FDA Clears First Rapid Handheld Blood Test For Concussions

Source: inside.upmc.com | Repost Duerson Fund 1/20/21 –

Nearly 5 million people go to the emergency room for a traumatic brain injury (TBI) in the U.S. each year. Survivors of TBI may experience physical impairments and changes in emotional functioning, including personality changes or psychological symptoms. These effects can last days or be permanent, and are often worsened by misdiagnosis.

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Earlier this week, Abbott Laboratories, a global health care company, received FDA clearance to market and sell the first rapid handheld TBI blood test. Based on years of research that involved University of Pittsburgh neuro-trauma experts, the test will run on Abbott’s handheld i-STAT Alinity platform, with results available within 15 minutes after plasma is placed in the test cartridge.

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