Levetiracetam (Levepil) Dosing in Children
For routine seizure management in children, start with 10 mg/kg twice daily and titrate to a maintenance dose of 20–30 mg/kg twice daily (maximum 1,500 mg per dose); for status epilepticus, administer a loading dose of 40 mg/kg IV (maximum 2,500 mg) followed by maintenance of 30 mg/kg every 12 hours for convulsive seizures or 15 mg/kg every 12 hours for non-convulsive seizures. 1, 2
Status Epilepticus Dosing
Loading Dose
- Administer 40 mg/kg IV bolus (maximum 2,500 mg) over 5–15 minutes as a second-line agent after benzodiazepines for both convulsive and non-convulsive status epilepticus 1, 2
- Higher loading doses of 20–60 mg/kg have been used safely in pediatric status epilepticus, with the 40 mg/kg dose showing moderate strength of evidence from the American Academy of Neurology 1
- The infusion can be given over 5 minutes without significant cardiovascular effects, making it safer than alternatives like fosphenytoin 3
Maintenance Dosing After Status Epilepticus
- For convulsive status epilepticus: 30 mg/kg IV every 12 hours (maximum 1,500 mg per dose) 1, 2
- For non-convulsive status epilepticus: 15 mg/kg IV every 12 hours (maximum 1,500 mg per dose) 1, 2
- Continue maintenance dosing for at least 3 doses after seizure termination 2
Routine Maintenance Dosing (Non-Emergency)
Starting Dose
- Begin with 10 mg/kg twice daily based on pharmacokinetic studies showing children require 30–40% higher clearance-adjusted doses than adults 4, 5
- This starting dose provides plasma concentrations similar to the adult 500 mg twice daily regimen 5
Target Maintenance Dose
- Titrate to 20 mg/kg twice daily to achieve the therapeutic trough concentration range of 6–20 mg/L 5
- The maximum recommended dose is 30 mg/kg twice daily (maximum 1,500 mg per dose) 2
- Some children with refractory seizures may tolerate and benefit from doses up to 60 mg/kg/day or higher, though this exceeds standard recommendations 6
Age-Specific Considerations
- Children 6 months to 12 years: Use weight-based dosing as outlined above; younger children may require higher mg/kg doses due to faster clearance 4, 7
- Infants under 6 months: Limited safety data exist; use with caution and consider lower initial doses 7
- Children have approximately 30–40% higher apparent body clearance (1.43 ± 0.36 mL/min/kg) compared to adults, necessitating higher weight-adjusted doses 4
Renal Dose Adjustments
- Levetiracetam requires dose reduction in renal dysfunction because 70% is excreted unchanged in urine 8
- Adjust dosing based on estimated glomerular filtration rate (eGFR), though specific pediatric renal dosing tables are not provided in the guidelines 8
- Monitor trough levels in patients with impaired renal function 8
Administration Guidelines
Intravenous Administration
- Loading dose: Infuse 40–50 mg/kg over 5–15 minutes 1, 7
- A single 50 mg/kg loading dose (maximum 2,500 mg) over 15 minutes is safe and well-tolerated, achieving mean levels of 83.3 mcg/mL 7
- No cardiac monitoring is required, unlike fosphenytoin 3
Oral Administration
- Administer twice daily without regard to meals 5
- Doses above 60 mg/kg/day may be considered in children who partially respond to standard doses, though behavioral adverse effects increase 6
Common Pitfalls to Avoid
- Do not underdose in status epilepticus: Use the full 40 mg/kg loading dose rather than lower prophylactic doses of 10–20 mg/kg 2
- Do not use adult fixed doses: Children require weight-based dosing due to higher clearance 4, 5
- Do not skip maintenance dosing: After status epilepticus resolves, continue maintenance therapy to prevent recurrence 2
- Monitor for behavioral adverse effects (irritability, aggression, mood changes), which occur in approximately 12% of children on high doses 6
Efficacy Data
- In status epilepticus, levetiracetam achieves seizure cessation in 68–73% of benzodiazepine-refractory cases 3
- For routine epilepsy management, 44% of children achieve >50% seizure reduction with high-dose therapy, and 16% achieve seizure freedom 6
- Levetiracetam shows equivalent efficacy to valproate and fosphenytoin as a second-line agent (approximately 45–47% seizure termination) but with superior safety profile 3