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ANTIMICROBIAL SUSCEPTIBILITY AND DETECTION METHODS FOR THE EXTENDED‑SPECTRUM β-LACTAMASES PRODUCING ENTEROBACTERIACEAE FROM CLINICAL SAMPLES

机译：扩展β-内酰胺酶从临床样品中产生肠杆菌的抗微生物敏感性和检测方法

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Kaviyarasan G; Rajamanikandan Kcp; Sabarimuthu M; Ramya S; Arvind Prasanth D;
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1. ANTIMICROBIAL SUSCEPTIBILITY AND DETECTION METHODS FOR THE EXTENDED?SPECTRUM β-LACTAMASES PRODUCING ENTEROBACTERIACEAE FROM CLINICAL SAMPLES [J] . Kaviyarasan G, Rajamanikandan Kcp, Sabarimuthu M, Asian Journal of Pharmaceutical and Clinical Research . 2018,第5期

机译：从临床样品中生产肠杆菌科细菌的广谱β-内酰胺酶的抗菌药敏性和检测方法
2. Antimicrobial susceptibility of clinical isolates of Enterobacteriaceae producing complex beta-lactamase patterns including extended-spectrum enzymes [J] . Segatore B, Setacci D, Perilli M, International journal of antimicrobial agents . 2004,第5期

机译：产复杂的β-内酰胺酶模式（包括广谱酶）的肠杆菌科临床分离株的抗菌敏感性
3. ANTIBIOTIC SUSCEPTIBILITY PATTERN AND PHENOTYPIC CHARACTERIZATION OF EXTENDED-SPECTRUM-BET A-LACTAMASE-PRODUCING Enterobacteriaceae ISOLATED FROM VARIOUS CLINICAL SAMPLES [J] . Mechai Abdelbasset, Debabza Manel, Fares Roufaida, Environmental engineering and management journal . 2020,第12期

机译：抗生素敏感性和表型表征延长光谱β-内酰胺酶产生的肠杆菌，各种临床样品分离
4. The Clinical Outcome of Infections Due to Extended Spectrum β-Lactamase Producing (ESBL) Enterobacteriaceae [C] . Perovic O., Brink A., Richards G., International Congress of Chemotherapy and Infection . 2009

机译：扩展β-内酰胺酶产生（ESBL）肠杆菌的感染临床结果
5. Prevalence of Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae with Focus on the Molecular Characterization of ESBL- and AmpC β-Lactamase-Producing Escherichia coli Isolated in Canadian Hospitals from 2005-2009 [D] . Simner, Patricia Jeanne 2011

机译：2005-2009年在加拿大医院分离的产广谱β-内酰胺酶肠杆菌的流行情况，侧重于生产ESBL和AmpCβ-内酰胺酶的大肠杆菌的分子表征
6. Use of an Enrichment Broth Improves Detection of Extended-Spectrum-Beta-Lactamase-Producing Enterobacteriaceae in Clinical Stool Samples [O] . Nathalie Jazmati, Rebecca Hein, Axel Hamprecht 2016

机译：使用丰富的肉汤可改善临床凳子样品中产生广谱β-内酰胺酶的肠杆菌科细菌的检测
7. The bacterial identification and antimicrobial susceptibility testing are usually performed manually. Recently, the number of samples has increased and the need for automatification has grown. BioMerieux has investigated Vitek2 for this purpose. HUSLAB has assigned us to compare the identification and antimicrobial results with respect to routine methods and Vitek2. Furthermore, we evaluate test reactions, ESBL (Extended Spectrum Beta-Lactamase) production and the time what it takes to get results with Vitek2. In this study, we examined a total of 183 bacterial isolates including 76 ESBL-strains, 40 nonfermenting rods, 41 fastidious bacteria and 26 fresh clinical isolates. The results of routine methods were gathered from the patient database and following this, compared to the results given by Vitek2. Vitek2 correctly identified more than 96 f the ESBL-strains and fresh clinical isolates. The results of nonfermenting rods and fastidious bacteri a were 70 oncordant with those of the routine methods. Test reaction results of Api20E were 94 nd Api20NE 70 n concordance with Vitek2 results. Approximately 80 f all Vitek2 antimicrobial results and 90 f ESBL test results were correct. Compared to earlier studies, Vitek2 performed the tests faster than the routine methods. These results suggest that Vitek2 is capable of giving rapid and accurate results. However, nonfermenting rods and fastidious bacteria should be studied further. [O] . Järveläinen Marika, Roslund Iira, Silander Maarit 2006

机译：细菌鉴定和抗菌药敏试验通常是手动进行的。最近，样品的数量增加了，并且对自动化的需求也在增长。 BioMerieux为此进行了Vitek2的研究。 HUSLAB已指派我们比较常规方法和Vitek2的鉴定和抗菌结果。此外，我们还评估了测试反应，ESBL（扩展频谱β-内酰胺酶）的产生以及使用Vitek2获得结果所需的时间。在这项研究中，我们检查了总共183个细菌分离株，包括76个ESBL菌株，40个非发酵棒，41个营养细菌和26个新鲜临床分离株。从患者数据库中收集常规方法的结果，然后将其与Vitek2给出的结果进行比较。 Vitek2正确鉴定出超过96种ESBL菌株和新鲜的临床分离株。与常规方法相比，非发酵棒和精制细菌的结果为70。 Api20E的测试反应结果与Vitek2结果一致为94nd Api20NE 70 n。所有Vitek2抗菌结果约80 f和ESBL测试结果90 f正确。与早期的研究相比，Vitek2的测试速度快于常规方法。这些结果表明Vitek2能够给出快速而准确的结果。但是，应进一步研究非发酵棒和营养细菌。

ANTIMICROBIAL SUSCEPTIBILITY AND DETECTION METHODS FOR THE EXTENDED‑SPECTRUM β-LACTAMASES PRODUCING ENTEROBACTERIACEAE FROM CLINICAL SAMPLES

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