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首页> 外文期刊>Journal of Clinical Microbiology >E Test versus Agar Dilution for Antimicrobial Susceptibility Testing of Viridans Group Streptococci
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E Test versus Agar Dilution for Antimicrobial Susceptibility Testing of Viridans Group Streptococci

机译:E测试与琼脂稀释法对Viridans组链球菌的药敏试验

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摘要

Viridans group streptococci (VGS) are commonly isolated from the blood of hospitalized patients. The E test represents a convenient method for determining the MICs for VGS, but for this purpose it has not been well validated against reference methods. In this study, 180 unselected VGS isolates were identified to a species level, and the MICs of penicillin, cefuroxime, cefotaxime, and vancomycin were determined by both agar dilution and the E test. Available data regarding demographic and laboratory variables for each VGS bacteremic episode were collected, the significance of each VGS isolate was assessed, and the associations between and among laboratory and clinical variables were investigated. Among all VGS isolates, 68.3% (median of three runs) were found to be fully susceptible to penicillin by agar dilution. The E test and agar dilution showed average agreements (within ±1 dilution) of 92.2% for penicillin, 95.7% for cefuroxime 91.3% for cefotaxime, and 86.7% for vancomycin. Agreements over serial E tests and serial agar dilutions were excellent for β-lactam agents (intraclass correlation coefficients, >0.9) but less impressive for vancomycin. Very major error rates for the E test were ≤0.7%, and combined major and minor error rates were within acceptable limits for all antimicrobial agents tested. Lysis-centrifugation culture methods were more often associated with clinically insignificant VGS isolates; otherwise, no associations between clinical and laboratory variables were noted.
机译:Viridans组链球菌(VGS)通常从住院患者的血液中分离出来。 E检验代表一种确定VGS MIC的便捷方法,但为此目的,尚未针对参考方法进行充分验证。在这项研究中,鉴定了180个未选择的VGS分离株至一个物种水平,并通过琼脂稀释和E检验确定了青霉素,头孢呋辛,头孢噻肟和万古霉素的MIC。收集有关每个VGS细菌发作的人口统计学和实验室变量的可用数据,评估每个VGS分离株的重要性,并研究实验室变量与临床变量之间的关联。在所有VGS分离株中,发现68.3%(三轮中值)对琼脂稀释完全敏感。 E试验和琼脂稀释度显示,青霉素的平均一致性(±1稀释内)为92.2%,头孢呋辛为95.7%,头孢噻肟为91.3%,万古霉素为86.7%。对于β-内酰胺类药物,系列E试验和琼脂稀释液的协议非常出色(类内相关系数> 0.9),而万古霉素的效果不佳。 E测试的主要错误率≤0.7%,所有主要和次要错误率的总和在所有测试的抗菌剂的可接受范围内。裂解-离心培养方法通常与临床上无关紧要的VGS分离物相关;否则,没有发现临床和实验室变量之间的关联。

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