Antiepileptic — Status Epilepticus (Second-Line)
Pregnancy: Use with caution; register with UK Epilepsy and Pregnancy Register; evidence suggests lower teratogenicity than older AEDs
Levetiracetam (IV)
Brand names: Keppra (IV), Desitrend
Adult dose
Dose: 60 mg/kg IV (max 4500 mg) over 10 minutes
Route: Intravenous infusion
Frequency: Single loading dose; maintenance 1000-3000 mg/day IV in divided doses if needed
Max: 4500 mg loading dose
NICE NG217: Second-line for established status epilepticus alongside phenytoin/fosphenytoin and sodium valproate IV — choice based on clinical context and comorbidities
Paediatric dose
Dose: 60 mg/kg IV (max 3000 mg) over 10 minutes mg/kg
Route: IV
Frequency: Single loading dose
Max: 3000 mg loading dose
Child 1 month to 17 years: 60 mg/kg (max 3000 mg) IV over 10 minutes. Neonates: seek specialist opinion
Dose adjustments
Renal
Reduce maintenance dose in renal impairment — eGFR 30-79: 750-1500 mg/day; eGFR under 30: 500-1000 mg/day
Hepatic
No dose adjustment required
Paediatric weight-based calculator
Child 1 month to 17 years: 60 mg/kg (max 3000 mg) IV over 10 minutes. Neonates: seek specialist opinion
Clinical pearls
- EsCCAPE, ConSEPT, and ESETT trials: levetiracetam IV equivalent in efficacy to fosphenytoin for established status epilepticus — now a first-choice second-line agent with more predictable pharmacokinetics
- Major practical advantages: no cardiac monitoring required (unlike phenytoin), no liver toxicity (unlike valproate), no teratogenicity concern, minimal drug interactions — ideal in polymedicated or pregnant patients
- Behavioural side effects (irritability, aggression) are more pronounced in patients with pre-existing brain injury or intellectual disability — monitor closely
- Renally cleared — dose reduction essential in eGFR under 80; otherwise broadly safe across organ function
- Can be given as fast bolus (10 minutes) versus slow phenytoin infusion (30-60 minutes) — faster seizure termination potential
Contraindications
- Hypersensitivity to levetiracetam
Side effects
- Somnolence and fatigue
- Behavioural disturbance (aggression, agitation — especially in brain injury patients)
- Dizziness
- Headache
- Thrombocytopenia (rare)
Interactions
- No significant pharmacokinetic interactions — advantage over phenytoin and valproate
- Additive CNS depression with other antiepileptics or sedatives
Monitoring
- Seizure activity
- Level of consciousness
- Renal function
- FBC (thrombocytopenia)
Reference: BNFc; BNF 90; NICE NG217 (Epilepsy); EsCCAPE Trial; ConSEPT Trial; ESETT Trial; APLS Guidelines. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
- ASA Physical Status Classification · Pre-operative Risk
- ASA Physical Status Classification · Perioperative Risk
- Duke Activity Status Index (DASI) · Functional Assessment
- ECOG / WHO Performance Status · Performance Status
- Karnofsky Performance Status Scale · Performance Status
- Duval/CIBMTR Score for AML in Second Complete Remission · Leukaemia
Pathways
- Paracetamol overdose · TOXBASE/NPIS; MHRA DSU 2012/2024; SNAP regimen (Lancet 2014); BNF
- TCA overdose · TOXBASE/NPIS; AACT/EAPCCT position statements; Resuscitation Council UK ALS
- Opioid overdose · TOXBASE/NPIS; Resuscitation Council UK; BNF
- Anticholinergic toxidrome · TOXBASE/NPIS; AACT/EAPCCT; BNF
- Benzodiazepine overdose · TOXBASE/NPIS; AACT/EAPCCT; BNF
- β-blocker overdose · TOXBASE/NPIS; AACT/EAPCCT; ESC; BNF