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dc.contributor.authorMasiá, Mar-
dc.contributor.authorFernández-González, Marta-
dc.contributor.authorSánchez-Molla, Manuel-
dc.contributor.authorCarvajal, Mar-
dc.contributor.authorGarcía, José Alberto-
dc.contributor.authorGonzalo Jiménez, Nieves-
dc.contributor.authorOrtiz de la Tabla, Victoria-
dc.contributor.authorAgulló, Vanesa-
dc.contributor.authorCandela, Inmaculada-
dc.contributor.authorGuijarro, Jorge-
dc.contributor.authorGutiérrez, José Antonio-
dc.contributor.authorde Gregorio, Carlos-
dc.contributor.authorGutiérrez, Félix-
dc.contributor.otherDepartamentos de la UMH::Medicina Clínicaes_ES
dc.date.accessioned2025-11-06T09:39:14Z-
dc.date.available2025-11-06T09:39:14Z-
dc.date.created2021-02-
dc.identifier.citationOpen Forum Infectious Diseases, 8(3), ofab059 - February 2021es_ES
dc.identifier.issn2328-8957-
dc.identifier.urihttps://hdl.handle.net/11000/37902-
dc.description.abstractBackground. Performance of point-of-care tests in different clinical scenarios and on different samples remains undetermined. We comprehensively evaluated the performance of the nasopharyngeal Panbio COVID-19 Ag Rapid Test Device. Methods. This is a prospective study that includes consecutive patients attending 3 primary care centers (PCCs) and an emergency department. The antigen test was performed at point-of-care in nasopharyngeal and nasal swabs and in saliva. Positive percent agreement (PPA) and negative percent agreement (NPA) were calculated with the reverse-transcription polymerase chain reaction (RT-PCR) assay as reference standard. Results. Of 913 patients included, 296 (32.3%) were asymptomatic and 690 (75.6%) came from the PCC. Nasopharyngeal swabs were collected from 913 patients, nasal swabs were collected from 659 patients, and saliva was collected from 611 patients. The RT-PCR was positive in 196 (21.5%) nasopharyngeal samples (NPS). Overall, PPA (95% CI) in NPS was 60.5% (53.3–67.4), and it was lower in nasal swabs (44.7%) and saliva (23.1%). Test performance in NPS was largely dependent on the cycle threshold (Ct) in RT-PCR, with PPA of 94% for Ct ≤25 and 80% for Ct <30. In symptomatic patients, the PPA was 95% for Ct ≤25, 85% for Ct <30, and 89% for the symptom triad of fever, cough, and malaise. Performance was also dependent on age, with a PPA of 100% in symptomatic patients >50 years with Ct <25. In asymptomatic patients, the PPA was 86% for Ct <25. In all cases, NPA was 100%. Conclusions. The nasopharyngeal Panbio COVID-19 Ag test performed at point-of-care has a good sensitivity in symptomatic patients with Ct <30 and older age. The test was useful to identify asymptomatic patients with lower Ct values.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent9es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectantigenes_ES
dc.subjectCOVID-19es_ES
dc.subjectPanbioes_ES
dc.subjectpoint-of-carees_ES
dc.subjectSARS-CoV-2es_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes_ES
dc.titleNasopharyngeal Panbio COVID-19 Antigen Performed at Point-of-Care Has a High Sensitivity in Symptomatic and Asymptomatic Patients With Higher Risk for Transmission and Older Agees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.1093/ofid/ofab059es_ES
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