Guides anaphylaxis recognition and epinephrine-first treatment protocol with observation timing. Use when managing allergic reactions, treating anaphylaxis, or planning post-anaphylaxis observation.
Guides anaphylaxis recognition using NIAID/FAAN diagnostic criteria, enforces epinephrine-first treatment protocol, and structures observation timing to capture biphasic reactions.
Anaphylaxis kills approximately 1,500 people annually in the United States, and the majority of deaths are associated with delayed epinephrine administration. Studies consistently show that patients who receive epinephrine within 5 minutes of symptom onset have near-zero mortality, while delays beyond 30 minutes dramatically increase the risk of fatal cardiovascular collapse. Despite this, epinephrine remains underused—only 50-60% of patients presenting with anaphylaxis to EDs receive epinephrine, often because clinicians fail to recognize anaphylaxis without classic urticaria or wait for "more severe" symptoms before acting.
The biphasic reaction rate of 5-20% means observation decisions directly impact patient safety. Premature discharge has resulted in deaths from recurrent anaphylaxis hours after initial resolution. This skill enforces the evidence-based standard: epinephrine is always first-line, antihistamines and steroids are adjuncts only, and observation duration is risk-stratified.
Anaphylaxis is highly likely when any ONE of these three criteria is met:
Criterion 1: Acute onset (minutes to hours) with skin/mucosal involvement (urticaria, angioedema, flushing, pruritus) PLUS at least one of:
Criterion 2: Two or more of the following occurring rapidly after exposure to a likely allergen:
Criterion 3: Reduced blood pressure after exposure to a known allergen for that patient:
Key point: Anaphylaxis can occur WITHOUT skin findings in 10-20% of cases. Do not wait for urticaria or angioedema to diagnose anaphylaxis if respiratory or cardiovascular symptoms are present.
| Population | IM Dose | Concentration | Injection Site |
|---|---|---|---|
| Adults (>30 kg) | 0.3-0.5 mg | 1:1,000 (1 mg/mL) | Anterolateral thigh (vastus lateralis) |
| Children (15-30 kg) | 0.15 mg (junior auto-injector equivalent) | 1:1,000 | Anterolateral thigh |
| Infants (<15 kg) | 0.01 mg/kg | 1:1,000 | Anterolateral thigh |
Repeat dosing: May repeat every 5-15 minutes if symptoms persist or recur. Most patients require 1-2 doses; refractory anaphylaxis may require 3+ doses or IV epinephrine infusion.
These are NOT substitutes for epinephrine and should never delay its administration:
| Medication | Dose | Purpose | Evidence Level |
|---|---|---|---|
| Diphenhydramine (H1) | 25-50 mg IV/IM | Pruritus and urticaria relief | Moderate—symptom control only |
| Ranitidine/Famotidine (H2) | 20 mg IV | Combined H1+H2 may improve urticaria resolution | Low |
| Methylprednisolone | 125 mg IV | Theoretically prevents biphasic reaction | Very low—no RCT evidence of benefit |
| Albuterol | 2.5-5 mg nebulized | Bronchospasm not responding to epinephrine | Moderate for isolated bronchospasm |
Steroids: Despite widespread use, no randomized controlled trial has demonstrated that corticosteroids prevent biphasic anaphylaxis. However, they remain standard practice in most guidelines pending definitive evidence. Document as "administered per current practice guidelines, evidence pending."
Angioedema-related airway compromise is the most common cause of anaphylaxis death:
| Risk Category | Minimum Observation | Disposition |
|---|---|---|
| Mild (single system, rapid response to single IM epi) | 4-6 hours | Discharge with epinephrine auto-injector |
| Moderate (multi-system, responded to 1-2 doses epi) | 8-12 hours | Observation unit; discharge if stable |
| Severe (required IV epi, intubation, or ICU-level care) | 24+ hours | ICU admission |
| Refractory (ongoing vasopressor or ventilator support) | Until resolved + 24 hours | ICU |
| # | Criterion | Pass/Fail |
|---|---|---|
| 1 | Anaphylaxis diagnosed using NIAID/FAAN criteria with criterion number documented | |
| 2 | Epinephrine IM administered as first medication | |
| 3 | Time from recognition to first epinephrine documented | |
| 4 | Epinephrine dose appropriate for weight | |
| 5 | Repeat epinephrine documented with timing intervals | |
| 6 | IV access established and fluid resuscitation given for hypotension | |
| 7 | Airway assessment and management plan documented | |
| 8 | Observation duration meets minimum for severity category | |
| 9 | Biphasic reaction risk factors assessed and documented | |
| 10 | Epinephrine auto-injector prescribed at discharge (two devices) | |
| 11 | Allergist referral placed with timeframe | |
| 12 | Trigger identified or documented as unknown with avoidance counseling | |
| 13 | Beta-blocker/ACE inhibitor use assessed and addressed | |
| 14 | Serum tryptase drawn within window if indicated |