| Literature DB >> 30883234 |
Rumiko Hosokawa1, Masanori Tsukamoto2, Saki Nagano2, Takeshi Yokoyama1.
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.Entities:
Keywords: Dental surgery; Hereditary angioedema; Intravenous sedation; Oral surgery
Mesh:
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Year: 2019 PMID: 30883234 PMCID: PMC6424165 DOI: 10.2344/anpr-65-04-01
Source DB: PubMed Journal: Anesth Prog ISSN: 0003-3006