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.