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急性感染中导致利奈唑胺血药谷浓度低的危险因素。

Risk factors for a low linezolid trough plasma concentration in acute infections.

机构信息

Department of Infectious Diseases, Hospital Clínic of Barcelona, Barcelona, Spain.

出版信息

Antimicrob Agents Chemother. 2013 Apr;57(4):1913-7. doi: 10.1128/AAC.01694-12. Epub 2013 Feb 12.

Abstract

Linezolid is an antibiotic with time-dependent activity, and both the percentage of time that plasma concentrations exceed the MIC and the area under the concentration-time curve over 24 h in the steady state divided by the MIC (AUC24/MIC ratio) are associated with clinical response. The aim of this study was to analyze the linezolid trough plasma concentration (C(min)) and to determine factors associated with a C(min) < 2 mg/liter and other clinically relevant thresholds. Characteristics of 78 patients receiving 600 mg/12 h of linezolid with a C(min) determination at the steady state and within the first 10 days of treatment were retrospectively reviewed. Concentrations were measured using high-pressure liquid chromatography. Univariate and multivariate analysis were performed to identify risk factors of low C(min). A total of 29.5% of patients had a C(min) < 2 mg/liter. The percentage was significantly higher in patients with an estimated glomerular filtration (eGF) > 80 ml/min, in intensive care unit (ICU) patients, and in patients with an infection due to Staphylococcus aureus. The independent predictors of C(min) < 2 mg/liter were an eGF > 80 ml/min (odds ratio [OR], 10; 95% confidence interval [CI], 2.732 to 37.037; P = 0.001) and infection due to S. aureus (OR, 5.906; 95% CI, 1.651 to 21.126; P = 0.006). A linezolid C(min) of <2 mg/liter was found in 29.5% of cases, and the risk was significantly higher among those with an eGF > 80 ml/min and in infections due to S. aureus. In patients with severe sepsis, a loading dose or continuous infusion and drug monitoring could improve the pharmacodynamic parameters associated with linezolid efficacy.

摘要

利奈唑胺是一种时间依赖性抗生素,血药浓度超过 MIC 的时间百分比和稳态下 24 小时内的浓度-时间曲线下面积(AUC24/MIC 比值)与临床疗效相关。本研究旨在分析利奈唑胺谷浓度(C(min)),并确定与 C(min) < 2 mg/L 及其他临床相关阈值相关的因素。回顾性分析了 78 例接受 600 mg/12 h 利奈唑胺治疗且在稳态和治疗开始后 10 天内进行 C(min)测定的患者的特征。使用高压液相色谱法测定浓度。采用单因素和多因素分析确定 C(min)低的危险因素。共有 29.5%的患者 C(min) < 2 mg/L。eGFR > 80 ml/min、重症监护病房(ICU)患者和金黄色葡萄球菌感染患者的 C(min) < 2 mg/L 的比例显著较高。C(min) < 2 mg/L 的独立预测因素为 eGFR > 80 ml/min(比值比[OR],10;95%置信区间[CI],2.732 至 37.037;P = 0.001)和金黄色葡萄球菌感染(OR,5.906;95% CI,1.651 至 21.126;P = 0.006)。29.5%的病例发现利奈唑胺 C(min) < 2 mg/L,eGFR > 80 ml/min 和金黄色葡萄球菌感染的风险显著较高。在严重脓毒症患者中,负荷剂量或连续输注和药物监测可能会改善与利奈唑胺疗效相关的药效学参数。

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