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使用FASTinov试剂盒进行流式细胞术抗菌药物敏感性试验对革兰氏阴性菌血症临床管理的潜在影响

Potential Impact of Flow Cytometry Antimicrobial Susceptibility Testing on the Clinical Management of Gram-Negative Bacteremia Using the FASTinov Kit.

作者信息

Costa-de-Oliveira Sofia, Teixeira-Santos Rita, Silva Ana P, Pinho Elika, Mergulhão Paulo, Silva-Dias Ana, Marques Nádia, Martins-Oliveira Inês, Rodrigues Acácio G, Paiva José A, Cantón Rafael, Pina-Vaz Cidália

机构信息

Division of Microbiology, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal.

CINTESIS - Center for Health Technology and Services Research, Faculty of Medicine, University of Porto, Porto, Portugal.

出版信息

Front Microbiol. 2017 Dec 12;8:2455. doi: 10.3389/fmicb.2017.02455. eCollection 2017.

Abstract

Laboratory assessment of antimicrobial susceptibility is a prerequisite for adequate management of infections. The aim of this research was to evaluate the performance of the novel FASTinov kit for antimicrobial susceptibility testing (AST) of Gram negative bacilli directly on positive blood cultures. One hundred and two positive blood cultures from patients of a Portuguese University Hospital were included. AST were performed with routine method, Vitek2, with FASTinov kit, and with the gold standard microdilution. Bacteria directly extracted from blood cultures were used to inoculate the FASTinov kit. Time-to-result as well as the number of patients receiving initially inappropriate therapy (and those in whom de-escalation would have been done) and length of stay (LOS) was recorded. Seventy percent of patients were over 70 years old and 18.6% were admitted in intensive care units. Regarding the isolates, 88.2% were Enterobacteriaceae, 9.8% spp. and 1% spp. Extended spectrum β-lactamases producing-Enterobacteriaceae were found in 7.8% of cases and 10.8% were multi-drug resistant. Fifty-one hours was the mean of time-to-result for routine test (Vitek2) vs. 2 h response regarding Fastinov test. The overall agreement between FASTinov and the reference microdilution method was 98%. According to the susceptibility phenotype, 16.7% of patients received initially inappropriate therapy and the mean hospital LOS of these patients was significantly higher. FASTinov kit revealed an excellent correlation with the AST standard method and provided much earlier results than Vitek2.

摘要

抗菌药物敏感性的实验室评估是感染恰当管理的前提条件。本研究的目的是评估新型FASTinov试剂盒直接对革兰氏阴性杆菌阳性血培养物进行抗菌药物敏感性测试(AST)的性能。纳入了葡萄牙一家大学医院102例患者的阳性血培养物。使用常规方法(Vitek2)、FASTinov试剂盒以及金标准微量稀释法进行AST。直接从血培养物中提取的细菌用于接种FASTinov试剂盒。记录结果报告时间以及最初接受不恰当治疗的患者数量(以及那些本应进行降阶梯治疗的患者)和住院时间(LOS)。70%的患者年龄超过70岁,18.6%的患者入住重症监护病房。关于分离菌株,88.2%为肠杆菌科细菌,9.8%为 菌属,1%为 菌属。7.8%的病例中发现产超广谱β-内酰胺酶的肠杆菌科细菌,10.8%为多重耐药菌。常规检测(Vitek2)的平均结果报告时间为51小时,而Fastinov检测的反应时间为2小时。FASTinov与参考微量稀释法的总体一致性为98%。根据药敏表型,16.7%的患者最初接受了不恰当治疗,这些患者的平均住院时间显著更长。FASTinov试剂盒与AST标准方法显示出极好的相关性,并且比Vitek2能更早给出结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be31/5733032/5233b6947842/fmicb-08-02455-g0001.jpg

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