Treatment of Acute Seizures in the ICU
For acute seizures in the ICU, immediately administer intravenous lorazepam 4 mg (0.1 mg/kg, maximum 4 mg) given slowly at 2 mg/min, and if seizures persist after 10-15 minutes, repeat with an additional 4 mg dose. 1, 2 This represents the standard first-line approach with the strongest evidence for both convulsive and non-convulsive seizures in critically ill patients.
Initial Management Algorithm
Immediate Actions
- Assess and secure airway, breathing, and circulation (ABCs) with equipment for airway management immediately available before administering any IV benzodiazepines 3, 1
- Provide high-flow oxygen and ensure adequate ventilation support is readily available 3
- Check blood glucose immediately and correct hypoglycemia if present 3
- Establish IV access and monitor vital signs continuously 3
First-Line Treatment: Benzodiazepines
- Administer lorazepam 0.1 mg/kg IV (maximum 4 mg per dose) at a rate of 2 mg/min 1, 2, 3
- For convulsive status epilepticus: repeat the dose after at least 1 minute if needed, up to a maximum of 2 doses 3
- For non-convulsive status epilepticus: repeat every 5 minutes up to a maximum of 4 doses 3
- Critical pitfall: Underdosing lorazepam (giving less than 4 mg in adults >40 kg) significantly increases progression to refractory status epilepticus (87% vs 62%) 4
Second-Line Treatment (If Seizures Persist After Benzodiazepines)
Administer one of the following agents immediately—all three have equivalent efficacy based on the highest quality evidence (ESETT trial): 2, 3
Option 1: Levetiracetam
- Dose: 40-60 mg/kg IV (maximum 2,500-4,500 mg) given as bolus 3, 2
- Infusion rate: 100 mg/min 2
- Advantages: Favorable side effect profile, minimal drug interactions, no cardiac monitoring required 2, 3
- Disadvantages: May cause nausea and rash 2
- Life-threatening hypotension rate: 0.7% 2
Option 2: Fosphenytoin
- Dose: 18-20 PE/kg IV at maximum rate of 150 PE/min 2, 3
- Advantages: Can be given IM if IV access lost 2
- Disadvantages: Risk of hypotension (3.2% life-threatening) and cardiac dysrhythmias, requires cardiac monitoring 2, 3
- Intubation rate: 26.4% (highest among the three options) 2
Option 3: Valproate
- Dose: 20-40 mg/kg IV at maximum rate of 10 mg/kg/min 2, 3
- Advantages: Rapid administration, minimal cardiorespiratory effects (1.6% life-threatening hypotension) 2, 3
- Disadvantages: Contraindicated in liver disease, risk of thrombocytopenia 2, 3
- Intubation rate: 16.8% (lowest among the three options) 2
The ESETT trial (Class I evidence) demonstrated no significant difference in seizure cessation at 60 minutes: levetiracetam 47%, fosphenytoin 45%, valproate 46%. 2 Selection should be based on patient-specific contraindications and side effect profiles rather than efficacy differences.
Third-Line Treatment: Refractory Status Epilepticus
- If seizures persist after adequate benzodiazepine and second-line agent, add phenobarbital 10-20 mg/kg IV loading dose (maximum 1,000 mg) 3
- Consider transfer to ICU if not already there 3
- Initiate continuous EEG monitoring for refractory seizures 3
Simultaneous Diagnostic Workup
While administering antiseizure medications, immediately investigate and treat reversible causes: 3, 2
- Hypoglycemia (check and treat immediately) 3, 2
- Hyponatremia and other electrolyte abnormalities 3, 2
- Hypoxia (ensure adequate oxygenation) 3, 2
- CNS or systemic infection 3, 2
- Drug toxicity (consider toxicology screen) 3, 2
- Intracranial hemorrhage, ischemic stroke, or mass lesion (neuroimaging if indicated) 3, 2
- Alcohol or benzodiazepine withdrawal 3
EEG Monitoring Recommendations
Urgent EEG (within 60 minutes) is strongly recommended in specific scenarios: 3
- All patients with acute brain injury and unexplained persistent altered consciousness 3
- Patients with convulsive status epilepticus who do not return to functional baseline within 60 minutes after seizure medication 3
- All comatose patients after cardiac arrest, both during therapeutic hypothermia and within 24 hours of rewarming 3
- Comatose ICU patients without primary brain condition but with unexplained mental status impairment or neurological deficits, particularly with severe sepsis or renal/hepatic failure 3
Continuous EEG monitoring is preferred over routine EEG when feasible, as routine EEG misses approximately 50% of non-convulsive seizures. 3
Maintenance Therapy After Seizure Control
After resolution of status epilepticus, continue maintenance dosing: 3
- Lorazepam: 0.05 mg/kg (maximum 1 mg) IV every 8 hours for 3 doses 3
- Levetiracetam: 15-30 mg/kg IV every 12 hours (maximum 1,500 mg) 3
- Phenobarbital: 1-3 mg/kg IV every 12 hours if used 3
Critical Pitfalls to Avoid
- Never underdose lorazepam: Adults >40 kg should receive the full 4 mg dose, as lower doses dramatically increase progression to refractory status epilepticus 4
- Do not overlook non-convulsive seizures: Up to 50% may be missed without continuous EEG monitoring 3
- Avoid abrupt discontinuation of sedatives after prolonged use: Taper over several days to prevent withdrawal seizures 3, 5
- Do not use prophylactic anticonvulsants for single self-limiting seizures: A single seizure within 24 hours of ischemic stroke should not be treated with long-term anticonvulsants 3
- Recognize that benzodiazepines may cause respiratory depression and hypotension: Have airway management equipment immediately available 1, 6
- Do not fail to address the underlying cause: Treating only the seizure without identifying and correcting the precipitant leads to recurrence 3, 2
Special Considerations for ICU Sedation
If ongoing sedation is required in ICU patients with seizures: 3, 5
- Prefer dexmedetomidine over benzodiazepine infusions to reduce delirium risk 3, 5
- Target light sedation levels using daily sedation interruption or light sedation protocols 3, 5
- Use EEG monitoring to detect non-convulsive seizure activity and to titrate burst suppression therapy in patients with elevated intracranial pressure 3