Gamma hydroxybutyrate withdrawal
Background
- Abbreviation: GHB
- Central nervous system depressant
- GABA-B agonist (as opposed to GABA-A agonists - alcohol, benzodiazepines, etc)
- Abused for:
- Body building or sleep enhancement
- euphoric, sexual, stimulant, and relaxant effects
- Surreptitious drugging to facilitate sexual assault
- Also used therapeutically in the treatment of narcolepsy[1]
Pharmacokinetics
- effect starts in 15-20min, peaks in 30-60 min,
- lipid soluble, no protein binding so crosses BBB readily
- elimination is dose-dependent with half life of 20-50 min
- The duration of GHB's clinical effects depends upon the dose, and ranges from 2.5 to 4 hours
Pharmacology
- Is a metabolite and precursor of GABA
- Interacts with GHB-specific receptors and also acts as a direct agonist of GABA-B receptors
- Affects multiple neurotransmitter systems, including those of opioids, dopamine, serotonin, glutamate, and acetylcholine
- Gamma butyrolactone (GBL) and 1,4 butanediol (BD) are GHB analogs that are rapidly metabolized to GHB after ingestion, with the same toxic and recreational effects
Clinical Features
- Similar to alcohol withdrawal
- tremor, agitation, hallucinations, tachycardia, hypertension
- Withdrawal only if have long term use, not episodic binging
- Occur a few hours after use
Differential Diagnosis
Sedative/hypnotic withdrawal
- Toxic alcohols
- Ethanol
- Ethylene glycol
- Methanol
- Isopropyl alcohol
- Benzodiazepines
- Flunitrazepam (Rohypnol)
- Gamma hydroxybutyrate (GHB)
- Baclofen
- Barbiturates
- Opioids
- Chloral hydrate
Evaluation
- Typically a clinical diagnosis
Management
- Benzodiazepines (may need large doses)
- Neuroleptics
- Beta-blockers
References
- Mamelak M, Scharf MB, Woods M. Treatment of narcolepsy with gamma-hydroxybutyrate. A review of clinical and sleep laboratory findings. Sleep. 1986;9(1 Pt 2):285-289. doi:10.1093/sleep/9.1.285
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