Department of Pharmacy, Kitasato University Hospital, Kanagawa, Japan
Department of Pharmacy, Medical Hospital, Tokyo Medical and Dental University, Tokyo, Japan.
Antimicrob Agents Chemother. 2021 Mar 18;65(4). doi: 10.1128/AAC.02114-20.
The objectives of this study were to evaluate the population pharmacokinetics of prophylactic cefazolin (CFZ) from its serum and hip joint capsule concentrations in patients undergoing total hip arthroplasty and to establish the pharmacodynamic target concentration exceeding the MIC for designing an effective dosing regimen for serum and the hip joint capsule. We analyzed 249 serum samples and 125 hip joint capsule samples from 125 individuals using a nonlinear mixed-effects model. The pharmacodynamic index target value obtained from our results indicates the probability of maintaining CFZ trough and hip joint capsule concentrations exceeding the MIC of 1 mg/liter to account for methicillin-susceptible (MSSA). We estimated the population pharmacokinetics using a two-compartment model. The estimated population pharmacokinetic parameters were as follows: clearance (CL) (liters/h) = 1.46 × (creatinine clearance [CL] [ml/min]/77), volume of distribution of the central compartment (V) (liters) = 7.5, central-hip joint capsule compartment clearance (Q) (liters/h) = 3.38, and volume of distribution in the hip joint capsule compartment (V) (liters) = 36.1. The probability of achieving concentrations exceeding the MIC for MSSA was approximately 100% for serum and 100% for the hip joint capsule at 3 h after the initial dose. Our findings suggest that population-based parameters are useful for evaluating CFZ pharmacokinetics and that individual dosages should be determined based on the dosage regimen that achieves and maintains adequate tissue CFZ concentration.
本研究的目的是评估接受全髋关节置换术患者的头孢唑林(CFZ)预防性治疗的血清和髋关节囊浓度的群体药代动力学,并确定超过 MIC 的药效学目标浓度,以设计有效的血清和髋关节囊给药方案。我们使用非线性混合效应模型分析了 125 名个体的 249 份血清样本和 125 份髋关节囊样本。从我们的结果中获得的药效学指标目标值表明,维持 CFZ 谷浓度和髋关节囊浓度超过 1mg/L 的 MIC 的概率以涵盖对甲氧西林敏感的金黄色葡萄球菌(MSSA)。我们使用两室模型估计群体药代动力学。估计的群体药代动力学参数如下:清除率(CL)(升/小时)= 1.46×(肌酐清除率[CL] [毫升/分钟]/77),中央室分布容积(V)(升)= 7.5,中央-髋关节囊腔清除率(Q)(升/小时)= 3.38,髋关节囊腔分布容积(V)(升)= 36.1。初始剂量后 3 小时,血清中 MSSA 超过 MIC 的浓度的概率约为 100%,髋关节囊中为 100%。我们的研究结果表明,基于人群的参数可用于评估 CFZ 的药代动力学,并且应该根据实现和维持足够组织 CFZ 浓度的给药方案来确定个体剂量。