Global Point of Care

C. DIFF QUIK CHEK コンプリート

C. DIFF QUIK CHEK コンプリートは、糞便中のC. difficile抗原及びトキシンを検出する迅速診断キットです。抗原とトキシンを同時に検出することで、30分以内にC. difficile感染の診断の補助として有用な結果を提供します。

  1. Updated IDSA/SHEA guidelines published in 2018 recommend:
    • Against the use of NAAT alone when there are no pre-agreed institutional criteria for patient stool submission, due to inadequate positive predictive value.
    • Use of a stool toxin test as part of a multi-step algorithm (ie, glutamate dehydrogenase [GDH] plus toxin; GDH plus toxin, arbitrated by nucleic acid amplification test [NAAT]; or NAAT plus toxin) for all specimens received in the clinical laboratory whether there are or are no pre-agreed institutional criteria for patient stool submission.
    • Or screening samples simultaneously with both a GDH and toxin A/B EIA with an assay that includes both these targets in one system (C. DIFF QUIK CHEK COMPLETE®).
  2. Updated ESCMID guidelines published in 2016 recommend:
    • Against the use of a single rapid test as a standalone test, due to inadequate positive predictive value.
    • The use of a 2-step algorithm starting with either GDH EIA or NAAT. Samples with a negative first test result can be reported as negative. Samples with a positive first test result should be tested further with a Toxin A & B EIA.
    • Or screen samples simultaneously with both a GDH and toxin A/B EIA with an assay that includes both these targets in one system (C. DIFF QUIK CHEK COMPLETE®).
  3. C. DIFF QUIK CHEK COMPLETE® Package Insert

  

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