Wolk D M, Picton E, Johnson D, Davis T, Pancholi P, Ginocchio C C, Finegold S, Welch D F, de Boer M, Fuller D, Solomon M C, Rogers B, Mehta M S, Peterson L R
The University of Arizona/BIO5 Institute, Tucson, Arizona 85724-5059, USA.
J Clin Microbiol. 2009 Mar;47(3):758-64. doi: 10.1128/JCM.01714-08. Epub 2009 Jan 7.
The first U.S. multicenter clinical trial to assess the performance of the Cepheid Xpert MRSA assay (Xpert MRSA) was conducted. The assay is a qualitative test designed for the rapid detection of methicillin-resistant Staphylococcus aureus (MRSA) directly from nares swabs. This novel test combines integrated nucleic acid extraction and automated real-time PCR for the detection of a MRSA-specific signature sequence. A total of 1,077 nares specimens were collected from seven geographically distinct health care sites across the United States with prevalence rates ranging from 5.2% to 44%. Nares specimens were tested by (i) the Xpert MRSA assay, (ii) direct culture on CHROMagar MRSA medium (direct CM culture), and (iii) broth-enriched culture (Trypticase soy broth with 6.5% sodium chloride) followed by plating onto CHROMagar MRSA medium (broth-enriched CM culture). When direct CM culture was designated the reference method, the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of the Xpert MRSA assay were 94.3%, 93.2%, 73.0%, and 98.8%, respectively. When broth-enriched CM culture was used as the reference method, the clinical sensitivity, specificity, PPV, and NPV of the Xpert MRSA assay were 86.3%, 94.9%, 80.5%, and 96.6%, respectively. The BD GeneOhm MRSA (BDGO) assay was performed as a comparative molecular method. No statistical performance differences were observed between the Xpert MRSA and BDGO assays when they were compared to culture methods. From this large-scale, multicenter clinical comparison, we conclude that the Xpert MRSA assay is a simple, rapid, and accurate method for performing active surveillance for MRSA in a variety of health care populations.
开展了美国首个评估赛沛Xpert MRSA检测法(Xpert MRSA)性能的多中心临床试验。该检测法是一种定性检测,旨在直接从鼻腔拭子中快速检测耐甲氧西林金黄色葡萄球菌(MRSA)。这项新型检测结合了集成核酸提取和自动化实时PCR技术,用于检测MRSA特异性特征序列。从美国七个地理位置不同、患病率在5.2%至44%之间的医疗保健机构共收集了1077份鼻腔标本。鼻腔标本通过以下方法进行检测:(i)Xpert MRSA检测法;(ii)在CHROMagar MRSA培养基上直接培养(直接CM培养);(iii)肉汤增菌培养(含6.5%氯化钠的胰蛋白酶大豆肉汤),随后接种到CHROMagar MRSA培养基上(肉汤增菌CM培养)。当将直接CM培养指定为参考方法时,Xpert MRSA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94.3%、93.2%、73.0%和98.8%。当将肉汤增菌CM培养用作参考方法时,Xpert MRSA检测法的临床灵敏度、特异性、PPV和NPV分别为86.3%、94.9%、80.5%和96.6%。BD GeneOhm MRSA(BDGO)检测法作为一种比较分子方法进行了检测。将Xpert MRSA和BDGO检测法与培养方法进行比较时,未观察到统计学上的性能差异。通过这项大规模、多中心的临床比较,我们得出结论,Xpert MRSA检测法是一种在各种医疗保健人群中对MRSA进行主动监测的简单、快速且准确的方法。