Anti-Infective Research Laboratory, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.
Department of Clinical Pharmacy, Touro University California College of Pharmacy, Vallejo, California, USA.
Clin Infect Dis. 2020 Jun 24;71(1):1-10. doi: 10.1093/cid/ciz746.
Mounting evidence suggests the addition of a β-lactam (BL) to daptomycin (DAP) results in synergistic in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA) and bolsters the innate immune response to infection. This study's objective was to provide clinical translation to these experimental data and determine if DAP+BL combination therapy results in improved clinical outcomes compared with treatment with DAP alone in patients with MRSA bloodstream infections (BSIs).
This was a retrospective, comparative cohort study conducted at 2 academic medical centers between 2008 and 2018. Adults with MRSA BSI treated with DAP for ≥72 hours and initiated ≤5 days of culture collection were included. Patients who received a BL for ≥24 hours and initiated ≤24 hours of DAP comprised the DAP+BL group. The primary outcome was composite clinical failure (60-day all-cause mortality and/or 60-day recurrence). Analyses were adjusted for confounding using inverse probability of treatment weighting (IPTW).
A total of 229 patients were included (72 DAP+BL and 157 DAP). In unadjusted and IPTW-adjusted analyses, DAP+BL was associated with significantly reduced odds of clinical failure (odds ratio [OR], 0.362; 95% confidence interval [CI], .164-.801; adjusted OR, 0.386; 95% CI, .175-.853). Adjusted analyses restricted to prespecified subgroups based on infection complexity and baseline health status were consistent with the main analysis.
The addition of a BL to DAP was associated with improved clinical outcomes in patients with MRSA BSI. This study provides support to ongoing and future studies evaluating the impact of combination therapy for invasive MRSA infections.Patients treated with daptomycin plus a β-lactam for MRSA bloodstream infection had lower odds of composite clinical failure defined as 60-day all-cause mortality and/or 60-day recurrence compared with patients treated with daptomycin monotherapy after adjusting for confounding variables using inverse probability of treatment weighting.
越来越多的证据表明,在达托霉素(DAP)中加入β-内酰胺(BL)可导致耐甲氧西林金黄色葡萄球菌(MRSA)的体外协同活性,并增强对感染的固有免疫反应。本研究的目的是将这些实验数据转化为临床应用,并确定与单独使用 DAP 相比,DAP+BL 联合治疗是否会改善 MRSA 血流感染(BSI)患者的临床结局。
这是一项在 2008 年至 2018 年期间在 2 所学术医疗中心进行的回顾性、比较队列研究。纳入接受 DAP 治疗≥72 小时且在培养物采集≤5 天内开始治疗的 MRSA BSI 成年患者。接受 BL 治疗≥24 小时且在开始使用 DAP≤24 小时的患者构成 DAP+BL 组。主要结局是复合临床失败(60 天全因死亡率和/或 60 天复发)。使用逆概率治疗加权(IPTW)对混杂因素进行调整分析。
共纳入 229 例患者(DAP+BL 组 72 例,DAP 组 157 例)。在未调整和 IPTW 调整分析中,DAP+BL 与临床失败的可能性显著降低相关(比值比 [OR],0.362;95%置信区间 [CI],.164-.801;调整 OR,0.386;95% CI,.175-.853)。根据感染复杂性和基线健康状况进行预先指定亚组的调整分析与主要分析一致。
在 MRSA BSI 患者中,DAP 联合 BL 治疗可改善临床结局。本研究为正在进行和未来评估联合治疗侵袭性 MRSA 感染影响的研究提供了支持。
患者接受达托霉素加β-内酰胺治疗 MRSA 血流感染的复合临床失败(定义为 60 天全因死亡率和/或 60 天复发)的可能性低于接受达托霉素单药治疗的患者,这是通过使用逆概率治疗加权(IPTW)调整混杂变量后得出的结果。