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首页> 外文期刊>The American Journal of the Medical Sciences >Empiric Weight-Based Vancomycin in Intensive Care Unit Patients With Methicillin-Resistant Staphylococcus aureus Bacteremia
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Empiric Weight-Based Vancomycin in Intensive Care Unit Patients With Methicillin-Resistant Staphylococcus aureus Bacteremia

机译:重症监护病房耐甲氧西林金黄色葡萄球菌细菌血症的经验性体重为基础的万古霉素

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Background: Previous studies were conducted in all hospitalized patients with methicillin-resistant Staphylococcus aureus (MRSA) bacteremia to determine safety and effectiveness of guideline-recommended, weight-based dosing of vancomycin. In these studies, it was observed that severely ill patients (Pitt bacteremia score >= 4 or intensive care unit [ICU] patients) were at an increased risk of mortality and/or nephrotoxicity. Therefore, a subanalysis of the effect of guideline-recommended vancomycin dosing on in-hospital mortality and nephrotoxicity in ICU patients with MRSA bacteremia was conducted. Methods: This multicenter, retrospective, cohort study was conducted in a subset of ICU patients from a previous MRSA bacteremia study. Patients were >= 18 years old and received >= 48 hours of empiric vancomycin from July 1, 2002, to June 30, 2008. The incidence of nephrotoxicity and in-hospital mortality was compared in patients who received guideline-recommended dosing (at least 15 mg/kg per dose) to patients who received non-guideline-recommended dosing of vancomycin. Multivariable generalized linear mixed-effects models were constructed to determine independent risk factors for in-hospital mortality and nephrotoxicity. Results: Guideline-recommended dosing was received by 34% of patients (n = 137). Nephrotoxicity occurred in 35% of patients receiving guideline-recommended dosing and 39% receiving non-guideline-recommended dosing (P = 0.67). In-hospital mortality rate was 24% among patients who received guideline-recommended dosing compared with 31% for non-guideline-recommended dosing (P = 0.40). Guideline-recommended dosing was not associated with nephrotoxicity (odds ratio: 1.10; 95% confidence interval: 0.43-2.79) or in-hospital mortality (odds ratio: 0.54; 95% confidence interval: 0.22-1.36) in the multivariable analysis. Conclusions: Guideline-recommended dosing of vancomycin in ICU patients with MRSA bacteremia is not significantly associated with nephrotoxicity or in-hospital mortality. However, the 7% absolute difference for in-hospital mortality suggests that larger studies are needed.
机译:背景:先前在所有住院的耐甲氧西林金黄色葡萄球菌(MRSA)菌血症的患者中进行了研究,以确定指南推荐的基于体重的万古霉素给药的安全性和有效性。在这些研究中,观察到重症患者(皮特菌血症评分> = 4或重症监护病房[ICU]患者)的死亡和/或肾毒性风险增加。因此,对指南推荐的万古霉素剂量对ICU MRSA菌血症患者的院内死亡率和肾毒性进行了亚分析。方法:这项多中心,回顾性队列研究是在先前MRSA菌血症研究的一部分ICU患者中进行的。从2002年7月1日至2008年6月30日,≥18岁的患者接受了48小时的经验性万古霉素治疗。比较接受指南推荐剂量的患者的肾毒性和院内死亡率发生率(至少接受万古霉素非指导性推荐剂量的患者,每剂15 mg / kg)。构建多变量广义线性混合效应模型,以确定院内死亡率和肾毒性的独立危险因素。结果:34%的患者接受了指南推荐的剂量(n = 137)。 35%接受指南推荐剂量的患者和39%接受非指南推荐剂量的患者发生肾毒性(P = 0.67)。接受指南推荐剂量的患者的院内死亡率为24%,而非指南推荐剂量为31%(P = 0.40)。在多变量分析中,指南推荐的剂量与肾毒性(赔率:1.10; 95%置信区间:0.43-2.79)或院内死亡率(赔率:0.54; 95%置信区间:0.22-1.36)无关。结论:ICU MRSA菌血症患者推荐的万古霉素剂量与肾毒性或院内死亡率无显着相关性。但是,院内死亡率的绝对差异为7%,表明需要进行更大的研究。

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