic imaging , Tomography, X-Ray Computed/methods , Algorithms , Betacoronavirus , COVID-19 , Databases, Factual , Diagnosis, Differential , Humans , Neural Networks, Computer , Pandemics , Pneumonia/diagnostic imaging , Radiography, Thoracic , Reproducibility of Results , SARS-CoV-2
SELECTION OF CITATIONS
SEARCH DETAIL