| Literature DB >> 35194866 |
Tahira Nazir1, Marriam Nawaz1, Ali Javed1, Khalid Mahmood Malik2, Abdul Khader Jilani Saudagar3, Muhammad Badruddin Khan3, Mozaherul Hoque Abul Hasanat3, Abdullah AlTameem3, Mohammad AlKathami3.
Abstract
The COVID-19 pandemic is spreading at a fast pace around the world and has a high mortality rate. Since there is no proper treatment of COVID-19 and its multiple variants, for example, Alpha, Beta, Gamma, and Delta, being more infectious in nature are affecting millions of people, further complicates the detection process, so, victims are at the risk of death. However, timely and accurate diagnosis of this deadly virus can not only save the patients from life loss but can also prevent them from the complex treatment procedures. Accurate segmentation and classification of COVID-19 is a tedious job due to the extensive variations in its shape and similarity with other diseases like Pneumonia. Furthermore, the existing techniques have hardly focused on the infection growth estimation over time which can assist the doctors to better analyze the condition of COVID-19-affected patients. In this work, we tried to overcome the shortcomings of existing studies by proposing a model capable of segmenting, classifying the COVID-19 from computed tomography images, and predicting its behavior over a certain period. The framework comprises four main steps: (i) data preparation, (ii) segmentation, (iii) infection growth estimation, and (iv) classification. After performing the pre-processing step, we introduced the DenseNet-77 based UNET approach. Initially, the DenseNet-77 is used at the Encoder module of the UNET model to calculate the deep keypoints which are later segmented to show the coronavirus region. Then, the infection growth estimation of COVID-19 per patient is estimated using the blob analysis. Finally, we employed the DenseNet-77 framework as an end-to-end network to classify the input images into three classes namely healthy, COVID-19-affected, and pneumonia images. We evaluated the proposed model over the COVID-19-20 and COVIDx CT-2A datasets for segmentation and classification tasks, respectively. Furthermore, unlike existing techniques, we performed a cross-dataset evaluation to show the generalization ability of our method. The quantitative and qualitative evaluation confirms that our method is robust to both COVID-19 segmentation and classification and can accurately predict the infection growth in a certain time frame. RESEARCH HIGHLIGHTS: We present an improved UNET framework with a DenseNet-77-based encoder for deep keypoints extraction to enhance the identification and segmentation performance of the coronavirus while reducing the computational complexity as well. We propose a computationally robust approach for COVID-19 infection segmentation due to fewer model parameters. Robust segmentation of COVID-19 due to accurate feature computation power of DenseNet-77. A module is introduced to predict the infection growth of COVID-19 for a patient to analyze its severity over time. We present such a framework that can effectively classify the samples into several classes, that is, COVID-19, Pneumonia, and healthy samples. Rigorous experimentation was performed including the cross-dataset evaluation to prove the efficacy of the presented technique.Entities:
Keywords: COVID-19 segmentation; DenseNet-77; UNET; classification; infection growth estimation
Mesh:
Year: 2022 PMID: 35194866 PMCID: PMC9088346 DOI: 10.1002/jemt.24088
Source DB: PubMed Journal: Microsc Res Tech ISSN: 1059-910X Impact factor: 2.893
FIGURE 1Architecture of the proposed method namely COVID‐DAI
FIGURE 2DenseUNet architecture
The DenseNet‐77 network structural details
| Layer | Densenet‐77 | ||
|---|---|---|---|
| Size | Stride | ||
| ConL 1 |
| 2 | |
| PoolL 1 |
| 2 | |
| DB 1 |
| 1 | |
| TL | ConL 2 |
| 1 |
| PoolL 2 |
| 2 | |
| DB 2 |
| 1 | |
| TL | ConL 3 |
| 1 |
| PoolL 3 |
| 2 | |
| DB 3 |
| 1 | |
| TL | ConL 4 |
| 1 |
| PoolL 4 |
| 2 | |
| DB 4 |
| 1 | |
| Classification_layer |
| ||
| Fully connected layer | |||
| SoftMax | |||
FIGURE 3Detailed architectural view of DenseNet‐77 with dense block and transition layer structure
Model hyperparameters
| Network parameters | Value |
|---|---|
| Epochs | 20 |
| Value of learning rate | 0.001 |
| Selected batch size | 8 |
| Validation frequency | 7000 |
| Optimizer | Stochastic gradient descent |
FIGURE 4Segmentation results using DenseUNet
FIGURE 5Segmentation evaluation results using different evaluation parameters
Comparative analysis of the introduced model with base networks
| Parameters | VGG‐16 | ResNet‐50 | ResNet‐101 | DenseNet‐121 | DenseNet‐77 |
|---|---|---|---|---|---|
| No of total model parameters (million) | 119.6 | 23.6 | 42.5 | 7.1 | 6.2 |
| Test time accuracy (%) | 81.83 | 83.59 | 84.21 | 87.54 | 90.21 |
| Execution time (s) | 1116 | 1694 | 2541 | 2073 | 1040 |
Evaluation of the introduced work with DL‐based approaches
| Technique | Parameters | Dice (%) | Sensitivity (%) | Specificity (%) | Training time (per day) |
|---|---|---|---|---|---|
| ENET | 363,069 | 72.28 | 77.10 | 70.84 | 3.47 |
| C‐ENET | 793,917 | 74.83 | 76.50 | 76.26 | 4.22 |
| ERFNET | 2,056,440 | 54.23 | 72.97 | 48.65 | 2.87 |
| Proposed | 361,624 | 84.67 | 87.24 | 88.62 | 0.42 |
Abbreviations: C‐ENET, custom ENET; ENET, Efficient Neural Network; ERFNET, Efficient Residual Factorized ConvNet.
FIGURE 6Patient‐wise samples with sizes of the covid region
Patient‐wise infection growth estimation of COVID_19 region
| Samples | Day_1 | Day_8 | Day_15 | Infection growth (mm2) | |
|---|---|---|---|---|---|
| Day 1–Day 8 | Day 8–Day 15 | ||||
| Patient_1 | 164.060 | 1251.918 | 2519.185 | 0.2903 | 0.0998 |
| Patient_2 | 46.573 | 322.307 | 333.422 | 0.2763 | 0.0048 |
| Patient_3 | 145.541 | 144.483 | 144.483 | −0.0010 | 0 |
| Patient_4 | 5588.780 | 5578.195 | 5334.745 | −0.0002 | −0.0063 |
| Patient_5 | 79.121 | 155.597 | 194.761 | 0.0966 | 0.03207 |
| Patient_6 | 93.146 | 139.720 | 128.076 | 0.0579 | −0.0124 |
| Patient_7 | 105.583 | 116.433 | 200.053 | 0.0139 | 0.0773 |
| Patient_8 | 305.636 | 333.422 | 346.653 | 0.0124 | 0.0055 |
| Patient_9 | 2267.266 | 2132.310 | 2119.608 | −0.0087 | −0.0008 |
| Patient_10 | 1603.334 | 1489.283 | 1263.297 | −0.0105 | −0.0235 |
FIGURE 7Error rate of estimated infection growth
FIGURE 8Classification results: (a) precision and (b) recall
FIGURE 9Classification results of the introduced work in terms of F1 score and error rate
FIGURE 10Confusion matrix of proposed method
FIGURE 11AUC‐ROC curve of the proposed model
Comparison of the presented work with base techniques of classification
| Technique | Accuracy (%) | ||
|---|---|---|---|
| COVID‐19 | Normal | Pneumonia | |
| AlexNet | 88.89 | 96.83 | 94.40 |
| GoogLeNet | 73.10 | 92.06 | 94.90 |
| InceptionV3 | 83.63 | 98.41 | 98.40 |
| VGG16 | 90.64 | 97.62 | 100.00 |
| ShuffleNet | 85.96 | 98.41 | 96.00 |
| MobileNetV2 | 77.78 | 98.41 | 100.00 |
| ResNet18 | 82.46 | 98.41 | 98.40 |
| ResNet50 | 66.08 | 99.21 | 96.00 |
| ResNet101 | 71.93 | 99.21 | 99.20 |
| Proposed | 98.83 | 99.84 | 98.98 |
FIGURE 12Comparison of introduced work with base approaches on entire dataset
Comparison with state‐of‐the‐art methods
| Technique | Accuracy (%) |
|---|---|
| Gunraj et al. ( | 98.10 |
| Zhao et al. ( | 99.20 |
| Loddo et al. ( | 98.87 |
| Proposed | 99.27 |
FIGURE 13Cross‐dataset validation results