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The flu assay offers a point-of-care molecular detection and flu A & B differentiation result in 13 minutes or less, with a compact storage system that allows streamlined tests. The test also allows for room temperature storage of all test components, based on a statement from Abbott, simplifying and streamlining test ordering and storage.
The Strep A 2 assay, which provides a molecular detection of Group A Streptococcus bacterial nucleic acid, is capable of providing results in 6 minutes or less. Positive results can be called in as early as 2 minutes, with no culture confirmation required.
The first CLIA-waived point-of-care molecular platform, with an instrument-based isothermal system for the qualitative detection of infectious diseases. The initial flu A & B Strep A assays for the platform were approved for use in 2014 and 2015, respectively, with a third assay indicated for respiratory syncytial virus was cleared 2016.
With the FDA approval, Abbot now anticipates offering new assays for this fall.
It has been a particularly busy week for marketed flu vaccines with baloxavir marboxil approval and updated indication for the quadrivalent flu vaccine to include pediatric patients
Gregory J. Berry, PhD, Director of Molecular Diagnostics, Northwell Health Laboratories in Lake Success, is a "game-changing development" for treatment purposes. , New York.
"Rapid testing may also help reduce antibiotic use, which may occur when a patient's symptoms, and to antibiotic resistance," said Berry in a statement.
This article originally appeared, "FDA Approves Rapid Flu & Strep Assays," on MD Magazine.com.
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