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1.
Research on Biomedical Engineering ; 2023.
Artículo en Inglés | Scopus | ID: covidwho-20236113

RESUMEN

Purpose: In December 2019, the Covid-19 pandemic began in the world. To reduce mortality, in addiction to mass vaccination, it is necessary to massify and accelerate clinical diagnosis, as well as creating new ways of monitoring patients that can help in the construction of specific treatments for the disease. Objective: In this work, we propose rapid protocols for clinical diagnosis of COVID-19 through the automatic analysis of hematological parameters using evolutionary computing and machine learning. These hematological parameters are obtained from blood tests common in clinical practice. Method: We investigated the best classifier architectures. Then, we applied the particle swarm optimization algorithm (PSO) to select the most relevant attributes: serum glucose, troponin, partial thromboplastin time, ferritin, D-dimer, lactic dehydrogenase, and indirect bilirubin. Then, we assessed again the best classifier architectures, but now using the reduced set of features. Finally, we used decision trees to build four rapid protocols for Covid-19 clinical diagnosis by assessing the impact of each selected feature. The proposed system was used to support clinical diagnosis and assessment of disease severity in patients admitted to intensive and semi-intensive care units as a case study in the city of Paudalho, Brazil. Results: We developed a web system for Covid-19 diagnosis support. Using a 100-tree random forest, we obtained results for accuracy, sensitivity, and specificity superior to 99%. After feature selection, results were similar. The four empirical clinical protocols returned accuracies, sensitivities and specificities superior to 98%. Conclusion: By using a reduced set of hematological parameters common in clinical practice, it was possible to achieve results of accuracy, sensitivity, and specificity comparable to those obtained with RT-PCR. It was also possible to automatically generate clinical decision protocols, allowing relatively accurate clinical diagnosis even without the aid of the web decision support system. © 2023, The Author(s), under exclusive licence to The Brazilian Society of Biomedical Engineering.

2.
Diagnostics (Basel) ; 13(3)2023 Jan 20.
Artículo en Inglés | MEDLINE | ID: covidwho-2199882

RESUMEN

The COVID-19 pandemic shed light on the need for quick diagnosis tools in healthcare, leading to the development of several algorithmic models for disease detection. Though these models are relatively easy to build, their training requires a lot of data, storage, and resources, which may not be available for use by medical institutions or could be beyond the skillset of the people who most need these tools. This paper describes a data analysis and machine learning platform that takes advantage of high-performance computing infrastructure for medical diagnosis support applications. This platform is validated by re-training a previously published deep learning model (COVID-Net) on new data, where it is shown that the performance of the model is improved through large-scale hyperparameter optimisation that uncovered optimal training parameter combinations. The per-class accuracy of the model, especially for COVID-19 and pneumonia, is higher when using the tuned hyperparameters (healthy: 96.5%; pneumonia: 61.5%; COVID-19: 78.9%) as opposed to parameters chosen through traditional methods (healthy: 93.6%; pneumonia: 46.1%; COVID-19: 76.3%). Furthermore, training speed-up analysis shows a major decrease in training time as resources increase, from 207 min using 1 node to 54 min when distributed over 32 nodes, but highlights the presence of a cut-off point where the communication overhead begins to affect performance. The developed platform is intended to provide the medical field with a technical environment for developing novel portable artificial-intelligence-based tools for diagnosis support.

3.
International Journal of Advanced Computer Science and Applications ; 13(6):564-570, 2022.
Artículo en Inglés | Scopus | ID: covidwho-1934698

RESUMEN

The COVID-19 infection was sparked by the severe acute respiratory syndrome SARS-CoV-2, as mentioned by the World Health Organization, and originated in Wuhan, Republic of China, eventually extending to every nation worldwide in 2020. This research aims to establish an efficient Medical Diagnosis Support System (MDSS) for recognizing COVID-19 in chest radiography with X-ray data. To build an ever more efficient classifier, this MDSS employs the concatenation mechanism to merge pretrained convolutional neural networks (CNNs) predicated on Transfer Learning (TL) classifiers. In the feature extraction phase, this proposed classifier employs a parallel deep feature extraction approach based on Deep Learning (DL). As a result, this approach increases the accuracy of our proposed model, thus identifying COVID-19 cases with higher accuracy. The suggested concatenation classifier was trained and validated using a Chest Radiography image database with four categories: COVID-19, Normal, Pneumonia, and Tuberculosis during this research. Furthermore, we integrated four separate public X-Ray imaging datasets to construct this dataset. In contrast, our mentioned concatenation classifier achieved 99.66% accuracy and 99.48% sensitivity respectively © 2022. International Journal of Advanced Computer Science and Applications.All Rights Reserved.

4.
J Med Internet Res ; 23(1): e25535, 2021 01 06.
Artículo en Inglés | MEDLINE | ID: covidwho-1011363

RESUMEN

BACKGROUND: Effectively identifying patients with COVID-19 using nonpolymerase chain reaction biomedical data is critical for achieving optimal clinical outcomes. Currently, there is a lack of comprehensive understanding in various biomedical features and appropriate analytical approaches for enabling the early detection and effective diagnosis of patients with COVID-19. OBJECTIVE: We aimed to combine low-dimensional clinical and lab testing data, as well as high-dimensional computed tomography (CT) imaging data, to accurately differentiate between healthy individuals, patients with COVID-19, and patients with non-COVID viral pneumonia, especially at the early stage of infection. METHODS: In this study, we recruited 214 patients with nonsevere COVID-19, 148 patients with severe COVID-19, 198 noninfected healthy participants, and 129 patients with non-COVID viral pneumonia. The participants' clinical information (ie, 23 features), lab testing results (ie, 10 features), and CT scans upon admission were acquired and used as 3 input feature modalities. To enable the late fusion of multimodal features, we constructed a deep learning model to extract a 10-feature high-level representation of CT scans. We then developed 3 machine learning models (ie, k-nearest neighbor, random forest, and support vector machine models) based on the combined 43 features from all 3 modalities to differentiate between the following 4 classes: nonsevere, severe, healthy, and viral pneumonia. RESULTS: Multimodal features provided substantial performance gain from the use of any single feature modality. All 3 machine learning models had high overall prediction accuracy (95.4%-97.7%) and high class-specific prediction accuracy (90.6%-99.9%). CONCLUSIONS: Compared to the existing binary classification benchmarks that are often focused on single-feature modality, this study's hybrid deep learning-machine learning framework provided a novel and effective breakthrough for clinical applications. Our findings, which come from a relatively large sample size, and analytical workflow will supplement and assist with clinical decision support for current COVID-19 diagnostic methods and other clinical applications with high-dimensional multimodal biomedical features.


Asunto(s)
COVID-19/diagnóstico , Sistemas de Apoyo a Decisiones Clínicas , Salud , Aprendizaje Automático , Neumonía Viral/diagnóstico , COVID-19/diagnóstico por imagen , Diagnóstico Diferencial , Humanos , Persona de Mediana Edad , Neumonía Viral/diagnóstico por imagen , SARS-CoV-2 , Máquina de Vectores de Soporte , Tomografía Computarizada por Rayos X
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