Aortic dissection is a serious life-threatening condition and is one of the most common potentially deadly conditions of the aorta. [1][2][3][4][5] In the United States, nearly 10,000 people are affected by this condition each year. 3,6 Aortic dissection is a tear in the aorta caused by a weakened wall in which the intima, or inner wall, separates from the media (middle wall layer). 3,7-12 The separation in the wall causes the formation of two separate lumens, a true lumen and a false lumen, with blood flow penetrating the intima into the false lumen. 5,8,9,11 Once the intima is penetrated, the dissection may propagate toward the iliac arteries (an antegrade dissection) or back toward the heart (a retrograde dissection). In either case, blood may pool in the false lumen, constricting the true lumen and causing a low volume of blood flow to other parts of the body, creating a fatal compromise of blood flow to essential organs at or downstream from the constriction. 3,8,9 The serious complications secondary to an aortic dissection may include stroke, heart attack, aortic insufficiency, congestive heart failure, cardiac tamponade, aortic rupture, renal and/or mesenteric ischemia, and hemorrhage. 5,7,9,10,[13][14][15] Dissection typically occurs in older patients. 1,7,13,16 Nearly 75% of patients are between the ages of 40 and 70, with the majority being 50 to 65 years old. 1,3,6,7,9 Men are more likely to have an aortic dissection compared with women and blacks more commonly than whites. 3,4,7,13,[16][17][18][19] The cause of aortic dissection is unknown, but several risk factors precipitate its occurrence in individuals. 7 Some of the most common risk factors are chronic hypertension, atherosclerosis, and a blunt-force trauma to the chest or abdomen. 3,7,9,16,17,20 Other risk factors may include a bicuspid aortic valve, prior heart surgery, narrowing of the aorta, connective tissue disorders, or genetic disorders such as Marfan syndrome. [1][2][3]7,9,13,16,20 There are two classification systems for aortic dissections. The Stanford classification divides dissections into type A and type B based on their location. 2,3,5,9,10,15,17 Type A dissections originate in the ascending aorta and may extend through the aortic arch to involve the descending aorta as well; type B dissections occur distal to the brachiocephalic (innominate) artery. 8,14,17,21 The DeBakey classification system helps distinguish dissections requiring surgical intervention from those not needing surgery. 1,2,5,8,[22][23][24] Type I dissections originate in the ascending aorta but propagate to involve both the ascending and descending aorta; these constitute approximately 60% of cases, tend to occur in younger patients, and are the most lethal of all dissection types. Type II dissections are the least common, making up approximately 10% to 15% of cases, and only involve the ascending aorta; type III dissections constitute approximately 25% to 30% of cases and involve only the descending aorta. 1,8,22 Stanford Type A dissections include both the DeBak...