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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the BD GeneOhm Assay Using the Rotor-Gene 6000 Platform for Rapid Detection of Methicillin-Resistant Staphylococcus aureus from Pooled Screening Swabs
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Evaluation of the BD GeneOhm Assay Using the Rotor-Gene 6000 Platform for Rapid Detection of Methicillin-Resistant Staphylococcus aureus from Pooled Screening Swabs

机译:使用Rotor-Gene 6000平台评估BD GeneOhm分析的效果,该平台可从汇集的拭子中快速检测耐甲氧西林的金黄色葡萄球菌

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As health services move toward universal methicillin-resistant Staphylococcus aureus (MRSA) screening for hospital admissions, the most cost-effective approach is yet to be defined. In this study, one of the largest to date, we evaluated the performance of the BD GeneOhm MRSA assay on the Rotor-Gene 6000 thermal cycler, using samples taken directly from pooled MRSA screens. Results were compared with the same assay performed on the Smart-Cycler II platform and overnight broth culture. Samples yielding discrepant results were subjected to detailed analysis with an in-house PCR and patient note review. A total of 1,428 pooled MRSA screens were tested. Sensitivities and specificities of 85.3% and 95.8% for the Rotor-Gene and 81% and 95.7% for the Smart-Cycler were obtained, compared with broth enrichment. The sensitivity of the BD GeneOhm assay was increased to 100% when the results of in-house PCR and patient note review were taken into account. This study demonstrates that the Rotor-Gene 6000 thermal cycler is a reliable platform for use with the BD GeneOhm assay. It also proves that commercial PCR can be performed direct on pooled samples in selective broth, without the need for overnight incubation.
机译:随着卫生服务朝着对耐甲氧西林的金黄色葡萄球菌(MRSA)的通用筛查入院,最经济有效的方法尚待确定。在这项迄今规模最大的研究中,我们使用直接从合并的MRSA筛选器中提取的样品,评估了Rotor-Gene 6000热循环仪上BD GeneOhm MRSA测定的性能。将结果与在Smart-Cycler II平台和过夜培养液上进行的相同测定进行比较。产生差异结果的样品将通过内部PCR和病历审查进行详细分析。总共对1,428个MRSA合并筛选进行了测试。与肉汤浓缩相比,Rotor-Gene的敏感性和特异性分别为85.3%和95.8%,Smart-Cycler的敏感性和特异性分别为81%和95.7%。考虑到内部PCR和患者注意事项审查的结果,BD GeneOhm分析的灵敏度提高到100%。这项研究表明Rotor-Gene 6000热循环仪是与BD GeneOhm分析一起使用的可靠平台。这也证明了商业PCR可以直接在选择性肉汤中的合并样品上进行,而无需过夜孵育。

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