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用于药敏试验的自动化系统与市售微量稀释板的同步可比性

Concurrent comparability of automated systems and commercially prepared microdilution trays for susceptibility testing.

作者信息

Hansen S L, Freedy P K

出版信息

J Clin Microbiol. 1983 May;17(5):878-86. doi: 10.1128/jcm.17.5.878-886.1983.

Abstract

Susceptibility test results from 100 clinical isolates, using the AMS, MS-2, Autobac MTS, Micro-Media system, and Sensititre, were compared with results from the proposed National Committee for Clinical Laboratory Standards reference microdilution method for minimum inhibitory concentrations and with Bauer-Kirby results. Isolates were tested concurrently by each method on consecutive days to obtain duplicate results. The data were computer analyzed, using National Committee for Clinical Laboratory Standards guidelines for break point interpretation. Analysis was centered on drug-organism combinations and not on overall percent correlation. Data were analyzed for comparability to the reference methods and for reproducibility within each system. Commercial system results were very reproducible. Results from 4- to 8-h tests (AMS, MS-2, MTS) gave more very major discrepancies when compared with either reference method than did results from 15- to 18-h systems (Micro-Media, Sensititre).

摘要

使用AMS、MS-2、Autobac MTS、Micro-Media系统和Sensititre对100株临床分离菌进行药敏试验,将结果与美国国家临床实验室标准委员会提出的参考微量稀释法测定最低抑菌浓度的结果以及鲍尔-柯克斯法的结果进行比较。每天连续用每种方法对分离菌进行检测,以获得重复结果。按照美国国家临床实验室标准委员会的折点解释指南对数据进行计算机分析。分析集中在药物-菌株组合上,而不是总体百分比相关性。分析数据与参考方法的可比性以及每个系统内的可重复性。商业系统的结果具有很高的可重复性。与15至18小时系统(Micro-Media、Sensititre)相比,4至8小时试验(AMS、MS-2、MTS)的结果与任何一种参考方法相比都有更多的极重大差异。

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