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首页> 外文期刊>The Journal of hospital infection >Epidemiology of infections caused by extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella spp.: a nested case-control study from a tertiary hospital in London.
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Epidemiology of infections caused by extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella spp.: a nested case-control study from a tertiary hospital in London.

机译:由产生广谱β-内酰胺酶的大肠杆菌和克雷伯菌属引起的感染的流行病学:来自伦敦一家三级医院的嵌套病例对照研究。

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摘要

Information on risk factors for acquisition of extended-spectrum ss-lactamase (ESBL)-producing organisms and their outcomes in patients with invasive infections is scant. The objectives of this study were to evaluate risk factors and all-cause mortality associated with infection due to ESBL-producing organisms using a nested case-control design, and to document transmission within a hospital employing molecular and conventional epidemiological methods. From December 2003 to April 2005, 50 patients with bloodstream infections (BSIs) due to ESBL-producing E. coli and Klebsiella spp. were recruited. Controls (N=50) were chosen, within the same period, from patients with non-ESBL-producing BSIs by simple random sampling; account was taken of potential confounding factors. Cases and controls were followed-up until November 2005, and outcomes were recorded as discharged or deceased. Molecular methods, supported by conventional epidemiology, were used to study the transmission of organisms. Logistic regression analyses showed prior ss-lactam antibiotics [odds ratio (OR) 11.57; 95% confidence intervals (CI) 2.31-51.15; P=0.003], hospital stay >15 days (OR 2.63; 95% CI 1.01-6.89; P=0.04) and prior admission to the intensive care unit (OR 13.98; 95% CI 1.88-19.15; P=0.006) to be independent risk factors for the acquisition of ESBL-producing organisms. In the first 15 days of follow-up, a significant proportion of patients with ESBL-producing organisms died; however, there was no difference in mortality between cases and controls at the end of the follow-up period. Molecular epidemiology identified five clusters amongst the ESBL-producing isolates. Conventional epidemiological analyses supported the evidence of transmission in three of these clusters.
机译:很少有关于获得广谱β-内酰胺酶(ESBL)的生物体获得感染的危险因素及其在侵入性感染患者中的预后的信息。这项研究的目的是使用巢式病例对照设计评估与生产ESBL的生物引起的感染相关的危险因素和全因死亡率,并记录采用分子和常规流行病学方法在医院内的传播情况。从2003年12月到2005年4月,有50例由于产生ESBL的大肠杆菌和克雷伯菌属而引起的血液感染(BSI)。被招募。在同一时期内,通过简单随机抽样从非ESBL产生BSI的患者中选择了对照组(N = 50);考虑了潜在的混杂因素。随访病例和对照直至2005年11月,并记录结局为出院或死亡。在常规流行病学的支持下,分子方法被用于研究生物的传播。 Logistic回归分析显示,以前使用的β-内酰胺类抗生素[比值比(OR)为11.57; 95%置信区间(CI)2.31-51.15; P = 0.003],住院时间超过15天(OR 2.63; 95%CI 1.01-6.89; P = 0.04),以及入院重症监护室(OR 13.98; 95%CI 1.88-19.15; P = 0.006)获得ESBL的生物的独立危险因素。在随访的前15天中,有很大比例的ESBL产生生物死亡。但是,在随访期结束时,病例与对照之间的死亡率没有差异。分子流行病学在产生ESBL的分离物中鉴定出五个簇。传统的流行病学分析支持了在这三个集群中传播的证据。

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