Johnson Alexis, Thomas Nolan, Blumenthal Max, Ikonomidou Chrysanthy, Lim Sin Yin
Pharmacy Practice and Translational Research Division, School of Pharmacy, University of Wisconsin-Madison, Madison, USA.
Department of Neurology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, USA.
J Clin Pharmacol. 2025 Oct;65(10):1246-1261. doi: 10.1002/jcph.70037. Epub 2025 May 2.
Seizures are the most common neurologic emergency in neonates and are associated with significant morbidity and mortality. Current first-line pharmacotherapy, phenobarbital, is associated with serious adverse effects, including impairment of the developing brain. Levetiracetam is a well-tolerated alternative; however, its use is limited because its optimal dosing in neonates remains unknown. Additionally, limited knowledge of levetiracetam pharmacokinetics in neonates, especially preterm neonates, means they generally receive the same weight-based dosing. This may put preterm neonates at risk of increased adverse events or insufficient drug effects. This study developed a physiologically based pharmacokinetic (PBPK) model for levetiracetam in term and preterm neonates to evaluate their pharmacokinetic differences. After accounting for the physiological changes, a 1.56-fold increase in drug tissue distribution was needed to represent the increased volume of distribution of levetiracetam in neonates. In term neonates, scaling renal clearance from children based on estimated glomerular filtration rate required a 61% increase to accurately describe renal clearance. Additionally, allometric scaling to extrapolate metabolic clearance required age-dependent corrections to account for the reduced metabolic clearance. In preterm neonates, extrapolated renal clearance was approximately equal to observed total clearance, suggesting renal clearance as the sole elimination route. Consistently, predicted metabolic clearance approached zero when the postmenstrual age was <37.5 weeks. Our simulations showed that common intravenous levetiracetam dosing regimens resulted in higher plasma concentrations in more premature neonates or those with reduced kidney function. In preterm neonates, these regimens may result in plasma concentrations exceeding toxicity thresholds, indicating a need for lower weight-based dosing.
癫痫发作是新生儿最常见的神经系统急症,且与显著的发病率和死亡率相关。当前的一线药物治疗药物苯巴比妥会产生严重的不良反应,包括对发育中大脑的损害。左乙拉西坦是一种耐受性良好的替代药物;然而,其应用受到限制,因为其在新生儿中的最佳剂量仍不清楚。此外,对于左乙拉西坦在新生儿尤其是早产儿中的药代动力学了解有限,这意味着他们通常接受相同的基于体重的剂量。这可能使早产儿面临不良事件增加或药物效果不足的风险。本研究建立了一个基于生理的左乙拉西坦在足月儿和早产儿中的药代动力学(PBPK)模型,以评估他们的药代动力学差异。在考虑生理变化后,需要将药物组织分布增加1.56倍,以代表左乙拉西坦在新生儿中增加的分布容积。在足月儿中,根据估计的肾小球滤过率按儿童比例缩放肾清除率需要增加61%,才能准确描述肾清除率。此外,通过异速生长缩放来推断代谢清除率需要进行年龄依赖性校正,以考虑代谢清除率的降低。在早产儿中,推断的肾清除率约等于观察到的总清除率,表明肾清除率是唯一的消除途径。同样,当孕龄<37.5周时,预测的代谢清除率接近零。我们的模拟结果表明,常见的静脉注射左乙拉西坦给药方案在更早产的新生儿或肾功能降低的新生儿中会导致更高的血浆浓度。在早产儿中,这些方案可能导致血浆浓度超过毒性阈值,这表明需要降低基于体重的剂量。