Angioedema

Background

• Angioedema is paroxysmal, nondemarcated swelling of dermal or submucosal layers of skin or mucosa
  • Swelling is asymmetric, nonpitting, and nonpruritic
• 4 etiologies:
  • 1. Congenital or acquired loss of C1 esterase inhibitor
  • 2. IgE–mediated type I allergic reaction
  • 3. ACEI adverse reaction
  • 4. Idiopathic

Hereditary Angioedema

Background

• Due to C1 esterase inhibitor deficiency
  • Leads to unregulated activity of vasoactive mediators associated with complement pathway
  • Autosomal dominant

Diagnosis

• Suspect in patients with history of recurrent peripheral angioedema and abdominal pain
  • 75% experience onset of symptoms before age 15yr
• Decreased levels of C1 and C4 esterase inhibitors confirms diagnosis

Treatment

• Epinephrine IM can produce some improvement in early acute attacks
• C1 esterase inhibitor (if available)
• FFP
  • Replaces the missing inhibitor protein
  • Not recommended in life-threatening laryngeal edema (some pts may become more edematous)
    • Instead, pt should undergo fiberoptic intubation w/ preparation for surgical airway

ACE Inhibitor-induced Angioedema

Background

• Incidence is highest within the first month; however, may occur at anytime
• Incidence is 0.1-2.2% (more common in blacks)

Treatment

• Epinephrine 0.3mg IM q15-20min prn
• Diphenhydramine 50mg IV OR cetirizine 10mg PO
• Methylprednisolone 125mg IV
• Awake fiberoptic intubation

Disposition

• Consider discharge after obs if there is no airway edema and pt improves

See Also

• Anaphylaxis
• Tongue pathology

Source

Tintinalli