Anaphylaxis Immediate Action Checklist (When Injecting Now)
Use when you are sure or sufficiently sure to treat for anaphylaxis. Work the list in order; do not delay IM adrenaline.
Immediate (0–10 minutes)
- Shout for help and call 999/112; state “suspected anaphylaxis”.
- Do not allow standing/walking/sitting up suddenly.
- Position now (tick one):
- Lay flat with legs raised (hypotension/shock).
- Semi‑recumbent with legs raised (breathing difficulty).
- Recovery position if unconscious with normal breathing.
- Left lateral if pregnant.
- Remove visible trigger if safe (stop infusion/remove stinger). Do not induce vomiting.
- Administer IM adrenaline now (1 mg/ml, 1:1000) into anterolateral mid‑thigh (through clothing if needed):
- Adult/adolescent (>12 y): 0.5 mg IM via syringe/needle (preferred in healthcare setting).
- If using AAI in adults: 0.3 mg (device standard dose).
- Child dosing:
- <6 months: 0.1 mg (0.1–0.15 ml).
- 7.5–26 kg (≈6 m–6 y): 0.15 mg.
- >26 kg (≈6–12 y): 0.3 mg.
- Start high‑flow oxygen (aim SpO₂ ≥ 94%).
- Attach monitoring: SpO₂, BP, ECG; record time and dose of adrenaline.
- Establish IV access.
- If wheeze: salbutamol via MDI + spacer or oxygen nebuliser ± ipratropium.
- Consider nebulised adrenaline for laryngeal oedema/stridor (adjunct only).
- If hypotensive: crystalloid bolus (not dextrose): adult 500 ml; child 10 ml/kg.
- Reassess at 5 minutes; repeat IM adrenaline if no improvement (repeat q5 min as needed).
Ongoing (next 10–60 minutes)
- Continue A/B/C reassessment; document vitals and responses.
- Arrange urgent transfer to hospital; continuous monitoring during transfer.
- If on β‑blocker and poor response, consider IM/IV glucagon (usually hospital protocol).
- Treat refractoriness (no improvement after ≥2 IM doses 5 min apart) with hospital IV adrenaline infusion pathway.
- Cardiorespiratory arrest: start high‑quality CPR; do not interrupt CPR to give IM adrenaline (IM absorption unreliable in arrest).
Avoid / Do Not
- Do not give IV adrenaline in primary care.
- Do not give chlorphenamine acutely (sedation confounds assessment); antihistamines only for skin itch once stable.
- Do not give routine oral prednisolone to prevent biphasic reactions (no benefit; potential harms in children).
- Do not allow the patient to stand or walk during an acute reaction.
Handover & Early Post‑Stabilisation Tasks
- Handover times/doses of adrenaline, response, triggers, co‑factors, vitals, treatments given, devices used (give used AAI to crew).
- Observe in hospital 6–12 h (12–24 h if circulatory collapse/severe features); warn about biphasic reactions (~5%).
- ED tryptase sampling requested if feasible: 30 min–2 h after onset, plus baseline at ~24 h.
- On discharge (hospital): supply two AAIs, written plan, and training; advise always carrying both; storage 20–25°C; avoid refrigeration.
Quick Device Notes (UK)
- EpiPen: 150 mcg (<15 kg); 300 mcg (≥15 kg; standard for >26 kg). Shelf ≈ 18 months; can use just‑expired in emergency.
- Jext: 150 mcg (<15 kg); 300 mcg (>31 kg; may be appropriate at 15–30 kg). Shelf ≈ 22 months; can use just‑expired in emergency.
- Emerade: 150/300/500 mcg — withdrawn 2023 (misfiring/faulty needles).
- Neffy (nasal adrenaline): approved EU/US; not yet available in UK; ≥30 kg.