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产超广谱β-内酰胺酶肺炎克雷伯菌引起的大规模疫情的流行病学及成功控制

Epidemiology and successful control of a large outbreak due to Klebsiella pneumoniae producing extended-spectrum beta-lactamases.

作者信息

Peña C, Pujol M, Ardanuy C, Ricart A, Pallares R, Liñares J, Ariza J, Gudiol F

机构信息

Infectious Disease Service, Hospital de Bellvitge, Universidad de Barcelona, Spain.

出版信息

Antimicrob Agents Chemother. 1998 Jan;42(1):53-8. doi: 10.1128/AAC.42.1.53.

Abstract

An outbreak due to extended-spectrum beta-lactamase-producing Klebsiella pneumoniae (ESBL-KP) was detected from May 1993 to June 1995. A total of 145 patients, particularly patients in intensive care units (ICUs) (107 patients [72%]), were colonized or infected. Infection developed in 92 (63%) patients, and primary bacteremia caused by ESBL-KP was the most frequent infection (40 of 92 patients [43%]). A single clone of ESBL-KP was identified by pulsed-field gel electrophoresis analysis throughout the whole period, and no molecular epidemiological relationship could be found between the epidemic strain and non-ESBL-KP isolates. To determine risk factors for ESBL-KP infection weekly rectal swabs were obtained in three serial incidence surveys (470 patients); the probabilities of carriage of ESBL-KP in the digestive tract were 33% (October and November 1993), 40% (May and June 1994), and 0% (October and November 1995) at 10 days of ICU admission. A logistic regression model identified prior carriage of ESBL-KP in the digestive tract (odds ratio, 3.4; 95% confidence interval 1.1 to 10.4) as an independent variable associated with ESBL-KP infection. A statistically significant correlation was observed between the restricted use of oxyimino-beta-lactams (189 defined daily doses [DDD]/ 1,000 patient-days to 24 DDD/1,000 patient-days) and the trends of ESBL-KP infection (r = 0.7; P = 0.03).

摘要

1993年5月至1995年6月期间,检测到一起由产超广谱β-内酰胺酶肺炎克雷伯菌(ESBL-KP)引起的暴发。共有145例患者被定植或感染,尤其是重症监护病房(ICU)的患者(107例[72%])。92例(63%)患者发生感染,由ESBL-KP引起的原发性菌血症是最常见的感染类型(92例患者中有40例[43%])。在整个期间,通过脉冲场凝胶电泳分析鉴定出单一克隆的ESBL-KP,并且在流行菌株与非ESBL-KP分离株之间未发现分子流行病学关联。为了确定ESBL-KP感染的危险因素,在三项连续发病率调查(470例患者)中每周采集直肠拭子;在入住ICU 10天时,消化道中携带ESBL-KP的概率分别为33%(1993年10月和11月)、40%(1994年5月和6月)和0%(1995年10月和11月)。逻辑回归模型确定消化道先前携带ESBL-KP(比值比,3.4;95%置信区间1.1至10.4)为与ESBL-KP感染相关的独立变量。在氧亚氨基β-内酰胺类药物的限制使用(从189限定日剂量[DDD]/1000患者日降至24 DDD/1000患者日)与ESBL-KP感染趋势之间观察到统计学显著相关性(r = 0.7;P = 0.03)。

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