Selected article for: "clinical variable and specificity sensitivity"

Author: Li, Wei Tse; Ma, Jiayan; Shende, Neil; Castaneda, Grant; Chakladar, Jaideep; Tsai, Joseph C.; Apostol, Lauren; Honda, Christine O.; Xu, Jingyue; Wong, Lindsay M.; Zhang, Tianyi; Lee, Abby; Gnanasekar, Aditi; Honda, Thomas K.; Kuo, Selena Z.; Yu, Michael Andrew; Chang, Eric Y.; Rajasekaran, Mahadevan “ Raj”; Ongkeko, Weg M.
Title: Using machine learning of clinical data to diagnose COVID-19: a systematic review and meta-analysis
  • Cord-id: a1lc5my5
  • Document date: 2020_9_29
  • ID: a1lc5my5
    Snippet: BACKGROUND: The recent Coronavirus Disease 2019 (COVID-19) pandemic has placed severe stress on healthcare systems worldwide, which is amplified by the critical shortage of COVID-19 tests. METHODS: 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 aim to investigate correlations between clinical variables, cluster COVID-19 pat
    Document: BACKGROUND: The recent Coronavirus Disease 2019 (COVID-19) pandemic has placed severe stress on healthcare systems worldwide, which is amplified by the critical shortage of COVID-19 tests. METHODS: 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 aim 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. RESULTS: 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. CONCLUSIONS: 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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