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产超广谱β-内酰胺酶肠杆菌科社区获得性血流感染的危险因素:全国基于人群的病例对照研究。

Risk factors for community-onset bloodstream infection with extended-spectrum β-lactamase-producing Enterobacteriaceae: national population-based case-control study.

机构信息

Department of Medicine Solna, Unit for Infectious Diseases, Karolinska Institutet, Stockholm, Sweden.

Department of Clinical Microbiology, Karolinska Institutet, Karolinska University Hospital Laboratory, Stockholm, Sweden.

出版信息

Clin Microbiol Infect. 2019 Nov;25(11):1408-1414. doi: 10.1016/j.cmi.2019.04.002. Epub 2019 Apr 13.

Abstract

OBJECTIVES

The aim was to investigate risk factors for community-onset bloodstream infections with extended-spectrum β-lactamase-producing Enterobacteriaceae (EPE BSI).

METHODS

It is mandatory to report EPE BSI to a national register at the Public Health Agency of Sweden. Using this register, we performed a population-based case-control study from 2007 to 2012 of 945 cases and 9390 controls. Exposure data on comorbidity, hospitalization, in- and outpatient antibiotic consumption and socio-economic status were collected from hospital and health registers.

RESULTS

The overall incidence of EPE BSI was 1.7 per 100 000 person-years. The 30-day mortality was 11.3%. Urological disorders inferred the highest EPE BSI risk, adjusted odds ratio (aOR) 4.32 (95% Confidence Interval (CI) 3.41-5.47), followed by immunological disorders, aOR 3.54 (CI 2.01-6.23), haematological malignancy, aOR 2.77 (CI 1.57-4.87), solid tumours, aOR 2.28 (1.76-2.94) and diabetes, aOR 2.03 (1.58-2.61). Consumption of fluoroquinolones or mostly non-EPE-active antibiotics with selective Gram-negative spectrum of activity within the previous 3 months was associated with EPE BSI, aORs 5.52 (CI 2.8-11.0) and 3.8, CI 1.9-7.7) respectively. There was a dose-response relationship in EPE BSI risk with increasing number of consecutive regimens. Antibiotic consumption >3 months before EPE BSI was not associated with increased risk. Higher age, malignancies and education ≤12 years (aORs >2) were associated with increased 30-day mortality.

CONCLUSIONS

Targeted interventions should be directed towards improving care for patients with immunosuppression, urological disorders and subjects with lower socio-economic status. Antibiotic stewardship should focus on reduction of fluoroquinolones.

摘要

目的

本研究旨在探讨产超广谱β-内酰胺酶肠杆菌科细菌(EPE BSI)社区获得性血流感染的危险因素。

方法

在瑞典公共卫生局,有一项强制性规定,要求向全国登记处报告 EPE BSI。我们利用该登记处,于 2007 年至 2012 年期间开展了一项以人群为基础的病例对照研究,共纳入 945 例病例和 9390 例对照。从医院和健康登记处收集了合并症、住院、门诊和住院抗生素使用以及社会经济状况等暴露数据。

结果

EPE BSI 的总发病率为 1.7/100000 人年。30 天死亡率为 11.3%。泌尿系统疾病与 EPE BSI 风险相关性最高,校正比值比(aOR)为 4.32(95%置信区间(CI)为 3.41-5.47),其次是免疫性疾病,aOR 为 3.54(CI 为 2.01-6.23),血液恶性肿瘤,aOR 为 2.77(CI 为 1.57-4.87),实体瘤,aOR 为 2.28(1.76-2.94)和糖尿病,aOR 为 2.03(1.58-2.61)。在过去 3 个月内使用氟喹诺酮类药物或大多数非 EPE 活性抗生素,具有选择性革兰氏阴性谱活性,与 EPE BSI 相关,aOR 分别为 5.52(CI 2.8-11.0)和 3.8(CI 1.9-7.7)。EPE BSI 风险与连续方案数量呈剂量反应关系。EPE BSI 前>3 个月使用抗生素与增加风险无关。年龄较大、恶性肿瘤和教育程度≤12 年(aOR>2)与 30 天死亡率增加相关。

结论

应针对免疫抑制、泌尿系统疾病和社会经济地位较低的患者加强针对性干预。抗生素管理应侧重于减少氟喹诺酮类药物的使用。

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