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Using Real-Time PCR Fluorescence Reaction Values to Improve SARS-CoV-2 Virus Detection and Benefit Clinical Decision-Making.

Wan-Wen YangChin-Wen HsuYu-Ju ChanShih-Bin SuI-Jung FengChia-Yi HouChien-Yuan Huang
Published in: Life (Basel, Switzerland) (2023)
This study aimed to compare the SARS-CoV-2 nucleic acid detection results of the BD MAX™ System and other platforms to formulate an optimized laboratory verification process. The re-examination of 400 samples determined as positive by BD MAX™ indicated that the inconsistency rate between BD MAX™ and the other platforms was 65.8%; the inconsistency rate of single-gene-positive results was as high as 99.2%. A receiver operating characteristic curve was drawn for the relative light unit (RLU) values of samples positive for a single gene, and RLU 800 was used as the cutoff. After setting the retest standard as single-gene positive and RLU ≥ 800, the number of the 260 BD MAX™ single-gene positives that needed to be confirmed again was 36 (13.8%) and the number that could be directly reported as negative was 224 (86.2%). This verification process can shorten the reporting period and speed up the epidemic adjustment time and turnover rate of special wards, thereby improving SARS-CoV-2 detection efficiency and clinical decision-making.
Keyphrases
  • sars cov
  • real time pcr
  • decision making
  • copy number
  • genome wide
  • respiratory syndrome coronavirus
  • nucleic acid
  • label free
  • loop mediated isothermal amplification
  • dna methylation
  • single molecule