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10.1038/s41579-020-00461-z

http://scihub22266oqcxt.onion/10.1038/s41579-020-00461-z
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33057203!7556561!33057203
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suck abstract from ncbi

pmid33057203      Nat+Rev+Microbiol 2021 ; 19 (3): 171-183
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  • Considerations for diagnostic COVID-19 tests #MMPMID33057203
  • Vandenberg O; Martiny D; Rochas O; van Belkum A; Kozlakidis Z
  • Nat Rev Microbiol 2021[Mar]; 19 (3): 171-183 PMID33057203show ga
  • 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.
  • |*COVID-19 Testing/economics/methods/standards[MESH]
  • |COVID-19/diagnosis[MESH]
  • |Developed Countries[MESH]
  • |Developing Countries[MESH]
  • |Diagnostic Test Approval[MESH]
  • |Humans[MESH]
  • |Manufacturing Industry[MESH]
  • |Pandemics[MESH]
  • |Point-of-Care Testing[MESH]
  • |SARS-CoV-2/genetics/*isolation & purification[MESH]
  • |Time Factors[MESH]


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