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Etest GRD 检测法在检测囊性纤维化患者中糖肽类药物低敏性金黄色葡萄球菌中的应用。

Utility of the Etest GRD for detecting Staphylococcus aureus with reduced susceptibility to glycopeptides in cystic fibrosis patients.

机构信息

Hôpital Arnaud de Villeneuve, Service de Pédiatrie Générale, Maladies Infectieuses, Immunologie Clinique, Centre Hospitalier Régional Universitaire de Montpellier, 371, Avenue du Doyen Gaston Giraud, 34295, Montpellier Cedex 5, France.

出版信息

Eur J Clin Microbiol Infect Dis. 2012 Apr;31(4):599-604. doi: 10.1007/s10096-011-1353-4. Epub 2011 Sep 9.

Abstract

Glycopeptide-intermediate S. aureus (GISA), particularly heterogeneous GISA (hGISA), remain difficult to detect in the routine practice of medical microbiology. Novel tools have been evaluated comparatively to the population analysis profile-area under the curve (PAP-AUC) reference method for detecting GISA/hGISA. Among them, the Etest GRD showed relatively high specificity (85.8-97%) and negative predictive value (97%) but lower sensibility (57-95%) and positive predictive value (30.8%). We investigated the utility of the Etest GRD for detecting GISA/hGISA among 180 strains isolated from 106 cystic fibrosis (CF) patients. Etest GRD was performed on all isolates, and those exhibiting a GISA/hGISA phenotype were further tested by PAP-AUC and other agar routine assays for GISA/hGISA detection. The Etest GRD allowed the detection of 15 GISA/hGISA strains, of which eight were confirmed by the reference method. Despite the 3.9% level of false positive results, the Etest GRD constitutes a useful routine tool for detecting GISA/hGISA overlooked by other routine assays, two strains being detected by the Etest GRD only. GISA/hGISA represented 7.7% of MRSA and 2.1% of MSSA, and were found in 4.7% of CF patients colonized/infected by S. aureus, which is the highest rate reported to date in this population.

摘要

糖肽中介金黄色葡萄球菌(GISA),特别是异质性 GISA(hGISA),在医学微生物学的常规实践中仍然难以检测。已经评估了一些新工具,以比较它们在检测 GISA/hGISA 方面的表现,与人群分析轮廓-面积下的曲线(PAP-AUC)参考方法相比。其中,Etest GRD 显示出相对较高的特异性(85.8-97%)和阴性预测值(97%),但敏感性较低(57-95%)和阳性预测值(30.8%)。我们调查了 Etest GRD 在检测 106 例囊性纤维化(CF)患者中 180 株分离株中的 GISA/hGISA 的应用价值。对所有分离株进行了 Etest GRD 检测,对表现出 GISA/hGISA 表型的分离株进一步进行了 PAP-AUC 和其他琼脂常规检测,以检测 GISA/hGISA。Etest GRD 能够检测到 15 株 GISA/hGISA 菌株,其中 8 株被参考方法证实。尽管存在 3.9%的假阳性结果,但 Etest GRD 仍然是一种有用的常规工具,可以检测到其他常规检测方法忽略的 GISA/hGISA,有两株仅通过 Etest GRD 检测到。GISA/hGISA 占 MRSA 的 7.7%和 MSSA 的 2.1%,在 4.7%的金黄色葡萄球菌定植/感染 CF 患者中发现,这是迄今为止在该人群中报告的最高比例。

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