About: Multicenter Evaluation of the QIAstat-Dx Respiratory Panel for Detection of Viruses and Bacteria in Nasopharyngeal Swab Specimens

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About: Multicenter Evaluation of the QIAstat-Dx Respiratory Panel for Detection of Viruses and Bacteria in Nasopharyngeal Swab Specimens Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Multicenter Evaluation of the QIAstat-Dx Respiratory Panel for Detection of Viruses and Bacteria in Nasopharyngeal Swab Specimens
Creator	Leber, Amy Young, Stephen Hansen, Glen Relich, Ryan Hannet, Irene Lisby, Jan Schneider, Uffe Granato, Paul Pareja, Josep
Source	Medline; PMC
abstract	The QIAstat-Dx Respiratory Panel (QIAstat-Dx RP) is a multiplex in vitro diagnostic test for the qualitative detection of 20 pathogens directly from nasopharyngeal swab (NPS) specimens. The assay is performed using a simple sample-to-answer platform with results available in approximately 69 min. The pathogens identified are adenovirus, coronavirus 229E, coronavirus HKU1, coronavirus NL63, coronavirus OC43, human metapneumovirus A and B, influenza A, influenza A H1, influenza A H3, influenza A H1N1/2009, influenza B, parainfluenza virus 1, parainfluenza virus 2, parainfluenza virus 3, parainfluenza virus 4, rhinovirus/enterovirus, respiratory syncytial virus A and B, Bordetella pertussis, Chlamydophila pneumoniae, and Mycoplasma pneumoniae. This multicenter evaluation provides data obtained from 1,994 prospectively collected and 310 retrospectively collected (archived) NPS specimens with performance compared to that of the BioFire FilmArray Respiratory Panel, version 1.7. The overall percent agreement between QIAstat-Dx RP and the comparator testing was 99.5%. In the prospective cohort, the QIAstat-Dx RP demonstrated a positive percent agreement of 94.0% or greater for the detection of all but four analytes: coronaviruses 229E, NL63, and OC43 and rhinovirus/enterovirus. The test also demonstrated a negative percent agreement of ≥97.9% for all analytes. The QIAstat-Dx RP is a robust and accurate assay for rapid, comprehensive testing for respiratory pathogens.
has issue date	2020-04-23(xsd:dateTime)
bibo:doi	10.1128/jcm.00155-20
bibo:pmid	32132186
has license	cc-by
sha1sum (hex)	ab3a4d6eaa47e161400af58c4c63bb62dfe36115
schema:url	https://doi.org/10.1128/jcm.00155-20
resource representing a document's title	Multicenter Evaluation of the QIAstat-Dx Respiratory Panel for Detection of Viruses and Bacteria in Nasopharyngeal Swab Specimens
has PubMed Central identifier	PMC7180242
has PubMed identifier	32132186
schema:publication	J Clin Microbiol
resource representing a document's body	covid:ab3a4d6eaa47e161400af58c4c63bb62dfe36115#body_text
is schema:about of	named entity 'TESTING' named entity 'INFLUENZA A' named entity 'DETECTION' named entity 'SIMPLE' named entity 'SAMPLE' named entity '99.5' named entity 'parainfluenza virus' named entity 'pathogens' named entity 'enterovirus' named entity 'enterovirus' named entity 'influenza' named entity 'Chlamydophila pneumoniae' named entity 'coronaviruses' named entity 'coronavirus HKU1' named entity 'parainfluenza virus 3' named entity 'H1N1' named entity 'Viruses' named entity 'Bacteria' named entity 'influenza' named entity 'pathogens' named entity 'respiratory syncytial virus' named entity 'coronavirus' named entity 'NL63' named entity '229E' named entity 'Bordetella pertussis' named entity 'adenovirus' named entity '229E' named entity 'PATHOGENS' named entity 'OC43' named entity 'VERSION' named entity 'MYCOPLASMA PNEUMONIAE' named entity 'diagnostic test' named entity 'influenza' named entity 'NL63' named entity 'nasopharyngeal swab' named entity 'parainfluenza virus' named entity 'pathogens' named entity 'influenza' named entity 'ROBUST' named entity 'APPROXIMATELY' named entity 'OBTAINED' named entity 'COMPARATOR' named entity 'INFLUENZA B' named entity 'NEGATIVE' named entity 'PARAINFLUENZA VIRUS 1' named entity 'COMPREHENSIVE' named entity 'DIRECTLY' named entity 'PLATFORM' named entity '310' named entity 'H1N1' named entity 'PANEL' named entity 'PARAINFLUENZA VIRUS 2' named entity 'PERFORMANCE' named entity 'COLLECTED' named entity 'ANALYTES' named entity 'DIAGNOSTIC TEST' named entity 'CORONAVIRUS OC43' named entity 'EVALUATION' named entity 'PERCENT' named entity 'IN VITRO' named entity 'PARAINFLUENZA VIRUS 4' named entity '229E' named entity 'NPS' named entity 'BORDETELLA PERTUSSIS' named entity 'VITRO DIAGNOSTIC' named entity 'SPECIMENS' named entity 'coronavirus' covid:arg/ab3a4d6eaa47e161400af58c4c63bb62dfe36115 named entity 'CORONAVIRUS NL63' named entity 'MIN' named entity 'RESPIRATORY PATHOGENS' named entity 'OVERALL' named entity 'CORONAVIRUS HKU1'

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