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首页> 外文期刊>Clinical therapeutics >Comparison of Outcomes From Daptomycin or Linezolid Treatment for Vancomycin-Resistant Enterococcal Bloodstream Infection: A Retrospective, Multicenter, Cohort Study
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Comparison of Outcomes From Daptomycin or Linezolid Treatment for Vancomycin-Resistant Enterococcal Bloodstream Infection: A Retrospective, Multicenter, Cohort Study

机译:达托霉素或利奈唑胺治疗耐万古霉素肠球菌血流感染的结果比较:一项回顾性,多中心,队列研究

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Background: The optimal treatment for bloodstream infections (BSIs) with vancomycin-resistant enterococci (VRE) is unknown.Objective: This study examined outcomes in patients treated with daptomycin or linezolid for VRE BSI.Methods: A retrospective, multicenter, cohort study was performed via chart review. Hospitalized patients treated for VRE BSI with daptomycin or linezolid from September 1,2003, to June 30,2007, were identified via pharmacy and microbiology reports at each institution. Patients aged <18 years or with polymicrobial bacter-emia were excluded from analysis. Linezolid and daptomycin were included because the participating institutions used either of the 2 agents as first-line treatment for VRE BSI. Univariate and multivariate analyses were performed to determine the effect of drug selection on mortality and duration of BSI. Duration of BSI was defined as the amount of time from the draw date of the first positive blood culture to the draw date of the first finalized negative blood culture. Adverse events were not assessed.Results: One-hundred one patients from 3 participating US hospitals experiencing VRE BSI were identified. Sixty-seven patients were treated with daptomycin and 34 with linezolid. Baseline characteristics appeared comparable between the daptomycin- and linezolid-treated groups, with the exception of shock (P = 0.049), prior vancomycin treatment (P = 0.002), and prior linezolid treatment (P < 0.001), all of which occurred significantly more often in daptomycin-treated patients. Inpatient mortality occurred in 31 daptomycin- and 10 linezolid-treated patients (46.3% vs 29.4%; P = NS). Linear regression found that shock (P = 0.015), infective endocarditis (P = 0.021), and concurrent rifampin or gentamicin treatment (P = 0.01) were associated with prolonged duration of positive cultures. Logistic regression revealed that shock (odds ratio [OR] = 14.24; P = 0.008), infection with Enterococcus faecium (OR = 53.10; P = 0.024), previous linezolid treatment (OR = 6.63; P = 0.031), concurrent rifampin or gentamicin treatment (OR = 6.48; P = 0.046), and a nonline source of infection (OR = 6.67; P = 0.019) were associated with increased mortality.Conclusions: In this retrospective cohort analysis, there were no significant differences in mortality of VRE BSI between patients receiving daptomycin or linezolid. Underlying comorbidities appeared to best predict outcome;however, given the retrospective nature of this study, larger, prospective, randomized, comparative studies are needed to control for potential biases and determine definitive outcome differences between these 2 antimicrobials.
机译:背景:耐万古霉素的肠球菌(VRE)不能最佳治疗血流感染(BSI)目的:这项研究检查了接受达托霉素或利奈唑胺治疗VRE BSI的患者的结果。方法:进行了一项回顾性,多中心,队列研究通过图表审查。在2003年9月1日至2007年6月30日期间,通过各机构的药房和微生物学报告确定了接受达托霉素或利奈唑胺治疗的VRE BSI住院患者。年龄<18岁或患有多菌血症的患者被排除在分析之外。包括利奈唑胺和达托霉素是因为参与研究的机构使用这两种药物中的任何一种作为VRE BSI的一线治疗药物。进行单因素和多因素分析以确定药物选择对BSI死亡率和持续时间的影响。 BSI的持续时间定义为从第一次阳性血液培养物的抽取日期到第一次最终阴性血液培养物的抽取日期的时间量。结果:确定了来自美国3家参与医院的VRE BSI的一百零一例患者。 67例患者接受达托霉素治疗,34例接受利奈唑胺治疗。除休克(P = 0.049),万古霉素治疗前(P = 0.002)和利奈唑胺治疗前(P <0.001)外,达托霉素和利奈唑胺治疗组的基线特征似乎相当。常在达托霉素治疗的患者中。 31例接受达托霉素和10例利奈唑胺治疗的患者发生住院死亡率(46.3%比29.4%; P = NS)。线性回归发现休克(P = 0.015),感染性心内膜炎(P = 0.021)以及同时利福平或庆大霉素治疗(P = 0.01)与阳性培养时间延长有关。 Logistic回归显示,休克(赔率比[OR] = 14.24; P = 0.008),粪便肠球菌感染(OR = 53.10; P = 0.024),先前使用利奈唑胺治疗(OR = 6.63; P = 0.031),同时使用利福平或庆大霉素治疗(OR = 6.48; P = 0.046)和非感染源(OR = 6.67; P = 0.019)与死亡率增加相关。结论:在这项回顾性队列分析中,VRE BSI的死亡率无显着差异接受达托霉素或利奈唑胺治疗的患者之间。潜在的合并症似乎可以最好地预测结果;但是,鉴于这项研究具有回顾性,因此需要进行更大,前瞻性,随机,比较的研究,以控制潜在的偏倚并确定这两种抗菌药物之间的确切结果差异。

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