Pharmacokinetics of Levetiracetam Seizure Prophylaxis in Severe Traumatic Brain Injury

Ann Pharmacother. 2024 Jul;58(7):705-714. doi: 10.1177/10600280231202246. Epub 2023 Sep 30.

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.

Keywords: levetiracetam; pharmacodynamics; pharmacokinetics; seizure prophylaxis; traumatic brain injury.

MeSH terms

  • Adult
  • Aged
  • Anticonvulsants* / administration & dosage
  • Anticonvulsants* / pharmacokinetics
  • Brain Injuries, Traumatic*
  • Critical Illness
  • Half-Life
  • Humans
  • Levetiracetam* / administration & dosage
  • Levetiracetam* / pharmacokinetics
  • Male
  • Middle Aged
  • Monte Carlo Method
  • Piracetam / administration & dosage
  • Piracetam / analogs & derivatives
  • Piracetam / pharmacokinetics
  • Prospective Studies
  • Seizures* / drug therapy
  • Seizures* / prevention & control

Substances

  • Levetiracetam
  • Anticonvulsants
  • Piracetam