| Literature DB >> 29142048 |
Daniel M Cohen1, Jennifer Kline2, Larissa S May3, Glenn Eric Harnett4, Jane Gibson5, Stephen Y Liang6, Zubaid Rafique7, Carina A Rodriguez8, Kevin M McGann9, Charlotte A Gaydos10, Donna Mayne11, David Phillips12, Jason Cohen13.
Abstract
The Xpert Flu+RSV Xpress Assay is a fast, automated in vitro diagnostic test for qualitative detection and differentiation of influenza A and B viruses and respiratory syncytial virus (RSV) performed on the Cepheid GeneXpert Xpress System. The objective of this study was to establish performance characteristics of the Xpert Flu+RSV Xpress Assay compared to those of the Prodesse ProFlu+ real-time reverse transcription-PCR (RT-PCR) assay (ProFlu+) for the detection of influenza A and B viruses as well as RSV in a Clinical Laboratory Improvement Amendments (CLIA)-waived (CW) setting. Overall, the assay, using fresh and frozen nasopharyngeal (NP) swabs, demonstrated high concordance with results of the ProFlu+ assay in the combined CW and non-CW settings with positive percent agreements (PPA) (100%, 100%, and 97.1%) and negative percent agreements (NPA) (95.2%, 99.5%, and 99.6%) for influenza A and B viruses and RSV, respectively. In conclusion, this multicenter study using the Cepheid Xpert Flu+RSV Xpress Assay demonstrated high sensitivities and specificities for influenza A and B viruses and RSV in ∼60 min for use at the point-of-care in the CW setting.Entities:
Keywords: CLIA-waived; DNA polymerase; influenza; respiratory syncytial virus
Mesh:
Substances:
Year: 2018 PMID: 29142048 PMCID: PMC5786727 DOI: 10.1128/JCM.01237-17
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948