Aortic dissection is a tear in the inner layer of the aorta, the largest blood vessel in the body. This is a very serious problem. When blood leaks through the tear, it collects between the inner and outer layers of the aorta and causes them to separate. The separation often enlarges quickly. It can block other important blood vessels, change the way the heart works, or cause the aorta to burst.
The most common causes are:
Over time, continuing high blood pressure can cause the aorta to widen. This widening weakens the aortic wall, and the high blood pressure increases the stress on the wall. These conditions may make it easier for the wall to tear, but no one knows exactly what makes this happen.
Among the inherited diseases that cause an abnormal aortic wall are Marfan syndrome, Turner's syndrome, and Ehlers-Danlos syndrome. These fairly uncommon disorders all have a common feature. The middle layer of the aortic wall is made of weak tissue. People with these diseases have a high risk of dissection and sudden death.
Symptoms may include:
Your healthcare provider will review your symptoms, examine you, and ask about your medical history. He or she may do the following tests:
Aortic dissection is a medical emergency. Treatment must be started as soon as possible. The choice of treatment depends mainly on the location of the dissection in the aorta. In some cases, you may be given a sedative and fast-acting IV medicine to lower high blood pressure. In other cases, you may need surgery to replace the weakened part of the aorta with a graft of man-made material. Sometimes bypass surgery and valve replacements are done at the same time.
With successful medical or surgical treatment, there are usually no lasting affects. You can usually resume normal living.
The best prevention is control of high blood pressure, even for people with the inherited forms of aortic wall weakness. For people with Marfan syndrome, taking drugs called beta blockers helps prevent aortic dissection.