Abstract
Hereditary angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of edema affecting various body regions. Upper airway edema is a life-threatening condition that can progress to complete airway obstruction. Patients are particularly likely to encounter several triggering factors for HAE attacks during the preoperative period, necessitating specialized management. An 80-year-old woman with an established diagnosis of HAE was scheduled to undergo bipolar hip arthroplasty following a femoral neck fracture. During pre-surgical hospitalization, she developed pharyngeal discomfort and hoarseness, which were diagnosed as HAE attacks. Immediate treatment with an intravenous plasma-derived C1 inhibitor (pdC1-INH) resulted in rapid resolution of the symptoms. Surgery was performed as scheduled under spinal anesthesia with the administration of a pdC1-INH as short-term prophylaxis. No postoperative HAE attacks were observed. Surgical intervention in patients with HAE requires specialized care, and short-term prophylaxis may be useful in preventing HAE attacks.