Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA.
CPT Pharmacometrics Syst Pharmacol. 2018 Nov;7(11):718-727. doi: 10.1002/psp4.12349. Epub 2018 Sep 28.
Diazepam is labeled for status epilepticus (SE) in children, but there are limited data characterizing its disposition in pediatric patients. We developed a population pharmacokinetic (PK) model of i.v. diazepam in children with SE. We evaluated relationships between PK parameters and both safety and efficacy, and simulated exposures using dosing regimens from the product label and clinical practice. The model was developed using prospective data from a pediatric clinical trial comparing diazepam to lorazepam for treatment of SE. Altogether, 87 patients aged ≥ 3 months to < 18 years contributed 162 diazepam concentrations. Diazepam PKs were well characterized by a two-compartment model scaled by body size. No significant or clinically important relationships were observed between diazepam PKs and safety or efficacy. Simulations demonstrated that, compared with label dosing, the study dose (0.2 mg/kg i.v., maximum 8 mg) resulted in greater frequency in rapidly achieving the target therapeutic range of 200-600 ng/mL.
地西泮被批准用于儿童癫痫持续状态(SE),但有关其在儿科患者中的药代动力学(PK)特征的数据有限。我们开发了一种儿童 SE 患者静脉注射地西泮的群体 PK 模型。我们评估了 PK 参数与安全性和疗效之间的关系,并使用产品标签和临床实践中的给药方案进行了模拟。该模型是使用一项比较地西泮和劳拉西泮治疗 SE 的儿科临床试验的前瞻性数据开发的。共有 87 名年龄≥3 个月至<18 岁的患者贡献了 162 次地西泮浓度。地西泮 PK 特征由一个按身体大小缩放的两室模型很好地描述。未观察到地西泮 PK 与安全性或疗效之间存在显著或具有临床意义的关系。模拟结果表明,与标签剂量相比,研究剂量(0.2mg/kg 静脉注射,最大 8mg)可更频繁地迅速达到 200-600ng/mL 的目标治疗范围。