Schmith V D, Fiedler-Kelly J, Phillips L, Grasela T H
Clinical Pharmacokinetics and Dynamics, Glaxo Wellcome Inc., RTP, North Carolina 27709, USA.
Pharm Res. 1997 Jan;14(1):91-7. doi: 10.1023/a:1012015719694.
The population PK/PD approach was prospectively used to determine the PK/PD of cisatracurium in various subgroups of healthy surgical patients.
Plasma concentration (Cp) and neuromuscular block data from 241 patients in 8 prospectively-designed Phase I-III trials were pooled and analyzed using NONMEM. The analyses included limited Cp-time data randomly collected from 186 patients in efficacy/safety studies and full Cp-time data from 55 patients in pharmacokinetic studies. The effects of covariates on the PK/PD parameters of cisatracurium were evaluated. The time course of neuromuscular block was predicted for various patient subgroups.
The population PK/PD model for cisatracurium revealed that anesthesia type, gender, age, creatinine clearance, and presence of obesity were associated with statistically significant (p < 0.01) effects on the PK/PD parameters of cisatracurium. These covariates were not associated with any clinically significant changes in the predicted recovery profile of cisatracurium. Slight differences in onset were predicted in patients with renal impairment and patients receiving inhalation anesthesia. Based on the validation procedure, the model appears to be accurate and precise.
The prospective incorporation of a population PK/PD strategy into the clinical development of cisatracurium generated information which influenced product labeling and reduced the number of studies needed during development.
前瞻性地采用群体药代动力学/药效学(PK/PD)方法来确定顺式阿曲库铵在健康手术患者各亚组中的PK/PD情况。
汇总并分析了8项前瞻性设计的I - III期试验中241例患者的血浆浓度(Cp)和神经肌肉阻滞数据,使用NONMEM软件进行分析。分析包括从186例患者在疗效/安全性研究中随机收集的有限Cp - 时间数据以及55例患者在药代动力学研究中的完整Cp - 时间数据。评估了协变量对顺式阿曲库铵PK/PD参数的影响。预测了各患者亚组神经肌肉阻滞的时间进程。
顺式阿曲库铵的群体PK/PD模型显示,麻醉类型、性别、年龄、肌酐清除率和肥胖情况对顺式阿曲库铵的PK/PD参数有统计学显著(p < 0.01)影响。这些协变量与顺式阿曲库铵预测恢复曲线的任何临床显著变化均无关联。预测肾功能损害患者和接受吸入麻醉患者的起效略有差异。基于验证程序,该模型似乎准确且精确。
将群体PK/PD策略前瞻性地纳入顺式阿曲库铵的临床开发中,产生了影响产品标签并减少开发期间所需研究数量的信息。