To the Editor: Faix et al. (Aug. 13 issue)1 highlight the moderate sensitivity of rapid antigen tests as compared with reverse-transcriptase–polymerase-chain-reaction (RT-PCR) assays in detecting the 2009 pandemic influenza A (H1N1) virus in infected patients. We found that the antigen tests had poor sensitivity to the virus when used in a subgroup of 21 patients in the Australian intensive care cohort with severe 2009 influenza A (H1N1) virus infection and acute lung injury that required mechanical ventilation.2 In these patients, rapid antigen tests (QuickVue A+B, Quidel) were performed on swabs from the nose and throat, and influenza type-specific immunofluorescent antigen . . .
CITATION STYLE
Blyth, C. C., Iredell, J. R., & Dwyer, D. E. (2009). Rapid-Test Sensitivity for Novel Swine-Origin Influenza A (H1N1) Virus in Humans. New England Journal of Medicine, 361(25), 2493–2493. https://doi.org/10.1056/nejmc0909049
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