last authored: July 2010, Caleb Zelenietz
last reviewed:
Anaphylaxis is a potentially fatal, systemic allergic reaction with an acute onset. Prompt recognition and treatment greatly reduces its mortality. As a clinician, anaphylaxis provides an excellent opportunity for life saving interventions.
A 12 year old boy presents to the emergency department with urticarial hives, mucous membrane swelling, stridor and diarrhea. The symptoms onset 30 minutes ago after ingestion of a peanut containing snack. The child has no previous history of allergic reactions.
There are many potential causes of anaphylaxis. Any allergen can evoke and anaphylactic response in a previously sensitized individual. Food allergens are the most common cause in children, while medication (especially penicillin) and insect stings (ie Hymenoptera) predominate in adults (Sampson et al, 1992). Fire ants, in the southern US and Central/South America, can cause anaphylaxis. Spider bites do NOT cause anaphylaxis.
Size of previous reaction does not relate to increased risk.
A major risk factor for anaphylaxis is a previous anaphylactic episode. Risk factors that increase the chance of death include asthma and cardiovascular disease. Other respiratory conditions such as chronic obstructive pulmonary disease also increase the risk of death.
Smelling food, kissing, etc does not cause anaphylaxis. The only rule is no sharing food.
Anaphylaxis is typically an immediate hypersensitivity reaction causing the release of immunoglobulin E (IgE). Autoimmune and non immune mechanisms can also be involved, although to a much lesser extent. The pathophysiology of the anaphylactic reaction does not alter management.
Anaphylaxis onsets in minutes to hours of an inciting event, though a biphasic presentation can result in the recurrence of symptoms 8-72 hours after initial resolution following treatment. Biphasic reactions occur in 1-20% of anaphylactic reactions. Occasionally protracted anaphylaxis can last for hours to days.
Anaphylaxis is highly likely when any one of the following 3 criteria are fulfilled: (Sampson et al, 2006)
1. Acute onset of an illness (minutes to several hours) with involvement of the skin, mucosal tissue, or both and at least one of the following:
2. Two or more of the following that occur rapidly after exposure to a likely allergen for that patient (minutes to several hours):
3. reduced BP after exposure to known allergen for that patient (minutes to several hours):
Approximately 90% of anaphylactic reactions involve the skin or mucosa. This can include
Respiratory symptoms occur in 70% of patients:
Gastrointestinal symptoms occur in 40% of patients:
Cardiovascular effects may be life-threatening, and include:
No laboratory investigations are indicated in the diagnosis and management of anaphylaxis. Respiratory and cardiovascular monitoring are an important part of anaphylaxis management.
The differential diagnosis of anaphylaxis includes many conditions, both benign and life threatening. The benign causes include:
Potentially fatal conditions include:
The treatment for anaphylaxis is to:
Epinephrine is the pharmacological intervention of choice. The preferred intramuscular dosing is 0.01 mg/kg (with a maximum dose of 0.5 mg) of a 1:1000 aqueous dilution of epinephrine should be given every 5 to 15 minutes as needed. The dosage range used is typically 0.3 mg to 0.5 mg in adults as well as children. The injection should be given in the mid-anterolateral thigh, the location of the vastus lateralis muscle.
In patients with severe hypotension or cardiac arrest intravenous infusion of epinephrine may be necessary. There is variability in the recommended dosing. In adults the dose is 2 - 10 micrograms per minute of a 1:10000 solution. In children 0.1 - 1 microgram per kilogram per minute of a 1:10000 solution is the preferred dose. In severe cases of cardiovascular collapse boluses as large as 0.1 - 0.5 mg have been suggested in the literature.
Patients who are on beta-blocker therapy may be resistant to epinephrine treatment and have refractory bradycardia and hypotension. In these patients glucagon must be administered as an adjuvant to epinephrine. In adults 1 - 2 mg intravenous bolus over 5 minutes is preferred. In children 20 - 30 micrograms per kilogram with a max dose of 1 mg is recommended. This initial bolus may be repeated as needed or an infusion of 5 - 15 micrograms per minute started.
There are no absolute contraindications to the use of epinephrine in the treatment of anaphylaxis. Patients with cardiac disease are at increased risk with the use of epinephrine, however the risks of delaying treatment outweigh the benefits.
Other medications to consider include:
If patients have a rapid response, they may be discharged after 8-10 hours. If, however, their symptoms are moderate or severe, they should be admitted.
Patients should be provided with an written anaphylaxis emergency plan and an Epi-pen on discharge. If etiology is unclear, allergy testing may be warranted. An allergy bracelet may be worn to advise others of the allergy.
Anaphylaxis can rapdily be fatal:
If promptly recognized and treated anaphylaxis has no long term sequela. A delay in the recognition and treatment can result in death. For this reason clinicians should begin treatment with epinephrine as soon as anaphylaxis is suspected. Patients who have had an anaphylactic reaction are at increased risk of having another episode if exposed to the same antigen.
Sampson HA, Mendelson LM, Rosen JP. Fatal and near-fatal anaphylactic reactions to food in children and adolescents. N Engl J Med. 1992;327:380-384.
Sheikh A, Shehata YA, Brown SGA, Simons FER. Adrenaline (epinephrine) for the treatment of anaphylaxis with and without shock. Cochrane Database of Systematic Reviews 2008, Issue 4. Art. No.: CD006312. DOI: 10.1002/14651858.CD006312.pub2.
Second symposium on the definition and management of anaphylaxis: summary report--second National Institute of Allergy and Infectious Disease/Food Allergy and Anaphylaxis Network symposium. Sampson HA, Muñoz-Furlong A, Campbell RL, Adkinson NF Jr, Bock SA, Branum A, Brown SG, Camargo CA Jr, Cydulka R, Galli SJ, Gidudu J, Gruchalla RS, Harlor AD Jr, Hepner DL, Lewis LM, Lieberman PL, Metcalfe DD, O'Connor R, Muraro A, Rudman A, Schmitt C, Scherrer D, Simons FE, Thomas S, Wood JP, Decker WW. Ann Emerg Med. 2006 Apr;47(4):373-80.
Lieberman, PL. Anaphylaxis. In: Middleton's Allergy Principles & Practice, Adkinson, NF Jr, Bochner, BS, Busse, WW, et al (Eds), 7th ed, St Louis 2009. p.1027.
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