Etiology
Ascending aortic dissection is associated with hypertension, cystic medial necrosis, Marfan and Ehlers-Danlos syndromes; descending dissections are commonly associated with atherosclerosis or hypertension. Incidence is increased in pts with coarctation of aorta, bicuspid aortic valve, and rarely in third trimester of pregnancy in otherwise normal women.
Symptoms
Sudden onset of severe anterior or posterior chest pain, with “ripping” quality; maximal pain may travel if dissection propagates. Additional symptoms relate to obstruction of aortic branches (stroke, MI), dyspnea (acute aortic regurgitation), or symptoms of low cardiac output due to cardiac tamponade (dissection into pericardial sac).
Physical Examination
Sinus tachycardia common; if cardiac tamponade develops, hypotension, pulsus paradoxus, and pericardial rub appear. Asymmetry of carotid or brachial pulses, aortic regurgitation, and neurologic abnormalities associated with interruption of carotid artery flow are possible findings.
Laboratory
CXR: Widening of mediastinum; dissection can be confirmed by CT, MRI, or transesophageal echocardiography. Aortography is rarely required, as sensitivity of these noninvasive techniques is >90%.
Aortic Dissection TREATMENT
Reduce cardiac contractility and treat hypertension to maintain systolic bp between 100 and 120 mmHg using IV agents , e.g., sodium nitroprusside accompanied by a beta blocker (e.g., IV metoprolol, labetolol, or esmolol, aiming for heart rate of 60 beats per min), followed by oral therapy. If beta blocker contraindicated, consider IV verapamil or diltiazem . Avoid direct vasodilators (e.g., hydralazine) because they may increase shear stress. Ascending aortic dissection (type A) requires surgical repair emergently or, if pt can be stabilized with medications, semielectively. Descending aortic dissections are stabilized medically (maintain systolic bp between 110 and 120 mmHg) with oral antihypertensive agents (esp. beta blockers); surgical repair is not usually indicated unless continued pain or extension of dissection is observed (by serial MRI or CT performed every 6–12 months).
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