Drug Intoxication
Drug intoxication from recreational substances requires toxidrome recognition, ABCDE management, specific treatments for complications, and awareness of novel psychoactive substances. TOXBASE and NPIS provide UK-specific guidance.
Key Facts
UK drug-related deaths: approximately 4,500/year — highest in Scotland; increasing trend Cocaine: Sympathomimetic toxidrome; treat hypertension/agitation with benzodiazepines; avoid beta-blockers (unopposed alpha stimulation) MDMA (ecstasy): Serotonergic effects + hyperthermia + hyponatraemia (from excess water intake); treat with cooling and dantrolene if severe Novel psychoactive substances (NPS): Formerly 'legal highs'; synthetic cannabinoids, cathinones — variable and unpredictable effects GHB/GBL: Rapid-onset coma, may recover spontaneously; narrow margin between recreational and lethal dose Spice/synthetic cannabinoids: Severe adverse effects (seizures, psychosis, AKI, rhabdomyolysis) unlike natural cannabis Chemsex drugs (GHB/GBL, mephedrone, crystal meth): Seen in MSM community; overdose risk from combination use FRANK (talktofrank.com) and TOXBASE provide information on novel substances
Overview
Key Facts
Recreational drug intoxication presents an evolving challenge with the emergence of novel psychoactive substances and changing patterns of drug use. Management is predominantly supportive with treatment of specific complications.
Epidemiology
Drug-related deaths in the UK exceed 4,500 per year and are increasing. Opioids remain the leading cause of drug death. Cocaine-related deaths have tripled over the past decade. NPS-related deaths are increasing. Scotland has the highest drug death rate in Europe.
Aetiology
- Stimulants: Cocaine, amphetamines, MDMA, methamphetamine, mephedrone
- Depressants: GHB/GBL, benzodiazepines (recreational), ketamine
- Cannabis and synthetic cannabinoids: 'Spice', K2
- Hallucinogens: LSD, psilocybin, DMT
- Dissociatives: Ketamine, PCP, nitrous oxide
- Novel psychoactive substances: Evolving range of synthetic drugs
Pathophysiology
Different drugs act on different neurotransmitter systems:
- Stimulants: Increase catecholamines (dopamine, noradrenaline) → sympathomimetic toxidrome
- MDMA: Serotonin and noradrenaline release → serotonergic syndrome, hyperthermia, SIADH
- GHB/GBL: GABA-B agonism → rapid-onset sedation
- Synthetic cannabinoids: Full CB1 agonism (unlike THC partial agonism) → unpredictable severe effects
Clinical Presentation
Stimulant Toxidrome (Cocaine, Amphetamines, MDMA)
- Agitation, psychosis, paranoia
- Tachycardia, hypertension, hyperthermia
- Dilated pupils (mydriasis)
- Seizures, arrhythmias, MI (cocaine), rhabdomyolysis
MDMA-Specific
- Hyponatraemia (dilutional — excess water drinking)
- Serotonin syndrome (clonus, hyperreflexia, hyperthermia)
- Hepatotoxicity
GHB/GBL
- Rapid deep sedation → coma (onset 15-30 min, duration 2-4h)
- Bradycardia, respiratory depression
- Agitated emergence from coma
Synthetic Cannabinoids
- Agitation, psychosis, seizures (unlike natural cannabis)
- Tachycardia, AKI, rhabdomyolysis
Red Flags
- Hyperthermia >40°C — actively cool (MDMA, cocaine, serotonin syndrome)
- Chest pain in cocaine user — ACS; treat with benzodiazepines, GTN, avoid beta-blockers
- Seizures — benzodiazepines first-line
- Hyponatraemia (Na⁺ <120) — hypertonic saline if symptomatic
- Body-packing — risk of massive drug release
Differential Diagnosis
| Substance | Key Features | Specific Treatment |
|---|---|---|
| Cocaine | Chest pain, agitation, MI risk | Benzodiazepines, GTN, NO beta-blockers |
| MDMA | Hyponatraemia, hyperthermia, serotonin syndrome | Cooling, fluid restriction, cyproheptadine |
| Amphetamines | Prolonged sympathomimetic effects | Benzodiazepines, cooling |
| GHB/GBL | Rapid coma, spontaneous recovery | Supportive, airway protection |
| Ketamine | Dissociative state, nystagmus, hypertension | Benzodiazepines if agitated |
| Synthetic cannabinoids | Seizures, psychosis, AKI | Benzodiazepines, supportive |
| Nitrous oxide | Peripheral neuropathy (B12 depletion), myelopathy | B12 supplementation |
Diagnosis / Investigation
Bedside
- ABCDE assessment: Priority
- Temperature: Hyperthermia is a medical emergency
- Blood glucose: Exclude hypoglycaemia
- ECG: Arrhythmias, QTc prolongation, Brugada-like (cocaine)
- GCS: Serial monitoring
Bloods
- U&Es: Sodium (MDMA — hyponatraemia), potassium, creatinine (AKI)
- CK: Rhabdomyolysis (stimulants, prolonged seizures, hyperthermia)
- Troponin: If chest pain (cocaine-associated MI)
- LFTs: Hepatotoxicity (MDMA, cocaine)
- ABG/VBG: pH, lactate
- Coagulation: DIC in severe hyperthermia
- Paracetamol level: Always check for co-ingestion
Imaging
- CXR: If respiratory symptoms
- CT head: If seizures, focal neurology, prolonged altered consciousness
- Abdominal X-ray/CT: If body-packing suspected
Special Tests
- Urine drug screen: Confirmatory but rarely changes acute management
- TOXBASE/NPIS: For NPS identification and management guidance
Management
Non-pharmacological
- Supportive care: ABCDE, calm environment, reassurance (for mild stimulant intoxication)
- Active cooling: For hyperthermia >39°C — remove clothing, cold IV fluids, ice packs, evaporative cooling; consider dantrolene if >41°C
- Fluid restriction: For MDMA-induced hyponatraemia (NOT IV fluids)
Pharmacological
Stimulant toxicity (cocaine/amphetamines):
- Benzodiazepines (diazepam 10-20mg IV) for agitation, hypertension, tachycardia
- GTN for cocaine-associated chest pain
- Avoid beta-blockers in cocaine toxicity (risk of unopposed alpha stimulation)
- Sodium bicarbonate if wide QRS on ECG
MDMA toxicity:
- Cooling measures
- Benzodiazepines for seizures/agitation
- Cyproheptadine 12mg PO for serotonin syndrome (then 4mg every 2h)
- Hypertonic saline 3% (100mL over 10 min) if Na⁺ <120 with seizures/severe symptoms
GHB/GBL:
- Supportive — airway protection; usually self-limiting
- Atropine if symptomatic bradycardia
- Do NOT use flumazenil (not effective)
Ketamine:
- Benzodiazepines for emergence reactions/agitation
- Monitoring of cardiovascular parameters
Surgical/Interventional
- Body-packer: Whole bowel irrigation; surgical retrieval if package rupture with clinical toxicity
Referral Criteria
- ICU: Hyperthermia >40°C, cardiovascular instability, refractory seizures, severe hyponatraemia
- Drug and alcohol services: All patients with recreational drug use
- Psychiatric: If self-harm or suicidal ideation
- Safeguarding: If children exposed to drug use in the home
Prognosis
- Cocaine-associated MI: 5-10% mortality if not recognised; excellent outcome with appropriate management
- MDMA fatalities: Primarily from hyperthermia, hyponatraemia, or serotonin syndrome
- GHB/GBL: Narrow therapeutic window; death from respiratory depression; usually recover fully if airway managed
- Synthetic cannabinoids: Increasing mortality and morbidity; unpredictable pharmacology
- Nitrous oxide: Prolonged use → B12 deficiency → subacute combined degeneration of the cord (irreversible if severe)
Other Relevant Information
Drug-Specific Emergency Management Summary
| Drug | Primary Danger | Key Treatment |
|---|---|---|
| Cocaine | MI, arrhythmia, seizures | Benzodiazepines, GTN, no beta-blockers |
| MDMA | Hyperthermia, hyponatraemia | Cooling, fluid restriction, cyproheptadine |
| Amphetamines | Hyperthermia, agitation, rhabdomyolysis | Benzodiazepines, cooling, IV fluids |
| GHB/GBL | Respiratory depression, coma | Supportive, airway protection |
| Ketamine | Emergence reaction, laryngospasm | Benzodiazepines |
| Synthetic cannabinoids | Seizures, psychosis, AKI | Benzodiazepines, supportive |
| Nitrous oxide | B12 deficiency, myelopathy | B12 replacement |
Serotonin Syndrome Diagnostic Criteria (Hunter)
| Criterion | Detail |
|---|---|
| Spontaneous clonus | Present |
| Inducible clonus + agitation/diaphoresis | Present |
| Ocular clonus + agitation/diaphoresis | Present |
| Tremor + hyperreflexia | Present |
| Temperature >38°C + clonus | Present |