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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分析法在从阳性阳性血培养瓶中检测耐甲氧西林和易感甲氧西林金黄色葡萄球菌分离物中的评价▿

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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结果,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金黄色葡萄球菌并确定其对甲氧西林(美西林)耐药性的有吸引力的方法。通过直接与其他分子分析(sa442和mecA实时PCR)和标准实验室程序进行比较,我们评估了BD GeneOhm StaphSR分析在从加标样品中检测金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌(MRSA)的用途血液培养瓶(n = 134)。在检测金黄色葡萄球菌的情况下(n = 90;对于易感甲氧西林的金黄色葡萄球菌,n = 45;对于MRSA,n = 45),BD GeneOhm StaphSR分析的灵敏度和特异性均为100%(95)。置信区间百分比[CIs]分别为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,此分析产生了五个差异结果,这是由于存在BD遗传基因StaphSR分析未检测到的甲氧西林敏感,可逆MRSA菌株(3/45)和MRSA菌株(2/45)。与其他基于实时PCR的分子方法和常规标准实验室方法相比,BD GeneOhm StaphSR被证明是从血培养中快速(约1.5 h)初步鉴定金黄色葡萄球菌和MRSA的合适诊断工具。 。

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