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Vitek系统对肠杆菌科血流感染分离株进行抗菌药物敏感性试验的准确性:采用从Bactec 9240血培养瓶“直接”接种的方法。

Accuracy of the Vitek system for antimicrobial susceptibility testing Enterobacteriaceae bloodstream infection isolates: use of "direct" inoculation from Bactec 9240 blood culture bottles.

作者信息

Putnam L R, Howard W J, Pfaller M A, Koontz F P, Jones R N

机构信息

Department of Pathology, University of Iowa College of Medicine, Iowa City 52242, USA.

出版信息

Diagn Microbiol Infect Dis. 1997 Jun;28(2):101-4. doi: 10.1016/s0732-8893(97)00014-x.

Abstract

A recent investigation indicates that rapid antimicrobial susceptibility tests (AST) can affect patient therapy leading to reductions in health-care costs for some patient populations. However, there is little information relative to the often performed direct inoculation of positive blood culture bottles into rapid AST systems. AST results of direct inoculated Vitek (bioMerieux Vitek, Hazelwood, MO, USA) GNS cards were compared to those inoculated per package insert recommendations and a reference broth microdilution test using 50 consecutive Enterobacteriaceae bloodstream infection isolates. Escherichia coli (44% of isolates), Klebsiella ssp. (30%), and six other members of this family were tested against 15 antimicrobial agents. The direct inoculation method produced only two false-susceptible (0.3%), seven false-resistant (0.9%; six different drugs), and 48 minor errors (6.4%). The GNS cards inoculated in the usual, recommended manner had no very major error, and 7.5% combined major and minor errors. If the results of the urinary infection-specific drugs (nitrofurantoin, trimethoprim/sulfamethoxazole; not appropriate for bacteremia therapy) and ampicillin/sulbactam were deleted, both Vitek inoculation methods yielded results well within acceptable limits (< or = 4.5% overall error). These results indicate that the direct inoculation method of Vitek GNS cards from Enterobacteriaceae bloodstream infections (detected by Bactec 9240, Becton-Dickinson, Cockeysville, MD, USA) performed as well as the NCCLS broth microdilution test. Thus, a procedural modification of this type could further accelerate rapid access to accurate AST data.

摘要

最近的一项调查表明,快速抗菌药敏试验(AST)可影响患者治疗,从而降低某些患者群体的医疗成本。然而,关于将阳性血培养瓶直接接种到快速AST系统中这一常见操作的信息却很少。使用50株连续的肠杆菌科血流感染分离株,将直接接种到Vitek(美国密苏里州黑兹尔伍德市bioMerieux Vitek公司)GNS卡中的AST结果与按照包装说明书建议接种的结果以及参考肉汤微量稀释试验的结果进行了比较。对大肠杆菌(占分离株的44%)、克雷伯菌属(30%)以及该菌科的其他六个成员进行了15种抗菌药物的测试。直接接种法仅产生了2例假敏感结果(0.3%)、7例假耐药结果(0.9%;六种不同药物)和48个小误差(6.4%)。以常规推荐方式接种的GNS卡没有非常重大的误差,主要和小误差的总和为7.5%。如果剔除尿路感染特异性药物(呋喃妥因、甲氧苄啶/磺胺甲恶唑;不适用于菌血症治疗)和氨苄西林/舒巴坦的结果,两种Vitek接种方法产生的结果均在可接受范围内(总误差≤4.5%)。这些结果表明,对于肠杆菌科血流感染(由美国马里兰州科基斯维尔市Becton-Dickinson公司的Bactec 9240检测),将Vitek GNS卡直接接种的方法与美国国家临床实验室标准化委员会(NCCLS)的肉汤微量稀释试验效果相当。因此,这种程序上的改进可以进一步加快快速获取准确AST数据的速度。

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