Algorithm


graph TD

classDef start fill:#1b5e20,color:#ffffff,stroke:#66bb6a;
classDef step fill:#0d47a1,color:#ffffff,stroke:#42a5f5;
classDef decision fill:#4a148c,color:#ffffff,stroke:#ab47bc;
classDef alert fill:#b71c1c,color:#ffffff,stroke:#ef5350;

A(<b>Poisoned Child</b><br>Emergency Presentation):::start
B{<b>Hemodynamically Stable</b>}:::decision
C[<b>Emergency Resuscitation</b><br>Airway Fluids Vasopressors]:::alert
D[<b>Bedside Interventions</b><br>Glucose and Naloxone trial]:::step

A --> B
B -->|No| C
C --> D
B -->|Yes| D

D --> E{<b>Clinical Action Path</b>}:::decision

E -->|History Exam| F1[<b>Toxidrome Identification</b><br>Assess odors and mucosa]:::step
E -->|Diagnostics| F2[<b>Labs and Imaging</b><br>ECG and Gap Analysis]:::step
E -->|Management| F3[<b>Decontamination</b><br>Dermal Ocular or GI]:::step

F1 --> G1[<b>Antidotal Therapy</b><br>Atropine Flumazenil etc]:::step
F2 --> G2[<b>Toxin Screening</b><br>Salicylates Acetaminophen]:::step
F3 --> G3[<b>Enhanced Elimination</b><br>Dialysis or Alkalinization]:::step

Initial Stabilization And Resuscitation

  • Emergency cardiorespiratory stabilization precedes comprehensive diagnostic testing.
  • Require rapid systematic assessment of airway, breathing, circulation, and neurological disability upon presentation.
  • Anticipate early elective endotracheal intubation for profound central nervous system depression, absent protective airway reflexes, or acute respiratory failure mitigating pulmonary aspiration risk.
  • Manage hypotension aggressively initially using rapid intravenous boluses of isotonic crystalloids including normal saline or lactated Ringer’s.
  • Utilize direct-acting vasopressors including epinephrine or norepinephrine if hypotension remains refractory to volume expansion.
  • Prefer vasopressors particularly if suspecting tricyclic antidepressant or calcium channel blocker toxicity.
  • Perform mandatory bedside serum glucose test for altered mental status.
  • Treat profound neuroglycopenia immediately using intravenous dextrose; condition perfectly mimics toxic encephalopathy.
  • Initiate diagnostic and therapeutic trial of naloxone in cases featuring unexplained coma or significant respiratory depression reversing potential opioid intoxication.

Clinical Evaluation And History Taking

Epidemiological And Historical Clues

  • Analyze child’s age providing critical epidemiological context.
  • Under 5 years: Exposures predominantly accidental, often involving single agents including common household products, cosmetics, or unsecured pharmaceuticals.
  • Adolescents: Ingestions largely intentional, driven by suicide attempts, substance abuse, or misuse, frequently involving severe polypharmacy.
  • Reconstruct scene via meticulous history.
  • Establish exact location child found.
  • Explore accessibility of medications belonging to older relatives or visitors.
  • Screen for underlying psychiatric stress or previous suicide attempts in older youths.

Physical Examination And Diagnostic Odors

  • Perform targeted physical examination identifying classic toxidromes.
  • Assess characteristic odors on breath or clothing.
  • Bitter almonds: Suggest cyanide.
  • Acetone: Suggest salicylates or isopropyl alcohol.
  • Garlic: Point to organophosphates or arsenic.
  • Mothballs: Indicate camphor or naphthalene exposure.
  • Inspect oral cavity revealing excessive salivation suggesting organophosphates or ketamine.
  • Identify oral mucosal burns indicating caustic or corrosive ingestion.
  • Detect pigmented gum lines establishing hallmark of heavy metal poisoning including lead, mercury, or bismuth.

Major Toxidromes And Clinical Features

ToxidromeCharacteristic Clinical FeaturesCommon Causative Agents
AnticholinergicDelirium, mydriasis, tachycardia, hyperthermia, dry skin, dry oral mucosa, flushing, urinary retention.Atropine, antihistamines, tricyclic antidepressants.
CholinergicDiarrhea, urination, miosis, bradycardia, bronchorrhea, emesis, lacrimation, salivation, muscle fasciculations.Organophosphates, carbamate pesticides.
SympathomimeticAgitation, seizures, mydriasis, tachycardia, hypertension, diaphoresis, hyperthermia.Amphetamines, cocaine, ADHD medications.
OpioidProfound central nervous system depression, respiratory depression, miosis, bradycardia, hypotension, hypothermia.Morphine, heroin, methadone, buprenorphine.
Sedative-HypnoticComa, respiratory depression, normal to decreased heart rate, normal to decreased blood pressure, normal or small pupils.Benzodiazepines, barbiturates, alcohols, zolpidem.

Diagnostic And Laboratory Evaluation

Basic Investigations

  • Require comprehensive laboratory testing assessing multi-organ dysfunction and screening specific highly toxic occult substances.
  • Include complete blood count, serum electrolytes, blood urea nitrogen, serum creatinine, liver transaminases, and blood gas analysis.

Acid-Base And Osmolar Gap Analysis

  • Calculate anion gap evaluating high anion gap metabolic acidosis revealing unmeasured toxic anions.
  • Identify toxins causing high anion gap metabolic acidosis

πŸ’‘MUDPILES Mnemonic for HAGMA

M – Methanol U – Uremia D – Diabetic Ketoacidosis P – Paraldehyde / Propylene Glycol I – Inborn Errors of Metabolism / Iron / Isoniazid L – Lactic Acidosis E – Ethylene Glycol S – Salicylates

  • Determine osmolar gap indicating unmeasured osmotically active substances including toxic alcohols like methanol, ethanol, ethylene glycol if elevated greater than 10 mOsm.

Electrocardiography

  • Utilize 12-lead electrocardiography rapidly assessing life-threatening cardiotoxicity and specific conduction delays.
  • Widened QRS interval suggests dangerous fast sodium channel blockade, classic finding in severe tricyclic antidepressant toxicity requiring immediate intervention.
  • Prolonged QTc interval demonstrates interference with potassium rectifier channels predisposing to torsades de pointes.
  • Observe prolonged QTc frequently with methadone, phenothiazines, and antipsychotics.

Specific Toxicology Screening And Radiography

  • Recommend quantitative serum screening for acetaminophen and salicylates in all cases of intentional or unknown poisoning.
  • Note early acetaminophen and salicylate toxicity may remain asymptomatic but highly amenable to time-sensitive antidotal therapy.
  • Note limited utility of urine drugs-of-abuse screens for acute management due to inherent delays and high false positive/negative rates.
  • Utilize plain abdominal radiography visualizing specific radiopaque toxins.

CHIPPED Mnemonic for Radio-opaque toxins

C – Chloral hydrate / Calcium carbonate H – Heavy metals I – Iron P – Phenothiazines P – Play-Doh E – Enteric-coated tablets D – Dental amalgam / Illicit drug packets

Decontamination Strategies

Dermal And Ocular Decontamination

  • Mandate immediate, extensive flushing using tepid water or normal saline for minimum 10-20 minutes.
  • Strictly avoid water irrigation for highly reactive compounds including elemental sodium, phosphorus, calcium oxide, and titanium tetrachloride.

Gastrointestinal Decontamination

  • Individualize decontamination based on suspected toxin properties, exposure route, clinical stability, and time elapsed.
  • Consider syrup of ipecac obsolete and contraindicated; produces variable toxin removal, delays definitive treatments, causes significant adverse outcomes.
  • Utilize gastric lavage rarely; consider only within 1 hour of massive, potentially lethal ingestion.
  • Avoid gastric lavage strictly in unprotected airway, corrosive ingestion, or volatile hydrocarbon exposure due to extreme aspiration and perforation risk.

Activated Charcoal

  • Represents single most effective gastrointestinal decontamination method.
  • Achieves maximum efficacy administered within 1 hour of toxin ingestion.
  • Requires completely patent and protected airway prior to administration preventing catastrophic pulmonary aspiration.
  • Dose at 1 g/kg.
  • Acts via physical adsorption onto highly porous surface.
  • Ineffective binding heavy metals, iron, lithium, mineral acids, strong alkalis, toxic alcohols, cyanide, and most hydrocarbons.

Whole-Bowel Irrigation

  • Instill massive volumes of polyethylene glycol electrolyte solution via nasogastric tube.
  • Administer 35 mL/kg/hr in children and 1-2 L/hr in adolescents.
  • Clears gastrointestinal tract of substances poorly adsorbed by charcoal including iron, heavy metals, lithium, sustained-release pharmaceuticals, and illicit drug packets.

Techniques For Enhanced Elimination

Urinary Alkalinization

  • Enhances renal excretion of weak acids trapping ionized, polar molecules within renal tubules preventing systemic circulation reabsorption.
  • Accomplish administering continuous intravenous sodium bicarbonate infusion maintaining target urine pH 7.5-8.0.
  • Serves as primary elimination strategy for severe salicylate, phenobarbital, and methotrexate toxicity.

Hemodialysis And Hemofiltration

  • Clears toxins possessing low volume of distribution, low molecular weight, low plasma protein affinity, and high water solubility rapidly.
  • Indicated specifically for severe, life-threatening poisonings involving toxic alcohols, lithium, salicylates, theophylline, and barbiturates.

Multiple-Dose Activated Charcoal

  • Accelerates systemic toxin clearance interrupting enterohepatic circulation.
  • Utilizes intestinal mucosa as gastrointestinal dialysis membrane pulling toxins back into gut lumen.
  • Administer 0.5 g/kg every 4-6 hours.
  • Recommend for life-threatening ingestions involving carbamazepine, dapsone, phenobarbital, quinine, and theophylline.

Intravenous Lipid Emulsion

  • Creates intravascular lipid sink sequestering highly fat-soluble toxins.
  • Reduces active concentration mitigating target organ impact.
  • Utilize as profound lifesaving intervention in severe cardiotoxicity secondary to bupivacaine, massive calcium channel blocker overdoses, and tricyclic antidepressant poisonings.

Diagnostic Trials And Antidotal Therapy

  • Administer specific, carefully titrated antidotes serving as lifesaving therapeutic intervention and definitive diagnostic tool in undifferentiated comatose child.
  • Utilize naloxone starting at 0.1 mg/kg intravenous dose for presumed opioid toxicity characterizing profound respiratory depression and pinpoint pupils.
  • Mandate significantly lower naloxone doses if chronic opioid dependence suspected preventing precipitation of severe acute withdrawal.
  • Administer flumazenil 0.01 mg/kg reversing severe benzodiazepine-induced central nervous system depression.
  • Exercise extreme caution using flumazenil; carries substantial risk unmasking intractable seizures particularly with co-ingested pro-convulsant drugs or underlying seizure disorder.
  • Provide rapid diagnostic trial intravenous atropine 0.05 to 0.1 mg/kg for profound cholinergic signs highly suspicious for organophosphate pesticide poisoning.
  • Reverse life-threatening muscarinic symptoms including severe bradycardia and bronchorrhea using atropine.