| Literature DB >> 33027042 |
Mary Kathryn Bohn1, Nicasio Mancini2, Tze Ping Loh3, Cheng-Bin Wang4, Matthias Grimmler5, Maurizio Gramegna6, Kwok-Yung Yuen7, Robert Mueller8, David Koch9, Sunil Sethi3, William D Rawlinson10, Massimo Clementi2, Rajiv Erasmus11, Marc Leportier12, Gye Cheol Kwon13, María Elizabeth Menezes14, Maria-Magdalena Patru15, Krishna Singh16, Maurizio Ferrari2, Osama Najjar17, Andrea R Horvath18, Khosrow Adeli1, Giuseppe Lippi19,20.
Abstract
The diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection globally has relied extensively on molecular testing, contributing vitally to case identification, isolation, contact tracing, and rationalization of infection control measures during the coronavirus disease 2019 (COVID-19) pandemic. Clinical laboratories have thus needed to verify newly developed molecular tests and increase testing capacity at an unprecedented rate. As the COVID-19 pandemic continues to pose a global health threat, laboratories continue to encounter challenges in the selection, verification, and interpretation of these tests. This document by the International Federation for Clinical Chemistry and Laboratory Medicine (IFCC) Task Force on COVID-19 provides interim guidance on: (A) clinical indications and target populations, (B) assay selection, (C) assay verification, and (D) test interpretation and limitations for molecular testing of SARS-CoV-2 infection. These evidence-based recommendations will provide practical guidance to clinical laboratories worldwide and highlight the continued importance of laboratory medicine in our collective pandemic response.Entities:
Keywords: COVID-19; SARS-CoV-2; molecular testing; virology
Mesh:
Year: 2020 PMID: 33027042 DOI: 10.1515/cclm-2020-1412
Source DB: PubMed Journal: Clin Chem Lab Med ISSN: 1434-6621 Impact factor: 3.694