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Bottom Line Recommendations: Summary of Pediatric Emergency Care Information for Healthcare Providers

Cannabis Intoxication

Developed by:Dr. Neil Desai (University of British Columbia) and Dr. Kaitlin Hogue (HSC Children's Hospital of Winnipeg)

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Last Updated
Jan 2025

Topic
Cannabis

Summary

Cannabis contains Delta-9 Tetrahydrocannabinol (Δ-9-THC) and Cannabidiol (CBD). The psychoactive properties of cannabis are typically attributed to Δ-9-THC, which is present in variable concentrations dependent on the strain and absorbed at variable rates dependent on the route of exposure. Acute intoxication is rare from CBD products unless given in excess or with high THC:CBD ratio. Canadian legalization of cannabis has been associated with an increased rate of hospitalization for cannabis exposures in children 14 years and younger.1

Presentation Types

UNINTENTIONAL INGESTION (PREDOMINANTLY TODDLERS)

  • Consider in any previously healthy afebrile child <12 years with acute onset of the following symptoms without another clear cause:2
    • Lethargy, coma
    • Tachycardia, hypoventilation/apnea (5% of children will need intubation), bradycardia, hypotension, hypothermia
    • Hypotonia, ataxia, hyperactivity/irritability, hypertonia, tremor, seizures (CBD alone has some anticonvulsant activity, but in overdose can cause seizures)
    • Delayed recognition of cannabis intoxication results in increased testing/interventions and longer Emergency Department length of stay.

INTENTIONAL AND/OR CHRONIC USE (PREDOMINANTLY ADOLESCENTS)

Formulations & Methods of Delivery

Methods of Delivery and Pharmacokinetic Effects

METHOD

ONSET

PEAK EFFECT

DURATION

Ingestion

30-120 minutes

Within 4 hours

Up to 12 hrs, longer in children (up to 24 hrs)

Inhalation

Within minutes

Within 15-30 minutes

Up to 6 hrs, some residual effects can last up to 24 hrs

For more detailed information see: TREKK Cannabis Formulations & Methods of Delivery and CPS Cannabis Tools

INGESTION

  • High concentration edible products are commercially available or can be made at home, making the dose difficult to determine reliably. Legal commercially available edibles are required to state the dose of THC and/or CBD per unit/total package.
  • Edibles are more easily accessible to young children who can ingest large doses unintentionally, potentially leading to altered LOC and respiratory depression. Edible ingestion is a strong predictor of ICU admissions in the pediatric population.3
  • Pharmaceutical cannabinoids, including nabilone and dronabinol (tablets) or Sativex® (rapid acting oral spray of THC and CBD), have similar time to peak effects as edibles.

INHALATION

  • Inhaled dose depends on depth of inhalation and duration of puffing/breath holding. Alternative methods of inhalation of highly concentrated cannabis (e.g., vaporizing, dabbing), can lead to very rapid effects.
  • Synthetic cannabinoids (e.g., “Spice”, “K2”) have similar symptoms of intoxication but are associated with more CNS depression/agitation and potentially life-threatening symptoms (e.g., seizures, respiratory depression).

Diagnostic Testing

  • Perform work up for other causes of altered LOC if no clear history for cannabis intoxication is provided.
  • With altered LOC, strongly consider: POCT glucose, venous blood gas, lactate and electrolytes. Consider CBC, liver enzymes, blood cultures, ECG and/or intracranial imaging, as required.
  • CAUTION: Urine drug screen for the urine metabolite of Δ-9-THC can remain positive for weeks and does not necessarily reflect acute intoxication or rule out other possible co-ingestions/causes for altered LOC. There is a risk of false positives. Results rarely change clinical management.
  • In order to assess for co-ingestions, ask patient/family what medications are in the home/accessible and check serum levels when possible (e.g., acetaminophen, salicylates).

Management

  • Consult Poison Control/Toxicology and/or Pediatric Referral Center early, especially with major derangements in neurologic or respiratory status.
  • Consider activated charcoal with appropriate timing of presentation and clinical circumstance.

Symptoms

Management

Altered LOC/Vital sign instability

ABCs, supportive care

Nausea/Vomiting

Establish IV access and give fluid replacement.

Ondansetron: oral disintegrating tablet preferred (8-15 kg: 2 mg/dose; >15-30 kg: 4 mg/dose; >30 kg: 8 mg/dose) x 1 dose PO

OR 0.1 mg/kg/dose (MAX 4 mg) IV if not able to tolerate PO.

Agitation

Consider using benzodiazepines if central respiratory failure is not a concern.

Seizures

Benzodiazepines are the recommended first-line treatment for toxicologic seizures. Avoid phenytoin/fosphenytoin in toxicologic seizures

  • Transfer to Pediatric Referral Centre/admit to hospital if persistent altered LOC or intractable vomiting.
  • If asymptomatic 6 hours post-exposure, patient may be discharged home.
  • If intentional exposure by a guardian is suspected, discuss case with Child Protection Specialist at Pediatric Referral Centre and report to Child Welfare Authority.

Counselling Families About Cannabis

  • With the exception of CBD for specific seizure disorders, there are very few proven indications for medical cannabis use in children and many concerns for acute and long-term risks.
  • Provide parental education on the dangers of cannabis in children and safe storage of dangerous medication and substances. For more information for parents, visit: Caring for Kids – Cannabis: what parents need to know.
  • Use harm reduction strategies to counsel teens regarding cannabis use and refer to local resources and services due to long-term concerns for their mental health (increased risk for psychosis), attention, concentration, memory and executive functioning.

Development Team

Thank you to the following content experts who led the development of the Cannabis Intoxication and Cannabinoid Hyperemesis Syndrome Bottom Line Recommendations and Cannabis Supplement Table:

Kaitlin Hogue, MD, Resident – Pediatric Emergency Medicine, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Health Sciences Centre Children’s Hospital of Winnipeg

Neil Desai, MD, Clinical Assistant Professor, Division of Emergency Medicine, Department of Pediatrics, Faculty of Medicine, University of British Columbia

Thank you to the TREKK Editorial Committee, Editor Dr. Sarah Reid (CHEO), and CHRIM Parent and Youth Advisory Committee who provided editorial support and expertise in the development of this resource. Thank you as well to Mateja Carevic, TREKK Project Coordinator (University of Manitoba) who coordinated the development process.

To see our resource development process please visit our website here.

Key References

Evidence Depository

For a complete list of the evidence that informed the creation of the Cannabis Intoxication Bottom Line Recommendations see the Evidence Repository here.

Disclaimer

The purpose of this document is to provide healthcare professionals with key facts and recommendations for the diagnosis and treatment of community acquired pneumonia in children in the emergency department. The TREKK Network is not liable for any damages, claims, liabilities, costs or obligations arising from the use of this document including loss or damages arising from any claims made by a third party. THIS DOCUMENT IS SUBJECT TO FULL DISCLAIMER HERE: trekk.ca/terms-of-use