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重症监护病房中产超广谱β-内酰胺酶细菌定植的临床影响和危险因素。

Clinical impact and risk factors for colonization with extended-spectrum β-lactamase-producing bacteria in the intensive care unit.

机构信息

Université Paris Est-Créteil, INSERM U955, Créteil, France.

出版信息

Intensive Care Med. 2012 Nov;38(11):1769-78. doi: 10.1007/s00134-012-2675-0. Epub 2012 Aug 15.

Abstract

PURPOSE

The changed epidemiology of extended spectrum beta-lactamases (ESBL), the spread to the community and the need for prudent use of carbapenems require updated knowledge of risk factors for colonization with ESBL-producing enterobacteriaceae (ESBL-PE).

METHODS

An 8-month prospective study in the medical ICU of an 850-bed general and university-affiliated hospital.

RESULTS

Of 610 patients admitted, 531 (87 %) had a rectal swab obtained at admission, showing a 15 % (82 patients) ESBL-PE carriage rate, mostly of E. coli (n = 51, 62 %); ESBL-PE caused 9 (3 %) infections on admission. By multivariable analysis, transfer from another ICU (OR = 2.56 [1, 22]), hospital admission in another country [OR = 5.28 (1.56-17.8)], surgery within the past year [OR = 2.28 (1.34-3.86)], prior neurologic disease [OR = 2.09 (1.1-4.0)], and prior administration of third generation cephalosporin (within 3-12 months before ICU admission) [OR = 3.05 (1.21-7.68)] were independent predictive factors of colonization by ESBL-PE upon ICU admission. Twenty-eight patients (13 % of those staying for more than 5 days) acquired ESBL carriage in ICU, mostly with E. cloacae (n = 13, 46 %) and K. pneumoniae (n = 10, 36 %). In carriers, ESBL-PE caused 10 and 27 % of first and second episodes of ICU-acquired infections, respectively.

CONCLUSION

We found a high prevalence of ESBLE-PE colonization on admission to our ICU, even in the subgroup admitted from the community, but few first infections. Identifying risk factors for ESBL-PE colonization may help identifying which patients may warrant empiric ESBL-targeted antimicrobial drug therapy as a means to limit carbapenem use.

摘要

目的

扩展型β-内酰胺酶(ESBL)的流行病学变化、向社区的传播以及对碳青霉烯类药物合理使用的需求,都要求我们更新对产 ESBL 肠杆菌科细菌(ESBL-PE)定植相关危险因素的认识。

方法

对一家 850 张床位的综合性大学附属医院的内科重症监护病房进行了为期 8 个月的前瞻性研究。

结果

在 610 名入院患者中,有 531 名(87%)在入院时获得了直肠拭子,定植 ESBL-PE 的检出率为 15%(82 名患者),主要为大肠埃希菌(n=51,62%);ESBL-PE 在入院时导致 9 例(3%)感染。多变量分析显示,从另一家重症监护病房转入(比值比[OR]=2.56[1,22])、在其他国家住院(OR=5.28[1.56-17.8])、过去 1 年内接受过手术(OR=2.28[1.34-3.86])、既往神经系统疾病(OR=2.09[1.1-4.0])以及在重症监护病房入住前 3-12 个月内使用过第三代头孢菌素(OR=3.05[1.21-7.68])是入院时定植 ESBL-PE 的独立预测因素。28 名(入住时间超过 5 天的患者中有 13%)在重症监护病房获得 ESBL 定植,主要为阴沟肠杆菌(n=13,46%)和肺炎克雷伯菌(n=10,36%)。在定植者中,ESBL-PE 分别导致 10%和 27%的首次和第二次 ICU 获得性感染。

结论

我们发现,即使在从社区转入的亚组患者中,我们的重症监护病房入院时 ESBL-PE 的定植率也很高,但初次感染却很少。确定 ESBL-PE 定植的危险因素可能有助于确定哪些患者可能需要经验性针对 ESBL 的抗菌药物治疗,以限制碳青霉烯类药物的使用。

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