Antimicrobial susceptibility testing in Sweden. IV. Quality assurance.

G Kahlmeter, B Olsson-Liljequist, S Ringertz
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Abstract

The performance of susceptibility testing depends on high-quality material (disks and media), good laboratory practice (robust methodology and correct handling of material) and antimicrobial breakpoints being set in such a way that they allow for some intralaboratory variation. Thus, breakpoints must not divide homogeneous bacterial populations. Routine susceptibility testing should be checked with both internal and external quality control programs. The internal quality control should be designed to demonstrate the importance of minimizing random errors and to rapidly disclose systematic errors. This can be achieved either through the repeated testing of defined control strains or by systematic comparison of histograms of routine zone diameters with reference histograms supplied by the Swedish Reference Group for Antibiotics (SRGA and SRGA-M). The SRGA-M offers an external quality control program which by its design also functions as an epidemiological surveillance program. The quality control programs are supported by an educational program for laboratory personnel.

瑞典的抗菌药物敏感性试验。四、质量保证。
药敏试验的性能取决于高质量的材料(磁盘和介质)、良好的实验室规范(稳健的方法和正确的处理材料)和以允许实验室内部一些变化的方式设置的抗菌断点。因此,断点不能分裂同质细菌群。常规药敏试验应通过内部和外部质量控制程序进行检查。内部质量控制的设计应体现出尽量减少随机误差和迅速发现系统误差的重要性。这可以通过重复检测确定的对照菌株或将常规区直径直方图与瑞典抗生素参考组(SRGA和SRGA- m)提供的参考直方图进行系统比较来实现。SRGA-M提供外部质量控制程序,其设计也可作为流行病学监测程序。质量控制程序由实验室人员的教育计划支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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