FDA approved new influenza detection method for molecular diagnosis within 15 minutes

Release date: 2014-06-30

US Airil announced on June 16 that the US Food and Drug Administration (FDA) approved a new on-site test kit produced by the company on June 13 for the first time to obtain a highly accurate flu within 15 minutes. Molecular diagnosis results. Medscape Medical News reported on this news.

According to the US Airil Company, the new Alere i Influenza A & B Rapid Diagnostic Kit facilitates clinicians to diagnose influenza on the outpatient site and start giving proper treatment in a timely manner.

At present, there are similar influenza rapid test (RIDTs) products on the market, and the diagnosis results are about 15 minutes, but these test kits rely on enzyme-linked immunosorbent technology to find seasonal influenza virus antigens in clinical specimens. CDC indicates that such RIDTs are sensitive between 50% and 70%, thus leading to higher false negative rates.

The company's new test kit is 90% sensitive to both influenza A and B, and the Alere i Influenza A & B kit inherits some of the advantages of other RIDTs. Differential diagnosis of influenza A and B.

The novel detection principle is the extraction and analysis of viral DNA and RNA strands for the discovery of pathogen nucleic acid sequences associated with viral and bacterial infections. For the detection accuracy that people care about, the US company said that the results show that it is similar to the slowdown rate of polymerase chain reaction detection (usually takes 1-6 hours).

Source: Lilac Garden

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