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November 25, 2009
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Takayasu Disease (cont.)

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How is Takayasu disease treated?

Takayasu disease is treated by suppressing the inflammation with cortisone medication. While most patients can improve, some do not or relapse. In cortisone-resistant patients, stronger medications which suppress the immune system (immunosuppressive drugs), thereby further decreasing active inflammation of the arteries, have been used. Examples include prednisone, prednisolone, methotrexate (Rheumatrex, Trexall), cyclosporine, cyclophosphamide (Cytoxan), and azathioprine (Imuran). Strict control of elevated blood pressure (hypertension) is important.

What is the long-term outlook for patients with Takayasu disease?

The long-term prognosis is not predictable. Some researchers have found that the prognosis is worse when the retinas of the eyes are affected, if the aorta is damaged, or when aneurysms develop. There is also some research that indicates that earlier, aggressive treatment with cortisone and immune-suppression medications may decrease the chances for requiring future surgical procedures for the blood-vessel abnormalities.

The effects of Takayasu arteritis vary greatly from patient to patient. These effects frequently depend on the impaired blood supply to body tissues (such as the brain leading to strokes or spinal cord leading to paralysis).


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