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Poisoning - management of childhood

Date last published:

Unintentional poisoning is most common in the 12 to 36 month age group. Most small children will only take 2 to 3 tablets or one mouthful of substance.

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Starship clinical guidelines

Introduction

  • Unintentional poisoning is most common in the 12 to 36 month age group.

  • Most small children will only take 2 to 3 tablets or one mouthful of substance.

  • Serious sequelae are rare.

  • Supportive care and observation are the mainstays of treatment.

  • Beware of causing harm - a risk assessment is essential before considering decontamination or treatment.

  • Small ingestions of some substances can cause very serious injury in a small child.

One or two tablets that can be lethal to a 10kg toddler

  • Calcium channel blockers (eg Diltiazem, Verapamil), especially high dose slow release (SR) preparations
  • Amphtetamines
  • Dextropropoxyphene (in "Paradex")
  • Tricyclic antidepressants
  • Chloroquine
  • Opioids
  • Sulphonylureas
  • Theophylline

Small volumes of non-pharmaceuticals than can result in severe toxicity

  • Organophosphates
  • Paraquat
  • Camphor
  • Naphthalene
  • Hydrocarbons, Solvents, Eucalyptus oil, Kerosene

Poisoning should be considered in the child with unexplained abnormal vital signs, altered neurology or metabolic disturbance.

Consider non accidental injury (NAI) in non-ambulatory children, older children or large ingestions.

Older children/adolescents may present with deliberate self harm (intentional poisoning).

Approach to Paediatric Toxicology

  1. Resuscitation

  2. Risk assessment

  3. Supportive care

  4. Decontamination

  5. Enhanced elimination

  6. Antidotes

  7. Disposition

Resuscitation

Resuscitation takes priority over decontamination and administration of antidotes (unless necessary for resuscitation e.g. NaHCO₃)

Airway

Intubation likely to be indicated in the following situations:

  • Cardio-respiratory arrest

  • Airway injury

    - Corrosive ingestion

    - Decreased level of consciousness (GCS<8) or anticipated decrease in GCS

    - Prolonged seizures

    - Severe agitation or to facilitate treatment/investigations

Breathing

Oxygen/ventilation if required

Circulation

  • Support perfusion as needed

    - IV fluids (20ml/kg 0.9% NaCl if shocked)

    - Inotropes

  • Treatment of hypertension (see Hypertension guideline)

    - Beta-blockers should be avoided in sympathomimetic toxicity

  • Arrhythmia

    - NaHCO3 (1mmol/kg repeated as necessary) if sodium channel blocker ingested (Suspect if prolonged QRS, large R wave in aVR)

    - Generally poor response to defibrillation in poisoning

Examples of sodium channel blockers
Tricyclic antidepressants
Propranolol
Class 1A and 1C antiarrhthmics
- Quinidine
- Flecanide
First generation antihistamines 
Local anaesthetics
- Cocaine
- Bupivicaine
Propranolol
Dextropropoxyphene
Carbamazepine 

Disability

  • Sedation (benzodiazepines are the mainstay)

    - Midazolam (0.1-0.2mg/kg) is most commonly used

  • Seizure control (note - NOT conventional treatment)

    - Repeat doses of Midazolam (0.15mg/kg IV)

    - Phenobarbitone (20mg/kg IV) as second line

    - Phenytoin should NOT be used - Prolongs sodium channel blockade

  • Treatment of hypoglycaemia

  • Maintain normothermia

    - Management of hyperthermia

    - Benzodiazepines

    - Physical cooling

    - May require intubation and paralysis

Risk assessment

Risk assessment is a distinct cognitive process through which the clinician attempts to predict the likely clinical course and potential complications for the individual patient at that particular presentation.

Risk assessment should be quantitative and take into account agent, dose, time of ingestion, current clinical status and individual patient factors (for example, weight and co-morbidities).

The risk assessment is essential to determine the course of the poisoning and will guide treatment, investigations, period of observation and disposition.

Attempt to elucidate and clearly document:

  • What substance(s) have been ingested?

  • How much of each substance has been ingested - including a calculation of amount of substance per kg?

  • What time the ingestion occurred?

  • What clinical features have occurred thus far?

  • What other relevant patient factors (patient weight, other medical problems etc) are present?

Then discuss with senior staff and/or consult poisons information

If the ingestant is unknown:
Consider all possible medications or toxins accessible in the house

  • All family members medications

  • Non-pharmaceutical agents

  • Drugs of abuse

Conduct tablet counts of missing medication

Consider the worst case scenario, including:

  • That all the missing tablets were taken

  • That the ingestion time is the latest time possible

  • That there has not been significant spillage

  • That one child has ingested all of the missing poison.

Focused clinical examination

  • Especially important if ingestant is unknown

  • Toxidromes

Screening tests
No tests are routine. These will be determined by risk assessment and may include:

  • Blood sugar level

  • ECG

  • Paracetamol level should be requested in all children/young people following any intentional ingestion

  • Other screening tests should be guided by risk assessment

    • Other drug levels

    • Blood gases

    • Radiology

Supportive care

For most children the only treatment required is good supportive care:

  • Observation

  • Hydration

  • Nutrition

  • Sedation

  • Treatment of

    • Hypo/hyperthermia

    • Hypo/hyperglycaemia

    • Agitation

    • Seizures

Decontamination

This is rarely required and must not distract from resuscitation and supportive care

Skin

Wash off with soapy water

Eyes

Irrigate with 0.9% NaCl until pH is <8.0

GI tract

  • Dilution with milk/water is generally not recommended

  • Emesis should never be induced

  • Gastric lavage is not recommended as no demonstrated benefit compared to a single dose of activated charcoal.

  • Activated charcoal (AC) Is rarely indicated in paediatric poisoning. The use of AC carries a risk of aspiration and subsequent chemical pneumonitis. Indicated only if ALL of the following are true:

    • Presentation within 1 hour of Ingestion

    • Toxin is adsorbed by AC

    • Patient is currently maintaining own airway and risk assessment determines that their GCS will remain normal

    • Otherwise only give if airway is protected

    • The substance has significant toxicity and is not easily treatable
      Dose = 1g/kg
      Can be made more palatable by mixing with ice-cream

Toxins not adsorbed by activated charcoal

Acids/alkalis
Alcohols
Metals and ionic compounds (iron, potassium, lithium)
Hydrocarbons

  • Whole bowel irrigation (WBI) is very rarely performed.

    Indicated if:

    • Ingestion of a slow release or extended release substance or a substance not bound to AC and

    • Presentation prior to symptom onset and

    • Ingestion is likely to result in significant toxicity despite supportive care or antidote therapy

    • Polyethylene glycol (Golytely) - 30ml/kg/h until effluent runs clear)

Possible indications for WBI

Iron (>60mg/kg elemental iron ingested)
Sustained release diltiazem/verapamil
Slow release potassium chloride

Enhanced Elimination

This is very rarely required and must not distract from resuscitation and supportive care

Multidose activated charcoal

  • Can interrupt enterohepatic circulation and promote gut dialysis

  • May be indicated with large ingestions of Carbemazepine, Dapsone, Phenobarbital, Quinine, Theophylline

  • 1g/kg activated charcoal q4h

Urinary alkalinisation

  • Alkalinisation promotes ionization of highly acidic drugs, therefore prevents reabsorbtion across tubule and increases renal excretion.

Indications

  • Salicylates (however if severe toxicity this should not detract from urgent haemodialysis)

  • Phenobarbitone

Administration

  • 1-2 mmol/kg NaHCO3 stat then titrate (can infuse further doses over 1-2 hours)

  • Aim for urinary pH >7.5

Extracorporeal elimination (haemodialysis)

  • Haemodialysis is effective if toxin is water soluble, low molecular weight, not protein bound and has a small volume of distribution - e.g. alcohols, lithium, chloral hydrate, amphetamine, camphor, heavy metals, salicylates, theophylline, valproate or carbamazepine

  • Indications are based on drug levels, biochemistry and clinical symptoms.

  • Intensive care required

Antidotes

  • Pharmacological antagonists and chelating agents

  • Only useful in a small minority of poisonings

  • Administered when the potential therapeutic effect outweighs the adverse effects

Examples of some available antidotes

POISON ANTIDOTE 
Paracetamol   N-acetylcysteine - see guideline
Opioids  Naloxone 
Benzodiazepines Flumazenil 
Sodium channel blockers  NaHCO3 
Iron  Desferroxamine 
Glipizide Octreotide 
Digoxin  Digoxin fab-fragments (Digi-bind) 
Organophosphates  Pralidoxime, atropine 
Beta blockers, Ca2+ channel blockers  Insulin/dextrose euglycaemic therapy 

For further information see Toxicology Handbook (Murray et al). Elsevier. 2007

Disposition

  • Should be directed by risk assessment

  • Some children can be safely discharged after brief or no observation.

  • Others may require admission for ongoing observation and treatment

Unknown ingestant

  • Assume worst case scenario - a potentially lethal ingestion

  • Observe for a minimum of 12 hours

    - Monitor cardio-respiratory status and neurology

    - Cardiac monitoring if any evidence of abnormal vital signs

  • IV access can be deferred unless evidence of toxicity present

  • Investigations

    - BSL at presentation and discharge

    - ECG

  • Discharge only in daylight hours

Other considerations

  • Child safety and parental education

    - Safe storage of toxins

    - Supervision

    - Social work review might be indicated

    - Consider non-accidental injury

  • Discharge instructions

Deliberate self harm

Psychiatric review is mandatory prior to discharge

Prevention

  • The prevention of unintentional poisoning should be promoted throughout the community.

  • Child resistant packaging and safe storage has been shown to decrease the incidence of childhood poisoning.

  • Other measures include:

    - Smaller volume prescribing

    - Child resistant lids

    - Education about safe storage of medications, out of reach of children

    - Store in cupboards with child resistant latches

    - Home visits to target this advice

Toxidromes

Toxidrome  Effects Examples 
Anticholinergic  Delirium + peripheral effects

Mad as a hatter
Confusion, hallucinations, seizures, coma
Red as a beet
Flushed skin
Blind as a bat
Mydriasis
Hot as a hare
Hyperthermia
Dry as a bone
Dry skin, urinary retention, ileus 

1st generation antihistamines
Tricyclic antidepressants
Antitussives
Antipsychotics
Anticonvulsants
Antimuscularinics
- Atropine, Scopolamine, Ipatroprium bromide
Plants
- Some mushrooms, Datura 

Cholinergic  D  Diaphoresis
    Diarrhoea (& abdo cramps)
U  Urination
M  Miosis (or mydriasis)
B   Bronchospasm
     Bronchorrhoea
     Bradycardia
E   Emesis
L   Lacrimation
S   Salivation
Insecticides
- Organophosphates
- Carbamates
Chemical warfare agents
- Ricin, Tabun, Soman, VX
Alzheimer's medication
- Donepezil
Agents used for myasthenia gravis 
Sympathomimetic  Alpha
- Hypertension
- Bradycardia
- Mydriasis

Beta
- Hypotension
- Tachycardia
- Miosis 
Alpha
- Phenylephrine, OTC cold preps

Beta
- Salbutamol, Theophylline, Caffeine

Alpha and beta
- Amphetamine, Cocaine,
Pseudo/ephedrine, OTC cold preps,MDMA (ecstasy) 
Sedative/hypnotics Decreased LOC
Hypoventilation
Hypotension
Bradycardia
Opioids and barbiturates
- Miosis
- Hypothermia 
Benzodiazepines
Barbiturates
Alcohols
Opioids
Anticonvulsants
Antipsychotics 
Serotonergic   CNS
- Anxiety, agitation, hallucinations, seizures, coma
Neuromuscular
- Tremor
- Hyper-reflexia and clonus (LL>UL)
- Myoclonus
- Rigidity
Autonomic
- Flushing/sweating
- Tachycardia
- Hypertension
- Hyperthermia
 Antidepressants
- SSRIs, SSNRIs, MAOIs, TCADs
Analgesics
- Tramadol, Pethidine, Fentanyl
Drugs of abuse
- Amphetamine, MDMA (ecstasy), LSD
"Dietary supplements"
- St John's Wort, Ginseng
Hallucinogenic  Hallucinations
Psychosis
Panic
Fever
Mydriasis
Hypertension
- Amphetamine
- Cannaboids
- Cocaine
- LSD
- PCP
- Magic mushroom - Psilocybin species 

Resources

Poisons information centre 0800POISON

Toxins database (https://www.toxinz.com/)
- This is an extensive database of most toxins
- Information is generally accurate but generic at times (particularly with regard to decontamination). Consider each case on its merits. If in doubt discuss with ED consultant.

Toxicology Handbook (Murray, Daly, Little, Cadogen). Elsevier. 2007.
- An excellent reference guide with a very sensible approach to poisoning

A risk assessment based approach to the management of acute poisoning. Daly FFS, Little M, Murray L. Emerg Med J 2006;23:396-399

Poisonous plants in New Zealand. http://www.landcareresearch.co.nz/publications/factsheets/poisonous-plants 

Safefkids New Zealand - Excellent resource for prevention information
http://www.safekids.nz/Resources/CatID/13/Poisoning

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