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首页> 外文期刊>Journal of Clinical Microbiology >Validation of the Automated Reading and Incubation System with Sensititre Plates for Antimicrobial Susceptibility Testing
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Validation of the Automated Reading and Incubation System with Sensititre Plates for Antimicrobial Susceptibility Testing

机译:带有敏感性板的自动读数和孵育系统用于抗菌药敏感性测试的验证

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The present study compared the antimicrobial susceptibility testing (AST) results generated by the Automated Incubation and Reading System (ARIS) with custom Sensititre plates (TREK Diagnostic Systems, Cleveland, Ohio) and MicroScan PC10 GP and NUMIC10 GN plates interpreted with the WalkAway-96 system (Dade Behring, West Sacramento, Calif.) for gram-positive (GP) and gram-negative (GN) organisms as part of an in-house validation. A total of 326 isolates (3,689 antimicrobial agent-organism combinations) were evaluated. Sensititre plates were inoculated according to the instructions of the manufacturer with a suspension adjusted to a 0.5 McFarland standard, while the Prompt Inoculation System was used for the MicroScan plates. ARIS and the WalkAway system were used for automated reading of the Sensititre and MicroScan plates, respectively, at 18 to 24 h. The results were analyzed for essential (±1 twofold dilution) and categorical (sensitive, intermediate, or resistant) agreements. Plates that resulted in ARIS interpretations with major (falsely resistant) or very major (falsely susceptible) errors compared to the results obtained with the WalkAway system were read manually to corroborate instrument readings. Isolates for which very major or major errors were obtained and for which the results were not resolved by manual reading were retested in parallel. Isolates for which very major or major errors were obtained and for which the results were not resolved upon repeat testing were tested by the National Committee for Clinical Laboratory Standards M7-A5 frozen reference microdilution method. Essential agreement was 95.8% for 246 GN isolates. The following categorical error rates were obtained for the GN isolates: 1.3% minor errors, 0% major errors, and 0.4% very major errors. For 95 GP isolates, there was 93.5% essential agreement. Categorical error rates for GP isolates were 0.9% minor errors, 0.6% major errors, and 0.4% very major errors. ARIS-Sensititre is a diagnostic system feasible for use for automated AST in a clinical laboratory.
机译:本研究比较了自动孵育和读数系统(ARIS)与定制的Sensititre板(TREK Diagnostic Systems,俄亥俄州克利夫兰)以及MicroScan PC10 GP和NUMIC10 GN板(用WalkAway-96解释)生成的抗菌药敏试验(AST)结果。内部验证的一部分,用于革兰氏阳性(GP)和革兰氏阴性(GN)生物的系统(Dade Behring,西萨克拉曼多,加利福尼亚)。总共评估了326种分离物(3,689种抗菌剂-有机物组合)。根据制造商的说明,将敏化平板接种到调整为0.5 McFarland标准的悬浮液中,同时将提示接种系统用于MicroScan平板。 ARIS和WalkAway系统分别用于在18至24小时自动读取Sensititre和MicroScan板。对结果进行了必要的(±1两倍稀释)和绝对(敏感,中间或耐药)协议的分析。与WalkAway系统获得的结果相比,人工读取导致ARIS解释有严重(错误抵抗)或非常严重(错误敏感)错误的板,以确认仪器读数。并行重新测试获得非常重大错误的分离物,以及无法通过手动读取解决结果的分离物。通过临床试验国家标准委员会M7-A5冷冻参考微量稀释方法测试了分离出非常重大或重大错误且结果在重复测试后仍未解决的分离株。 246个GN分离株的基本一致性为95.8%。对于GN分离株,获得以下分类错误率:1.3%的次要错误,0%的主要错误和0.4%的非常重大的错误。对于95株GP分离株,有93.5%的基本一致性。 GP分离株的分类错误率是0.9%的次要错误,0.6%的主要错误和0.4%的非常重大错误。 ARIS-Sensititre是一种诊断系统,可用于临床实验室中的自动AST。

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