聚合抗生素敏感性测试对多微生物尿路感染在CLSI验证标准内执行
Richard A Festa1, Frank R Cockerill2, Rick L Pesano2
1Department of Research and Development, Pathnostics, Irvine, CA 92618, USA.
Antibiotics (Basel, Switzerland)
|February 26, 2025
概括
聚合抗生素敏感性测试 (P-AST) 与诊断尿路感染 (UTI) 的标准方法相比显示出高一致性和低错误率. 这种新的方法符合抗菌素耐药性测试的临床标准.
科学领域:
- 临床微生物学 临床微生物学
- 诊断试验的发展.
- 抗微生物耐药性 抗微生物耐药性
背景情况:
- 尿路感染 (UTI) 由于抗菌素耐药性增加而构成越来越大的挑战.
- 新的诊断测试正在出现,以克服标准尿液培养的局限性.
- 对新测试与已建立的抗生素敏感性测试 (AST) 方法进行验证至关重要.
研究的目的:
- 为了验证一种新的诊断测试,聚合抗生素敏感性测试 (P-AST),与标准的AST方法相比.
- 评估多微生物尿道感染样本中P-AST的一致性和错误率.
- 为了评估生物体负载对抗生素敏感性结果的影响.
主要方法:
- 使用P-AST和标准微稀释/盘扩散 (BMD/DD) 方法测试了多微生物尿样.
- 性能特征包括基本协议 (EA%),非常重大错误 (VMEs) 和重大错误 (ME) 根据临床和实验室标准研究所 (CLSI) 的指导方针进行评估.
- 评估了异质抗性和生物体数量与抗生素敏感性之间的关联.
主要成果:
- 与标准AST相比,P-AST显示了≥90%的基本一致性,并满足了CLSI对VMEs (<2.0%) 和MEs (<3.0%) 的指导方针.
- 在计算异阻力时,VMEs和ME均为<1.5%.
- 生物数量的增加显著减少了每个样本检测到的"敏感"抗生素的数量.
结论:
- 作为Guidance®尿道感染检测的一部分,P-AST在多微生物尿道感染诊断样本中执行AST的CLSI标准.
- 这些发现支持P-AST用于准确的尿路感染诊断的实用性.
- 该研究强调了在解释AST结果时考虑生物体负荷的重要性.
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