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Metallo-Betalactamase Producing Clinical Isolates of Pseudomonas aeruginosa from Intensive Care Unit Patients of a Tertiary Care Hospital

机译:三重护理医院重症监护病房患者铜绿假单胞菌产生铜绿假单胞菌的临床分离株

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Background and Objectives: Pseudomonas aeruginosa is an important nosocomial pathogen in the health care settings. Increasing resistance to carbapenems mediated by metallo-betalactamase (MBL) and other mechanisms is a cause for concern because they adversely affect clinical outcomes and add to treatment costs. This study was undertaken to determine the prevalence of MBL production in carbapenem-resistant isolates and to study the factors influencing the clinical outcomes of infections.Materials and Methods: One hundred tweleve consecutive P. aeruginosa isolates obtained from hospitalised patients were subjected to susceptibility testing to anti-pseudomonal drugs by disc diffusion, and minimum inhibitory concentration (MIC) of imipenem was determined. The production of MBL was detected by 4-fold reduction in MIC with imipenem-ethylene diamine tetraacetic acid (EDTA) and the zone size enhancement with EDTA impregnated imipenem and ceftazidime discs.Results: By disc diffusion method, 31.2% of the P. aeruginosa isolates tested were found resistant to imipenem. 15 resistant isolates, showed a significant enhancement in zone size with the EDTA impregnated discs as well as a 4-fold reduction in MIC with imipenem EDTA. Thus 42.8% isolates of imipenem resistant Pseudomonas aeruginosa were found to be MBL producers. Overall prevalence of MBL production was 13.4% among all the Pseudomonas aeruginosa isolates.Conclusion: MBL-mediated imipenem resistance in P. aeruginosa is a cause for concern in the therapy of critically ill patients. Intensity of selection pressure for usage of broad spectrum antibiotics is high in ICUs. Therefore, a strict antibiotic policy should be followed in intensive care areas to prevent further spread of MBLs. Detection of MBLs by Disk potentiation test should be routinely performed in all microbiology laboratories for all imipenem-resistant isolates, which will help to reduce morbidity and mortality in these patients.
机译:背景与目的:铜绿假单胞菌是医疗机构中重要的医院病原体。金属β-内酰胺酶(MBL)和其他机制介导的碳青霉烯类药物的耐药性增加令人担忧,因为它们会对临床结果产生不利影响并增加治疗费用。这项研究是为了确定耐碳青霉烯分离株中MBL产生的流行率,并研究影响感染临床结果的因素。材料与方法:对来自住院患者的12例连续的12株铜绿假单胞菌分离物进行药敏测试,通过椎间盘扩散抗假性药物,并测定亚胺培南的最低抑菌浓度(MIC)。用亚胺培南-乙二胺四乙酸(EDTA)将MIC降低4倍,并用EDTA浸渍亚胺培南和头孢他啶盘片增加区域大小,从而检测到MBL的产生。结果:通过盘片扩散法,铜绿假单胞菌占31.2%。发现测试的分离株对亚胺培南具有抗性。 15个抗性分离株显示,用EDTA浸渍的椎间盘可显着增加区域大小,并使用亚胺培南EDTA可降低MIC 4倍。因此,发现亚胺培南抗性铜绿假单胞菌的42.8%分离株是MBL的产生者。在所有铜绿假单胞菌菌株中,MBL产生的总体患病率为13.4%。结论:铜绿假单胞菌MBL介导的亚胺培南耐药性是危重患者治疗中值得关注的一个原因。重症监护病房使用广谱抗生素的选择压力很高。因此,在重症监护区应遵循严格的抗生素政策,以防止MBL进一步传播。在所有微生物实验室中,应对所有亚胺培南耐药的分离株常规进行圆盘增强试验检测MBL,这将有助于降低这些患者的发病率和死亡率。

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