Antibiotic resistance pattern and identification of Extended -Spectrum BetaLactamase producing Gram-Negative Bacteria obtained from patients admitted in educational hospitals of Shohada Qaen

Z. B. Esfeden, A. Ghaderi, A. Dashtgard, Marzie Moghanni
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Abstract

Background and Aim: Determination of antibiotic resistance pattern and awareness of current resistance in each region, it can help to take appropriate therapeutic measures. The purpose of this study to identification of bacterial agents causing infection, and was the determination of their antibiotic resistance in patients admitted to educational hospital of Shohada Qaen, through the years 20182019. Materials and Methods: In this descriptive-analytic study, in the period of one year, 1980 samples were collected from patients admitted to educational hospitals of Shohada Qaen. The specimens were cultured in blood agar and EMB, and were incubated at 37 ° C for 24 hours, then the infection-causing bacteria were identified by differential biochemical tests, depending on gram positive or gram negative bacteria. The Disk diffusion method was applied to determine antibiotic resistance pattern, and the combined disk phenotypic method was applied to determine the strains producing e extended -spectrum beta-lactamase enzymes (ESBLs). Results: of 1980 samples collected from patients admitted, 183 bacterial isolates were collected from which 151 gram negative and 32 gram-positive bacteria were identified. The most common isolated bacteria were Escherichia coli with a frequency of 60.1%, followed by Staphylococcus aureus and Klebsiella, with a frequency of 11.5% and 10.9% respectively. Generally, gram-positive bacteria had the least resistance to Ciprofloxacin and Imipenem and gram-negative bacteria had the least resistance to Amikacin. 44.7% of the gram-negative bacteria produced ESBL. Conclusion: Antibiotic administration based on the antibiotic resistance pattern can be more effective and useful. The high prevalence of ESBL producing strains indicates the necessity of rapid monitoring and identification of these strains.
Shohada qen教育医院患者产β -内酰胺酶的革兰氏阴性菌的耐药模式及鉴定
背景与目的:了解各地区抗生素耐药模式及现状,有助于采取相应的治疗措施。本研究的目的是鉴定引起感染的细菌病原体,并确定2018 - 2019年在Shohada Qaen教育医院住院的患者的抗生素耐药性。材料与方法:本描述性分析研究在一年的时间里,收集了1980例在Shohada qen教育医院住院的患者样本。将标本分别置于血琼脂和EMB中培养,37℃孵育24小时,根据革兰氏阳性菌和革兰氏阴性菌进行鉴别生化试验。采用盘片扩散法测定耐药模式,联合盘片表型法测定产生e -扩展谱β -内酰胺酶(ESBLs)的菌株。结果:1980例住院患者标本中,分离细菌183株,检出革兰氏阴性菌151株,革兰氏阳性菌32株。最常见的分离细菌是大肠杆菌,频率为60.1%,其次是金黄色葡萄球菌和克雷伯氏菌,频率分别为11.5%和10.9%。革兰氏阳性菌对环丙沙星和亚胺培南的耐药性最低,革兰氏阴性菌对阿米卡星的耐药性最低,产生ESBL的革兰氏阴性菌占44.7%。结论:基于抗生素耐药模式给药更为有效和有用。ESBL产生菌株的高流行率表明有必要对这些菌株进行快速监测和鉴定。
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