Abstract
Hereditary angioedema (HAE) is a rare genetic disease that results from deficiency or dysfunction of C1 inhibitor (C1-INH). This disease is characterized by sudden attacks of angioedema. When edema occurs in the pharynx or larynx, it can lead to serious airway compromise, including death. Physical and/or psychological stress can trigger an attack. Dental treatment, including tooth extraction, is also a recognized trigger. We report a case of a 20-year-old male with HAE who required impacted third molar extractions. C1-INH concentrate was administered 1 hour before surgery, which was completed under deep intravenous sedation. This report describes the anesthetic management of a patient with HAE and reviews treatment options and concerns.
Original language | English |
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Pages (from-to) | 30-32 |
Number of pages | 3 |
Journal | Anesthesia progress |
Volume | 66 |
Issue number | 1 |
DOIs | |
Publication status | Published - Mar 1 2019 |
All Science Journal Classification (ASJC) codes
- Anesthesiology and Pain Medicine