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Diagnostic performance and characteristics of anterior nasal collection for the SARS-CoV-2 antigen test: a prospective study
The clinical utility of antigen test using anterior nasal samples has not been well evaluated. We conducted a prospective study in a drive-through testing site located at a PCR center to evaluate the diagnostic performance of the antigen test QuickNavi-COVID19 Ag using anterior nasal samples and to...
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Published in: | Scientific reports 2021-05, Vol.11 (1), p.10519-10519, Article 10519 |
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description | The clinical utility of antigen test using anterior nasal samples has not been well evaluated. We conducted a prospective study in a drive-through testing site located at a PCR center to evaluate the diagnostic performance of the antigen test QuickNavi-COVID19 Ag using anterior nasal samples and to compare the degrees of coughs or sneezes induction and the severity of pain between anterior nasal collection and nasopharyngeal collection. The study included a total of 862 participants, of which 91.6% were symptomatic. The median duration from symptom onset to sample collection was 2.0 days. Fifty-one participants tested positive for severe acute respiratory syndrome coronavirus 2 on reverse transcription PCR (RT-PCR) with nasopharyngeal samples, and all of them were symptomatic. In comparison to the findings of RT-PCR, the antigen test using anterior nasal samples showed 72.5% sensitivity (95% confidence interval [CI] 58.3–84.1%) and 100% specificity (95% CI 99.3–100%). Anterior nasal collection was associated with a significantly lower degree of coughs or sneezes induction and the severity of pain in comparison to nasopharyngeal collection (
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doi_str_mv | 10.1038/s41598-021-90026-8 |
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p
< 0.001). The antigen test using anterior nasal samples showed moderate sensitivity in symptomatic patients who were at the early stages of the disease course but was less painful and induced fewer coughs or sneezes.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-021-90026-8</identifier><identifier>PMID: 34006975</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/2521 ; 631/326/596/4130 ; 692/308 ; Antigens ; Coronaviruses ; COVID-19 ; Humanities and Social Sciences ; multidisciplinary ; Pain ; Polymerase chain reaction ; Reverse transcription ; Science ; Science (multidisciplinary) ; Severe acute respiratory syndrome coronavirus 2</subject><ispartof>Scientific reports, 2021-05, Vol.11 (1), p.10519-10519, Article 10519</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-cd5a3bafeb561439ed02cb3a046058884dd6a4771c358ea7873ba0f97fb3960b3</citedby><cites>FETCH-LOGICAL-c540t-cd5a3bafeb561439ed02cb3a046058884dd6a4771c358ea7873ba0f97fb3960b3</cites><orcidid>0000-0001-9789-8301 ; 0000-0002-6643-6208</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2528635200/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2528635200?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34006975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeuchi, Yuto</creatorcontrib><creatorcontrib>Akashi, Yusaku</creatorcontrib><creatorcontrib>Kato, Daisuke</creatorcontrib><creatorcontrib>Kuwahara, Miwa</creatorcontrib><creatorcontrib>Muramatsu, Shino</creatorcontrib><creatorcontrib>Ueda, Atsuo</creatorcontrib><creatorcontrib>Notake, Shigeyuki</creatorcontrib><creatorcontrib>Nakamura, Koji</creatorcontrib><creatorcontrib>Ishikawa, Hiroichi</creatorcontrib><creatorcontrib>Suzuki, Hiromichi</creatorcontrib><title>Diagnostic performance and characteristics of anterior nasal collection for the SARS-CoV-2 antigen test: a prospective study</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The clinical utility of antigen test using anterior nasal samples has not been well evaluated. We conducted a prospective study in a drive-through testing site located at a PCR center to evaluate the diagnostic performance of the antigen test QuickNavi-COVID19 Ag using anterior nasal samples and to compare the degrees of coughs or sneezes induction and the severity of pain between anterior nasal collection and nasopharyngeal collection. The study included a total of 862 participants, of which 91.6% were symptomatic. The median duration from symptom onset to sample collection was 2.0 days. Fifty-one participants tested positive for severe acute respiratory syndrome coronavirus 2 on reverse transcription PCR (RT-PCR) with nasopharyngeal samples, and all of them were symptomatic. In comparison to the findings of RT-PCR, the antigen test using anterior nasal samples showed 72.5% sensitivity (95% confidence interval [CI] 58.3–84.1%) and 100% specificity (95% CI 99.3–100%). Anterior nasal collection was associated with a significantly lower degree of coughs or sneezes induction and the severity of pain in comparison to nasopharyngeal collection (
p
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We conducted a prospective study in a drive-through testing site located at a PCR center to evaluate the diagnostic performance of the antigen test QuickNavi-COVID19 Ag using anterior nasal samples and to compare the degrees of coughs or sneezes induction and the severity of pain between anterior nasal collection and nasopharyngeal collection. The study included a total of 862 participants, of which 91.6% were symptomatic. The median duration from symptom onset to sample collection was 2.0 days. Fifty-one participants tested positive for severe acute respiratory syndrome coronavirus 2 on reverse transcription PCR (RT-PCR) with nasopharyngeal samples, and all of them were symptomatic. In comparison to the findings of RT-PCR, the antigen test using anterior nasal samples showed 72.5% sensitivity (95% confidence interval [CI] 58.3–84.1%) and 100% specificity (95% CI 99.3–100%). Anterior nasal collection was associated with a significantly lower degree of coughs or sneezes induction and the severity of pain in comparison to nasopharyngeal collection (
p
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subjects | 631/326/2521 631/326/596/4130 692/308 Antigens Coronaviruses COVID-19 Humanities and Social Sciences multidisciplinary Pain Polymerase chain reaction Reverse transcription Science Science (multidisciplinary) Severe acute respiratory syndrome coronavirus 2 |
title | Diagnostic performance and characteristics of anterior nasal collection for the SARS-CoV-2 antigen test: a prospective study |
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