Diagnosing and predicting risk in children with SARS-CoV-2- related illness

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 3R61HD105590-02S1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2021.0
    2022.0
  • Known Financial Commitments (USD)

    $400,000
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    PROFESSOR JANE BURNS
  • Research Location

    United States of America
  • Lead Research Institution

    UNIVERSITY OF CALIFORNIA, SAN DIEGO
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Children (1 year to 12 years)Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

In the wake of COVID-19 pandemic, Multisystem Inflammatory Syndrome in Children (MIS-C) has evolved as a new threat to children exposed to SARS-CoV-2. Currently there are no diagnostic tests to readily identify these patients nor are there tools to predict disease progression. Through established, funded, multi-center consortia in the U.S. (CHARMS: Characterization of MIS-C and its Relationship to Kawasaki Disease funded by PCORI) and the UK (DIAMONDS), we have collected clinical data and samples to support development and testing of diagnostic and prognostic tests for MIS-C. In phase 1 of this project (R61HD105590, years 1-2), we used these data to devise machine learning-based clinical decision support tool (KIDMATCH) to assist clinicians in diagnosis of MIS-C and other causes of fever in children. This proposal focuses on the development of a Software as a Medical Device (SaMD) and clinical deployment of this SaMD in a clinical setting. Additionally, we aim to develop a quality management system (QMS) to minimize and manage unintentional outcomes related to patient safety as required for FDA regulatory approval. To this end, this proposal aims to further develop a cross-platform SMART- on-FHIR app for display of the KIDMATCH outputs for integration within electronic health records. In close collaboration between our clinical and data science teams, we will evaluate the KIDMATCH app set-up, user workflow and physician preferences through structured interviews, simulations, and direct feedback. Finally, we aim to complete an ongoing application for Emergency Use Authorization (EUA) to enable wider deployment and commercialization of the KIDMATCH SaMD. The synergistic expertise of the investigative team in this proposal provides a unique opportunity to create diagnostic tools for children suffering from the spectrum of SARS- CoV-2 illnesses. 1