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Restrictive Cardiomyopathy
(RCM) is an uncommon form of heart muscle disease in which the
walls of the heart become abnormally stiff while maintaining a near-normal
thickness and pumping ability. Because the ventricles cannot relax properly
between heartbeats, they fill with less blood, reducing the
amount of blood delivered to the body. This condition may develop due to
inherited genetic disorders or secondary causes such as amyloidosis,
hemochromatosis, sarcoidosis, radiation therapy, or connective tissue diseases.
People with Restrictive
Cardiomyopathy often experience fatigue, shortness of breath, reduced exercise
tolerance, swelling in the legs or abdomen, and irregular heart rhythms. As the
disease progresses, it may lead to heart failure, blood clots, or pulmonary
hypertension if left untreated.
Diagnosis typically involves
echocardiography, electrocardiography (ECG), cardiac MRI, blood tests,
and, in selected cases, heart tissue biopsy to determine the underlying cause.
Treatment focuses on managing symptoms, improving heart function, and
addressing the condition responsible for the disease. Medications such as diuretics,
antiarrhythmic drugs, and anticoagulants may be prescribed. In
advanced cases where symptoms cannot be controlled, heart transplantation
may be considered. Early diagnosis, ongoing monitoring, and specialized medical
care can significantly improve quality of life and long-term outcomes.