What is the recommended emergency department approach for managing generalized tonic‑clonic seizures or status epilepticus in a primary‑care hospital, including initial assessment and first‑line and second‑line treatment for pediatric and adult patients?

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Last updated: February 10, 2026View editorial policy

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Emergency Department Approach to Seizures: Pediatric vs Adult Management

Benzodiazepines are first-line treatment for both pediatric and adult patients with generalized tonic-clonic seizures or status epilepticus, followed by immediate escalation to second-line agents if seizures persist beyond 5 minutes, with key differences in dosing, administration rates, and drug selection between age groups. 1

Initial Assessment & Stabilization (0-5 minutes)

Both pediatric and adult patients require:

  • Immediate assessment of airway, breathing, and circulation with high-flow oxygen 2
  • Fingerstick glucose check and correction of hypoglycemia 1
  • Establishment of IV access with simultaneous fluid resuscitation 1
  • Airway equipment immediately available before any benzodiazepine administration due to respiratory depression risk 1, 3
  • Continuous vital sign monitoring, particularly oxygen saturation and blood pressure 1, 2

Simultaneously search for reversible causes: hypoglycemia, hyponatremia, hypoxia, drug toxicity or withdrawal, CNS infection, stroke, intracerebral hemorrhage 1, 2

First-Line Treatment: Benzodiazepines

Adult Dosing

Lorazepam 4 mg IV at 2 mg/min is the preferred first-line agent, with 65% efficacy in terminating status epilepticus and superior efficacy over diazepam (59.1% vs 42.6%) 1, 3

  • May repeat once after 10-15 minutes if seizures continue 1, 3
  • Lorazepam preferred due to longer duration of action compared to other benzodiazepines 1

Pediatric Dosing

Lorazepam 0.1 mg/kg IV (maximum 2 mg) for convulsive status epilepticus 1, 2

  • May repeat once after at least 1 minute 1
  • For non-convulsive status epilepticus: 0.05 mg/kg IV (maximum 1 mg), may repeat every 5 minutes up to maximum 4 doses 1

Alternative Routes When IV Access Unavailable

  • IM midazolam 0.2 mg/kg (maximum 6 mg) for both adults and children, may repeat every 10-15 minutes 1, 4
  • Intranasal midazolam with onset of action within 1-2 minutes 1
  • Rectal diazepam 0.5 mg/kg if buccal/intranasal routes not feasible 1

Critical pitfall: Never use IM diazepam due to erratic absorption—use rectal route instead 1

Second-Line Treatment (5-20 minutes)

If seizures persist after adequate benzodiazepine dosing, immediately escalate to one of the following agents—do not delay beyond 5-10 minutes: 1, 2

Adult Second-Line Options (in order of safety profile)

1. Valproate 20-30 mg/kg IV (maximum 3000 mg) over 5-20 minutes

  • 88% efficacy with 0% hypotension risk 1, 2
  • Superior safety profile compared to phenytoin 1
  • Absolute contraindication in women of childbearing potential due to teratogenic risk 1

2. Levetiracetam 30 mg/kg IV (maximum 2500-3000 mg) over 5 minutes

  • 68-73% efficacy with minimal cardiovascular effects 1, 2
  • No cardiac monitoring required 1
  • Approximately 0.7% hypotension risk 1

3. Fosphenytoin 20 mg PE/kg IV at maximum rate of 150 PE/min

  • 84% efficacy but 12% hypotension risk 1, 2, 5
  • Requires continuous ECG and blood pressure monitoring 1, 5
  • Traditional and most widely available option 1

4. Phenobarbital 20 mg/kg IV over 10 minutes

  • 58.2% efficacy as initial second-line agent 1
  • Higher risk of respiratory depression and hypotension 1, 2

Pediatric Second-Line Options

Key difference: Maximum infusion rates are weight-based and slower than adults 1, 5

1. Valproate 20-30 mg/kg IV over 5-20 minutes

  • Pediatric data shows 90% seizure termination vs 77% with phenobarbital, with significantly fewer adverse effects (24% vs 74%) 1

2. Levetiracetam 40 mg/kg IV (maximum 2500 mg) over 5-15 minutes

  • Higher loading dose than adults 1

3. Fosphenytoin 20 mg PE/kg IV

  • Maximum rate: 2 mg PE/kg/min OR 150 mg PE/min, whichever is slower 1, 5
  • This is the critical pediatric difference—rate must not exceed 1-3 mg/kg/min 1

4. Phenobarbital 20 mg/kg IV over 10 minutes (maximum 1000 mg)

  • May be preferred in very young children 1

Refractory Status Epilepticus (20+ minutes)

Definition: Seizures continuing despite benzodiazepines and one second-line agent 1

Initiate continuous EEG monitoring at this stage—25% of patients with apparent seizure cessation have continuing electrical seizures 1, 2

Third-Line Anesthetic Agents (Both Pediatric & Adult)

1. Midazolam continuous infusion (first choice)

  • Loading: 0.15-0.20 mg/kg IV 1, 4
  • Maintenance: 1 mg/kg/min, titrate up by 1 mg/kg/min every 15 minutes to maximum 5 mg/kg/min 1
  • 80% efficacy with 30% hypotension risk 1
  • Before tapering midazolam, load with a long-acting anticonvulsant (phenytoin/fosphenytoin, valproate, levetiracetam, or phenobarbital) 1

2. Propofol

  • Loading: 2 mg/kg bolus 1, 4
  • Maintenance: 3-7 mg/kg/hour infusion 1
  • 73% efficacy with 42% hypotension risk 1
  • Requires mechanical ventilation but shorter duration than barbiturates (4 days vs 14 days) 1

3. Pentobarbital (highest efficacy but most adverse effects)

  • Loading: 13 mg/kg 1, 4
  • Maintenance: 2-3 mg/kg/hour 1
  • 92% efficacy but 77% hypotension risk requiring vasopressors 1
  • Mean 14 days mechanical ventilation 1

All anesthetic agents require:

  • Mechanical ventilation readiness 1, 4
  • Continuous blood pressure monitoring with vasopressors available 1
  • Continuous EEG monitoring to guide titration 1

Maintenance Dosing After Seizure Control

Adult Maintenance

  • Levetiracetam: 30 mg/kg IV every 12 hours OR increase to 20 mg/kg every 12 hours (maximum 1500 mg) for convulsive SE 1
  • Valproate: Continue at maintenance doses based on clinical response 1
  • Phenobarbital: 1-3 mg/kg IV every 12 hours if used 1, 2

Pediatric Maintenance

  • Levetiracetam: 30 mg/kg IV every 12 hours (maximum 1500 mg) for convulsive SE; 15 mg/kg every 12 hours for non-convulsive SE 1
  • Phenobarbital: 1-3 mg/kg IV every 12 hours 1
  • Lorazepam: 0.05 mg/kg (maximum 1 mg) IV every 8 hours for 3 doses 2

Critical Pitfalls to Avoid

1. Dosing errors with fosphenytoin: Do not confuse PE (phenytoin equivalents) with actual drug concentration in vial 1, 5

2. Excessive infusion rates in pediatrics: Fosphenytoin rate must not exceed 2 mg PE/kg/min in children vs 150 mg PE/min in adults 1, 5

3. Delaying second-line agents: Move to next treatment step if seizures continue after 5-10 minutes 2

4. Using neuromuscular blockers alone: They only mask motor manifestations while allowing continued electrical seizure activity and brain injury 1

5. Skipping to third-line agents: Do not use pentobarbital or propofol until benzodiazepines and a second-line agent have been tried 1

6. Failure to monitor for respiratory depression: Especially critical with benzodiazepines and barbiturates in both age groups 2

7. Assuming seizures have stopped clinically: Obtain EEG if patient does not awaken within expected timeframe—nonconvulsive status epilepticus occurs in >50% of refractory cases 1

Key Pediatric vs Adult Differences Summary

Parameter Adult Pediatric
Lorazepam dose 4 mg IV 0.1 mg/kg (max 2 mg)
Levetiracetam loading 30 mg/kg 40 mg/kg
Fosphenytoin max rate 150 mg PE/min 2 mg PE/kg/min OR 150 mg PE/min (whichever slower)
Valproate efficacy 88% 90%
Preferred second-line Valproate or levetiracetam Valproate (superior pediatric data)

Mortality for status epilepticus ranges from 5-22% overall, reaching 65% in refractory cases, making aggressive time-based treatment essential. 1

References

Guideline

Status Epilepticus Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Status Epilepticus Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Myoclonic Status Epilepticus

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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