Author: Li, W. T.; Ma, J.; Shende, N.; Castaneda, G.; Chakladar, J.; Tsai, J. C.; Apostol, L.; Honda, C. O.; Xu, J.; Wong, L. M.; Zhang, T.; Lee, A.; Gnanasekar, A.; Honda, T. K.; Kuo, S. Z.; Yu, M. A.; Chang, E. Y.; Rajasekaran, M. R.; Ongkeko, W. M.
                    Title: Using Machine Learning of Clinical Data to Diagnose COVID-19  Cord-id: ymlfitp0  Document date: 2020_6_24
                    ID: ymlfitp0
                    
                    Snippet: The recent pandemic of Coronavirus Disease 2019 (COVID-19) has placed severe stress on healthcare systems worldwide, which is amplified by the critical shortage of COVID-19 tests. In this study, we propose to generate a more accurate diagnosis model of COVID-19 based on patient symptoms and routine test results by applying machine learning to reanalyzing COVID-19 data from 151 published studies. We aimed to investigate correlations between clinical variables, cluster COVID-19 patients into subty
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: The recent pandemic of Coronavirus Disease 2019 (COVID-19) has placed severe stress on healthcare systems worldwide, which is amplified by the critical shortage of COVID-19 tests. In this study, we propose to generate a more accurate diagnosis model of COVID-19 based on patient symptoms and routine test results by applying machine learning to reanalyzing COVID-19 data from 151 published studies. We aimed to investigate correlations between clinical variables, cluster COVID-19 patients into subtypes, and generate a computational classification model for discriminating between COVID -19 patients and influenza patients based on clinical variables alone. We discovered several novel associations between clinical variables, including correlations between being male and having higher levels of serum lymphocytes and neutrophils. We found that COVID-19 patients could be clustered into subtypes based on serum levels of immune cells, gender, and reported symptoms. Finally, we trained an XGBoost model to achieve a sensitivity of 92.5% and a specificity of 97.9% in discriminating COVID-19 patients from influenza patients. We demonstrated that computational methods trained on large clinical datasets could yield ever more accurate COVID-19 diagnostic models to mitigate the impact of lack of testing. We also presented previously unknown COVID-19 clinical variable correlations and clinical subgroups.
 
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