Evaluation of a new, rapid, simple test for the detection of influenza virus

dc.contributor.authorHurtado, Juan Carlos
dc.contributor.authorMosquera, Maria Mar
dc.contributor.authorLazzari, Elisa de
dc.contributor.authorMartínez Chamorro, Esteban José
dc.contributor.authorTorner Gràcia, Núria
dc.contributor.authorIsanta, Ricard
dc.contributor.authorMolina, Patricia de
dc.contributor.authorPumarola Suñé, Tomàs
dc.contributor.authorMarcos, Ma. Angeles
dc.contributor.authorVila Estapé, Jordi
dc.date.accessioned2016-11-14T12:28:16Z
dc.date.available2016-11-14T12:28:16Z
dc.date.issued2015-02-06
dc.date.updated2016-11-14T12:28:22Z
dc.description.abstractBackground: Influenza virus infections are responsible for significant morbidity and mortality in both pediatric and adult populations worldwide. Rapid and accurate diagnosis of influenza is necessary for appropriate patient management during the influenza season and for optimal utilization of anti-influenza therapy. We prospectively tested the accuracy of a simple and rapid diagnostic method. Methods: Ninety-eight samples (nasal and pharyngeal swabs) from patients with upper respiratory tract infection symptoms who presented to primary healthcare centres in Barcelona (Spain) were prospectively analyzed. The samples were collected as part of influenza surveillance program. Samples that had enough volume to make the new test after aliquoting the amount needed to perform routine tests were included. None of the samples were pre-selected as a result of their status in relation to influenza virus. Samples were analyzed by in-house real-time PCR and AlereTM i Influenza A & B (AlereTM i), which uses isothermal amplification of nucleic acids for the qualitative detection of influenza A and B in nasal swabs transported in viral transport media. The two techniques were compared by positive percent agreement (PPA) and negative percent agreement (NPA). Statistical analysis was performed with Stata. Results: Of the 98 samples analysed 90 were concordant; 46 (46.9%) were positive and 44 (44.9%) were negative. Five samples showed invalid results with the AlereTM i test and could be not re-tested due to insufficient sample volume and were not included in the final statistical analysis. In the 93 remaining samples, the AlereTM i test showed 97% of accuracy having correctly classified 90 samples. We obtained discordant results in 3 samples (3%). The PPA was 93.8% for influenza A and 94.1% for influenza B, and NPA was 100% for influenza A and influenza B virus. In addition, the AlereTM i was very rapid (15 minutes or less) and extremely easy to use. Conclusions: The AlereTM i test provided a good correlation compared to the real-time PCR test for the diagnosis of influenza. Since this method can be performed in minutes, it allows immediate, accurate clinical decisions to prescribe appropriate antiviral treatment or isolation of patients. Keywords: Influenza Virus A and B, Isothermal amplification, Real time PCR, Rapid test
dc.format.extent4 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec647616
dc.identifier.issn1471-2334
dc.identifier.pmid25656393
dc.identifier.urihttps://hdl.handle.net/2445/103664
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1186/s12879-015-0775-5
dc.relation.ispartofBmc Infectious Diseases, 2015, vol. 15, num. 44
dc.relation.urihttps://doi.org/10.1186/s12879-015-0775-5
dc.rightscc-by (c) Hurtado, J. C. et al., 2015
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationInfluenzavirus
dc.subject.classificationÀcids nucleics
dc.subject.otherInfluenza viruses
dc.subject.otherNucleic acids
dc.titleEvaluation of a new, rapid, simple test for the detection of influenza virus
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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