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A two minute liquid based sample preparation for rapid SARS-CoV2 real-time PCR screening: A multicentre evaluation.
Claas, Eric C J; Smit, Pieter W; van Bussel, Mario J A W M; Verbakel, Harold; Taouil, Mohammed; Verweij, Jaco J; Thijsen, Steven F T.
Afiliação
  • Claas ECJ; Leiden University Medical Center, Department of Medical Microbiology, Leiden, the Netherlands. Electronic address: e.claas@lumc.nl.
  • Smit PW; Maasstad Hospital, Medical Microbiology Laboratory, Rotterdam, the Netherlands.
  • van Bussel MJAWM; Leiden University Medical Center, Department of Medical Microbiology, Leiden, the Netherlands.
  • Verbakel H; Elisabeth-Tweesteden Hospital, Microvida Laboratory for Medical Microbiology and Immunology, Tilburg, the Netherlands.
  • Taouil M; Maasstad Hospital, Medical Microbiology Laboratory, Rotterdam, the Netherlands.
  • Verweij JJ; Elisabeth-Tweesteden Hospital, Microvida Laboratory for Medical Microbiology and Immunology, Tilburg, the Netherlands.
  • Thijsen SFT; Diakonessenhuis Hospital, Department of Medical Microbiology and Immunology, the Netherlands.
J Clin Virol ; 135: 104720, 2021 02.
Article em En | MEDLINE | ID: mdl-33418142
ABSTRACT

BACKGROUND:

Apart from major health concerns associated to the SARS-coronavirus-2 (SARS-CoV-2) pandemic, also the diagnostic workflow encountered serious problems. Limited availability of kit components, buffers and even plastics has resulted in suboptimal testing procedures worldwide. Alternative workflows have been implemented to overcome these difficulties. Recently a liquid based sample prep has been launched as solution to overcome limitations in relation to nucleic acid extraction.

OBJECTIVE:

Multicenter evaluation of the QIAprep& Viral RNA UM kit (QIA P&A) for rapid sample preparation and real-time PCR detection of SARS-CoV-2 in comparison to standardized laboratory testing methods. STUDY

DESIGN:

Selected samples of the routine diagnostic workflow at Clinical Microbiology Laboratories of four Dutch hospitals have been subjected to the rapid QIA P&A protocol and the results have been compared to routine diagnostic data.

RESULTS:

Combining results of manual and automated procedures, a total of 377 clinical samples of which 202 had been tested positive with a wide range of CT values, showed almost complete concordance in the QIA P&A assay for samples up to CT values of 33 with one exception of CT 31. Prospectively 60 samples were tested and also showed 100 % concordance with 5 positives. The method has been automated by two centres.

CONCLUSIONS:

Despite an input of only 8 µL of clinical sample, the QIA P&A kit showed good performance for sample preparation and amplification of SARS-CoV-2 and can contribute as a rapid molecular testing strategy in managing the CoV-2 pandemic.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Programas de Rastreamento / Reação em Cadeia da Polimerase em Tempo Real / Teste para COVID-19 / SARS-CoV-2 / COVID-19 Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Programas de Rastreamento / Reação em Cadeia da Polimerase em Tempo Real / Teste para COVID-19 / SARS-CoV-2 / COVID-19 Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article