首页> 外文期刊>Journal of Microbiological Methods >Different antimicrobial susceptibility testing methods to detect ertapenem resistance in enterobacteriaceae: VITEK2, MicroScan, Etest, disk diffusion, and broth microdilution
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Different antimicrobial susceptibility testing methods to detect ertapenem resistance in enterobacteriaceae: VITEK2, MicroScan, Etest, disk diffusion, and broth microdilution

机译:检测肠杆菌科细菌对厄他培南耐药性的不同抗菌药敏测试方法:VITEK2,MicroScan,Etest,磁盘扩散和肉汤微量稀释

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We investigated different antimicrobial susceptibility testing methods to detect ertapenem resistance in Enterobacteriaceae. A total of 72 Enterobacteriaceae isolates were collected from a clinical microbiology laboratory of a tertiary university hospital, all of which were detected ertapenem resistance by the VITEK2 system. Bacterial identification and antimicrobial susceptibility were determined using the VITEK2. Ertapenem susceptibility test was performed using the MicroScan, Etest and a disk diffusion test. Ertapenem MICs were confirmed using the broth microdilution (BMD). Sensitivity, specificity, and positive and negative predictive values (PPV and NPV, respectively) of each method for the detection of ertapenem resistance were calculated. Carbapenemases and AmpC beta-lactamase were screened using phenotypic methods. Among the 72 isolates, 20 isolates (27.8%) were resistant to ertapenem. Etest showed high sensitivity and specificity (85.0% and 88.5%, respectively) and excellent concordance with BMD. The disk diffusion test had the lowest sensitivity of 50.0%. The VITEK2 showed the lowest essential and categorical agreement (30.5% and 27.8%, respectively). The MicroScan showed relatively good agreement with BMD compared to the VITEK2. Most category disagreements were minor errors. There were 3 very major errors in both the MicroScan and disk diffusion test. Only 1 isolate was positive for carbapenemase screening test and all of the isolates were positive for AmpC screening test. In conclusion, the detection of ertapenem resistance in Enterobacteriaceae has limitations using routine testing such as an automated system or disk diffusion. Confirmation of results by an additional MIC test is recommended for accurate resistance results of ertapenem. (C) 2015 Elsevier B.V. All rights reserved.
机译:我们调查了不同的抗菌药敏试验方法,以检测肠杆菌科细菌对厄他培南的耐药性。从三级大学医院的临床微生物学实验室收集了总共72株肠杆菌科细菌,通过VITEK2系统检测到所有这些细菌对厄他培南的耐药性。使用VITEK2确定细菌鉴定和抗菌药敏性。厄他培南敏感性试验使用MicroScan,Etest和磁盘扩散试验进行。使用肉汤微稀释液(BMD)确认了厄他培南MIC。计算了每种检测厄他培南耐药性的方法的灵敏度,特异性以及阳性和阴性预测值(分别为PPV和NPV)。使用表型方法筛选了碳青霉烯酶和AmpCβ-内酰胺酶。在72种分离物中,有20种(27.8%)对厄他培南有抗药性。 Etest显示出高灵敏度和特异性(分别为85.0%和88.5%),并且与BMD具有极好的一致性。磁盘扩散测试的最低灵敏度为50.0%。 VITEK2显示最低的基本和绝对一致性(分别为30.5%和27.8%)。与VITEK2相比,MicroScan与BMD具有相对较好的一致性。大多数类别上的分歧都是次要错误。 MicroScan和磁盘扩散测试都存在3个非常主要的错误。碳青霉烯酶筛选试验只有1株呈阳性,而所有AmpC筛选试验均为阳性。总之,使用常规测试(例如自动化系统或磁盘扩散)检测肠杆菌科中的ertapenem耐药性具有局限性。建议通过额外的MIC测试对结果进行确认,以使厄他培南具有准确的耐药性。 (C)2015 Elsevier B.V.保留所有权利。

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