Baclofen toxicity: Difference between revisions

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==Clinical Features==
==Clinical Features==
*Nausea and vomiting
*Nausea and vomiting
*Drowsziness
*Depressed level of consciousness
*Delirium
*Delirium
*Seizures
*Seizures
*Coma
**Tonic-clonic
*Respiratory compromise
**Non-convulsive status epilepticus
*Myoclonus
*Airway compromise and respiratory failure
*Hypothermia
*Hypothermia
*Hypotension
*Bradycardia and conduction abnormalities


==Differential Diagnosis==
==Differential Diagnosis==

Revision as of 15:36, 13 October 2025

Background

  • Baclofen is a synthetic derivative of GABA used to reduce spasticity in conditions such as multiple sclerosis and cerebral palsy, or to reduce muscular spasm in lower back pain.
  • At therapeutic doses, baclofen acts as a GABA-B receptor agonist in the spinal cord, causing inhibition of muscular tone.
  • At higher doses, baclofen loses selectivity and can cause sedation.
  • Primarily (80%) excreted by the kidneys
    • Dosage must be reduced in renal dysfunction and should be avoided with GFR < 30 mL/min/1.73 m2.
    • Patients on chronic therapy may become toxic with new AKI.

Clinical Features

  • Nausea and vomiting
  • Depressed level of consciousness
  • Delirium
  • Seizures
    • Tonic-clonic
    • Non-convulsive status epilepticus
  • Myoclonus
  • Airway compromise and respiratory failure
  • Hypothermia
  • Hypotension
  • Bradycardia and conduction abnormalities

Differential Diagnosis

Sedative/hypnotic toxicity

Evaluation

  • Diagnosis of exclusion

Management

  • Activated charcoal for recent ingestion
  • Supportive care:
    • IV fluids, respiratory care
    • Vasopressors for persistent hypotension
    • Benzodiazepines for seizures
  • Hemodialysis for very severe toxicity

Disposition

See Also

References

  • Jung, M. “Baclofen Overdoses”. Maryland Poison Center, University of Maryland School of Pharmacy. www.mdpoison.com Accessed April 29th, 2014.
  • Nicola Y Leung, Ian M Whyte, Geoffrey K Isbister Baclofen overdose: defining the spectrum of toxicity. Emerg Med Australas: 2006, 18(1);77-82