| Literature DB >> 33298612 |
Carlo Fischer1, Ramona Mögling2, Jan Felix Drexler3,4, Chantal B E M Reusken5, Angeliki Melidou6, Arne Kühne1, Edmilson F Oliveira-Filho1, Thorsten Wolff7, Janine Reiche7, Eeva Broberg6, Christian Drosten1,4, Adam Meijer2, Katrin Leitmeyer6.
Abstract
During the ongoing coronavirus disease 2019 (COVID-19) outbreak, robust detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a key element for clinical management and to interrupt transmission chains. We organized an external quality assessment (EQA) of molecular detection of SARS-CoV-2 for European expert laboratories. An EQA panel composed of 12 samples, containing either SARS-CoV-2 at different concentrations to evaluate sensitivity or other respiratory viruses to evaluate specificity of SARS-CoV-2 testing, was distributed to 68 laboratories in 35 countries. Specificity samples included seasonal human coronaviruses hCoV-229E, hCoV-NL63, and hCoV-OC43, as well as Middle East respiratory syndrome coronavirus (MERS-CoV), SARS-CoV, and human influenza viruses A and B. Sensitivity results differed among laboratories, particularly for low-concentration SARS-CoV-2 samples. Results indicated that performance was mostly independent of the selection of specific extraction or PCR methods.Entities:
Keywords: COVID-19; EQA; Europe; SARS-CoV-2; diagnostics; molecular
Mesh:
Year: 2021 PMID: 33298612 DOI: 10.1128/JCM.02676-20
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948