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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the VITEK 2 System for Rapid Direct Identification and Susceptibility Testing of Gram-Negative Bacilli from Positive Blood Cultures
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Evaluation of the VITEK 2 System for Rapid Direct Identification and Susceptibility Testing of Gram-Negative Bacilli from Positive Blood Cultures

机译:VITEK 2系统的评估,用于从阳性血液培养物中快速直接鉴定和药敏检测革兰氏阴性杆菌

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This study explores the possibility of combining the BacT/Alert Microbial Detection System with the VITEK 2 system to achieve rapid bacterial identification and susceptibility testing. Direct inoculation of bacterial suspension to the VITEK 2 ID-GNB card and AST-NO09 card was made by differential centrifugation of blood cultures of organisms with gram-negative enteric bacillus-like morphology. A total of 118 strains were investigated; of these, 97 (82.2%) strains were correctly identified to the species level and 21 (17.8%) strains were not identified; by comparing the results with those of the reference method of API identification systems using a pure culture, it was found that no strain had been misidentified. Among the 21 strains with no identification, 13 (61.9%) strains were nonfermenters. The direct-identification reporting time of VITEK 2 was 3.3 h. Direct testing of susceptibility to 11 antibiotics, i.e., amikacin, cefepime, ceftazidime, ciprofloxacin, gentamicin, imipenem, meropenem, netilmicin, piperacillin, piperacillin-tazobactam, and tobramycin, was also performed by using the broth microdilution (MB) method according to the NCCLS guidelines as a reference. After comparing the MICs of the VITEK 2 system with those obtained by the MB method within ±twofold dilution, it was determined that the 1,067 organism-antibiotic combinations had an overall correct rate of 97.6% (1,041 combinations). The rates of susceptibility to the 11 antibiotics ranged from 88.7 to 100%, respectively. Only two (0.2%) and four (0.4%) combinations of the susceptibility tests gave very major errors (i.e., reported as sensitive by the VITEK 2 system but shown to be resistant by the MB method) and major errors (i.e., reported as resistant by the VITEK 2 system but shown to be sensitive by the MB method), respectively. The reporting time for the direct testing of susceptibility against the 11 antibiotics for 97 blood culture isolates by the VITEK 2 system ranged from 3.3 to 17.5 h. Compared with conventional methods that require 1 or 2 days, this method can make same-day reporting possible and thus permit better patient management.
机译:这项研究探索了将BacT / Alert微生物检测系统与VITEK 2系统结合使用以实现快速细菌鉴定和药敏测试的可能性。将细菌悬浮液直接接种到VITEK 2 ID-GNB卡和AST-NO09卡上,方法是对具有革兰氏阴性肠杆菌样形态的生物体的血液培养物进行离心分离。共调查了118株。其中,正确鉴定出97种(82.2%)菌株至物种水平,未鉴定出21种(17.8%)菌株;通过将结果与使用纯培养物的API鉴定系统的参考方法的结果进行比较,发现没有菌株被错误鉴定。在21株未鉴定的菌株中,有13株(61.9%)是非发酵菌。 VITEK 2的直接识别报告时间为3.3小时。还通过根据肉汤微量稀释(MB)方法对阿米卡星,头孢吡肟,头孢他啶,环丙沙星,庆大霉素,亚胺培南,美罗培南,奈替米星,哌拉西林,哌拉西林-他唑巴坦和妥布霉素等11种抗生素的敏感性进行了直接测试。 NCCLS指南作为参考。在将VITEK 2系统的MIC与通过MB方法在两倍稀释度下获得的MIC进行比较之后,确定了1,067种生物-抗生素组合的总体正确率为97.6%(1,041组合)。对11种抗生素的敏感性分别为88.7%至100%。磁化率测试中只有两种(0.2%)和四种(0.4%)组合给出了非常大的错误(即,被VITEK 2系统报告为敏感,但被MB方法证明是可以抵抗的)和主要错误(即,被报告为VITEK 2系统具有抗性,但MB方法显示具有敏感性)。通过VITEK 2系统直接测试针对97种血液培养菌株的11种抗生素的敏感性的报告时间为3.3到17.5 h。与需要1或2天的常规方法相比,此方法可以实现当日报告,从而可以更好地管理患者。

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