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POSTED ON 12-04-2023

The latest in Medical Technology: 12 April 2023


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Abbott's lab blood test for concussions receives FDA approval.

 

The first commercially accessible laboratory blood test to assist assess traumatic brain injury (TBI), generally known as concussion, has been approved by the U.S. Food and Drug Administration.

 

According to the business, the test provides a response in 18 minutes, enabling doctors to promptly examine and triage concussed patients. An unneeded CT scan can be ruled out by a negative test result, saving time at the hospital.

 

 

An innovative urine test to identify bladder cancer

 

A test for the non-invasive diagnosis of bladder cancer has been introduced at the Annual Meeting of the European Association of Urology as a consequence of cooperation between researchers from the University of Birmingham and the liquid biopsy cancer detection and screening firm Nonacus.

 

The urine-based molecular test, known as GALEAS Bladder, can lessen the need for invasive cystoscopies by swiftly and effectively identifying bladder cancer.

 

In order to detect the presence of bladder cancer by detecting DNA from tumour cells present in the urine, it uses susceptible liquid biopsy technology created by Nonacus in conjunction with a panel of biomarkers.

 

Log my Care and PainChek collaborate to improve care coordination

 

A regulatory-cleared medical gadget for pain assessment and a care management platform called Log my Care have announced their collaboration to improve the care management process.

 

Under this collaboration, care providers will have access to PainChek's AI technology via the Log my Care app, which offers pain assessment for those who might not be able to vocally express their discomfort. A user-friendly tool called Log my Care enables caregivers to offer person-centred care while also helping them save time and money.

 

The QuidelOrtho COVID test is the first to get FDA approval through premarket evaluation.

 

For the first time ever, the U.S. Food and Drug Administration's premarket assessment procedure resulted in the COVID-19 antigen test being given marketing approval.

 

The Sofia 2 SARS Antigen+ FIA, a prescription-only lateral flow assay appropriate for use in point-of-care settings, has been given the De Novo authorisation by QuidelOrtho Corp.

 

The authorisation heralds the beginning of the COVID-19 antigen test regulation's subsequent phase. The approach has prepared the way for more tests to enter the market via the 510(k) pathway, with the FDA instituting extra restrictions as part of the De Novo review.

 

A smartphone app monitors the frequency of coughs in a TB experiment

 

Researchers have assessed cough frequency in patients with TB and other respiratory illnesses using a smartphone app, indicating that the technology potentially enables remote monitoring.

 

The researchers report how they kept track of 565 individuals with respiratory diseases using the Hyfe Research cough tracking app in the International Journal of Tuberculosis and Lung Disease.

 

According to the study, individuals with TB responded to therapy differently and coughed more frequently than those with other respiratory illnesses. The study might promote the adoption of the digital biomarker to reduce overtreating TB and enhance illness identification if it is verified in additional research.

 

 

Predictive Health Intelligences tool for undiagnosed liver disease

 

HepatoSIGHT, a data-driven technology from Predictive Health Intelligence, uses historical blood tests to identify persons with undetected liver illness.

 

HepatoSIGHT can swiftly and easily identify persons at risk of developing severe liver disease, enabling them to be treated much sooner, according to pilot tests conducted by Somerset NHS Foundation Trust.

 

HepatoSIGHT was created in collaboration with the public and patients with an eye on the needs of the NHS and is intended to assist medical professionals in proactively identifying individuals with the liver disease before it worsens. I

 

 

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