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Evaluation of water gargle samples for SARS-CoV-2 detection using Abbott ID NOW COVID-19 assay.
Lévesque, Simon; Beauchemin, Stéphanie; Vallée, Maud; Longtin, Jean; Jacob-Wagner, Mariève; Dumaresq, Jeannot; Dulcey, Carlos; Labbé, Annie-Claude.
  • Lévesque S; Service de microbiologie, CIUSSS de l'Estrie-Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Québec, Canada.
  • Beauchemin S; Département de microbiologie et infectiologie, Université de Sherbrooke, Sherbrooke, Québec, Canada.
  • Vallée M; Département des laboratoires de biologie médicale, Grappe Optilab-CHUM, Centre hospitalier de l'Université de Montréal, Montréal, Québec, Canada.
  • Longtin J; Laboratoire de santé publique du Québec, Institut national de santé publique du Québec, Ste-Anne-de-Bellevue, Québec, Canada.
  • Jacob-Wagner M; Département de microbiologie et d'infectiologie du centre hospitalier universitaire (CHU) de Québec-Université Laval, Québec, Québec, Canada.
  • Dumaresq J; Département de microbiologie-infectiologie et d'immunologie, Faculté de Médecine, Université Laval, Québec, Québec, Canada.
  • Dulcey C; Département de microbiologie et d'infectiologie du centre hospitalier universitaire (CHU) de Québec-Université Laval, Québec, Québec, Canada.
  • Labbé AC; Département de microbiologie et d'infectiologie du centre hospitalier universitaire (CHU) de Québec-Université Laval, Québec, Québec, Canada.
J Med Virol ; 94(9): 4522-4527, 2022 09.
Article in English | MEDLINE | ID: covidwho-1826060
ABSTRACT
The Abbott ID NOW™ COVID-19 assay has been shown as a reliable and sensitive alternative to reverse transcription-polymerase chain reaction (RT-PCR) testing from nasopharyngeal or nasal samples in symptomatic patients. Water gargle is an acceptable noninvasive alternative specimen for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) detection by RT-PCR. The objective of this study was to evaluate the performance of water gargle samples for the detection of SARS-CoV-2 using the ID NOW. Residual gargle samples were randomly selected among positive standard of care (SOC)-nucleic acid amplification test (NAAT) samples. For testing on ID NOW, the manufacturer's instructions were followed, except for the specimen addition step 500 µl of the gargle specimen was added to the blue sample receiver with a pipette and gently mixed. Among the 202 positive samples by SOC-NAAT, 185 were positive by ID NOW (positive percent agreement [PPA]) = 91.6% (95% confidence interval [CI] 86.9-95.0). For the 17 discordant samples, cycle threshold (Ct ) values were all ≥31.0. The PPA was significantly lower among asymptomatic patients (84.4%; 95% CI 73.2-92.3) versus symptomatic patients (95.2%; 95% CI 89.8-98.2). The performance of the ID NOW for the detection of SARS-CoV-2 infection on gargle samples is excellent when Ct values are <31.0 and for patients that have COVID-19 compatible symptoms.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: J Med Virol Year: 2022 Document Type: Article Affiliation country: Jmv.27847

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: J Med Virol Year: 2022 Document Type: Article Affiliation country: Jmv.27847