Service of Pharmacy, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva, Switzerland.
Antimicrob Agents Chemother. 2018 Aug 27;62(9). doi: 10.1128/AAC.00505-18. Print 2018 Sep.
The objective of this study was to investigate the population pharmacokinetics (PK) of amoxicillin in ICU burn patients and the optimal dosage regimens. This was a prospective study involving 21 consecutive burn patients receiving amoxicillin. PK data were analyzed using nonlinear mixed-effects modeling. Monte-Carlo simulations assessed the influence of various amoxicillin dosage regimens with identified covariates on the probability to achieve a target (PTA) value of time during which free amoxicillin concentrations in plasma exceeded the MIC (T>MIC). A two-compartment model best described the data. Creatinine clearance (CL) and body weight (BW) influenced amoxicillin CL and central volume of distribution (), respectively. The median CL (Cockcroft-Gault formula) was high (128 ml/min), with 25% of patients having CLs of >150 ml/min. The CL, , and half-life () values at steady state for a patient with a CL of 110 ml/min and BW of 70 kg were 13.6 liters/h, 9.7 liters, and 0.8 h, respectively. Simulations showed that a target T>MIC of ≥50% was achieved (PTA > 90%) with standard amoxicillin dosage regimens (1 to 2 g every 6 to 8 h [q6-8h]) when the MIC was low (<1 mg/liter). However, increased dosages of up to 2 g/4 h were necessary in patients with augmented CLs or higher MICs. Prolonging amoxicillin infusion from 30 min to 2 h had a favorable effect on target attainment. In conclusion, this population analysis shows an increased amoxicillin CL and substantial CL PK variability in burn patients compared to literature data with nonburn patients. Situations of augmented CL and/or high bacterial MIC target values may require dosage increases and longer infusion durations. (This study has been registered at ClinicalTrials.gov under identifier NCT01965340.).
本研究旨在探讨 ICU 烧伤患者中阿莫西林的群体药代动力学(PK)和最佳剂量方案。这是一项涉及 21 例连续接受阿莫西林治疗的烧伤患者的前瞻性研究。采用非线性混合效应模型分析 PK 数据。蒙特卡罗模拟评估了具有已确定协变量的各种阿莫西林剂量方案对达到目标(PTA)值的影响,即游离阿莫西林在血浆中的浓度超过 MIC(T>MIC)的时间。两室模型最能描述数据。肌酐清除率(CL)和体重(BW)分别影响阿莫西林 CL 和中央分布容积()。按 Cockcroft-Gault 公式计算,中位 CL 较高(128 ml/min),25%的患者 CL>150 ml/min。CL、、和稳态时半衰期()值为 110 ml/min 且 BW 为 70 kg 的患者分别为 13.6 升/小时、9.7 升和 0.8 小时。模拟表明,在 MIC 较低(<1 mg/L)时,标准阿莫西林剂量方案(q6-8h 时每 6-8 小时 1 至 2 g)即可实现目标 T>MIC≥50%(PTA>90%)。然而,在 CL 增加或 MIC 较高的患者中,需要增加至 2 g/4 h 的剂量。将阿莫西林输注时间从 30 分钟延长至 2 小时对目标实现有积极影响。总之,与非烧伤患者的文献数据相比,该群体分析显示烧伤患者的阿莫西林 CL 增加且 CL PK 变异性较大。CL 增加和/或高细菌 MIC 靶值的情况可能需要增加剂量和延长输注时间。(本研究已在 ClinicalTrials.gov 注册,标识符为 NCT01965340。)