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dc.contributor.authorMesquita Ramírez, Mirta
dc.contributor.authorZárate, Mirian Noemí 
dc.contributor.authorRodríguez, Leonidas Adelaida
dc.contributor.authorAquino Quintana, Víctor Hugo 
dc.contributor.otherSalud y Nutrición - Paraguay SRLes
dc.date.accessioned2024-01-30T00:42:55Z
dc.date.available2024-01-30T00:42:55Z
dc.date.issued2023-10-05
dc.identifier.citationMesquita Ramírez, M., Zarate, M. N., Rodríguez, L. A., & Aquino, V. H. (2023). Performance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital setting. PloS one, 18(10), Artículo e0292314. https://doi.org/10.1371/journal.pone.0292314en
dc.identifier.otherhttps://doi.org/10.1371/journal.pone.0292314es
dc.identifier.urihttp://hdl.handle.net/20.500.14066/4366
dc.descriptionAutor de correspondencia: vhaquino@iics.una.pyes
dc.description.abstractThe highly contagious nature of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of Coronavirus Disease 2019 (COVID-19), requires rapid diagnostic tests to prevent the virus from spreading within hospitals and communities. Reverse transcription followed by the polymerase chain reaction (RT-PCR) test is the gold standard for detecting SARS-CoV-2 infections but is time-consuming, labor-intensive, and restricted to centralized laboratories. There is a growing need to develop and implement point-of-care and rapid tests for SARS-CoV-2 detection to address these limitations. We aimed to evaluate the performance of BioFire Film Array Respiratory Panel 2.1 (BioFire FA-RP2.1) for SARS-CoV-2 detection in a pediatric hospital setting. The BioFire FA-RP2.1 test provides rapid results and can identify several viral and bacterial infections in a single test. This prospective, cross-sectional, diagnostic accuracy study enrolled participants ranging from 0 to 18 years of age, seeking medical consultation for any reason, who had been in contact with individuals confirmed to have COVID-19 or managed at the hospital for medical or surgical reasons. We employed a systematic sampling technique to ensure a representative sample. The study included 339 participants with a median age of 5 years. The BioFire FA-RP2.1 test detected SARS-CoV-2 in 18.6% of cases, while the reference RT-PCR test in 14% of cases. The BioFire FA-RP2.1 sensitivity and specificity for SARS CoV-2 detection were 98% and 94%, respectively. The positive probability coefficient (LR+) was 18. The agreement between the two tests was 0.80. In addition, the BioFire FA-RP2.1 test detected coinfection with two viruses in 7,6% of cases. The BioFire FA-RP2.1 is a reliable solution to meet pediatric healthcare needs and improve prognosis in the post-pandemic era thanks to its friendly interface and rapid testing process.es
dc.description.sponsorshipConsejo Nacional de Ciencia y Tecnologíaes
dc.language.isoenges
dc.publisherPublic Library of Sciencees
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.otherCOVID-19/diagnósticoes
dc.subject.otherEstudios prospectivoses
dc.subject.otherEstudios transversaleses
dc.subject.otherHospitales pediátricoses
dc.subject.otherNiñoes
dc.subject.otherPreescolares
dc.subject.otherSARS-CoV-2/genéticaes
dc.subject.otherSensibilidad y especificidades
dc.subject.otherCOVID-19/diagnosises
dc.subject.otherProspective studieses
dc.subject.otherCross-sectional studieses
dc.subject.otherHospitals, Pediatrices
dc.subject.otherChildes
dc.subject.otherChild, Preschooles
dc.subject.otherSARS-CoV-2/geneticses
dc.subject.otherSensitivity and specificityen
dc.titlePerformance evaluation of Biofire Film Array Respiratory Panel 2.1 for SARS-CoV-2 detection in a pediatric hospital settinges
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1371/journal.pone.0292314es
dc.description.fundingtextPrograma Paraguayo para el Desarrollo de la Ciencia y Tecnología. Proyectos de investigación y desarrolloes
dc.identifier.essn1932-6203es
dc.issue.number10es
dc.journal.titlePLOS ONEes
dc.relation.projectCONACYTPINV20-287es
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.copyright© 2023 Ramirez et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es
dc.volume.number18es


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Atribución 4.0 Internacional
Except where otherwise noted, this item's license is described as Atribución 4.0 Internacional