Spontaneous coronary artery dissection: An often unrecognized cause of acute coronary syndrome
ABSTRACT
Spontaneous coronary artery dissection (SCAD), an intramural hemorrhage leading to a separation of the layers of the coronary artery wall, is traditionally considered a rare condition associated mainly with pregnancy but is likely underdiagnosed in other settings. Its recognition by coronary angiography is key. Medical management is usually indicated, except in certain circumstances in which coronary artery bypass grafting or percutaneous coronary intervention should be considered.
KEY POINTS
- SCAD often presents with symptoms of acute coronary syndrome but can be asymptomatic or cause sudden death.
- Management is generally conservative, but a left main or severe proximal 2-vessel dissection, hemodynamic instability, or ongoing ischemic symptoms may warrant revascularization.
- All patients with SCAD should be screened for other vascular problems, especially fibromuscular dysplasia.
- Long-term aspirin therapy and 1 year of clopidogrel are recommended after an episode of SCAD.
A 12-lead electrocardiogram (Figure 1) showed ST-segment elevation of more than 2 mm in leads V2, V3, V4, and V5, with no reciprocal changes.
Based on the classic angiographic appearance and the absence of atherosclerotic disease in other coronary arteries, type 2 spontaneous coronary artery dissection (SCAD) was diagnosed.
CORONARY ARTERY WALL SEPARATION
SCAD is defined as a nontraumatic, noniatrogenic intramural hemorrhage leading to separation of the coronary arterial wall and the formation of a false lumen. The separation can occur between any of the coronary artery wall layers and may or may not involve an intimal tear. The bleeding may result in an intramural hematoma and possible narrowing of the arterial lumen. Depending on the severity of narrowing, blood supply to the myocardium could be compromised, resulting in symptoms of ischemia.1
SCAD usually involves a single coronary artery, although multiple coronary artery involvement has been reported.2
CASE CONTINUED: MANAGEMENT
The patient recovered completely and was discharged home with plans to return for outpatient imaging for fibromuscular dysplasia.