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ICU 入院时的产 ESBL 细菌定植:对后续感染、碳青霉烯类药物使用和结局的影响。

ESBL-colonization at ICU admission: impact on subsequent infection, carbapenem-consumption, and outcome.

机构信息

Division of Infectious Diseases and Hospital Epidemiology,University Hospital Basel,Basel,Switzerland.

Department of Anesthesiology, Operative Intensive Care, Preclinical Emergency Medicine and Pain Management,University Hospital Basel,Basel,Switzerland.

出版信息

Infect Control Hosp Epidemiol. 2019 Apr;40(4):408-413. doi: 10.1017/ice.2019.5. Epub 2019 Feb 21.

DOI:10.1017/ice.2019.5
PMID:30786948
Abstract

OBJECTIVE

To determine whether colonization with extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-PE) predicts the risk for subsequent infection and impacts carbapenem-consumption and outcome in intensive care unit (ICU) patients.

DESIGN

Prospective cohort study.

SETTING

The 2 ICUs in the University Hospital Basel in Switzerland.

PATIENTS

All patients admitted to the 2 ICUs providing mechanical ventilation and an expected ICU stay >48 hours.

METHODS

Patients were routinely screened for ESBL-PE carriage by rectal swab on admission. Competing risk regression analyses were applied to calculate hazard ratios (HRs) for infection with ESBL-PE and mortality. Length of hospital stay, length of ICU stay, and duration of carbapenem exposure were compared using the Mann-Whitney U test.

RESULTS

Among 302 patients, 24 (8.0%) were colonized with ESBL-PE on ICU admission. Infections with ESBL-PE occurred in 4 patients, of whom 3 (75%) were identified as ESBL-PE colonized on admission. ESBL-PE colonization on admission was associated with subsequent ESBL-PE infection (hazard ratio [HR], 25.52; 95% confidence interval [CI], 2.40-271.41; P = .007) and exposure to carbapenems (HR, 2.42; 95% CI, 1.01-5.79; P = .047), whereas duration of carbapenem exposure did not differ in relation to ESBL-PE colonization (median, 7 days [IQR, 3-8 days] vs median, 6 days [IQR 3-9 days]; P = 0.983). Patients colonized with ESBL-PE were not at increased risk for death overall (HR, 1.00; 95% CI, 0.44-2.30; P = .993) or death attributable to infection (HR, 1.20; 95% CI, 0.28-5.11; P = .808).

CONCLUSIONS

Screening strategies for detection of ESBL-PE colonization on ICU admission may allow the identification of patients at highest risk for ESBL-PE infection and the correct allocation of empiric carbapenem treatment.

摘要

目的

确定产超广谱β-内酰胺酶肠杆菌科(ESBL-PE)定植是否预测随后感染的风险,并影响重症监护病房(ICU)患者的碳青霉烯类药物使用和结局。

设计

前瞻性队列研究。

地点

瑞士巴塞尔大学医院的 2 个 ICU。

患者

所有入住提供机械通气和预计 ICU 住院时间>48 小时的 2 个 ICU 的患者。

方法

患者在入院时通过直肠拭子常规筛查 ESBL-PE 定植。应用竞争风险回归分析计算 ESBL-PE 感染和死亡率的风险比(HR)。使用 Mann-Whitney U 检验比较住院时间、ICU 住院时间和碳青霉烯类药物暴露时间。

结果

在 302 名患者中,有 24 名(8.0%)在入住 ICU 时定植 ESBL-PE。4 名患者发生 ESBL-PE 感染,其中 3 名(75%)入院时被确定为 ESBL-PE 定植。入住 ICU 时 ESBL-PE 定植与随后的 ESBL-PE 感染(HR,25.52;95%置信区间 [CI],2.40-271.41;P=.007)和碳青霉烯类药物暴露(HR,2.42;95%CI,1.01-5.79;P=.047)相关,而碳青霉烯类药物暴露时间与 ESBL-PE 定植无关(中位数,7 天 [IQR,3-8 天] vs 中位数,6 天 [IQR,3-9 天];P=0.983)。定植 ESBL-PE 的患者总体死亡率无增加(HR,1.00;95%CI,0.44-2.30;P=.993)或归因于感染的死亡率(HR,1.20;95%CI,0.28-5.11;P=.808)。

结论

在 ICU 入院时进行 ESBL-PE 定植筛查策略可能有助于识别感染 ESBL-PE 风险最高的患者,并正确分配经验性碳青霉烯类药物治疗。

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