Hypertrophic Cardiomyopathy is a genetic disorder, where the muscle wall (septum) between the lower chambers of heart, thickens abnormally resulting in improper functioning of the heart.
It’s often undiagnosed due to lack of significant clinical manifestations.
What are the symptoms of Hypertrophic Cardiomyopathy?
Shortness of breath, especially during exercise or lying position
Chest pain or discomfort
Abnormal heartbeat
Dizziness
Fainting during physical activity
Fatigue
Swelling in legs, feet or ankles
What are the causes of Hypertrophic Cardiomyopathy?
Echocardiogram: This is commonly used to diagnose Hypertrophic Cardiomyopathy. Utilizes ultrasounds to see abnormally thickened heart muscle. It also examines heart chambers and valves.
Electrocardiogram: To measure electrical signals of the heart.
Cardiac MRI
Exercise test: Record’s EEG while treadmill or physical activity
Genetic testing for Hypertrophic Cardiomyopathy: To identify the gene mutation
How is Hypertrophic Cardiomyopathy treated?
Non-pharmacological treatment:
ICD (Implantable cardioverter-defibrillator)
Septal ablation (Catheter-based therapy)
Septal myectomy (Surgery based therapy)
A pacemaker in case of abnormal heartbeat
Pharmacological treatment:
Anticoagulants such as warfarin, rivaroxaban, dabigatran or apixaban in case of atrial fibrillation to prevent blood clots
CCB’s( Calcium channel blockers) such as verapamil or diltiazem
Beta-blockers such as metoprolol, propranolol or atenolol
Amiodarone or disopyramide to control over heart rhythm