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首页> 外文期刊>Infection and Drug Resistance >Extended-spectrum beta-lactamase- and carbapenemase-producing Enterobacteriaceae among Ethiopian children
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Extended-spectrum beta-lactamase- and carbapenemase-producing Enterobacteriaceae among Ethiopian children

机译:埃塞俄比亚儿童中产生广谱β-内酰胺酶和碳青霉烯酶的肠杆菌科

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Background: Infections by extended-spectrum beta-lactamase- (ESBL) and carbapenem-resistant Enterobacteriaceae (CRE) are an emerging problem in children nowadays. Hence, the aim of this study was to determine the prevalence of ESBL- and carbapenemase-producing Enterobacteriaceae among children suspected of septicemia and urinary tract infections (UTIs). Methods: A cross-sectional study was conducted from January to March 2014. A total of 322 study participants suspected of septicemia and UTIs were recruited. All blood and urine samples were cultured on blood and MacConkey agar. All positive cultures were characterized by colony morphology, Gram stain, and standard biochemical tests. Antimicrobial susceptibility test was performed on Muller-Hinton agar using disk diffusion. ESBL was detected using combination disk and double-disk synergy methods, and the results were compared. Carbapenemase was detected by modified Hodge method using meropenem. Data were analyzed using SPSS version 20. Results: The overall prevalence of ESBL- and carbapenemase-producing Enterobacteriaceae was 78.57% (n=22/28) and 12.12%, respectively. Among the Enterobacteriaceae tested, Klebsiella pneumoniae (84.2%, n=16/19), Escherichia coli (100%, n=5/5), and Klebsiella oxytoca (100%, n=1/1) were positive for ESBL. Double-disk synergy method showed 90.9% sensitivity, 66.7% specificity, 95.2% positive predictive value, and 50% negative predictive value. Carbapenemase-producing Enterobacteriaceae were K. pneumoniae (9.09%, n=3/33) and Morganella morganii (3.03%, n=1/33). Conclusion: Screening Enterobacteriaceae for ESBL production is essential for better antibiotics selection and preventing its further emergence and spread. In resource-limited settings, double-disk synergy method can be implemented for screening and confirming ESBL production. Moreover, occurrence of CRE in countries where no carbapenems are sold is worrying microbiologists as well as clinicians. Hence, identifying factors that induce carbapenemase production in the absence of carbapenems prescription is essential for control of CRE dissemination within the community.
机译:背景:广谱β-内酰胺酶(ESBL)和对碳青霉烯类耐药的肠杆菌科(CRE)的感染已成为当今儿童的新问题。因此,本研究的目的是确定怀疑败血病和尿路感染(UTI)的儿童中产生ESBL和碳青霉烯酶的肠杆菌的患病率。方法:2014年1月至2014年3月进行了一项横断面研究。总共招募了322名怀疑有败血病和泌尿道感染的研究参与者。所有血液和尿液样本均在血液和MacConkey琼脂上培养。所有阳性培养物均以菌落形态,革兰氏染色和标准生化测试为特征。使用圆盘扩散法在Muller-Hinton琼脂上进行了药敏试验。使用组合磁盘和双磁盘协同方法检测ESBL,并比较结果。使用美罗培南通过改良的Hodge方法检测碳青霉烯酶。使用SPSS 20版分析数据。结果:产ESBL和碳青霉烯酶的肠杆菌科细菌的总患病率分别为78.57%(n = 22/28)和12.12%。在测试的肠杆菌科中,肺炎克雷伯菌(84.2%,n = 16/19),大肠杆菌(100%,n = 5/5)和产酸克雷伯菌(100%,n = 1/1)对ESBL呈阳性。双盘协同法显示出90.9%的敏感性,66.7%的特异性,95.2%的阳性预测值和50%的阴性预测值。产生碳青霉烯酶的肠杆菌科是肺炎克雷伯氏菌(9.09%,n = 3/33)和摩根氏摩根氏菌(3.03%,n = 1/33)。结论:筛选肠杆菌科细菌产生ESBL对更好地选择抗生素并防止其进一步出现和扩散至关重要。在资源有限的环境中,可以实施双盘协同方法来筛选和确认ESBL的生产。此外,在没有出售碳青霉烯的国家中发生CRE令微生物学家和临床医生感到担忧。因此,在缺乏碳青霉烯处方的情况下,识别诱导碳青霉烯酶产生的因素对于控制社区内CRE的传播至关重要。

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