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Anaphylaxis — Causes, Symptoms, Emergency Treatment & Prevention Guide — Symptoms, Causes & Treatment | MyMedicPlus

Updated: 2026-07-06
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Quick Facts

Type
Acute life-threatening systemic allergic reaction
Specialist
Allergist / Immunologist / Emergency Physician
Key Treatment
Intramuscular adrenaline (epinephrine) 0.3–0.5 mg — immediate first response
Prevalence
Lifetime prevalence 0.5–2%; incidence 50–112 per 100,000 person-years

Overview: Anaphylaxis

Anaphylaxis is a severe, potentially fatal systemic allergic reaction involving multiple organ systems simultaneously. It occurs when the immune system is re-exposed to a trigger allergen, causing massive mast cell and basophil degranulation with release of histamine, tryptase, leukotrienes, and prostaglandins. This cascade produces rapid vasodilation, bronchospasm, and mucosal oedema. Without immediate treatment with intramuscular adrenaline, anaphylaxis can be fatal within minutes. Globally, anaphylaxis affects approximately 0.5–2% of people over a lifetime, with incidence rising over recent decades. Approximately 1–3 people per million die from anaphylaxis annually, though the true mortality rate is likely under-reported due to misclassification. The UK Anaphylaxis Register reports approximately 20 deaths per year from anaphylaxis in the UK alone, the majority from food allergy. Anaphylaxis is more common in atopic individuals and those with prior anaphylactic reactions, though it can occur in anyone without prior history of allergy, emphasising the importance of broad public awareness and the wide availability of adrenaline auto-injectors in public settings.

Causes & Risk Factors

The most common triggers are foods (peanuts, tree nuts, shellfish, fish, milk, eggs, wheat — accounting for 33–56% of cases), insect venom (bee and wasp stings — particularly in adults), medications (penicillin and beta-lactam antibiotics, NSAIDs, radiocontrast agents, neuromuscular blocking agents, chemotherapy), and latex. Exercise-induced anaphylaxis can occur with or without food cofactors. Risk factors for severe or fatal anaphylaxis include prior anaphylaxis, asthma or chronic lung disease, cardiovascular disease, mastocytosis (elevated baseline tryptase), and beta-blocker or ACE inhibitor use — beta-blockers antagonize the effects of adrenaline, making treatment more difficult. Idiopathic anaphylaxis (no identifiable cause despite full investigation) accounts for 20–30% of adult cases.

Symptoms & Signs

Anaphylaxis typically develops within minutes of allergen exposure. Skin and mucosal symptoms (present in 80–90% of cases): urticaria (hives), angioedema, flushing, pruritus. Respiratory symptoms: bronchospasm, wheeze, stridor, hoarse voice, dyspnoea — laryngeal oedema causing stridor is an emergency sign. Cardiovascular symptoms: hypotension, tachycardia, dizziness, collapse, loss of consciousness — cardiovascular collapse (anaphylactic shock). Gastrointestinal symptoms: nausea, vomiting, abdominal cramps, diarrhoea. Neurological: confusion, anxiety, sense of impending doom. Anaphylaxis can occur without skin symptoms — isolated cardiovascular or respiratory collapse — requiring high clinical suspicion especially in medication or anaesthesia-related reactions. Symptoms can progress from mild skin reactions to life-threatening cardiovascular and respiratory collapse within minutes. Any two or more organ system involvement following allergen exposure should be treated as anaphylaxis without delay, and adrenaline administered immediately.

How It Is Diagnosed

Anaphylaxis is a clinical diagnosis based on the characteristic rapid-onset multi-system reaction following allergen exposure. The Brighton Collaboration and WAO clinical criteria require involvement of skin/mucosa plus at least one of: respiratory compromise, hypotension, or end-organ dysfunction. Serum tryptase drawn at 1–3 hours after reaction onset — elevated levels (above 20 mcg/L or above 1.2 x baseline + 2) support the diagnosis. Tryptase returns to baseline within 6–8 hours, so timing of blood draw is critical. After recovery (4–6 weeks), allergy investigation includes skin prick testing and specific IgE (radioallergosorbent tests — RAST) to identify the causative allergen. Allergy testing must NEVER be performed during or immediately after anaphylaxis. Baseline tryptase should be measured in all patients to screen for underlying mastocytosis.

Treatment Options

Intramuscular adrenaline (epinephrine) 0.3–0.5 mg (or 0.15 mg for children under 25 kg) into the outer mid-thigh is the definitive first-line treatment and must be given immediately — any delay worsens prognosis. Call emergency services immediately (999/112/911). Position: supine with legs elevated unless respiratory distress requires sitting upright; avoid standing the patient up suddenly. Supplemental high-flow oxygen, IV crystalloid fluids (1–2 L bolus for hypotension). Antihistamines (chlorphenamine H1 blocker + ranitidine H2 blocker) and corticosteroids (hydrocortisone 200 mg IV or prednisolone 40 mg oral) are useful adjuncts but are NOT first-line and must not delay adrenaline administration. Observe for 4–12 hours post-reaction to monitor for biphasic anaphylaxis (recurrence in 5–20% at 1–72 hours). Discharge with two prescribed adrenaline auto-injectors (EpiPen or Jext) plus a written emergency action plan.

Complications If Untreated or Inadequately Managed

Anaphylaxis that is untreated or inadequately managed with delayed epinephrine carries a high risk of fatal outcome. Laryngeal oedema causing complete airway obstruction is the most common cause of death in fatal anaphylaxis, followed by cardiovascular collapse. Even non-fatal anaphylaxis without epinephrine can cause prolonged hypoxia leading to hypoxic brain injury, myocardial infarction (demand ischaemia from severe hypotension), and acute kidney injury. Biphasic anaphylaxis occurs in 5-20% of patients — a second, sometimes more severe wave of symptoms 4-72 hours after the initial reaction without re-exposure — underscoring the importance of at least 4-6 hours of hospital observation after every anaphylactic episode. Patients who carry but do not use their epinephrine auto-injector promptly face significantly worse outcomes. Psychologically, anaphylaxis survivors frequently develop food anxiety, social avoidance, and significant reduction in quality of life — up to 50% experience anxiety disorders. Without formal allergy investigation and immunotherapy where available (for venom anaphylaxis), the risk of recurrent potentially fatal reactions persists.

Prevention & Lifestyle Management

Strict avoidance of identified allergen triggers is the cornerstone of anaphylaxis prevention. Always carry two adrenaline auto-injectors at all times and know how to use them. Wear a medical alert bracelet or necklace identifying known allergens. For food allergy: read all food labels meticulously, declare allergy to restaurants and catering staff, be vigilant about cross-contamination. For insect venom allergy: venom immunotherapy (VIT) for bee or wasp sting allergy is highly effective — reducing the risk of future anaphylaxis by over 95% — and is recommended for adults with venom allergy. Develop and rehearse a personalised emergency action plan with family, carers, schools, and workplaces. Seek annual review with an allergist to assess ongoing risk and review immunotherapy suitability.

When to Seek Medical Help

Anaphylaxis is a medical emergency — call 999/112/911 immediately and administer adrenaline without delay if symptoms suggest anaphylaxis: sudden urticaria with throat tightening, wheeze, or collapse following allergen exposure. Use the EpiPen immediately and call for emergency help even if symptoms initially appear mild. Always attend emergency services after using an EpiPen — effects last only 15–20 minutes and a second dose may be needed. After any anaphylactic episode, seek urgent referral to an allergy clinic for full allergen investigation. Consult your GP or allergist before travelling, for reviewing your emergency plan, when changing medications, or if venom immunotherapy is being considered. Do not wait for a second reaction — act on the first episode.

Frequently Asked Questions

Remove the EpiPen from its carrier and pull off the blue safety cap. Grip firmly in your dominant hand and press the orange tip firmly against the outer mid-thigh (can be used through clothing) until a click is heard. Hold in place for 10 seconds, then remove and massage the injection site. Call 999/911 immediately, even after using the EpiPen — effects last only 15–20 minutes and a second dose may be needed after 5–15 minutes if symptoms do not improve. Always go to hospital even if symptoms resolve rapidly.
Biphasic anaphylaxis is a recurrence of anaphylactic symptoms 1–72 hours after apparent recovery, without re-exposure to the trigger allergen. It occurs in approximately 5–20% of anaphylaxis cases. Biphasic reactions can be as severe as or more severe than the initial reaction. This is why all patients who experience anaphylaxis should be observed in hospital for at least 4–12 hours after treatment, even if initial recovery appears complete. Systemic corticosteroids are given during the acute episode to reduce the risk of biphasic reactions.
The most common food triggers worldwide are peanuts, tree nuts (cashew, walnut, almond, pistachio), shellfish (shrimp, crab, lobster), fish, cow's milk, hen's eggs, and wheat — the 'Big 9' allergens required to be declared on food labels in most countries. Sesame is also a significant trigger. Peanut and tree nut allergies are most likely to cause severe or fatal anaphylaxis and are least likely to be outgrown in childhood. Any food that has caused a previous significant reaction must be strictly avoided, and accidental exposure protocols should be reviewed with an allergist.
Yes — anaphylaxis can occur on first or subsequent exposure, and the trigger may not always be identified before the event. In 20–30% of adults with anaphylaxis, no cause is found despite full investigation (idiopathic anaphylaxis). Even after idiopathic anaphylaxis, patients require adrenaline auto-injectors, allergy specialist referral, and investigation for underlying conditions such as mastocytosis, which significantly increases anaphylaxis risk. A baseline serum tryptase is an important first test to screen for mastocytosis in all patients after their first anaphylactic episode.
Yes — venom immunotherapy (VIT) is highly effective, reducing the risk of a future systemic reaction to bee or wasp stings from approximately 50–65% to less than 5%. It involves a course of desensitising injections of gradually increasing doses of purified insect venom over 3–5 years. VIT is recommended for adults who have had anaphylaxis to insect stings and confirmed specific IgE or skin prick test sensitisation. It does not eliminate the need to carry an EpiPen during treatment. Most patients achieve long-term protection even after stopping treatment.

References

  1. World Allergy Organization (WAO) — Anaphylaxis Guidance, 2020
  2. NICE Guideline CG134 — Anaphylaxis: Assessment and Referral After Emergency Treatment, 2020
  3. European Academy of Allergy and Clinical Immunology (EAACI) — Anaphylaxis Guidelines, 2021
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Last updated: 2026-07-06

Important: This information is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider for diagnosis and treatment.

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