Department of Laboratory Medicine and Research Institute of Bacterial Resistance, Yonsei University College of Medicine, 211 Eonju-ro, Gangnam-gu, Seoul 135-720, Korea.
Yonsei Med J. 2014 Mar;55(2):467-75. doi: 10.3349/ymj.2014.55.2.467.
Inadequate empirical therapy for severe infections caused by extended-spectrum β-lactamase-producing Escherichia coli (ESBLEC) is associated with poor outcomes. This study was designed to investigate risk factors for community-onset ESBLEC bacteremia at admission to a tertiary care hospital.
A case-control study was performed that included all episodes of ESBLEC bacteremia in the outpatient department or within 48 hours of admission from January 2005 to March 2009. Data on predisposing factors were collected. The molecular epidemiology of ESBLEC clinical isolates was also determined.
Among 25281 blood cultures, 60 episodes of ESBLEC bacteremia were studied, which accounted for 7% of all E. coli bacteremia at admission. Healthcare-associated infection [odds ratio (OR), 8.3; 95% confidence interval (CI), 2.4-28.7; p=0.001], malignancy (OR, 4.6; 95% CI, 1.3-16.3; p=0.018), urinary tract infection (OR, 139.1; 95% CI, 24.6-788.2; p<0.001), hepatobiliary infection (OR, 79.1; 95% CI, 13.5-463.8; p<0.001), third generation cephalosporin usage during preceding 3 months (OR, 16.4; 95% CI, 2.0-131.8; p=0.008), and severe sepsis/septic shock (OR, 73.7; 95% CI, 12.4-438.5; p<0.001) were determined as independent risk factors for community-onset ESBLEC bacteremia. The most common extended-spectrum β-lactamase (ESBL) gene identified was blaCTX-M-15 (n=31) followed by blaCTX-M-14 (n=23).
The most common types of ESBLs in E. coli causing community-onset bacteremia were CTX-M-15 and CTX-M-14 in Korea. By result of decision tree analysis, the empirical use of carbapenems is suggested only for patients with severe sepsis/septic shock, hepatobiliary infection, or healthcare-associated urinary tract infection.
产超广谱β-内酰胺酶(ESBL)大肠埃希菌(E. coli)引起的严重感染如果经验性治疗不充分,其预后往往较差。本研究旨在调查三级医院住院患者社区获得性产 ESBL 大肠埃希菌菌血症的发病危险因素。
采用病例对照研究,纳入 2005 年 1 月至 2009 年 3 月期间在我院门诊或住院 48 小时内的所有产 ESBL 大肠埃希菌菌血症患者。收集易患因素的数据,并对产 ESBL 大肠埃希菌临床分离株的分子流行病学进行了分析。
在 25281 份血培养中,有 60 例产 ESBL 大肠埃希菌菌血症患者,占所有大肠埃希菌菌血症患者的 7%。医源性感染(比值比[OR],8.3;95%置信区间[CI],2.4-28.7;p=0.001)、恶性肿瘤(OR,4.6;95%CI,1.3-16.3;p=0.018)、尿路感染(OR,139.1;95%CI,24.6-788.2;p<0.001)、肝胆感染(OR,79.1;95%CI,13.5-463.8;p<0.001)、在过去 3 个月中使用第三代头孢菌素(OR,16.4;95%CI,2.0-131.8;p=0.008)和严重脓毒症/感染性休克(OR,73.7;95%CI,12.4-438.5;p<0.001)是社区获得性产 ESBL 大肠埃希菌菌血症的独立危险因素。最常见的超广谱β-内酰胺酶(ESBL)基因是 blaCTX-M-15(n=31),其次是 blaCTX-M-14(n=23)。
韩国引起社区获得性菌血症的大肠埃希菌中最常见的 ESBL 类型为 CTX-M-15 和 CTX-M-14。通过决策树分析,建议仅对严重脓毒症/感染性休克、肝胆感染或医源性尿路感染患者经验性使用碳青霉烯类药物。