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Accurate PCR Detection of Influenza A/B and Respiratory Syncytial Viruses by Use of Cepheid Xpert Flu+RSV Xpress Assay in Point-of-Care Settings: Comparison to Prodesse ProFlu.
Cohen, Daniel M; Kline, Jennifer; May, Larissa S; Harnett, Glenn Eric; Gibson, Jane; Liang, Stephen Y; Rafique, Zubaid; Rodriguez, Carina A; McGann, Kevin M; Gaydos, Charlotte A; Mayne, Donna; Phillips, David; Cohen, Jason.
Afiliação
  • Cohen DM; Division of Emergency Medicine, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio, USA daniel.cohen@nationwidechildrens.org.
  • Kline J; Division of Emergency Medicine, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio, USA.
  • May LS; Department of Emergency Medicine, University of California-Davis, Sacramento, California, USA.
  • Harnett GE; No-Resistance Consulting Group, Birmingham, Alabama, USA.
  • Gibson J; University of Central Florida College of Medicine, Orlando, Florida, USA.
  • Liang SY; Washington University School of Medicine, Saint Louis, Missouri, USA.
  • Rafique Z; Baylor College of Medicine, Houston, Texas, USA.
  • Rodriguez CA; University of South Florida, Tampa, Florida, USA.
  • McGann KM; Healthplex Family Clinic, LLC, Shreveport, Louisiana, USA.
  • Gaydos CA; Johns Hopkins University, Baltimore, Maryland, USA.
  • Mayne D; Sacred Heart Hospital, Pensacola, Florida, USA.
  • Phillips D; Pensacola Research Consultants, Inc., Pensacola, Florida, USA.
  • Cohen J; Albany Medical Center Hospital, Albany, New York, USA.
J Clin Microbiol ; 56(2)2018 02.
Article em En | MEDLINE | ID: mdl-29142048
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus da Influenza A / Vírus da Influenza B / Vírus Sincicial Respiratório Humano / Sistemas Automatizados de Assistência Junto ao Leito / Técnicas de Diagnóstico Molecular / Reação em Cadeia da Polimerase em Tempo Real Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus da Influenza A / Vírus da Influenza B / Vírus Sincicial Respiratório Humano / Sistemas Automatizados de Assistência Junto ao Leito / Técnicas de Diagnóstico Molecular / Reação em Cadeia da Polimerase em Tempo Real Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos