Initial Assessment in Poisoning - Spotting Poison's Play
- Airway, Breathing, Circulation (ABCs): Secure, ventilate, circulate. Utmost priority!
- History (AMPLE & Poisoning Specific):
- 📌 Allergies, Medications, Past medical Hx, Last meal, Events.
- Substance, Dose, Time, Route (📌 SDTR).
- Intent, symptoms onset, co-ingestants.
- Examination (Head-to-Toe):
- Vitals (HR, BP, RR, T, SpO2).
- Pupils (size, reactivity: miosis/mydriasis).
- Skin (color, temp, moisture, marks, diaphoresis).
- Odors (breath, body fluids - e.g., garlic, almonds).
- Neuro status (GCS, seizures, reflexes).
- Recognize Toxidromes (e.g., Opioid, Cholinergic, Anticholinergic, Sympathomimetic, Sedative-hypnotic).
- Initial Stabilization:
- Oxygen, IV access, cardiac monitoring.
- Correct immediate life threats (hypoxia, hypotension, hypoglycemia, seizures, arrhythmias).
⭐ Toxidrome recognition is key to guiding empirical treatment before definitive lab results.

Toxicological Screening Methods - Culprit Catchers
- Purpose: Identify toxins, guide antidote use, medico-legal.
- Common Samples:
- Urine: Preferred for screening (wide window).
- Blood (Serum/Plasma): For quantification, correlates with acute toxicity.
- Gastric Aspirate: If recent, large ingestion.

- Key Techniques:
- Immunoassays (e.g., ELISA, EMIT): Rapid, qualitative; common for drugs of abuse (DOA).
- Chromatography:
- GC-MS (Gas Chromatography-Mass Spectrometry): Gold standard for many volatiles; confirmatory.
- HPLC (High-Performance Liquid Chromatography): For non-volatile, thermolabile substances.
- Atomic Absorption Spectroscopy: For heavy metals.
- Considerations:
- Screening panels detect common toxins only.
- False positives/negatives possible. Clinical correlation is paramount.
⭐ Urine drug screens often detect metabolites, not parent drug; window varies (e.g., cannabis weeks, cocaine days).
Key Toxidromes - Symptom Signposts
Pattern recognition aids rapid diagnosis.
- Opioid:
- ↓LOC, ↓RR, miosis (pinpoint pupils)
- Hypotension, bradycardia, hypothermia
- Sympathomimetic:
- Agitation, mydriasis
- Tachycardia, hypertension, hyperthermia, diaphoresis
- Seizures
- Anticholinergic:
- "Mad as a hatter" (delirium)
- "Blind as a bat" (mydriasis)
- "Red as a beet" (flushed skin)
- "Hot as a hare" (hyperthermia)
- "Dry as a bone" (dry mucous membranes, urinary retention)
- Tachycardia
- Cholinergic:
- Muscarinic: 📌 SLUDGEM (Salivation, Lacrimation, Urination, Defecation, GI distress, Emesis, Miosis)
- Nicotinic: Weakness, fasciculations
- Killer B's: Bradycardia, Bronchorrhea, Bronchospasm
- Sedative-Hypnotic:
- ↓LOC, slurred speech, ataxia
- Respiratory depression (esp. barbiturates)
- Serotonin Syndrome:
- Mental status changes (agitation)
- Autonomic hyperactivity (tachycardia, hyperthermia)
- Neuromuscular: Clonus, hyperreflexia (esp. lower limbs)
⭐ Mydriasis is seen in sympathomimetic and anticholinergic toxidromes, while miosis is characteristic of opioid and cholinergic (organophosphate) poisoning.
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Ancillary Labs & Tox Screen Limits - Deeper Dive Dx
- Key Ancillary Labs:
- ABG:
- Anion Gap (AG): $AG = (Na^+) - (Cl^- + HCO_3^-)$. Normal: 8-12 mEq/L.
- 📌 MUDPILES for ↑AG.
- Osmolal Gap (OG): $OG = Measured Osmolality - Calculated Osmolality$. Normal < 10-15 mOsm/kg.
- ↑ in toxic alcohols (e.g., methanol, ethylene glycol).
- Anion Gap (AG): $AG = (Na^+) - (Cl^- + HCO_3^-)$. Normal: 8-12 mEq/L.
- ECG: QRS duration (e.g., TCAs), QT interval (e.g., antipsychotics).
- Electrolytes (K+, Ca2+), LFTs, RFTs, Glucose.
- ABG:
- Toxicology Screen Limitations:
- Not comprehensive; many drugs missed (e.g., synthetic opioids, novel psychoactive substances, many cardiovascular drugs).
- Primarily qualitative; concentration not typically given.
- Turnaround time often slow, may not guide emergency care.
- False positives/negatives common.
⭐ Many common drugs like beta-blockers, calcium channel blockers, and digoxin are NOT detected on standard urine toxicology screens.
- Clinical picture & specific assays guide management, not just broad screen.
High‑Yield Points - ⚡ Biggest Takeaways
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