首页> 外文期刊>Journal of neurosurgical sciences >A Population Pharmacokinetic Model-Guided Evaluation of Ceftolozane-Tazobactam Dosing in Critically Ill Patients Undergoing Continuous Venovenous Hemodiafiltration
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A Population Pharmacokinetic Model-Guided Evaluation of Ceftolozane-Tazobactam Dosing in Critically Ill Patients Undergoing Continuous Venovenous Hemodiafiltration

机译:一种人口药代动力学模型引导式指导评价持续的血管血管血管症的危重病患者患者

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The aim of this work was to describe optimized dosing regimens of ceftolozane-tazobactam for critically ill patients receiving continuous venovenous hemodiafiltration (CVVHDF). We conducted a prospective observational pharmacokinetic study in adult critically ill patients with clinical indications for ceftolozane-tazobactam and CVVHDF. Unbound drug concentrations were measured from serial prefilter blood, postfilter blood, and ultrafiltrate samples by a chromatographic assay. Population pharmacokinetic modeling and dosing simulations were performed using Pmetrics. A four-compartment pharmacokinetic model adequately described the data from six patients. The mean (+/- standard deviation [SD]) extraction ratios for ceftolozane and tazobactam were 0.76 +/- 0.08 and 0.73 +/- 0.1, respectively. The mean +/- SD sieving coefficients were 0.94 +/- 0.24 and 1.08 +/- 0.30, respectively. Model-estimated CVVHDF clearance rates were 2.7 +/- 0.8 and 3.0 +/- 0.6 liters/h, respectively. Residual non-CVVHDF clearance rates were 0.6 +/- 0.5 and 3.3 +/- 0.9 liters/h, respectively. In the initial 24 h, doses as low as 0.75 g every 8 h enabled cumulative fractional response of >= 85% for empirical coverage against Pseudomonas aeruginosa, considering a 40% fT (>MIC) (percentage of time the free drug concentration was above the MIC) target. For 100% fT (>MIC), doses of at least 1.5 g every 8 h were required. The median (interquartile range) steady-state trough ceftolozane concentrations for simulated regimens of 1.5 g and 3.0 g every 8 h were 28 (21 to 42) and 56 (42 to 84) mg/liter, respectively. The corresponding tazobactam concentrations were 6.1 (5.5 to 6.7) and 12.1 (11.0 to 13.4) mg/liter, respectively. We suggest a front-loaded regimen with a single 3.0-g loading dose followed by 0.75 g every 8 h for critically ill patients undergoing CVVHDF with study blood and dialysate flow rates.
机译:这项工作的目的是描述接受连续血管血液过滤(CVVHDF)的批判性患者的Ceftolozane-Tazobactam的优化剂量治疗方案。我们在成人临床适用于Ceftolozane-Tazobactam和CVVHDF的临床适应症进行了一项前瞻性观察药代动力学研究。通过色谱法测定从串行预流血液,后滤液和超滤液样品测量未结合的药物浓度。使用Pmetrics进行人口药代动力学建模和给药模拟。四室药代动力学模型充分描述了六名患者的数据。 Ceftolozane和Tazobactam的平均值(+/-标准偏差[SD])提取比分别为0.76 +/- 0.08和0.73 +/- 0.1。平均+/-SD筛分系数分别为0.94 +/- 0.24和1.08 +/- 0.30。模型估计的CVVHDF间隙率分别为2.7 +/- 0.8和3.0 +/- 0.6升/ h。残留的非CVVHDF间隙率分别为0.6 +/- 0.5和3.3 +/- 0.9升/ h。在初始24小时内,每8小时的剂量低至0.75克,累积分数响应> = 85%的累积分数反对假单胞菌铜绿假单胞菌的实证覆盖,考虑到40%Ft(> MIC)(可自由药物浓度上方的时间百分比麦克风)目标。对于100%Ft(> MIC),需要每8小时至少1.5克的剂量。模拟中位数(胎面范围)稳态槽的稳态槽浓度为1.5g和3.0g,每8小时的模拟方案分别为28(21至42)和56(42至84)mg /升。相应的TaZobactam浓度分别为6.1(5.5至6.7)和12.1(11.0至13.4)mg /升。我们建议一个3.0g加载剂量的前负载方案,然后每8小时进行0.75克,用于治疗血液和透析液流量的CVVHDF患者。

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