Aortic dissection is a life-threatening condition characterized by a tear in the intimal layer of the aorta, allowing blood to enter the medial layer and create a false lumen. This separates the aortic wall layers, potentially compromising blood flow to vital organs and causing aortic rupture.
[KEY_CONCEPT] The Stanford Classification System is the most clinically relevant classification for aortic dissection:
DeBakey Classification provides additional anatomical detail:
- Type I: Originates in ascending aorta, extends to arch and beyond
- Type II: Limited to ascending aorta only
- Type III: Originates distal to left subclavian artery
[HIGH_YIELD] Type A dissections account for 60-70% of cases and carry higher mortality due to potential complications including:
- Aortic regurgitation
- Coronary artery compromise
- Cardiac tamponade
- Stroke from carotid involvement
Epidemiology:
- Incidence: 3-4 per 100,000 person-years
- Peak age: 60-80 years
- Male predominance (2-5:1)
- Risk factors: Hypertension (most important), connective tissue disorders (Marfan syndrome, Ehlers-Danlos), bicuspid aortic valve, coarctation of aorta, pregnancy, cocaine use
[CLINICAL_PEARL] Acute dissection occurs within 14 days of symptom onset, while chronic dissection is >14 days. The distinction is crucial as chronic Type B dissections may require different management approaches.