Department of Clinical Pharmacy and Outcomes Sciences, University of South Carolina College of Pharmacy, Columbia, SC, USA; Department of Pharmacy, Palmetto Health Richland, Columbia, SC, USA.
Department of Pharmacy, Palmetto Health Richland, Columbia, SC, USA.
Int J Antimicrob Agents. 2018 Mar;51(3):488-492. doi: 10.1016/j.ijantimicag.2017.09.007. Epub 2017 Sep 14.
The utility of empirical combination antimicrobial therapy for Gram-negative bloodstream infection (BSI) remains unclear. This retrospective, quasi-experimental matched cohort study examined the impact of empirical combination therapy on mortality in patients with Gram-negative BSI. Hospitalized adults with Gram-negative BSI from 1 January 2010 to 31 December 2013 at Palmetto Health Hospitals in Columbia, SC, USA were identified. Patients receiving combination therapy or beta-lactam monotherapy were matched 1:1 based on age, sex and Bloodstream Infection Mortality Risk Score (BSIMRS). Multivariate Cox proportional hazards regression with propensity score adjustment was used to examine overall 28-day mortality and within predefined BSIMRS categories (<5 and ≥5). A total of 380 patients receiving combination therapy or monotherapy for Gram-negative BSI were included in the study. Median age was 66 years and 204 (54%) were female. Overall, 28-day mortality in patients who received combination therapy and monotherapy was 13% and 15%, respectively (P = 0.51). After stratification by BSIMRS, mortality in both combination therapy and monotherapy groups was 1.1% in patients with BSIMRS <5 (P = 0.98) and 27% and 32%, respectively, in patients with BSIMRS ≥5 (P = 0.47). After adjusting for propensity to receive combination therapy, risk of mortality was not significantly different for combination therapy compared to monotherapy (hazard ratio [HR] 0.90, 95% confidence interval [CI] 0.51-1.60). This finding persisted for both subgroups of BSIMRS <5 (HR 0.96, 95% CI 0.04-24.28) and BSIMRS ≥5 (HR 0.83, 95% CI 0.46-1.48). There is no survival benefit from empirical combination therapy over monotherapy in patients with Gram-negative BSI, regardless of predicted prognosis at initial presentation.
对于革兰氏阴性菌血流感染(BSI),经验性联合抗菌治疗的效用尚不清楚。本回顾性、准实验性匹配队列研究旨在探讨经验性联合治疗对革兰氏阴性菌 BSI 患者死亡率的影响。研究对象为 2010 年 1 月 1 日至 2013 年 12 月 31 日期间在美国南卡罗来纳州哥伦比亚市 Palmetto Health 医院住院的革兰氏阴性菌 BSI 成年患者。根据年龄、性别和血流感染死亡率风险评分(BSIMRS),对接受联合治疗或β-内酰胺单药治疗的患者进行 1:1 匹配。采用多变量 Cox 比例风险回归和倾向评分调整,比较 28 天总死亡率和预先设定的 BSIMRS 分类(<5 和≥5)内的死亡率。共纳入 380 例接受革兰氏阴性菌 BSI 联合治疗或单药治疗的患者。中位年龄为 66 岁,204 例(54%)为女性。联合治疗组和单药治疗组的 28 天死亡率分别为 13%和 15%(P=0.51)。按 BSIMRS 分层后,BSIMRS<5 的患者中,联合治疗组和单药治疗组的死亡率均为 1.1%(P=0.98),BSIMRS≥5 的患者中,死亡率分别为 27%和 32%(P=0.47)。调整接受联合治疗的倾向评分后,联合治疗组的死亡率与单药治疗组相比无显著差异(风险比 [HR] 0.90,95%置信区间 [CI] 0.51-1.60)。这一结果在 BSIMRS<5 亚组(HR 0.96,95% CI 0.04-24.28)和 BSIMRS≥5 亚组(HR 0.83,95% CI 0.46-1.48)中均保持不变。对于革兰氏阴性菌 BSI 患者,无论初始表现的预测预后如何,经验性联合治疗并不能带来生存获益,优于单药治疗。