Aortic Dissection: A High-Yield USMLE Review
Aortic dissection is a life-threatening vascular emergency in which an intimal tear allows blood to enter the media and create a false lumen. It is a cannot-miss diagnosis in any patient with acute chest pain and is a critical mimic of ACS on the exam. Recognizing it—and distinguishing Stanford Type A from Type B—determines both workup and whether the patient goes to surgery or medical management.
Pathophysiology
An intimal tear allows blood to enter the aortic media, creating a false lumen that propagates along the vessel. As the dissection extends it can involve branch vessels and produce the downstream complications: extension into the coronary ostia (particularly the right coronary artery near where Type A dissections begin) causes true myocardial infarction, extension to the aortic root causes acute aortic regurgitation, and involvement of the subclavian arteries produces the inter-arm blood pressure differential. Because it is an acute process, there is no time for compensation, so complications like acute AR present as an immediate hemodynamic crisis.
Presentation
- Sudden, severe tearing or ripping chest pain classically radiating to the back (interscapular region)
- Blood pressure asymmetry between arms (>20 mmHg differential) and possible pulse deficit
- New diastolic murmur of aortic regurgitation when the dissection extends to the aortic root (acute AR)
- Syncope
- Widened mediastinum on chest imaging in a hypertensive patient
- Signs of downstream branch involvement—e.g., inferior ST elevation (II, III, aVF) from extension into the right coronary ostium causing true myocardial ischemia
Diagnosis
- CT angiography is the confirmatory test when any dissection feature is present—and must be obtained before any anticoagulation
- Clinical examination: check for BP differential in both arms, pulse deficit, and a new diastolic (aortic regurgitation) murmur
- Chest imaging may show a widened mediastinum in a hypertensive patient with tearing chest pain
- ECG may show ischemic changes (e.g., inferior ST elevation) if the dissection extends into a coronary ostium
Management
- Immediate heart rate and blood pressure control for all patients
- Stanford Type A (involves the ascending aorta): surgical emergency
- Stanford Type B (does not involve the ascending aorta, starting at or beyond the left subclavian): usually managed medically
- Always look for complications, since dissection can affect any aortic branch
High-yield
- Buzzword: sudden "tearing" or "ripping" chest pain radiating to the back
- BP asymmetry >20 mmHg between arms suggests aortic dissection
- Widened mediastinum in a hypertensive patient with tearing chest pain is aortic dissection until proven otherwise
- Stanford Type A = ascending aorta = surgery; Type B = does not involve ascending aorta = usually medical
- DeBakey: Type I (ascending + descending), Type II (ascending only), Type III (descending only)
- Aortic dissection is a classic cause of acute aortic regurgitation (an emergency)
- Associated with connective tissue disorders—Marfan, Loeys-Dietz, vascular Ehlers-Danlos—and aortic root dilation/hypertension
Pitfalls
- Never give thrombolytics for a suspected STEMI if aortic dissection is possible—it doesn't treat the dissection, promotes bleeding into the false lumen, and can cause rupture. Suspected dissection is a contraindication to fibrinolytics.
- Don't anchor on ACS: dissection into the coronary ostium causes true ischemia with real ECG changes and troponin elevation, mimicking inferior MI. Always ask whether dissection features are present before anticoagulating.
- Don't overlook the inter-arm BP differential, pulse deficit, or new diastolic murmur—these bedside findings point away from simple ACS toward dissection.
Don't just memorize Dissection of aorta — practice reasoning through it on branching cases where your decisions shape the patient.