一种基于生理学的建模方法来评估足月和早产儿静脉注射左乙拉西坦的剂量。

IF 2.9 4区 医学
Alexis Johnson, Nolan Thomas, Max Blumenthal, Chrysanthy Ikonomidou, Sin Yin Lim
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引用次数: 0

摘要

癫痫发作是新生儿最常见的神经系统急症,与显著的发病率和死亡率相关。目前的一线药物治疗苯巴比妥与严重的不良反应有关,包括对发育中的大脑的损害。左乙拉西坦是一种耐受性良好的替代品;然而,它的使用受到限制,因为它在新生儿中的最佳剂量仍然未知。此外,由于对左乙拉西坦在新生儿(尤其是早产儿)体内的药代动力学的了解有限,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作用不足的风险。本研究建立了一个基于生理的左乙拉西坦在足月新生儿和早产儿体内的药代动力学(PBPK)模型,以评估它们的药代动力学差异。在考虑生理变化后,药物组织分布增加1.56倍才能表示左乙拉西坦在新生儿中的分布体积增加。在足月新生儿中,根据肾小球滤过率估算儿童肾脏清除率需要增加61%才能准确描述肾脏清除率。此外,外推代谢清除率的异速缩放需要年龄相关的校正来解释减少的代谢清除率。在早产儿中,推断的肾脏清除率大约等于观察到的总清除率,表明肾脏清除率是唯一的消除途径。一致地,预测的代谢清除率接近零时,经后年龄
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Physiologically Based Modeling Approach to Evaluate Intravenous Levetiracetam Dosing in Term and Preterm Neonates.

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.

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来源期刊
Journal of Clinical Pharmacology
Journal of Clinical Pharmacology PHARMACOLOGY & PHARMACY-
自引率
3.40%
发文量
0
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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