首页> 美国卫生研究院文献>PLoS Clinical Trials >Same Day Identification and Full Panel Antimicrobial Susceptibility Testing of Bacteria from Positive Blood Culture Bottles Made Possible by a Combined Lysis-Filtration Method with MALDI-TOF VITEK Mass Spectrometry and the VITEK2 System
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Same Day Identification and Full Panel Antimicrobial Susceptibility Testing of Bacteria from Positive Blood Culture Bottles Made Possible by a Combined Lysis-Filtration Method with MALDI-TOF VITEK Mass Spectrometry and the VITEK2 System

机译:MALDI-TOF VITEK质谱和VITEK2系统相结合的裂解-过滤方法可实现从阳性血液培养瓶中细菌的当日鉴定和全面板抗菌敏感性测试

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摘要

Rapid identification and antimicrobial susceptibility testing of microorganisms causing bloodstream infections or sepsis have the potential to improve patient care. This proof-of-principle study evaluates the Lysis-Filtration Method for identification as well as antimicrobial susceptibility testing of bacteria directly from positive blood culture bottles in a clinical setting. A total of 100 non-duplicated positive blood cultures were tested and 1012 microorganism-antimicrobial combinations were assessed. An aliquot of non-charcoal blood culture broth was incubated with lysis buffer briefly before being filtered and washed. Microorganisms recovered from the filter membrane were first identified by using Matrix-Assisted Laser Desorption/Ionization Time-of-Flight VITEK® Mass Spectrometry (VITEK MS). After quick identification from VITEK MS, filtered microorganisms were inoculated to VITEK®2 system for full panel antimicrobial susceptibility testing analysis. Of 100 bottles tested, the VITEK MS resulted in 94.0% correct organism identification to the species level. Compared to the conventional antimicrobial susceptibility testing methods, direct antimicrobial susceptibility testing from VITEK®2 resulted in 93.5% (946/1012) category agreement of antimicrobials tested, with 3.6% (36/1012) minor error, 1.7% (7/1012) major error, and 1.3% (13/1012) very major error of antimicrobials. The average time to identification and antimicrobial susceptibility testing was 11.4 hours by using the Lysis-Filtration method for both VITEK MS and VITEK®2 compared to 56.3 hours by using conventional methods (p<0.00001). Thus, the same-day results of microorganism identification and antimicrobial susceptibility testing directly from positive blood culture can be achieved and can be used for appropriate antibiotic therapy and antibiotic stewardship.
机译:对引起血液感染或脓毒症的微生物进行快速鉴定和抗菌药敏试验,有可能改善患者护理水平。这项原理验证研究评估了在临床环境中直接从阳性血培养瓶中进行细菌鉴定和抗菌药敏试验的溶菌过滤方法。总共测试了100种非重复的阳性血液培养物,并评估了1012种微生物-抗菌剂组合。将非木炭血液培养液的等分试样与裂解缓冲液短暂孵育,然后过滤和洗涤。首先使用基质辅助激光解吸/电离飞行时间质谱(VITEK MS)鉴定从滤膜中回收的微生物。从VITEK MS快速鉴定后,将过滤后的微生物接种到VITEK®2系统中,以进行全面的抗菌药敏测试分析。在100个经过测试的瓶子中,VITEK MS可以正确识别94.0%的物种。与常规抗菌药敏测试方法相比,VITEK®2进行的直接抗菌药敏测试得出的抗菌剂类别一致性为93.5%(946/1012),次要误差为3.6%(36/1012),1.7%(7/1012)重大错误和1.3%(13/1012)抗菌药物的重大错误。对于VITEK MS和VITEK®2,使用裂解过滤方法进行鉴定和抗菌药敏试验的平均时间为11.4小时,而使用传统方法则为56.3小时(p <0.00001)。因此,可以获得直接来自阳性血液培养物的微生物鉴定和抗菌药敏测试的当天结果,并可用于适当的抗生素治疗和抗生素管理。

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