Concannon Cathleen, van Wijngaarden Edwin, Stevens Vanessa, Dumyati Ghinwa
Center for Community Health, University of Rochester Medical Center, Rochester, New York.
Infect Control Hosp Epidemiol. 2014 Sep;35(9):1140-6. doi: 10.1086/677634. Epub 2014 Jul 28.
The current central line-associated bloodstream infection (CLABSI) surveillance rate calculation does not account for multiple concurrent central venous catheters (CVCs). The presence of multiple CVCs creates more points of entry into the bloodstream, potentially increasing CLABSI risk. Multiple CVCs may be used in sicker patients, making it difficult to separate the relative contributions of multiple CVCs and comorbidities to CLABSI risk. We explored the relative impact of multiple CVCs, patient comorbidities, and disease severity on the risk of CLABSI.
Case-control study.
A total of 197 case patients and 201 control subjects with a CVC inserted during hospitalization at a tertiary care academic medical center from January 1, 2008, to December 31, 2010.
Multiple CVCs was the exposure of interest; the primary outcome was CLABSI. Multivariable logistic regression was conducted to estimate odds ratios (ORs) and 95% confidence intervals (CIs) describing the association between CLABSI and multiple CVCs with and without controlling for Acute Physiology and Chronic Health Evaluation (APACHE) II and Charlson comorbidity index (CCI) scores as measures of disease severity and patient comorbidities, respectively.
Patients with multiple CVCs (n = 78) showed a 4.2 (95% CI, 2.2-8.4) times greater risk of CLABSI compared with patients with 1 CVC after adjusting for CLABSI risk factors. When including APACHE II and CCI scores, multiple CVCs remained an independent risk factor for CLABSI (OR, 3.4 [95% CI, 1.7-6.9]).
Multiple CVCs is an independent risk factor for CLABSI even after adjusting for severity of illness. Adjustment for this risk may be necessary to accurately compare rates between hospitals.
当前中心静脉导管相关血流感染(CLABSI)监测率的计算未考虑多个同时存在的中心静脉导管(CVC)。多个CVC的存在会增加进入血流的入口点,可能增加CLABSI风险。多个CVC可能用于病情更重的患者,因此难以区分多个CVC和合并症对CLABSI风险的相对影响。我们探讨了多个CVC、患者合并症和疾病严重程度对CLABSI风险的相对影响。
病例对照研究。
2008年1月1日至2010年12月31日期间,在一家三级医疗学术医学中心住院期间插入CVC的197例病例患者和201例对照受试者。
将多个CVC作为感兴趣的暴露因素;主要结局为CLABSI。进行多变量逻辑回归以估计比值比(OR)和95%置信区间(CI),描述CLABSI与多个CVC之间的关联,同时分别控制急性生理与慢性健康状况评估(APACHE)II和查尔森合并症指数(CCI)评分作为疾病严重程度和患者合并症的指标。
在调整CLABSI危险因素后,与有1个CVC的患者相比,有多个CVC的患者(n = 78)发生CLABSI的风险高4.2倍(95% CI,2.2 - 8.4)。当纳入APACHE II和CCI评分时,多个CVC仍然是CLABSI的独立危险因素(OR,3.4 [95% CI,1.7 - 6.9])。
即使在调整疾病严重程度后,多个CVC仍是CLABSI的独立危险因素。为准确比较医院之间的发生率,可能需要对这一风险进行调整。