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Comparing machine learning screening approaches using clinical data and cytokine profiles for COVID-19 in resource-limited and resource-abundant settings.
Rashidi, Hooman H; Ikram, Aamer; Dang, Luke T; Bashir, Adnan; Zohra, Tanzeel; Ali, Amna; Tanvir, Hamza; Mudassar, Mohammad; Ravindran, Resmi; Akhtar, Nasim; Sikandar, Rana I; Umer, Mohammed; Akhter, Naeem; Butt, Rafi; Fennell, Brandon D; Khan, Imran H.
Affiliation
  • Rashidi HH; Computational Pathology and AI Center of Excellence (CPACE), University of Pittsburgh Medical Center, and University of Pittsburgh School of Medicine, Pittsburgh, USA. rashidihh@upmc.edu.
  • Ikram A; National Institutes of Health, Islamabad, Pakistan.
  • Dang LT; Department of Pathology and Laboratory Medicine, University of California, 4400 V Street, DavisSacramento, CA, 95817, USA.
  • Bashir A; Health Information Systems Program (HISP), Islamabad, Pakistan.
  • Zohra T; National Institutes of Health, Islamabad, Pakistan.
  • Ali A; National Institutes of Health, Islamabad, Pakistan.
  • Tanvir H; National Institutes of Health, Islamabad, Pakistan.
  • Mudassar M; National Institutes of Health, Islamabad, Pakistan.
  • Ravindran R; Department of Pathology and Laboratory Medicine, University of California, 4400 V Street, DavisSacramento, CA, 95817, USA.
  • Akhtar N; Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
  • Sikandar RI; Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
  • Umer M; Rawalpindi Medical University-Rawalpindi, Rawalpindi, Pakistan.
  • Akhter N; Rawalpindi Medical University-Rawalpindi, Rawalpindi, Pakistan.
  • Butt R; Isolation Hospital and Infectious Treatment Centre, Islamabad, Pakistan.
  • Fennell BD; Department of Medicine, University of California, San Francisco, USA.
  • Khan IH; Department of Pathology and Laboratory Medicine, University of California, 4400 V Street, DavisSacramento, CA, 95817, USA. ihkhan@ucdavis.edu.
Sci Rep ; 14(1): 14892, 2024 06 28.
Article in En | MEDLINE | ID: mdl-38937503
ABSTRACT
Accurate screening of COVID-19 infection status for symptomatic patients is a critical public health task. Although molecular and antigen tests now exist for COVID-19, in resource-limited settings, screening tests are often not available. Furthermore, during the early stages of the pandemic tests were not available in any capacity. We utilized an automated machine learning (ML) approach to train and evaluate thousands of models on a clinical dataset consisting of commonly available clinical and laboratory data, along with cytokine profiles for patients (n = 150). These models were then further tested for generalizability on an out-of-sample secondary dataset (n = 120). We were able to develop a ML model for rapid and reliable screening of patients as COVID-19 positive or negative using three approaches commonly available clinical and laboratory data, a cytokine profile, and a combination of the common data and cytokine profile. Of the tens of thousands of models automatically tested for the three approaches, all three approaches demonstrated > 92% sensitivity and > 88 specificity while our highest performing model achieved 95.6% sensitivity and 98.1% specificity. These models represent a potential effective deployable solution for COVID-19 status classification for symptomatic patients in resource-limited settings and provide proof-of-concept for rapid development of screening tools for novel emerging infectious diseases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cytokines / Machine Learning / COVID-19 Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cytokines / Machine Learning / COVID-19 Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: United States Country of publication: United kingdom