Medical Disclaimer
- Educational Only: Not for clinical decision-making.
- Verify Information: Always consult protocols and authoritative sources.
AI Assistance Notice
AI was used to assist in organizing and formatting this information. All content is reviewed for accuracy.
Bedside Snapshot
- Primary Uses: Procedural anesthesia, electroconvulsive therapy (ECT), brief procedural sedation when rapid on/off sedation is desired
- Typical Dosing: Induction 1–1.5 mg/kg IV for anesthesia; procedural sedation 0.5–1 mg/kg IV; ECT dose ~0.75–1 mg/kg
- Onset & Duration: Onset within seconds; hypnotic duration ~5–10 minutes after bolus; prolonged infusions accumulate
- Key Risks: Profound respiratory depression/apnea, hypotension and myocardial depression; pro-convulsant activity (used intentionally in ECT)
- Environment: Requires full airway/resuscitation capability, continuous monitoring, and experienced anesthesia-level personnel
- Comparison: Faster onset but shorter duration than propofol; more hemodynamic instability and higher risk of myoclonus
Brand & Generic Names
- Generic Name: Methohexital sodium
- Brand Names: Brevital (Brevital Sodium); availability varies by region
Medication Class
Ultra–short-acting barbiturate sedative–hypnotic. Enhances GABAergic inhibition at the GABA-A receptor; at higher doses can directly activate GABA-A receptors causing rapid loss of consciousness. Rapid redistribution leads to short duration after bolus, but accumulation with repeated dosing extends recovery time.
Pharmacology
Mechanism of Action:
- Binds to barbiturate site on the GABA‑A receptor complex, increasing duration of chloride channel opening and enhancing inhibitory GABAergic transmission
- At higher doses, may directly activate GABA‑A receptors even without GABA, producing profound CNS depression
- Decreases cerebral metabolic rate and cerebral blood flow; can lower intracranial pressure (specialist use)
- Pro‑convulsant in some settings—facilitates seizure induction (useful for ECT) and can produce myoclonic or tonic–clonic movements
Pharmacokinetics:
- Route: IV (primary); occasionally rectal in pediatrics
- Onset: Within 10–30 seconds after IV bolus
- Duration: Hypnosis ~5–10 minutes after a single bolus due to rapid redistribution
- Distribution: Highly lipophilic with rapid brain penetration and large volume of distribution
- Metabolism: Hepatic oxidative metabolism to inactive metabolites
- Elimination: Renal excretion of metabolites; context‑sensitive half‑time increases with repeated doses/infusions
Indications
- Induction of anesthesia for short procedures (preferably in OR/monitored environments)
- Anesthetic agent for electroconvulsive therapy (ECT) due to rapid onset and short duration
- Brief procedural sedation when rapid on/off sedation is required and full airway support is available
- Neuroanesthesia situations requiring rapid control of ICP and cerebral metabolic rate (specialist use)
Dosing & Administration
Available Forms:
- Lyophilized powder for reconstitution; commonly provided as 0.5 g or 2.5 g vials; reconstitute to concentrations such as 10 mg/mL
- IV use only in most acute care settings (rectal forms have historical pediatric use in some protocols)
Adult Dosing (General – Follow anesthesia/clinical protocols):
| Indication | Dose | Route | Notes |
|---|---|---|---|
| Induction of Anesthesia | 1–1.5 mg/kg IV | IV bolus (slowly over 30–60 sec) | Titrate to loss of consciousness; expect apnea and be prepared to ventilate or intubate |
| ECT Anesthesia | 0.75–1 mg/kg IV | IV bolus | Titrate to adequate anesthesia while preserving seizure quality |
| Procedural Sedation (brief) | 0.5–1 mg/kg IV initial; increments of 0.25–0.5 mg/kg as needed | IV bolus | Use only with full airway/resuscitation readiness; elderly or hypovolemic patients require dose reduction |
Warning: Expect apnea after an induction dose — be ready to assist ventilation or intubate. Use only in monitored settings with experienced personnel.
Contraindications
Absolute Contraindications:
- Known hypersensitivity to barbiturates
- Porphyria (acute intermittent or variegate) — barbiturates can precipitate porphyric crises
- Marked hypotension or shock where further myocardial depression would be dangerous (unless full hemodynamic support available)
Precautions:
- Severe cardiovascular disease: risk of hypotension and decreased cardiac output — reduce dose and titrate slowly
- Respiratory disease: causes significant respiratory depression and apnea — airway must be secured or immediately supportable
- Hepatic or renal impairment: prolonged sedation possible — dose adjustments and monitoring required
- Elderly and frail patients: increased sensitivity — use reduced dosing and slow titration
- Concomitant CNS depressants (opioids, benzodiazepines, alcohol): synergistic respiratory and CNS depression — monitor closely
Adverse Effects
Common:
- Hypotension
- Tachycardia
- Apnea, hypoventilation, oxygen desaturation
- Injection site pain or thrombophlebitis
- Myoclonic movements or muscle twitching; tonic–clonic movements (particularly in ECT)
Serious:
- Profound cardiovascular collapse and refractory hypotension in hypovolemia or severe cardiac disease
- Prolonged apnea requiring intubation and mechanical ventilation
- Laryngospasm or bronchospasm
- Porphyric crises in susceptible individuals
Special Populations
Elderly / Frail:
- Markedly increased sensitivity; start at lower doses and titrate carefully
- Higher risk of hypotension and prolonged sedation
Hepatic / Renal Impairment:
- Hepatic impairment may prolong effect due to slower metabolism; use caution and consider lower doses
- Renal impairment may increase duration of metabolites — monitor recovery time
Respiratory Disease:
- Avoid or use extreme caution in patients with limited respiratory reserve; ensure airway support is immediately available
Monitoring
- Continuous ECG, blood pressure, and pulse oximetry during and after administration
- End‑tidal CO2 (capnography) when used for procedural sedation or anesthesia
- Monitor depth of sedation and recovery of airway reflexes and mental status
- Monitor hemodynamics closely, especially in patients with limited cardiac reserve
- For repeated doses/infusions: track cumulative dose and recovery time
Overdose Management
- Profound CNS and respiratory depression or apnea — secure airway and provide assisted ventilation; intubate if necessary
- Support blood pressure with fluids and vasopressors if refractory hypotension occurs
- No specific antagonist for barbiturate overdose; management is supportive and may include activated charcoal if recent oral ingestion in pediatrics (not commonly relevant for IV use)
- Consider ICU admission for monitoring and prolonged supportive care after large overdose
Clinical Pearls
Anesthesia-level drug: Only use when airway skills, resuscitation gear, and continuous monitoring are immediately available.
Expect apnea: After an induction dose, apnea is common—be prepared to ventilate or intubate.
ECT use: Methohexital lowers seizure threshold and is useful for ECT; in non‑ECT patients it may cause myoclonic or tonic–clonic movements.
ED Context: Propofol, etomidate, and ketamine commonly replace methohexital for procedural sedation in many EDs, but methohexital remains in specialty protocols.
Documentation: Record dose, timing, airway status, and hemodynamic course clearly for medico-legal and clinical handoff purposes.
References
- 1. Brevital (methohexital sodium) prescribing information.
- 2. Miller, R. D. (latest ed.). Miller’s Anesthesia. Elsevier.
- 3. American College of Emergency Physicians. Clinical Policy on Procedural Sedation in the Emergency Department.