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December 31, 2020

Episode 15 | AI Weekly Gossip | First Artificial Intelligence Tool To Detect COVID-19 | DataTrained

Research in the Journal of Medical Internet Research introduced Biocogniv’s new AI-Covid software that can quickly predict the COVID-19 infection.

A number of researchers from the University of Vermont and Cedars-Sinai found larger accuracy in predicting the probability of COVID-19 infection making use of ordinary blood tests, that help hospitals decrease the number of patients referred for PCR testing.

Lead author and University of Vermont Assistant Professor Timothy Plante, M.D., M.H.S stated, "9 months into this pandemic, we today have a clear comprehension of exactly how to care for patients with COVID-19, but there is still a huge bottleneck in COVID-19 diagnosis with PCR testing."

PCR testing is the present standard diagnostic for COVID-19 and requires certain sampling, such as a nasal swab, and then laboratory equipment to run.

Tanya Kanigan, Biocogniv Chief Operating Officer, Ph.D., said "According to data from more than 100 US clinics, the national average turnaround period for COVID-19 testing purchased in emergency rooms is above 24 hours, much from the focused one-hour turnaround,". Complete Blood Count along with Complete Metabolic Panels are popular lab tests purchased by emergency departments and have a fast turnaround time. These tests offer insight directly into the immune system, kidney, electrolytes, and liver. The scientists had the ability to teach a design that analyzes changes in these routine tests and assigns a probability of the patient being COVID-19 negative with high accuracy.

AI-COVID takes seconds to produce its informative result when these blood tests return, they may then be integrated by the laboratory into a test interpretation."

The Biocogniv staff thinks a secondary advantage of laboratories incorporating AI-COVID may be reduced time for conventional PCR results.

The AI-COVID model was validated on real-world data offered by Cedars Sinai and on data from geographically and demographically different patient encounters from 22 U.S. hospitals, achieving a location underneath the curve of 0.91 of 1.00.

This enables the design to attain a high sensitivity of 95% while maintaining reasonable specificity of 49%, and that is pretty similar to the overall performance of other widely used rule-out tests.

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