Aortic dissection natural history, complications and prognosis: Difference between revisions

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*[[Pericardial tamponade]] due to extension of the dissection into the pericardium
*[[Pericardial tamponade]] due to extension of the dissection into the pericardium
*[[Acute aortic regurgitation]]due to the aortic dilation and dissection into the valve structure which can then cause acute [[pulmonary edema]]
*[[Acute aortic regurgitation]]due to the aortic dilation and dissection into the valve structure which can then cause acute [[pulmonary edema]]
*[[Myocardial ischemia]] or [[myocardial infarction]] due to dissection into either the right or left coronary ostium (but most commonly the [[right coronary artery]])
*[[Myocardial ischemia]] or [[myocardial infarction]] due to dissection into either the right or left coronary ostium (but most commonly the [[right coronary artery]]). [[Myocardial infarction]] (heart attack) occurs in 1-2% of aortic dissections.  The etiology of the infarction is involvement of the [[coronary artery|coronary arteries]] (the [[artery|arteries]] that supply the heart) in the dissection.  The right coronary artery is involved more commonly than the left coronary artery.  If the myocardial infarction is treated with [[thrombolytic]] therapy, the mortality increases to over 70%, mostly due to hemorrhage into the pericardial sac causing [[pericardial tamponade]]. Because aortic dissection may present to the [[emergency room]] [[physician]] similar to a myocardial infarction, the physician must be careful to make the proper diagnosis prior to initiating treatment for myocardial infarction, since the treatment regimen for myocardial infarction can be lethal to an individual presenting with aortic dissection.
*Redissection and aortic diameter enlargement
*Redissection and aortic diameter enlargement
*Aneurysmal dilatation and [[saccular aneurysm]] chronically
*Aneurysmal dilatation and [[saccular aneurysm]] chronically

Revision as of 00:10, 29 October 2012

Aortic dissection Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Aortic dissection from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Special Scenarios

Management during Pregnancy

Case Studies

Case #1


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

Aortic dissection carries a very poor prognosis. 90% of patients who are untreated will be dead at one year. Type A dissection is associated with a worse prognosis than type B dissection. Aortic dissection can be complicated by extension to the coronary arteries resulting in myocardial infarction, involvement of the aortic arch to cause stroke, dilation of the route to cause aortic insufficiency, extension into the pericardium to cause pericardial tamponade, and heart failure, and aortic rupture.

Natural History

If the patient remains untreated, the mortality is:

  • 1% per hour during the first day
  • 75% at 2 weeks
  • 90% at 1 year

Complications

The complications of aortic dissection include:

Cardiac

Kidney

Peripheral Arterial

  • Claudication due to an extension of the dissection into the iliac arteries

Neurologic

Compression of Nearby Organs

Prognosis

The mortality rate is in large part determined by the patient's age and comorbidities.

  • 30% in hospital mortality
  • 60% 10-year survival rate among treated patients

Type A aortic dissection

  • Surgical treatment-30% mortality rate
  • Medical treatment-60% mortality rate

Type B aortic dissection

  • Surgical treatment-10% mortality rate
  • Medical treatment- 30% mortality rate

References

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