Emergency Department Management of Acute Seizures
Immediate First-Line Treatment (0-5 Minutes)
Administer IV lorazepam 4 mg at 2 mg/min immediately for any actively seizing patient—this terminates status epilepticus in 65% of cases and is superior to diazepam (59.1% vs 42.6% seizure cessation). 1
- Have airway equipment immediately available before administering any benzodiazepine due to respiratory depression risk 1
- Check fingerstick glucose simultaneously while administering treatment—hypoglycemia is rapidly reversible but rare (only 1.2% of seizure patients) 1, 2
- Do not delay benzodiazepine administration to obtain glucose testing—this causes a 2.1-5.9 minute delay without meaningful clinical benefit 2
- Status epilepticus is defined as seizure lasting ≥5 minutes or recurrent seizures without regaining consciousness 1
Alternative Benzodiazepine Routes When IV Access Unavailable
- IM midazolam 0.2 mg/kg (maximum 6 mg) if IV access is challenging—equally efficacious to IV lorazepam 1, 3, 4
- Intranasal midazolam provides onset within 1-2 minutes with peak effect at 3-4 minutes 1
- Rectal diazepam 0.5 mg/kg if buccal/intranasal routes not feasible 1
- Never use IM diazepam due to erratic absorption—use rectal route instead 1
Pediatric Benzodiazepine Dosing
- Lorazepam 0.1 mg/kg IV (maximum 2 mg) for convulsive status epilepticus, repeat after 1 minute up to 2 doses 1
- Lorazepam 0.05 mg/kg IV (maximum 1 mg) for non-convulsive status epilepticus, repeat every 5 minutes up to 4 doses 1
Second-Line Anticonvulsant Therapy (5-20 Minutes)
If seizures persist after adequate benzodiazepine dosing, immediately escalate to one of the following second-line agents—do not skip to third-line agents until these have been tried. 1
Valproate (Preferred for Safety Profile)
- Dose: 20-30 mg/kg IV (maximum 3000 mg) over 5-20 minutes 1
- Efficacy: 88% seizure cessation with 0% hypotension risk—superior safety profile compared to phenytoin 1
- Absolute contraindication in women of childbearing potential due to fetal teratogenic risk 1
- No cardiac monitoring required 1
Levetiracetam (Preferred for Minimal Adverse Effects)
- Dose: 30 mg/kg IV (maximum 2500-3000 mg) over 5 minutes 1
- Efficacy: 68-73% seizure cessation with minimal cardiovascular effects 1
- Hypotension risk ≈0.7%, intubation rate 20% 1
- No cardiac monitoring required 1
- Maintenance dosing: 30 mg/kg IV every 12 hours (maximum 1500 mg) for convulsive SE; 15 mg/kg every 12 hours for non-convulsive SE 1
Levetiracetam Renal Dose Adjustments
- CrCl >80 mL/min: 500-1500 mg every 12 hours 1
- CrCl 50-80 mL/min: 500-1000 mg every 12 hours 1
- CrCl 30-50 mL/min: 250-750 mg every 12 hours 1
- CrCl <30 mL/min: 250-500 mg every 12 hours 1
- ESRD on dialysis: 500-1000 mg every 24 hours 1
Fosphenytoin (Traditional Agent, Higher Risk)
- Dose: 20 mg PE/kg IV at maximum rate of 50 mg/min (150 PE/min) 1
- Efficacy: 84% seizure cessation but 12% hypotension risk 1
- Requires continuous ECG and blood pressure monitoring due to cardiovascular toxicity 1
- Intubation rate 26.4% 1
- Pediatric rate should not exceed 1-3 mg/kg/min or 50 mg/min, whichever is slower 1
Phenobarbital (Highest Respiratory Depression Risk)
- Dose: 20 mg/kg IV over 10 minutes (maximum 1000 mg) 1
- Efficacy: 58.2% seizure cessation as initial second-line agent 1
- Higher risk of respiratory depression and hypotension due to vasodilatatory and cardiodepressant effects 1
- Pediatric maintenance: 1-3 mg/kg IV every 12 hours 1
Refractory Status Epilepticus (20+ Minutes)
Refractory SE is defined as seizures continuing despite benzodiazepines and one second-line agent—initiate continuous EEG monitoring at this stage. 1
Midazolam Infusion (First-Choice Anesthetic)
- Loading dose: 0.15-0.20 mg/kg IV 1
- Maintenance: 1 mg/kg/min continuous infusion, titrate up by 1 mg/kg/min every 15 minutes to maximum 5 mg/kg/min 1
- Efficacy: 80% seizure control with 30% hypotension risk 1
- Load with phenytoin/fosphenytoin, valproate, levetiracetam, or phenobarbital during midazolam infusion to ensure adequate long-acting anticonvulsant levels before tapering 1
Propofol (Requires Mechanical Ventilation)
- Loading dose: 2 mg/kg bolus 1
- Maintenance: 3-7 mg/kg/hour infusion 1
- Efficacy: 73% seizure control with 42% hypotension risk 1
- Requires mechanical ventilation but shorter duration than barbiturates (4 days vs 14 days) 1
- Continuous blood pressure monitoring essential—propofol causes hypotension in 42% of patients 1
Pentobarbital (Highest Efficacy, Highest Risk)
- Loading dose: 13 mg/kg bolus 1
- Maintenance: 2-3 mg/kg/hour infusion 1
- Efficacy: 92% seizure control but 77% hypotension risk requiring vasopressors 1
- Prolonged mechanical ventilation (mean 14 days) 1
- Have vasopressors immediately available (norepinephrine or phenylephrine) as hypotension is nearly universal 1
Simultaneous Evaluation for Reversible Causes
While administering anticonvulsants, promptly identify and treat underlying etiologies—do not postpone anticonvulsant therapy to obtain neuroimaging. 1
Critical Laboratory Tests
- Serum glucose and sodium—the only laboratory tests that consistently alter acute ED management 5, 6
- Complete blood count to evaluate for infection, anemia, or hematologic abnormalities 5
- Basic metabolic panel for electrolyte disturbances, renal function, and acid-base status 5
- Hyponatremia is the most common electrolyte disturbance precipitating seizures 6
- Pregnancy test in women of childbearing age 5, 6
- Antiepileptic drug levels in patients with known epilepsy to assess non-compliance 5
- Toxicology screening if substance use, withdrawal, or overdose suspected 5
Additional Testing Based on Clinical Presentation
- Arterial blood gas if respiratory compromise or metabolic acidosis suspected 5
- Lumbar puncture if meningitis or encephalitis suspected (fever with meningeal signs, immunocompromised status) 5, 6
- Emergent EEG if persistent altered consciousness to detect non-convulsive status epilepticus—occurs in 25% of patients with generalized convulsive SE 1
Neuroimaging Strategy
Emergent Non-Contrast Head CT Indications
Perform emergent head CT without contrast when any high-risk feature is present: 6
- Age >40 years 6
- Recent head trauma 6
- Focal seizure onset before generalization 6
- Fever or persistent headache 6
- Anticoagulation use 6
- Known malignancy or immunocompromised state 6
- Focal neurologic deficit 6
- Persistent altered mental status 6
CT abnormalities are identified in 23-41% of first-time seizure presentations. 6
Deferred Outpatient MRI
If patient has returned to baseline, normal neurologic exam, no high-risk features, and reliable outpatient follow-up, neuroimaging can be deferred to outpatient MRI—MRI is more sensitive for epileptogenic lesions in temporal and orbitofrontal regions. 6
Disposition Criteria
Safe for Discharge
Patients who have returned to their clinical baseline in the ED can be safely discharged without admission. 6
- Arrange outpatient EEG—abnormal EEG predicts higher seizure recurrence risk 6
- Ensure reliable follow-up arrangements 6
Admission Criteria
- Persistent abnormal neurologic examination 6
- Abnormal investigation results requiring inpatient management 6
- Failure to return to baseline 6
- Unreliable follow-up or social concerns 6
Critical Pitfalls to Avoid
- Never use neuromuscular blockers alone (e.g., rocuronium)—they only mask motor manifestations while allowing continued electrical seizure activity and brain injury 1
- Do not skip to third-line agents until benzodiazepines and a second-line agent have been tried 1
- Do not delay benzodiazepine administration for glucose testing—causes 2.1-5.9 minute delay without benefit 2
- Maintain continuous EEG monitoring throughout tapering of anesthetic agents and for 24-48 hours after discontinuation—breakthrough seizures occur in >50% and are often only detectable by EEG 1
- Avoid attributing altered mental status solely to post-ictal state—obtain urgent EEG if patient does not awaken within expected timeframe, as non-convulsive SE occurs in >50% of cases 1