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Clinical evaluation of the Diagnostic Analyzer for Selective Hybridization (DASH): a point-of-care PCR test for rapid detection of SARS-CoV-2 infection
Chad J Achenbach; Matthew Caputo; Claudia Hawkins; Lauren C Balmert; Chao Qi; Joseph Odorisio; Etienne Dembele; Alema Jackson; Hiba Abbas; Jennifer K Frediani; Joshua M Levy; Paulina Alejandra Rebolledo; Russell R Kempker; Annette M Esper; Wilbur A Lam; Greg S Martin; Robert L Murphy.
Afiliação
  • Chad J Achenbach; Northwestern University
  • Matthew Caputo; Northwestern University
  • Claudia Hawkins; Northwestern University
  • Lauren C Balmert; Northwestern University
  • Chao Qi; Northwestern University
  • Joseph Odorisio; Northwestern University
  • Etienne Dembele; Northwestern University
  • Alema Jackson; Access Community Health Network
  • Hiba Abbas; Access Community Health Network
  • Jennifer K Frediani; Emory University
  • Joshua M Levy; Emory University
  • Paulina Alejandra Rebolledo; Rollis School of Public Health, Emory University
  • Russell R Kempker; Emory University
  • Annette M Esper; Emory University
  • Wilbur A Lam; Emory University
  • Greg S Martin; Emory University
  • Robert L Murphy; Northwestern University
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22269785
ABSTRACT
BackgroundRapid and accurate testing for SARS-CoV-2 is an essential tool in the medical and public health response to the COVID-19 pandemic. An ideal test for COVID-19 would combine the sensitivity of laboratory-based PCR combined with the speed and ease of use of point-of-care (POC) or home-based rapid antigen testing. MethodsTo evaluate the performance of the Diagnostic Analyzer for Selective Hybridization (DASH) SARS-CoV-2 POC PCR (sample insertion to result time of 16 minutes), we conducted a cross-sectional study of adults with and without symptoms of COVID-19 at four clinical sites. We collected two bilateral anterior nasal swabs from each participant and information on COVID-19 symptoms, vaccination, and exposure. One swab was tested with the DASH SARS-CoV-2 POC PCR and the second in a central laboratory using Cepheid Xpert Xpress SARS-CoV-2 PCR. We assessed test concordance and calculated sensitivity, specificity, negative and positive predictive values using Xpert as the "gold standard." ResultsWe enrolled 315 and analyzed 313 participants with median age 42 years; 65% were female, 62% symptomatic, 75% had received [≥]2 doses of mRNA COVID-19 vaccine, and 16% currently COVID-19 positive. There were concordant results for 307 tests indicating an overall agreement for DASH of 0.98 [95% CI 0.96, 0.99] compared to Xpert. DASH performed at 0.96 [95% CI 0.86, 1.00] sensitivity and 0.98 [95% CI 0.96, 1.00] specificity, with a positive predictive value of 0.85 [95% CI 0.73, 0.96] and negative predictive value of 0.996 [95% CI 0.99, 1.00]. The six discordant tests between DASH and Xpert all had high Ct values (>30) on the respective positive assay. DASH and Xpert Ct values were highly correlated (R=0.89 [95% CI 0.81, 0.94]). ConclusionsDASH POC SARS-CoV-2 PCR was accurate, easy to use, and provided fast results in real-life clinical settings with an overall performance similar to an EUA-approved laboratory-based PCR. Its compact design and ease of use are optimal for a variety of healthcare, and potentially community settings, including areas with lack of access to central laboratory-based PCR testing. SummaryDASH is an accurate, easy to use, and fast point-of-care test with applications for diagnosis and screening of SARS-CoV-2 infection.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo diagnóstico / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo diagnóstico / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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