Poisoning - management of childhood
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.
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
|
Small volumes of non-pharmaceuticals than can result in severe toxicity
|
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
Resuscitation
Risk assessment
Supportive care
Decontamination
Enhanced elimination
Antidotes
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 |
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) |
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 |
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