August 15, 2012
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CDC: All rapid flu tests do not detect H3N2v

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Just because a rapid influenza test comes back negative for influenza A H3N2v, does not mean an influenza diagnosis can be ruled out, according to CDC researchers.

Perspective from Pedro A. Piedra, MD

In an early release of the Morbidity and Mortality Weekly Report this week, Joseph Bresee, MD, of the Influenza Division in the National Center for Immunization and Respiratory Diseases at CDC, and colleagues reported that in an evaluation of seven FDA-cleared different rapid testing systems used to detect the H3N2, only four detected all influenza A H3N2v viruses. The four tests included, Directigen (Becton, Dickinson and Company), Sofia (Quidel Fluorescence), Veritor (Becton, Dickinson and Company) and Xpect (Oxoid).

“BinaxNOW (Alere) detected five of seven, and QuickVue (Quidel) detected three of seven. FluAlert (Thermo Fisher Scientific) detected only one of seven,” the researchers wrote. The researchers noted detection of influenza is important because there were 153 H3N2v infections reported from four states between July 12 and Aug. 9, 2012.

“Results from [rapid influenza tests], both positive and negative, always should be interpreted in the broader context of the circulating influenza strains present in the area, level of clinical suspicion, severity of illness, and risk for complications in a patient with suspected infection,” the researchers concluded.

In their report, the CDC and other researchers noted that the best way for clinicians to avoid false results is to “following the manufacturer’s instructions, collecting specimens soon after onset of influenza-like illness (ideally within the first 72 hours), and confirming results by sending a specimen to a public health laboratory.”

Disclosure: Dr. Bresee reports no relevant financial disclosures.