Cardiac amyloidosis
From DrKoop's partner site on heart disease, MyHeartCentral.com
Amyloidosis - cardiac; Primary cardiac amyloidosis - AL type; Secondary cardiac amyloidosis - AA type; Stiff heart syndrome; Senile amyloidosis; Amyloidosis - senile Treatment You can continue to exercise as long as feel like you can. Your doctor may tell you to make changes to your diet. This may include salt and fluid restrictions. Diuretics (water pills) may be given to help the body remove excess fluid. The doctor may tell you to weigh yourself everyday. A weight gain of three or more pounds over 1 or 2 days can mean there is too much fluid in the body. Digoxin, calcium channel blockers, and beta blockers may be used with caution in patients with atrial fibrillation. However, the dosage must be carefully monitored, since patients with cardiac amyloidosis may be unusually sensitive to any side effects. advertisement
Other treatments may include:
A heart transplant may be considered for some patients with very poor heart function. However, it is not done in those with AL type amyloidosis, since the disease weakens many other organs. A liver transplant is needed in those with hereditary amyloidosis. Expectations (prognosis) Cardiac amyloidosis is a long-term (chronic) condition that slowly gets worse. On average, persons with cardiac amyloidosis live less than 1 year. Complications
Calling your health care provider Call your health care provider if you have this disorder and new symptoms develop, particularly:
Review Date: 01/17/2007 ![]() | ||||||||||||||||||||
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