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Development of a national EUCAST challenge panel for antimicrobial susceptibility testing

机译:开发国家EUCAST挑战小组以进行抗微生物药敏试验

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A challenge panel of bacterial strains useful for clinical laboratories to validate their European Committee on Antimicrobial Susceptibility Testing (EUCAST) antimicrobial susceptibility test (AST) system was established. A total of 117 strains, obtained from Belgian Reference Centres (n = 57) and from routine clinical samples (n = 60) was selected based on resistance pattern. These strains were analysed in seven different laboratories by three different automated AST systems (Vitek (n = 2), Phoenix (n = 2) and Microscan (n = 2)) and by disc diffusion from five different manufacturers (Rosco (n = 2), Becton-Dickinson (n = 2), Biomerieux (n = 1), Bio-rad (n = 1) and i2a (n = 1)). To select the challenge panel, selection criteria were set for categorical agreement between the different systems and the number of very major errors, major errors and minor errors. Very major and major errors for at least two antibiotics were observed in 43% of all strains, leading to the exclusion of these strains from the selected panel. In only 10% of all tested strains was there 100% categorical agreement for all antibiotics. Finally, 28 strains (14 Gram-positive and 14 Gram-negative) covering a wide spectrum of resistance mechanisms were selected. Pilot-testing of this challenge panel in 20 laboratories mainly confirmed the results of the validation study. Only six strains withheld for the pilot study could not be used as challenge strain due to an overall (very) major error rate of >5% for a particular antibiotic (n = 5) or for two antibiotics (n = 1). To conclude, this challenge panel should facilitate the implementation and use of EUCAST breakpoints in laboratories. S. Desmet, (C) 2016 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
机译:建立了一个可用于临床实验室的细菌菌株挑战小组,以验证其欧洲抗微生物药敏试验(EUCAST)抗微生物药敏试验(AST)系统。根据耐药模式选择了从比利时参考中心(n = 57)和常规临床样品(n = 60)获得的117株菌株。通过三个不同的自动AST系统(Vitek(n = 2),Phoenix(n = 2)和Microscan(n = 2))以及来自五个不同制造商的光盘扩散(Rosco(n = 2),在七个不同的实验室中对这些菌株进行了分析。 ),Becton-Dickinson(n = 2),Biomerieux(n = 1),Bio-rad(n = 1)和i2a(n = 1))。为了选择挑战小组,为不同系统之间的类别一致性以及非常重大,重大和次要错误的数量设定了选择标准。在所有菌株中有43%观察到了至少两种抗生素的非常严重的错误,导致将这些菌株排除在所选小组之外。在所有测试菌株中,只有10%对所有抗生素都有100%的绝对一致性。最后,选择了涵盖广泛耐药机制的28株菌株(14革兰氏阳性和14革兰氏阴性)。在20个实验室对该挑战小组进行的试点测试主要证实了验证研究的结果。由于特定抗生素(n = 5)或两种抗生素(n = 1)的总体(非常)主要错误率大于5%,因此不能将仅用于前期研究的6株菌株用作挑战菌株。总而言之,该挑战小组应促进实验室中EUCAST断点的实施和使用。 S. Desmet,(C)2016年欧洲临床微生物学和传染病学会。由Elsevier Ltd.出版。保留所有权利。

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