Rapid diagnosis of bacteria and determination of sensitivity in blood culture

Münevver KAYIN DİNÇ, V. Özenci, S. Aydemir
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Abstract

Aim: In patients with bloodstream infection; identifying the causative agent in a short time and applying appropriate antimicrobial therapy is very important in terms of reducing morbidity and mortality. In this study, it was aimed to evaluate a new method developed for direct identification and antibiotic susceptibility testing from blood culture. Materials and Methods: Bacterial pellet was obtained from blood culture samples that showed positive signals in the BacT/Alert 3D system by washing and centrifugation. Identification was made from this pellet using Vitek MS, followed by direct antibiotic susceptibility testing in the VITEK 2 automated system. The results were compared with the standard method. Results: Identification was performed on 80 blood culture samples. In the direct identification process, 73 samples were identified, of which 72 (90%) resulted in agreement with the standard method. Direct antibiotic susceptibility tests were found to be compatible with a rate of 97.9%. Among the evaluated 635 antibiotic susceptibility results; it was observed that 10 of them had major errors and 3 of them had minor errors. Conclusions: Using the procedures applied in the study from blood culture samples, without the need for costly reagents or long processing time, it has been observed that identification and antibiotic susceptibility results can be obtained within 24 hours, similar to standard results.
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血培养细菌快速诊断及敏感性测定
目的:血液感染患者;在短时间内识别病原菌并进行适当的抗菌治疗对于降低发病率和死亡率非常重要。本研究旨在评价一种血培养直接鉴定和药敏试验的新方法。材料与方法:对在BacT/Alert 3D系统中显示阳性信号的血培养样本进行洗涤和离心,获得细菌微球。使用Vitek MS对该颗粒进行鉴定,然后在Vitek 2自动化系统中进行直接抗生素药敏试验。结果与标准方法进行了比较。结果:对80份血培养标本进行了鉴定。在直接鉴定过程中,鉴定了73个样品,其中72个(90%)与标准方法一致。直接药敏试验的配伍率为97.9%。在评价的635例药敏结果中;其中10个存在较大误差,3个存在较小误差。结论:使用本研究中应用的血液培养样品的程序,无需昂贵的试剂或较长的处理时间,可以在24小时内获得鉴定和抗生素敏感性结果,与标准结果相似。
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审稿时长
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