2020
DOI: 10.1101/2020.10.03.20205278
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Validation of self-collected buccal swab and saliva as a diagnostic tool for COVID-19

Abstract: Background: Effective management of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) requires large-scale testing. Collection of nasopharyngeal swab (NPS) by healthcare workers (HCW) is currently used to diagnose SARS-CoV-2, which increases the risk of transmission to HCWs. Self-administered saliva and buccal swabs are convenient, painless and safe alternative sample collection methods. Methods: A cross-sectional single centre study was conducted on 42 participants who were tested positive for SARS… Show more

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Cited by 12 publications
(19 citation statements)
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“…The second study included 42 individual who tested positive for SARS-CoV-2 by NP swab RT-qPCR within seven days prior to self-collected buccal swab (both cheeks, above and below the tongue, both gums, and on the hard palate), and a positive agreement of 56.7% was observed. (13) Herein we tested gingival fluid as a specimen for SARS-CoV-2 detection by RT-qPCR, and we found a poor concordance rate (15.38%) among RT-qPCR positive samples from NP swabs. Although our data is in agreement with previous data, our concordance rate among positive results was lower than the those reported by Ku et al (14) and Kam et al (12) .…”
Section: Discussionmentioning
confidence: 84%
“…The second study included 42 individual who tested positive for SARS-CoV-2 by NP swab RT-qPCR within seven days prior to self-collected buccal swab (both cheeks, above and below the tongue, both gums, and on the hard palate), and a positive agreement of 56.7% was observed. (13) Herein we tested gingival fluid as a specimen for SARS-CoV-2 detection by RT-qPCR, and we found a poor concordance rate (15.38%) among RT-qPCR positive samples from NP swabs. Although our data is in agreement with previous data, our concordance rate among positive results was lower than the those reported by Ku et al (14) and Kam et al (12) .…”
Section: Discussionmentioning
confidence: 84%
“… In patients with signs and symptoms compatible with severe or critical COVID-19 for the diagnosis of COVID-19 infection, we suggest the use of NAAT in nasopharyngeal swab samples versus NAAT in saliva samples for diagnosis of COVID-19. Weak against Very low [ 13 , 92 , [98] , [99] , [100] , [101] , [102] , [103] , [104] , [105] , [106] , [107] , [108] , [109] , [110] , [111] , [112] , [113] , [114] , [115] , [116] ] 22 In patients with signs and symptoms compatible with COVID-19 of equal or less than 7 days onset , should saliva sampling be used, compared with nasopharyngeal swab sampling for diagnosis of COVID-19 with NAAT? In patients with signs and symptoms compatible with COVID-19 of equal or less than 7 days-onset, we suggest the use of NAAT in saliva samples versus NAAT in nasopharyngeal swab samples for diagnosis of COVID-19.…”
Section: Recommendationsmentioning
confidence: 99%
“…Sample types such as anterior-nares or mid-turbinate nasal swabs [20][21][22][23] and saliva [24][25][26][27] To understand the required test sensitivity and the optimal sample type for earliest SARS-CoV-2 detection, we designed a case-ascertained study of household transmission with high-frequency sampling of both saliva and anterior-nares nasal swabs. Building on our earlier work, 14 we enrolled individuals ages 6 years and older who had recently tested positive (household index case), and their exposed household contacts at risk of infection.…”
Section: Introductionmentioning
confidence: 99%