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Jason S. Finkelstein, M.D. Cardiology Fellow Tulane University 8/11/03

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1 Jason S. Finkelstein, M.D. Cardiology Fellow Tulane University 8/11/03
Aortic Dissection Jason S. Finkelstein, M.D. Cardiology Fellow Tulane University 8/11/03

2 Overview Incidence of aortic dissection is at least 2000 new cases per year Peak incidence is in the sixth to seventh decade Men are affected twice as commonly as women Mortality in the first 48 hours is 1% per hour Early diagnosis is essential

3 Pathophysiology The chief predisposing factor is degeneration of collagen and elastin in the aortic intima media Blood passes through the tear into the aortic media, separating the media from the intima and creating a false lumen Dissection can occur both distal and proximal to the tear

4 Classification Debakey system Type I Type II Type III
Originates in the ascending aorta, propagates to the aortic arch and beyond it distally Type II Confined to the ascending aorta Type III Confined to the descending aorta, and extends distally, or rarely retrograde into the aortic arch

5 Classification The Stanford system Type A Type B
All dissections involving the ascending aorta Type B All other dissections regardless of the site of the primary intimal tear Ascending aortic dissections are twice as common as descending

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7 Predisposing factors Age, 60-80 yrs old
Long standing history of hypertension 80% of cases have co-existing HTN Takayasu’s arteritis Giant cell arteritis Syphilis Collagen disorders Marfan syndrome (6-9% of aortic dissections) Ehlers-Danlos syndrome

8 Other Risk Factors Congenital Cardiac Anomalies
Bicuspid aortic valve (7-14% of cases) Coarctation of the aorta Cocaine Abrupt HTN, due to catecholamine release Trauma Pregnancy (50% of dissections in women <40 yrs) Iatrogenic (cardiac cath, IABP, cardiac surgery, s/p valve replacement)

9 Clinical Symptoms Severe, sharp, “tearing” posterior chest pain or back pain (occurs in 74-90% of pts) Pain may be associated with syncope, CVA, MI, or CHF Painless dissection relatively uncommon Chest pain is more common with Type A dissections Back or abdominal pain is more common with Type B dissections

10 Physical Exam Pulse deficit Acute Aortic Insufficiency
Weak or absent carotid, brachial, or femoral pulses these patients have a higher rate of mortality Acute Aortic Insufficiency Diastolic decrescendo murmur Best heard along the right sternal border

11 Clinical signs Acute MI Cardiac tamponade Pleural effusions
RCA most commonly involved Cardiac tamponade Pleural effusions Hypertension or hypotension Hemothorax Variation in BP between the arms (>30mmHg) Neurologic deficits Stroke or decreased consciousness

12 Clinical Signs Involvement of the descending aorta Splanchnic ischemia
Renal insufficiency Lower extremity ischemia Spinal cord ischemia

13 Diagnosis Generally suspected from the history and PE
In a recent study in 2000, 96% of acute dissection patients could be identified based upon a combination of three clinical features Immediate onset of chest pain Mediastinal widening on CXR A variation in pulse and/or blood pressure (>20 mmHg difference between R & L arm Incidence >83% when any combination of all three variables occurred

14 Differential Diagnosis
Acute Coronary Syndrome Pericarditis Pulmonary embolus Pleuritis Cholecystitis Perforating ulcer

15 Diagnostic Tests EKG CXR Cardiac Enzymes
Absence of EKG changes usually helps distinguish dissection from angina Usually non-specific ST-T wave changes seen CXR Cardiac Enzymes

16 Chest X-Ray May show widening of the aorta with ascending aorta dissections Present in 63 % of patients with Type A dissections

17 Diagnostic Imaging Not performed until the patient is medically stable
Has been a dramatic shift from invasive to non-invasive diagnostic strategy Spiral CT scan TEE MRI Angiography

18 Imaging Can identify aortic dissection and other features such as:
Involvement of the ascending aorta Extent of dissection Thrombus in the false lumen Branch vessel or coronary artery involvement Aortic insufficiency Pericardial effusion with or without tamponade Sites of entry and re-entry

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20 Angiography First definitive test for aortic dissection
Traditionally considered “the gold standard” Involves injection of contrast media into the aorta Identifies the site of the dissection Major branches of the aorta Communication site between true & false lumen Can detect thrombus in the false lumen Disadvantages Not very practical in critically ill patients Nephrotoxic contrast Risks of an invasive procedure

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22 Spiral CT Sensitivity 83% Specificity 90 - 100%
Two distinct lumens with a visible intimal flap can be identified Advantages Noninvasive Readily available at most hospitals on an emergency basis Can differentiate dissection from other causes of aortic widening (tumor, periaortic hematoma, fat) Disadvantages Sensitivity lower than TEE and MRI Intimal flap is seen < 75% of cases Nephrotoxic contrast is required Cannot reliably detect AI, or delineate branch vessels

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26 TTE First used to diagnose aortic dissections in the ’70s
Sensitivity 59-85%, specificity 63-96% Image quality limited by obesity, lung disease, and chest wall deformities

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28 TEE Sensitivity 98% Specificity 95% Advantages
Close proximity of the esophagus to the thoracic aorta Portable procedure Yields diagnosis in < 5 minutes Useful in patients too unstable for MRI True and false lumens can be identified Thrombosis, pericardial effusion, AI, and proximal coronary arteries can be readily visualized

29 TEE Lower specificity attributed to reverberations atherosclerotic vessels or calcified aortic disease producing echo images that resemble an aortic flap Disadvantages Contraindicated in patients with esophageal varices, tumors, or strictures Potential complications: bradycardia, hypotension, bronchospasm

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32 MRI Most accurate noninvasive for evaluating the thoracic aorta
Sensitivity 98% Specificity 98% Advantages Safe Can visualize the whole extent of the aorta in multiple planes Ability to assess branch vessels, AI, and pericardial effusion No contrast or radiation Disadvantages Not readily available on an emergency basis Time consuming Limited applicability in pts with pacemakers or metallic clips

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34 Conclusions Conventional TTE is of limited diagnostic value in assessment of the thoracic aorta Both TEE and MRI have excellent sensitivity, however MRI is more specific MRI is the study of choice for stable patients TEE is the study of choice for unstable patients

35 Treatment Acute dissections involving the ascending aorta are considered surgical emergencies Dissections confined to the descending aorta are treated medically Unless patient demonstrates continued hemorrhage into the pleural or retroperitoneal space

36 Surgical Options Excision of the intimal tear
Obliteration of entry into the false lumen proximally Reconstitution of the aorta with interposition of a synthetic vascular graft

37 Type A Dissections Operative mortality varies from 7-35%
27% post-op mortality Patients who died had a higher rate of in-hospital complications such as strokes, renal failure, limb ischemia, & mesenteric ischemia

38 Poor prognostic factors
Hypotension or shock Renal failure Age> 70 yrs Pulse deficit Prior MI Underlying pulmonary disease Preoperative neurologic impairment Renal and/or visceral ischemia Abnormal EKG, particularly ST elevation

39 Medical therapy Reduce systolic BP to 100 to 120 mmHg or the lowest level that is tolerated IV Beta blockers Propanolol (1-10 mg load, 3mg/hr) Labetalol (20 mg bolus, 0.5 to 2 mg/min) If SBP remains >100mmHg, nitroprusside should be added Do not use without beta blockade Avoid hydralazine Surgical intervention for Type B dissections reserved for patients with a complicated course

40 Long Term Outcome Type A Type B Survival at 5 yrs – 68%
Spontaneous healing of dissection is uncommon

41 Long-Term Management Medical therapy Serial imaging
Oral Beta-blockers (reduces aortic wall stress) Keep BP < 135/80 mmHg (combination therapy) Avoidance of strenuous physical activity Serial imaging Thoracic MR scan prior to discharge f/u scans at 3, 6, and 12 months Subsequent screening studies done every 1-2 yrs if no evidence of progression


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