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10.1016/j.diagmicrobio.2021.115469

http://scihub22266oqcxt.onion/10.1016/j.diagmicrobio.2021.115469
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34280773!8230941!34280773
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suck abstract from ncbi


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pmid34280773      Diagn+Microbiol+Infect+Dis 2021 ; 101 (2): 115469
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  • Practical strategies for SARS-CoV-2 RT-PCR testing in resource-constrained settings #MMPMID34280773
  • Muller MS; Chhetri SB; Basham C; Rapp T; Lin FC; Lin K; Westreich D; Cerami C; Juliano JJ; Lin JT
  • Diagn Microbiol Infect Dis 2021[Oct]; 101 (2): 115469 PMID34280773show ga
  • Alternatives to nasopharyngeal sampling are needed to increase capacity for SARS-CoV-2 testing. Among 275 participants, we piloted the collection of nasal mid-turbinate swabs amenable to self-testing, including polyester flocked swabs as well as 3D-printed plastic lattice swabs, placed into viral transport media or an RNA stabilization agent. Flocked nasal swabs identified 104/121 individuals who were PCR-positive for SARS-CoV-2 by nasopharyngeal sampling (sensitivity 87%, 95% CI 79-92%), missing those with low viral load (<10(6) viral copies/mL). 3D-printed nasal swabs showed similar sensitivity. When nasal swabs were placed directly into RNA preservative, the mean 1.4 log decrease in viral copies/uL compared to nasopharyngeal samples was reduced to <1 log, even when samples were left at room temperature for up to 7 days. We also evaluated pooling strategies that involved pooling specimens in the lab versus pooling swabs at the point of collection, finding both successfully detected samples with >10(5) viral copies/mL.
  • |COVID-19 Nucleic Acid Testing/*methods[MESH]
  • |COVID-19/*diagnosis[MESH]
  • |Health Resources/supply & distribution[MESH]
  • |Humans[MESH]
  • |Limit of Detection[MESH]
  • |Nasopharynx/virology[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2/genetics/*isolation & purification[MESH]
  • |Self-Testing[MESH]
  • |Specimen Handling/instrumentation/methods[MESH]
  • |Turbinates/virology[MESH]


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