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10.1002/jmv.26673

http://scihub22266oqcxt.onion/10.1002/jmv.26673
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33200414!7753543!33200414
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suck abstract from ncbi


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pmid33200414      J+Med+Virol 2021 ; 93 (4): 1837-1842
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  • Guidelines on newly identified limitations of diagnostic tools for COVID-19 and consequences #MMPMID33200414
  • Syal K
  • J Med Virol 2021[Apr]; 93 (4): 1837-1842 PMID33200414show ga
  • Coronavirus disease 2019 (COVID-19) caused by coronavirus has spread worldwide and has become the deadliest pandemic of the 21st century. Such rapid spread is predominantly attributed to the poor diagnosis and its asymptomatic transmission. In the absence of treatment regime, timely diagnosis is the best available remedy that can restrict its spread. An early diagnosis of COVID-19 is critical for determining the line of treatment and preventing long term complications in the infected subject. Unfortunately, available rapid antigen and antibody kits are known to be erroneous whereas reverse transcription polymerase chain reaction based tests are expensive, viral load dependent and at times inconclusive. In current scenario, the false-negative results imposed a major risk to the individual patient care and also to the efforts for containing the spread at the population level, where as false positives are traumatic for families and can lead to improper treatment resulting in severe complications. In this article, the limitations of available diagnostic procedures have been elaborated and plausible combination approach has been advised.
  • |*COVID-19 Nucleic Acid Testing/standards[MESH]
  • |*COVID-19 Serological Testing/standards[MESH]
  • |*COVID-19 Testing/standards[MESH]
  • |Antibodies, Viral/blood[MESH]
  • |Antigens, Viral/analysis[MESH]
  • |COVID-19/*diagnosis[MESH]
  • |False Negative Reactions[MESH]
  • |False Positive Reactions[MESH]
  • |Humans[MESH]
  • |SARS-CoV-2/immunology/isolation & purification[MESH]
  • |Sensitivity and Specificity[MESH]


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