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Comparison of the BD GeneOhm methicillin-resistant Staphylococcus aureus (MRSA) PCR assay to culture by use of BBL CHROMagar MRSA for detection of MRSA in nasal surveillance cultures from intensive care unit patients.使用 BBL CHROMagar MRSA 比较 BD GeneOhm 耐甲氧西林金黄色葡萄球菌 (MRSA) PCR 检测与培养法在 ICU 患者鼻腔监测培养物中检测 MRSA 的效果。
J Clin Microbiol. 2010 Apr;48(4):1305-9. doi: 10.1128/JCM.01326-09. Epub 2010 Feb 24.
2
Rapid detection of methicillin-resistant Staphylococcus aureus (MRSA) in diverse clinical specimens by the BD GeneOhm MRSA assay and comparison with culture.BD GeneOhm MRSA 检测法对不同临床标本中耐甲氧西林金黄色葡萄球菌(MRSA)的快速检测与培养法的比较
J Clin Microbiol. 2010 Mar;48(3):981-4. doi: 10.1128/JCM.01990-09. Epub 2010 Jan 13.
3
A selective broth enrichment combined with real-time nuc-mecA-PCR in the exclusion of MRSA.选择性肉汤增菌与实时 nuc-mecA-PCR 联合在排除 MRSA 中的应用。
APMIS. 2010 Jan;118(1):74-80. doi: 10.1111/j.1600-0463.2009.02562.x.
4
Comparison of PCR and culture for screening of vancomycin-resistant Enterococci: highly disparate results for vanA and vanB.PCR 与培养法筛查万古霉素耐药肠球菌的比较:vanA 和 vanB 结果差异显著。
J Clin Microbiol. 2009 Dec;47(12):4136-7. doi: 10.1128/JCM.01547-09. Epub 2009 Oct 21.
5
Comparison of the Xpert methicillin-resistant Staphylococcus aureus (MRSA) assay, BD GeneOhm MRSA assay, and culture for detection of nasal and cutaneous groin colonization by MRSA.比较 Xpert 耐甲氧西林金黄色葡萄球菌(MRSA)检测、BD GeneOhm MRSA 检测与培养法对鼻和腹股沟皮肤 MRSA 定植的检测。
J Clin Microbiol. 2009 Nov;47(11):3769-72. doi: 10.1128/JCM.00303-09. Epub 2009 Aug 26.
6
A common variant of staphylococcal cassette chromosome mec type IVa in isolates from Copenhagen, Denmark, is not detected by the BD GeneOhm methicillin-resistant Staphylococcus aureus assay.丹麦哥本哈根分离株中葡萄球菌盒式染色体mec IVa型的一种常见变体无法通过BD GeneOhm耐甲氧西林金黄色葡萄球菌检测法检测到。
J Clin Microbiol. 2009 May;47(5):1524-7. doi: 10.1128/JCM.02153-08. Epub 2009 Mar 18.
7
Current trends in rapid diagnostics for methicillin-resistant Staphylococcus aureus and glycopeptide-resistant enterococcus species.耐甲氧西林金黄色葡萄球菌和耐糖肽肠球菌快速诊断的当前趋势。
J Clin Microbiol. 2008 May;46(5):1577-87. doi: 10.1128/JCM.00326-08. Epub 2008 Mar 5.
8
High rates of fecal carriage of nonenterococcal vanB in both children and adults.儿童和成人中非肠球菌vanB粪便携带率均很高。
Antimicrob Agents Chemother. 2008 Mar;52(3):1195-7. doi: 10.1128/AAC.00531-07. Epub 2008 Jan 7.
9
2007 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Health Care Settings.《2007年隔离预防指南:医疗机构中预防感染性因子的传播》
Am J Infect Control. 2007 Dec;35(10 Suppl 2):S65-164. doi: 10.1016/j.ajic.2007.10.007.
10
Comparison of the BD GeneOhm methicillin-resistant Staphylococcus aureus (MRSA) PCR assay to culture by use of BBL CHROMagar MRSA for detection of MRSA in nasal surveillance cultures from an at-risk community population.使用BD GeneOhm耐甲氧西林金黄色葡萄球菌(MRSA)聚合酶链反应检测法与使用BBL CHROMagar MRSA培养基培养法对高危社区人群鼻腔监测培养物中的MRSA进行检测的比较。
J Clin Microbiol. 2008 Feb;46(2):743-6. doi: 10.1128/JCM.02071-07. Epub 2007 Dec 5.

评估BD GeneOhm MRSA和VanR检测方法作为沙特阿拉伯一家三级医院检测耐甲氧西林金黄色葡萄球菌和耐万古霉素肠球菌的快速筛查工具。

Evaluation of the BD GeneOhm MRSA and VanR Assays as a Rapid Screening Tool for Detection of Methicillin-Resistant Staphylococcus aureus and Vancomycin-Resistant Enterococci in a Tertiary Hospital in Saudi Arabia.

作者信息

Hassan H, Shorman M

机构信息

Department of Pathology and Laboratory Medicine, King Fahad Specialist Hospital-Dammam (KFSHD), Dammam 31444, Saudi Arabia.

出版信息

Int J Microbiol. 2011;2011:861514. doi: 10.1155/2011/861514. Epub 2011 Dec 1.

DOI:10.1155/2011/861514
PMID:22187558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3236454/
Abstract

Objectives. The aim of this study was to evaluate the diagnostic performance of BD GeneOhm VanR Assay, a rapid PCR test that detects the presence of vanA and/or vanB genes and the performance of BDGeneOhm MRSA Assay which detects the staphylococcal cassette chromosomemec (SCCmec cassette) carrying the mecA gene and Staphylococcus aureus specific sequence located within the orfX gene. Methods. 300 duplicate rectal swabs collected consecutively were analyzed for the presence of VRE by culture and BD PCR. 2267 duplicate swabs were collected (728 nasal and 1539 groin swabs) and analyzed for the presence of MRSA by culture method and BD PCR. Results. Compared to culture, the BD GeneOhm VanR Assay showed a sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of 100%, 91.1%, 23.5%, and 100%, respectively. The BD GeneOhm MRSA Assay revealed sensitivity, specificity, PPV, and NPV of 97.2%, 99.4%, 89.7%, and 99.9%, respectively, for nasal swabs. For groin swabs, it was 100%, 98.7%, 61.5% and 100%, respectively. Conclusion. The BD GeneOhm vanR Assay is a good screening test for rapid exclusion of VRE carriers in hospitals. The BD GeneOhm MRSA Assay represents a reliable screening test. The true strength of the BD GeneOhm Assay for MRSA and VRE is its exceptionally high NPV making the test an ideal tool for rapid exclusion of MRSA and VRE carriers in hospitals. As a consequence, this would dramatically shorten the patient isolation time.

摘要

目的。本研究旨在评估BD GeneOhm VanR检测法的诊断性能,这是一种快速聚合酶链反应(PCR)检测方法,可检测vanA和/或vanB基因的存在,同时评估BD GeneOhm MRSA检测法的性能,该检测法可检测携带mecA基因的葡萄球菌盒式染色体mec(SCCmec盒式结构)以及位于orfX基因内的金黄色葡萄球菌特异性序列。方法。对连续收集的300份重复直肠拭子进行培养和BD PCR分析,以检测耐万古霉素肠球菌(VRE)的存在。收集了2267份重复拭子(728份鼻拭子和1539份腹股沟拭子),并通过培养方法和BD PCR分析耐甲氧西林金黄色葡萄球菌(MRSA)的存在。结果。与培养法相比,BD GeneOhm VanR检测法的灵敏度、特异性、阳性预测值(PPV)和阴性预测值(NPV)分别为100%、91.1%、23.5%和100%。BD GeneOhm MRSA检测法对鼻拭子的灵敏度、特异性、PPV和NPV分别为97.2%、99.4%、89.7%和99.9%。对于腹股沟拭子,其灵敏度、特异性、PPV和NPV分别为100%、98.7%、61.5%和100%。结论。BD GeneOhm vanR检测法是医院中快速排除VRE携带者 的良好筛查试验。BD GeneOhm MRSA检测法是一种可靠的筛查试验。BD GeneOhm检测法对MRSA和VRE的真正优势在于其极高的NPV,使其成为医院中快速排除MRSA和VRE携带者的理想工具。因此,这将大大缩短患者的隔离时间。