Pharmacokinetics of Levetiracetam Seizure Prophylaxis in Severe Traumatic Brain Injury.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-01 Epub Date: 2023-09-30 DOI:10.1177/10600280231202246
Sarah Schuman Harlan, Carolyn D Philpott, Shaun P Keegan, Molly E Droege, Aniruddha S Karve, Brandon Foreman, Devin Wakefield, Eric W Mueller, Kiranpal Sangha, Laura B Ngwenya, Joshua D Courter, Pankaj Desai, Christopher Droege
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Abstract

Background: Drug pharmacokinetics (PK) are altered in neurocritically ill patients, and optimal levetiracetam dosing for seizure prophylaxis is unknown.

Objective: This study evaluates levetiracetam PK in critically ill patients with severe traumatic brain injury (sTBI) receiving intravenous levetiracetam 1000 mg every 8 (LEV8) to 12 (LEV12) hours for seizure prophylaxis.

Methods: This prospective, open-label study was conducted at a level 1 trauma, academic, quaternary care center. Patients with sTBI receiving seizure prophylaxis with LEV8 or LEV12 were eligible for enrollment. Five sequential, steady-state, postdose serum levetiracetam concentrations were obtained. Non-compartmental analysis (NCA) and compartmental approaches were employed for estimating pharmacokinetic parameters and projecting steady-state trough concentrations. Pharmacokinetic parameters were compared between LEV8 and LEV12 patients. Monte Carlo simulations (MCS) were performed to determine probability of target trough attainment (PTA) of 6 to 20 mg/L. A secondary analysis evaluated PTA for weight-tiered levetiracetam dosing.

Results: Ten male patients (5 LEV8; 5 LEV12) were included. The NCA-based systemic clearance and elimination half-life were 5.3 ± 1.2 L/h and 4.8 ± 0.64 hours. A one-compartment model provided a higher steady-state trough concentration for the LEV8 group compared with the LEV12 group (13.7 ± 4.3 mg/L vs 6.3 ± 1.7 mg/L; P = 0.008). Monte Carlo simulations predicted regimens of 500 mg every 6 hours, 1000 mg every 8 hours, and 2000 mg every 12 hours achieved therapeutic target attainment. Weight-tiered dosing regimens achieved therapeutic target attainment using a 75 kg breakpoint.

Conclusion and relevance: Neurocritically ill patients exhibit rapid levetiracetam clearance resulting in a short elimination half-life. Findings of this study suggest regimens of levetiracetam 500 mg every 6 hours, 1000 mg every 8 hours, or 2000 mg every 12 hours may be required for optimal therapeutic target attainment. Patient weight of 75 kg may serve as a breakpoint for weight-guided dosing to optimize levetiracetam therapeutic target attainment for seizure prophylaxis.

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左乙拉西坦预防严重颅脑损伤癫痫发作的药代动力学。
背景:神经疾病患者的药物药代动力学(PK)发生了改变,预防癫痫发作的最佳左乙拉西坦剂量尚不清楚。目的:本研究评估左乙拉西坦PK在重症颅脑损伤(sTBI)患者中的作用,该患者每8至12小时静脉注射1000 mg左乙拉西坦(LEV8)以预防癫痫发作。方法:这项前瞻性的开放标签研究在一级创伤、学术、四级护理中心进行。接受LEV8或LEV12癫痫预防的sTBI患者有资格入选。获得了五个连续的、稳态的、给药后的血清左乙拉西坦浓度。非房室分析(NCA)和房室方法用于估计药代动力学参数和预测稳态谷浓度。比较了LEV8和LEV12患者的药代动力学参数。进行蒙特卡罗模拟(MCS)以确定6至20mg/L的目标谷达到概率(PTA)。二次分析评估了左乙拉西坦重量分级给药的PTA。结果:纳入10例男性患者(5例LEV8;5例LEV12)。基于NCA的系统清除和消除半衰期分别为5.3±1.2 L/h和4.8±0.64小时。与LEV12组相比,单室模型为LEV8组提供了更高的稳态谷浓度(13.7±4.3 mg/L vs 6.3±1.7 mg/L;P=0.008)。蒙特卡罗模拟预测每6小时500 mg、每8小时1000 mg和每12小时2000 mg的方案实现了治疗目标。重量分级给药方案使用75 kg断点实现了治疗目标。结论和相关性:神经危重症患者表现出左乙拉西坦清除迅速,导致清除半衰期短。这项研究的结果表明,可能需要每6小时500毫克、每8小时1000毫克或每12小时2000毫克的左乙拉西坦方案才能达到最佳治疗目标。75公斤的患者体重可以作为体重指导给药的断点,以优化左乙拉西坦预防癫痫发作的治疗目标实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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