What is the immediate emergency management of an active seizure (status epilepticus) in adults and children?

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Immediate Emergency Management of Active Seizure (Status Epilepticus)

Administer intravenous lorazepam 4 mg at 2 mg/min immediately for any actively seizing patient—this terminates seizures in 65% of cases and is superior to all other first-line options. 1, 2

Critical Pre-Treatment Actions (0–2 minutes)

  • Have airway equipment (bag-valve-mask, intubation set) immediately available before giving any benzodiazepine, as respiratory depression requiring intervention is predictable. 1, 2
  • Check fingerstick glucose immediately and correct hypoglycemia while administering lorazepam—this is a rapidly reversible cause that must not be missed. 1, 3
  • Establish IV access, start high-flow oxygen, and monitor vital signs continuously. 3

First-Line Treatment: Benzodiazepines (0–5 minutes)

Lorazepam (Preferred Agent)

  • Give lorazepam 4 mg IV at 2 mg/min for adults ≥18 years. 1, 2
  • Lorazepam achieves 59.1% seizure termination versus 42.6% for diazepam and has longer duration of action than other benzodiazepines. 1
  • If seizures continue after 10–15 minutes, give a second 4 mg dose (maximum 8 mg total). 2
  • Pediatric dose: 0.1 mg/kg IV (maximum 2 mg per dose) for convulsive SE; may repeat once after ≥1 minute. 1

Alternative Routes When IV Access Unavailable

  • Intramuscular midazolam 0.2 mg/kg (maximum 6 mg) if IV access is delayed—this has 97% relative efficacy compared to IV lorazepam. 1
  • Intranasal midazolam or buccal midazolam are acceptable alternatives with onset within 1–2 minutes. 1
  • Rectal diazepam 0.5 mg/kg if IM/intranasal routes are not feasible. 1
  • Never use intramuscular diazepam due to erratic absorption. 1

Second-Line Treatment: Non-Sedating Anticonvulsants (5–20 minutes)

If seizures persist after adequate benzodiazepine dosing, immediately escalate to one of the following second-line agents—do not delay. 1, 3

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: Women of childbearing potential due to fetal teratogenicity. 1

Levetiracetam (Preferred for Minimal Monitoring)

  • Dose: 30 mg/kg IV (maximum 2500–3000 mg) over 5 minutes. 1, 3
  • Efficacy: 68–73% seizure cessation with minimal cardiovascular effects (0.7% hypotension risk). 1
  • No cardiac monitoring required—ideal for elderly patients or those with cardiac disease. 1
  • Requires renal dose adjustment: reduce by 50% if CrCl <30 mL/min. 1

Fosphenytoin (Traditional Agent)

  • Dose: 20 mg PE/kg IV at maximum rate of 150 PE/min (not to exceed 50 mg/min in elderly). 1
  • Efficacy: 84% but 12% hypotension risk—requires continuous ECG and blood pressure monitoring. 1
  • May be ineffective in alcohol withdrawal or toxin-related seizures. 3

Phenobarbital (Reserve Option)

  • Dose: 20 mg/kg IV over 10 minutes (maximum 1000 mg). 1
  • Efficacy: 58.2% but higher risk of respiratory depression and hypotension. 1
  • Pediatric maintenance: 1–3 mg/kg IV every 12 hours. 1

Simultaneous Evaluation for Reversible Causes

While administering anticonvulsants, immediately search for and treat underlying etiologies—do not delay treatment to obtain imaging. 1, 3

  • Hypoglycemia: Check fingerstick glucose; give dextrose 50% 50 mL IV if <60 mg/dL. 1
  • Hyponatremia: Most common electrolyte cause; check sodium and correct cautiously. 1
  • Hypoxia: Maintain SpO₂ >94% with supplemental oxygen. 3
  • Drug toxicity or withdrawal: Alcohol, benzodiazepines, anticonvulsants. 1, 3
  • CNS infection: Check temperature; consider meningitis/encephalitis. 3
  • Acute stroke or hemorrhage: Especially in patients >40 years. 1

Refractory Status Epilepticus (20+ minutes): Third-Line Anesthetic Agents

Refractory SE is defined as seizures continuing despite benzodiazepines and one second-line agent—initiate continuous EEG monitoring and transfer to ICU immediately. 1, 3

Midazolam Infusion (First-Choice Anesthetic)

  • Loading dose: 0.15–0.20 mg/kg IV bolus. 1, 4
  • Continuous infusion: 1 mg/kg/min, 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—lowest hypotension rate among anesthetics. 1, 4
  • Before tapering midazolam, load a long-acting anticonvulsant (phenytoin, valproate, or levetiracetam) to prevent breakthrough seizures. 1

Propofol (Alternative Anesthetic)

  • Loading dose: 2 mg/kg IV bolus. 1, 4
  • Continuous infusion: 3–7 mg/kg/hour. 1
  • Efficacy: 73% with 42% hypotension risk—requires mechanical ventilation but shorter duration (4 days) than barbiturates (14 days). 1, 4
  • Mean time to seizure control: 2.6 minutes (fastest among anesthetics). 4

Pentobarbital (Highest Efficacy, Highest Risk)

  • Loading dose: 13 mg/kg IV bolus. 1, 4
  • Continuous infusion: 2–3 mg/kg/hour. 1
  • Efficacy: 92%—highest among all anesthetic agents—but 77% hypotension risk requiring vasopressor support. 1, 4
  • Prolonged mechanical ventilation (mean 14 days). 4

Critical Monitoring Requirements for Anesthetic Agents

  • Continuous EEG monitoring is mandatory—not optional—to titrate anesthetic depth and detect electrographic seizures (25% of patients have ongoing electrical seizures despite cessation of motor activity). 1, 4, 3
  • Mechanical ventilation is required for all anesthetic agents due to respiratory depression. 4
  • Prepare vasopressors (norepinephrine, phenylephrine) before initiating therapy, as hypotension is nearly universal. 4
  • Continue EEG monitoring for at least 24–48 hours after anesthetic discontinuation, as breakthrough seizures occur in >50% of patients. 1

Super-Refractory Status Epilepticus (SRSE)

SRSE is defined as seizures continuing despite anesthetic therapy or recurring during anesthetic wean—mortality approaches 40%. 4, 5

  • Immediately administer continuous IV anesthetic infusions titrated to EEG burst suppression. 4
  • Consider ketamine (0.45–2.1 mg/kg/hour) as a fourth-line agent—64% efficacy when started early (within 3 days) but only 32% if delayed. 1
  • Patients with toxic/metabolic causes or anoxia have worse outcomes (29% control) versus chronic epilepsy, infections, or stroke (91% control). 4

Critical Pitfalls to Avoid

  • Never use neuromuscular blockers (e.g., rocuronium) alone—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 assume seizures have stopped based on cessation of motor activity alone—obtain EEG to confirm, as nonconvulsive SE occurs in 25% of cases. 1, 3
  • Do not delay second-line treatment—every minute of ongoing seizures increases morbidity and mortality (5–22% overall, up to 65% in refractory cases). 1
  • Do not underdose anticonvulsants—use full weight-based dosing to avoid treatment failure. 3

Maintenance Dosing After Seizure Control

  • Levetiracetam: 30 mg/kg IV every 12 hours (maximum 1500 mg per dose) for convulsive SE; 15 mg/kg every 12 hours for nonconvulsive SE. 1
  • Valproate: Continue at maintenance dose based on serum levels. 1
  • Fosphenytoin/Phenytoin: Transition to oral phenytoin 300–400 mg daily in divided doses. 6

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

Super Refractory Status Epilepticus Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Status epilepticus in the ICU.

Intensive care medicine, 2024

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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