Considerations for diagnostic COVID-19 tests

被引:0
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作者
Olivier Vandenberg
Delphine Martiny
Olivier Rochas
Alex van Belkum
Zisis Kozlakidis
机构
[1] Laboratoire Hospitalier Universtaire de Bruxelles — Universitair Laboratorium Brussel,Innovation and Business Development Unit
[2] Université Libre de Bruxelles,Center for Environmental Health and Occupational Health, School of Public Health
[3] Université Libre de Bruxelles,Division of Infection and Immunity, Faculty of Medical Sciences
[4] University College London,Department of Microbiology
[5] Laboratoire Hospitalier Universtaire de Bruxelles — Universitair Laboratorium Brussel,Strategic Intelligence, Corporate Business Development
[6] Université Libre de Bruxelles,Open Innovation and Partnerships
[7] bioMérieux,Laboratory Services and Biobank Group
[8] bioMérieux,undefined
[9] International Agency for Research on Cancer,undefined
[10] World Health Organization,undefined
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摘要
During the early phase of the coronavirus disease 2019 (COVID-19) pandemic, design, development, validation, verification and implementation of diagnostic tests were actively addressed by a large number of diagnostic test manufacturers. Hundreds of molecular tests and immunoassays were rapidly developed, albeit many still await clinical validation and formal approval. In this Review, we summarize the crucial role of diagnostic tests during the first global wave of COVID-19. We explore the technical and implementation problems encountered during this early phase in the pandemic, and try to define future directions for the progressive and better use of (syndromic) diagnostics during a possible resurgence of COVID-19 in future global waves or regional outbreaks. Continuous global improvement in diagnostic test preparedness is essential for more rapid detection of patients, possibly at the point of care, and for optimized prevention and treatment, in both industrialized countries and low-resource settings.
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页码:171 / 183
页数:12
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