Ulrich Robert J, Santhosh Kavitha, Mogle Jill A, Young Vincent B, Rao Krishna
Department of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA; Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI 48105, USA.
Department of Internal Medicine, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA; Division of Infectious Diseases, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA.
Anaerobe. 2017 Dec;48:27-33. doi: 10.1016/j.anaerobe.2017.06.020. Epub 2017 Jun 29.
Clostridium difficile infection (CDI) is a common nosocomial diarrheal illness increasingly associated with mortality in United States. The underlying factors and mechanisms behind the recent increases in morbidity from CDI have not been fully elucidated. Murine models suggest a mucosal barrier breakdown leads to bacterial translocation and subsequent bloodstream infection (BSI). This study tests the hypothesis that CDI is associated with subsequent BSI in humans.
We conducted a retrospective cohort study on 1132 inpatients hospitalized >72 h with available stool test results for toxigenic C. difficile. The primary outcome was BSI following CDI. Secondary outcomes included 30-day mortality, colectomy, readmission, and ICU admission. Unadjusted and adjusted logistic regression models were developed.
CDI occurred in 570 of 1132 patients (50.4%). BSI occurred in 86 (7.6%) patients. Enterococcus (14%) and Klebsiella (14%) species were the most common organisms. Patients with BSI had higher comorbidity scores and were more likely to be male, on immunosuppression, critically ill, and have a central venous catheter in place. Of the patients with BSI, 36 (42%) had CDI. CDI was not associated with subsequent BSI (OR 0.69; 95% CI 0.44-1.08; P = 0.103) in unadjusted analysis. In multivariable modeling, CDI appeared protective against subsequent BSI (OR 0.57; 95% CI 0.34-0.96; P = 0.036). Interaction modeling suggests a complicated relationship among CDI, BSI, antibiotic exposure, and central venous catheter use.
In this cohort of inpatients that underwent testing for CDI, CDI was not a risk factor for developing subsequent BSI.
艰难梭菌感染(CDI)是一种常见的医院获得性腹泻疾病,在美国其与死亡率的关联日益增加。近期CDI发病率上升背后的潜在因素和机制尚未完全阐明。小鼠模型表明,黏膜屏障破坏会导致细菌移位及随后的血流感染(BSI)。本研究检验CDI与人类后续BSI相关的假说。
我们对1132例住院时间超过72小时且有艰难梭菌毒素检测结果的住院患者进行了一项回顾性队列研究。主要结局是CDI后的BSI。次要结局包括30天死亡率、结肠切除术、再次入院和入住重症监护病房(ICU)。构建了未调整和调整后的逻辑回归模型。
1132例患者中有570例(50.4%)发生CDI。86例(7.6%)患者发生BSI。肠球菌(14%)和克雷伯菌属(14%)是最常见的病原体。发生BSI的患者合并症评分更高,更可能为男性、正在接受免疫抑制治疗、病情危重且已留置中心静脉导管。在发生BSI的患者中,36例(42%)有CDI。在未调整分析中,CDI与后续BSI无关(比值比[OR]0.69;95%置信区间[CI]0.44 - 1.08;P = 0.103)。在多变量建模中,CDI似乎对后续BSI有保护作用(OR 0.57;95% CI 0.34 - 0.96;P = 0.036)。交互作用建模表明CDI、BSI、抗生素暴露和中心静脉导管使用之间存在复杂关系。
在这组接受CDI检测的住院患者中,CDI不是发生后续BSI的危险因素。