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Hypertrophic cardiomyopathy



Heart, section through the middle
Heart, section through the middle
Heart, front view
Heart, front view
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy


Hypertrophic cardiomyopathy

Alternative Names:

Cardiomyopathy - hypertrophic (HCM); IHSS; Idiopathic hypertrophic subaortic stenosis; Asymmetric septal hypertrophy (ASH).
Treatment:

Treatment is aimed at control of symptoms and prevention of complications. Some patients may require hospitalization until the condition is stabilized.



The thick ventricles of HCM contract and relax abnormally, and to assist the relaxation phase some drugs may be necessary. These include beta-blockers and calcium channel blockers such as verapamil, which improve exercise tolerance and reduce chest pain.

When severe blood outflow blockage exists, an operation called myotomy-myectomy (heart muscle cutting-heart muscle removal) often results in marked improvement. Replacement of the mitral valve during the same surgery is necessary in some HCM patients with mitral valve regurgitation.

Some people with arrhythmias may need anti-arrhythmic medications. If the arrhythmia is atrial fibrillation, the risk of blood clots breaking away from the atrium and clogging arteries in the body may need to be reduced with blood thinner medicine.

Patients with HCM and high risk factors may need to receive an implantable-cardioverter defibrillator (ICD) to prevent sudden cardiac death. These risks include severe heart muscle thickness, potentially lethal heart rhythms, a history of passing out, or a family history of sudden cardiac death.


Expectations (prognosis):

Some affected individuals remain without symptoms for many years and have a normal life span, yet some may deteriorate gradually or rapidly. Progression into dilated cardiomyopathy occurs in some patients.

Patients with hypertrophic cardiomyopathy are at higher risk for sudden death than the normal population, and can be affected at a young age. Hypertrophic cardiomyopathy is a well known cause of sudden death in athletes. People with HCM should follow their doctor's advice about physical exercise and medical appointments.

Young patients with HCM planning to start a family may benefit from genetic counseling.


Complications:
  • severe injury or trauma from fainting
  • cardiac arrhythmias, including lethal arrhythmias
  • congestive heart failure
  • dilated cardiomyopathy

Calling your health care provider:

Call for an appointment with your health care provider if:

  • You have any symptoms of hypertrophic cardiomyopathy
  • Chest pain, palpitations, faintness or other new or unexplained symptoms develop



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