...
首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the BD GeneOhm StaphSR Assay for Detection of Methicillin-Resistant and Methicillin-Susceptible Staphylococcus aureus Isolates from Spiked Positive Blood Culture Bottles
【24h】

Evaluation of the BD GeneOhm StaphSR Assay for Detection of Methicillin-Resistant and Methicillin-Susceptible Staphylococcus aureus Isolates from Spiked Positive Blood Culture Bottles

机译:BD GeneOhm StaphSR检测试剂盒对从阳性阳性血培养瓶中分离出的耐甲氧西林和耐甲氧西林金黄色葡萄球菌的检测的评估

获取原文
           

摘要

To improve the clinical outcome of Staphylococcus aureus septicemia, the early selection of appropriate antibiotic treatment is crucial. Molecular diagnostics represents an attractive approach for the rapid identification of S. aureus and the determination of its methicillin (meticillin) resistance. In direct comparison to other molecular assays (sa442 and mecA real-time PCRs) and standard laboratory procedures, we evaluated the BD GeneOhm StaphSR assay for its use in the detection of S. aureus and methicillin-resistant S. aureus (MRSA) from spiked blood culture bottles (n = 134). In the case of detecting S. aureus (n = 90; for methicillin-susceptible S. aureus, n = 45; for MRSA, n = 45), the BD GeneOhm StaphSR assay had a sensitivity and a specificity of 100% each (95% confidence intervals [CIs], 96.0 to 100% and 82.4 to 100%, respectively). For MRSA (n = 45), the test was 95.6% (95% CI, 84.9 to 99.5%) sensitive and 95.3% (95% CI, 86.9 to 99.0%) specific. Overall, five discrepant results arose with this assay due to the presence of methicillin-susceptible, revertant MRSA strains (3/45) and MRSA strains that were not detected by the BD GeneOhm StaphSR assay (2/45). Compared to other real-time PCR-based molecular approaches and to conventional standard laboratory methods, the BD GeneOhm StaphSR turned out to be an appropriate diagnostic tool for a rapid (~1.5 h), preliminary identification of S. aureus and MRSA from blood cultures.
机译:为了改善金黄色葡萄球菌败血症的临床疗效,早期选择合适的抗生素治疗至关重要。分子诊断学是一种快速鉴定 S的有吸引力的方法。金黄色葡萄球菌及其耐甲氧西林的测定与其他分子测定法( sa442 mecA 实时PCR)和标准实验室程序直接进行比较,我们评估了BD GeneOhm StaphSR测定法在检测< em> S。金黄色葡萄球菌和耐甲氧西林的 S。尖峰血液培养瓶中的金黄色葡萄球菌(MRSA)( n = 134)。在检测 S的情况下。金黄色 n = 90;对于易受甲氧西林影响的金黄色葡萄球菌 n = 45;对于MRSA, n = 45),BD GeneOhm StaphSR分析的灵敏度和特异性均为100%(95%置信区间[CIs],96.0至100%和82.4至100%)。对于MRSA( n = 45),测试的敏感性为95.6%(95%CI,84.9至99.5%),特异性为95.3%(95%CI,86.9至99.0%)。总体而言,该分析产生了五个不一致的结果,这是由于存在BD GeneOhm StaphSR分析未检测到的甲氧西林敏感性,可逆MRSA菌株(3/45)和MRSA菌株(2/45)。与其他基于实时荧光定量PCR的分子方法和常规标准实验室方法相比,BD GeneOhm StaphSR证明是快速(〜1.5 h)初步鉴定 S的合适诊断工具。血液培养中的金黄色葡萄球菌和MRSA。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号