Bottom Line Recommendations: Summary of Pediatric Emergency Care Information for Healthcare Providers
Anaphylaxis
Developed by:Dr. Waleed Alqurashi (CHEO); Dr. Anne Ellis (Queen's University)
Last Updated
Jul 2025
Topic
Anaphylaxis
Summary
Anaphylaxis is a serious systemic hypersensitivity reaction that is rapid in onset and can be fatal.1 The highest incidence of anaphylaxis is in children and youth. The three principal triggers of anaphylaxis are foods, insect stings, and drugs. In Canada, there is an Emergency Department (ED) visit for food allergy approximately every 10 minutes,2 and up to 80% of anaphylactic reactions in children are triggered by foods such as peanuts, tree nuts, and milk.3
Refer to TREKK’s Anaphylaxis treatment algorithm for emergent management and drug dosing.
Establishing the diagnosis of anaphylaxis1
HISTORY & PHYSICAL EXAMINATION
- Any acute onset of hypotension/signs of shock, or signs of upper or lower airway obstruction after exposure to known or highly probable allergen, even if typical skin features are not present; OR
- Any acute onset illness with typical skin features (diffuse urticarial rash or erythema/flushing, and/or angioedema), AND at least ONE of the following: respiratory signs, cardiovascular signs, or severe gastrointestinal symptoms (e.g., repetitive vomiting, persistent abdominal pain).
Risk factors for severe anaphylaxis
These factors may increase the risk for severe anaphylaxis and influence duration of monitoring in ED post-stabilization:4
- Concurrent medications: NSAIDs, ACE-inhibitors, β-blockers.
- Comorbidities: Chronic respiratory conditions (uncontrolled asthma), cardiovascular diseases, psychiatric conditions, mast cell disorders.
- Cofactors: Onset of anaphylaxis during physical exercise, menstruation, acute illness or infection, alcohol intake.
Management of anaphylaxis
IMMEDIATE INTERVENTIONS
- Remove allergic trigger, if applicable.
- Place patient in supine position (unless precluded by vomiting or respiratory distress). Trendelenburg position is not recommended. Do NOT allow patient to stand or walk.
- Administer Intramuscular (IM) Epinephrine into outer mid-thigh (0.01 mg/kg, MIN 0.1 mg/dose, MAX 0.5 mg/dose).
- Use epinephrine auto-injector or epinephrine 1 mg/mL injection.
- Assess and monitor airway, breathing, circulation, and mental status.
- Prepare age-appropriate airway equipment.
- Provide O2 (10-15 L) by non-rebreather mask if signs of shock or respiratory distress.
- Use basic airway management maneuvers to maximize oxygen delivery and call for help/assemble team. Upper airway obstruction should be managed by the most skilled clinician available.
- Proceed with intubation if persistent stridor, signs of significant upper airway obstruction, and/or respiratory arrest.
- If the child is hypotensive or signs of shock are not responding after 2 doses of IM epinephrine, establish vascular access and PUSH NS or Ringer’s Lactate 20 mL/kg IV over 5-10 minutes, repeat x 2 if necessary.
FIRST LINE THERAPY: EPINEPHRINE
- Immediate IM epinephrine administration is the most important therapy that prevents progression to refractory and biphasic anaphylaxis. There are NO absolute contraindications for IM epinephrine in anaphylaxis.
- AVOID common medication administration errors:
- Use the epinephrine 1 mg/mL preparation for IM dosing in anaphylaxis. Do NOT use epinephrine 0.1 mg/mL for this indication.
- Do NOT give epinephrine as an IV/IO bolus dose for anaphylaxis as this may result in serious cardiac adverse events.
- Start epinephrine IV infusion if anaphylactic shock persists after THREE doses of IM epinephrine and fluid resuscitation – continue to give epinephrine IM every 10 min while preparing epinephrine infusion (Refer to TREKK Anaphylaxis Order Set for dosing).
ADJUNCT THERAPIES
NEVER DELAY IM EPINEPHRINE TO GIVE ADJUNCT THERAPIES. ADJUNCT THERAPIES NEVER REPLACE THE NEED FOR IM EPINEPHRINE.
ANTIHISTAMINES
- Use second-generation H1 antihistamines (e.g., cetirizine PO or rupatadine PO) to relieve cutaneous symptoms. They may reduce the progression to severe anaphylaxis when used with IM epinephrine. 3
- Do NOT use first-generation H1 antihistamines (e.g., diphenhydramine PO/IV/IM or hydroxyzine PO) due to risk of drowsiness/ somnolence, dizziness, orthostatic hypotension (that may mimic anaphylaxis) and fatal cardiac arrhythmias.5
INHALED EPINEPHRINE
- Administer if stridor or signs of upper airway obstruction persist after IM epinephrine.
- Prepare for intubation and contact Pediatric Referral Centre if symptoms persist after two doses.
INHALED BRONCHODILATOR
- Give inhaled salbutamol (Ventolin®) for wheezing or persistent signs of lower airway obstruction.
CORTICOSTEROIDS
Emergency department monitoring
- Up to 15% of children are at risk of biphasic reactions, which typically occur within 3-24 hours of initial anaphylaxis.
- The following risk factors increase the risk of biphasic reaction5,7:
- Anaphylaxis due to drug or unknown trigger
- Severe anaphylaxis defined as any of the following: cardiac signs (hypotension, wide pulse pressure), respiratory signs (hypoxia, persistent wheeze, or respiratory distress), or anaphylaxis requiring more than one dose of IM epinephrine
- Delayed epinephrine administration (i.e. more than 60 minutes from the onset of the reaction)
- ED monitoring and disposition should be individualized according to the presence of risk factors for severe anaphylaxis (see above) and biphasic reactions. The following criteria can be used as a general guide:
Criteria | Disposition Plan |
|---|---|
Mild anaphylaxis that resolved after one dose of timely epinephrine and remained asymptomatic for at least 1 hour after epinephrine administration | Monitor for 2 hours from the onset of the reaction |
Any of the following: required two doses of epinephrine to treat the reaction, presented late in evening, lives alone or far from emergency care, has no immediate access to epinephrine auto-injector, history of severe or currently uncontrolled asthma | Monitor for 6 hours from the onset of the reaction or overnight |
Any of the following: severe anaphylaxis (e.g., anaphylactic shock, severe respiratory distress), required > 2 doses of IM epinephrine, drug-induced anaphylaxis | Admit to hospital for at least 24 hours |
STEPS FOR A SAFE DISCHARGE PLAN
- Refer to an allergy specialist. Infants less than 1 year of age with potential food allergies should be referred URGENTLY.
- Provide anaphylaxis emergency plan and counseling:
- Provide the Canadian Anaphylaxis Action Plan for Kids (Kids’ CAP)8
- Counsel patient/caregiver on: recognition of symptoms and signs of anaphylaxis, management steps, and prevention strategies. Use the Kids’ CAP teaching video for these discharge instructions.
- Discharge prescription:
- Provide an epinephrine auto-injector prescription and instruct patient/caregiver to fill the prescription immediately upon discharge.
- epinephrine auto-injectors should be prescribed for any patient with, or at risk of, anaphylaxis
- For children < 15 kg, prescribe the 0.15 mg epinephrine auto-injector9 (given the lack of a suitable alternative in Canada)
- Demonstrate the proper use of epinephrine auto-injector using a trainer device to allow patient/caregiver to practice.
- A prescription for two epinephrine auto-injectors should be considered for patients with ANY of the following:
- Co-existing mast cell disease, or asthma and a food allergy; OR
- Lack of rapid access to medical care; OR
- History of severe anaphylaxis or previous requirement of more than 1 dose of epinephrine; OR
- Any patient/caregiver who requests two epinephrine auto-injectors
- Second generation H1 antihistamine treatment (e.g., cetirizine or rupatadine) is rarely needed after discharge, but may be recommended/prescribed for ongoing, mild urticaria – it should never be used in place of epinephrine auto- injector for anaphylaxis.
- Never recommend/prescribe a first-generation H1 antihistamine (e.g., diphenhydramine and hydroxyzine).
- Provide an epinephrine auto-injector prescription and instruct patient/caregiver to fill the prescription immediately upon discharge.
Development Team
Thank you to the following content experts who led the development of the Anaphylaxis Resources:
Waleed Alqurashi, MD, MSc, FAAP, FRCPC, Assistant Professor, University of Ottawa;
Emergency Medicine Pediatrician, Children’s Hospital of Eastern Ontario (CHEO);
Scientist, CHEO Research Institute.
Anne Ellis, MD, MSc, FRCP(C), FAAAAI, Director, Allergy Research Unit/Environmental Exposure Unit, Kingston Health Sciences Centre, KGH site;
Professor, Department of Medicine, School of Medicine, and Department of Biomedical and Molecular Sciences, Queen’s University;
Chair, Allergy & Immunology, and James H. Day Chair in Allergic Diseases and Allergy Research, Faculty of Health Sciences, Queen’s University.
Thank you to the TREKK Editorial Committee, editor Dr. Sarah Reid (CHEO) 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.
Key References
- Alqurashi W, Stiell I, Chan K, et al. Epidemiology and clinical predictors of biphasic reactions in children with anaphylaxis. Ann Allergy Asthma Immunol. 2015;115(3):217-223.e2. doi:10.1016/j.anai.2015.06.018
- Food Allergy Canada, Canadian Society of Allergy and Clinical Immunology. National Food Allergy Action Plan. Published July 2019.
- Gabrielli S, Clarke A, Morris J, et al. Evaluation of prehospital management in a Canadian emergency department anaphylaxis cohort. J Allergy Clin Immunol Pract. 2019;7(7):2232-2238.e3. doi:10.1016/j.jaip.2019.04.018
- Worm M, Francuzik W, Renaudin J-M, et al. Factors increasing the risk for a severe reaction in anaphylaxis: an analysis of data from the European Anaphylaxis Registry. Allergy. 2018;73(6):1322-1330. doi:10.1111/all.13380
- Alqurashi W, Ellis AK. Do corticosteroids prevent biphasic anaphylaxis?. J Allergy Clin Immunol Pract. 2017;5(5):1194-1205. doi:10.1016/j.jaip.2017.05.022
- Cardona V, Ansotegui IJ, Ebisawa M, El-Gamal Y, Fernandez Rivas M, Fineman S, et al. World allergy organization anaphylaxis guidance 2020. World Allergy Organ J. 2020;13(10):100472. doi:10.1016/j.waojou.2020.100472
- Shaker MS, Wallace DV, Golden DBK, et al. Anaphylaxis – a 2020 practice parameter update, systematic review, and grading of recommendations, assessment, development and evaluation (GRADE) analysis. J Allergy Clin Immunol. 2020;145(4):1082-1123. doi:10.1016/j.jaci.2020.01.017
- Alqurashi W, Awadia A, Pouliot A, et al. The Canadian anaphylaxis action plan for kids: development and validation. Patient Educ Couns. 2020;103(1):227-233. doi:10.1016/j.pec.2019.07.028
- Halbrich M, Mack DP, Carr S, Watson W, Kim H. CSACI position statement: epinephrine auto-injectors and children <15 kg. Allergy Asthma Clin Immunol. 2015;11(1):20. doi:10.1186/s13223-015-0090-8
For a complete list of the evidence that informed the creation of the Eating Disorders Bottom Line Recommendations, see the Evidence Repository.
To see our resource development process please visit our website here.
Evidence Repository
For a complete list of the evidence that informed the creation of the Anaphylaxis Bottom Line Recommendations and Algorithm 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 anaphylaxis 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