Department of Medicine Solna, Unit for Infectious Diseases, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Microbiology, Karolinska Institutet, Karolinska University Hospital Laboratory, Stockholm, Sweden.
Clin Microbiol Infect. 2019 Nov;25(11):1408-1414. doi: 10.1016/j.cmi.2019.04.002. Epub 2019 Apr 13.
The aim was to investigate risk factors for community-onset bloodstream infections with extended-spectrum β-lactamase-producing Enterobacteriaceae (EPE BSI).
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.
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.
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.
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。
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。
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。
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。