Zasowski Evan J, Claeys Kimberly C, Lagnf Abdalhamid M, Davis Susan L, Rybak Michael J
Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University.
Department of Pharmacy Services, Henry Ford Hospital.
Clin Infect Dis. 2016 May 15;62(10):1242-1250. doi: 10.1093/cid/ciw110. Epub 2016 Mar 3.
With increasing prevalence of vancomycin-resistant enterococci (VRE), appropriate antibiotic therapy for enterococcal bloodstream infections (EBSI) can be delayed. Data regarding the impact of delayed therapy on EBSI outcomes are conflicting, and the time delay most strongly associated with poor outcomes has not been defined.
This was a single-center, retrospective cohort study of adult, nonneutropenic patients with hospital-onset EBSI from 2010 to 2014. Classification and regression tree (CART) analysis was used to determine the delay in appropriate therapy most predictive of 30-day mortality. Appropriate therapy was defined as antibiotic therapy to which the enterococci and copathogen, where applicable, were susceptible. Outcomes and clinical characteristics were compared between patients receiving early or delayed therapy, defined by CART timepoint. Poisson regression was employed to determine the independent association of delayed therapy on 30-day mortality and predictors of delayed therapy.
Overall, 190 patients were included. A breakpoint in time to appropriate therapy was identified at 48.1 hours, where 30-day mortality was substantially increased (14.6% vs 45.3%; P < .001). Patients receiving appropriate therapy after 48.1 hours also experienced higher in-hospital mortality and longer EBSI duration. After adjustment for severity of illness and comorbidity, delayed therapy ≥48.1 hours was associated with a 3-fold increase in 30-day mortality (risk ratio, 3.16 [95% confidence interval, 1.96-5.09]). Vancomycin resistance was the only independent predictor of delayed therapy.
In patients with hospital-onset EBSI, receipt of appropriate therapy within the first 48 hours was associated with reduced mortality, underscoring the potential role of rapid diagnostic testing for early identification of VRE.
随着耐万古霉素肠球菌(VRE)的患病率不断上升,肠球菌血流感染(EBSI)的适当抗生素治疗可能会延迟。关于延迟治疗对EBSI结局影响的数据相互矛盾,且与不良结局最密切相关的时间延迟尚未明确。
这是一项对2010年至2014年成人非中性粒细胞减少的医院获得性EBSI患者进行的单中心回顾性队列研究。使用分类与回归树(CART)分析来确定最能预测30天死亡率的适当治疗延迟时间。适当治疗定义为肠球菌和(如适用)共病原体敏感的抗生素治疗。根据CART时间点定义,比较接受早期或延迟治疗的患者的结局和临床特征。采用泊松回归确定延迟治疗与30天死亡率的独立关联以及延迟治疗的预测因素。
总共纳入了190例患者。确定适当治疗的时间断点为48.1小时,此时30天死亡率大幅增加(14.6%对45.3%;P <.001)。在48.1小时后接受适当治疗的患者住院死亡率也更高,EBSI持续时间更长。在调整疾病严重程度和合并症后,延迟治疗≥48.1小时与30天死亡率增加3倍相关(风险比,3.16 [95%置信区间,1.96 - 5.09])。万古霉素耐药是延迟治疗的唯一独立预测因素。
在医院获得性EBSI患者中,在最初48小时内接受适当治疗与死亡率降低相关,这突出了快速诊断检测在早期识别VRE方面的潜在作用。