Possibility of inferring drug susceptibility using UF-5000, a fully automated analyzer of formed elements in urine

DOI
  • MIWA Yuka
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • TAKEZAWA Riko
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • FUKUDA Yayoi
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • HASENO Yusaku
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • INOUE Marina
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • UBARA Hitomi
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • ONO Yuka
    Department of Clinical Laboratory, Mitsui Memorial Hospital
  • ISHIZAKI Kazuho
    Department of Clinical Laboratory, Mitsui Memorial Hospital

Bibliographic Information

Other Title
  • 全自動尿中有形成分分析装置UF-5000を利用した薬剤感受性推測の可能性

Abstract

<p>As an approach to resistant bacteria in urinary tract infections, we investigated whether it is possible to estimate the drug susceptibility of such bacteria from changes bacterial count in which a susceptibility disc is directly placed in urine using the UF-5000’s bacterial count measurement function. The drugs used were levofloxacin (LVFX), which is often prescribed for urinary tract infections, and cefotaxime (CTX), which is also used for extended-spectrum β-lactamase (ESBL) judgement. Changes bacterial count after 30, 60, 90, and 120 min were compared. Drug administration/blank value was calculated to determine the cut-off value at which antimicrobial agents can be judged to be effective. For LVFX, if the drug administration/blank value was less than 0.8 within 90 min, the bacteria were assumed to be sensitive, and if it was 0.8 or higher within 90 to 120 min, the bacteria were assumed to be 70 to 80% resistant. For CTX, if the drug administration/blank value was less than 0.8 within 60 min, the bacteria were estimated to be sensitive, and if it was 0.8 or higher, the bacteria were estimated to be 70% resistant. Since CTX alone yielded only 70% accuracy, cefotaxime clavulanate (CTX/C) was added and compared with CTX, focusing on the inhibition of ESBL by clavulanic acid. When the difference in bacterial count between CTX and CTX/C was compared, ESBL could be determined if the difference bacterial count was 800 or larger at each time point, and ESBL could be determined if the difference is a positive integer in CTX and CTX/C at 120 min.</p>

Journal

Details 詳細情報について

  • CRID
    1390580394707701376
  • DOI
    10.14932/jamt.23-32
  • ISSN
    21885346
    09158669
  • Text Lang
    ja
  • Data Source
    • JaLC
  • Abstract License Flag
    Disallowed

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