Cardiomyopathy : Types, Causes, Symptoms, Diagnosis, Treatment, Complications

Cardiomyopathy : Types, Causes, Symptoms, Diagnosis, Treatment, Complications

Myocardium (heart muscle) is impacted by the illness known as cardiomyopathy. Cardiomyopathy can develop scar tissue and cause your heart to stiffen, expand, or thicken. Your heart is unable to adequately pump blood to the rest of your body as a result.

Your heart may deteriorate over time, and cardiomyopathy may result in heart failure. Treatment is beneficial. Some cardiomyopathy sufferers eventually require a heart transplant.

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Types of Cardiomyopathy

Different forms of cardiomyopathy include:

  • Dilated cardiomyopathy - The left ventricle, the heart’s primary pumping chamber, enlarges (dilates) in this type of cardiomyopathy and is unable to efficiently pump blood out of the heart.Although this variety can affect people of all ages.Coronary artery disease or a heart attack are the most frequent causes. However, genetic alterations may also be to blame.
  • Hypertrophy cardiomyopathy- This type results in aberrant heart muscle thickening, which makes the heart’s job more difficult. It mostly affects the left ventricle’s (the heart’s main pumping chamber) muscle. Although hypertrophic cardiomyopathy can appear at any age, it usually worsens if it does. Although hypertrophic cardiomyopathy can manifest at any age, it usually worsens if it does so in a young child. A family history of the condition is common among those who have this kind of cardiomyopathy. Hypertrophic cardiomyopathy has a hereditary component.
  • Restrictive cardiomyopathy-. Due to the heart muscle’s stiffness and decreased flexibility, this type prevents the heart from expanding and filling with blood in between heartbeats. Although it can afflict anyone at any age, the most typical demographic for this least common type of cardiomyopathy is the elderly.

Restrictive cardiomyopathy can be the result of a heart illness that affects other parts of the body, such as amyloidosis, or it can develop for no apparent reason (idiopathic).

Right ventricular dysplasia that is arrhythmogenic. Genetic alterations are frequently the cause.

  • Cardiomyopathy that is unclassified. This includes many forms of cardiomyopathy.

Restrictive Cardiomyopathy

It is the Rarest form of cardiomyopathy. In this we find a condition which is known as STIFF HEART.In this condition there is normal size ventricle but atria is dilated to work against stiff ventricles. Pink Hyaline deposits (amyloid protein) in the myocardium occurs causing the stiffness of the ventricles which is shown in the below image

Restrictive Cardiomyopathy

Causes of Restrictive Cardiomyopathy

  • Amyloidosis
  • Radiation
  • Sarcoidosis
  • Hemochromatosis
  • Storage disorders: Gaucher disease and Fabry disease
  • Scleroderma
  • Endocardial fibroelastosis

Clinical Features

  • Decreased Right ventricular compliance
    • Pitting pedal edema/Ankle edema
    • Ascites
    • Hepatomegaly/ RUQ (Right upper quadrant) discomfort
    • Kussmaul sign: Jugular venous pressure rises with Inspiration
  • Decreased Left ventricular compliance
    • Pulmonary edema due to pooling of blood in the lungs, Dyspnea on exertion, Orthopnea, Paroxysmal nocturnal dyspnea
    • Fibrosis triggers clots in Left atria and ventricle leading to increased chances of embolic stroke
    • Effort intolerance


  • ECG- Low voltage leads due to fibrosis in the heart
  • Chest x-ray
    • To rule out Constrictive pericarditis (forms calcification around the heart)
    • To demonstrate Pulmonary edema
  • Trans thoracic echocardiography/ Trans esophageal echocardiography
    • Thickness of the Left ventricular and right ventricular wall is normal
    • Left ventricular end diastolic pressure is increased
  • Cardiac catheterization
    • The blood hits the ventricular wall, but it bounces of the wall instead of stretching of the wall due to fibrosis of the ventricular wall
    • This is called Square root wave sign due to non-compliant ventricular wall

Cardiac catheterization

  • Gold standard tool: Endomyocardial Biopsy
  • Cardiac MRI- preferred imaging modality in Hypertrophic cardiomyopathy


  • Implantable cardioverter defibrillator- To increase the chances of survival
  • Warfarin: given to reduce the risk of cerebral thrombosis
  • Diuretics- Lowest possible dose is given due to low blood pressure
  • Cardiac transplant

Dilated Cardiomyopathy

  • Globular enlarged flabby heart is seen in dilated cardiomyopathy
  • The histopathology shows multinucleated myocytes
  • Dicrotic pulse is a feature sign of dilated cardiomyopathy

Causes of dilated cardiomyopathy:

  • Sequelae to Viral myocarditis
    • Parvovirus B19
    • HHV6
    • Coxsackie B
    • Covid-19
  • Toxins- Alcohol
  • Sarcoidosis
  • Duchenne’s muscular dystrophy
  • Functional mitral regurgitation, tricuspid regurgitation- due to the annulus dilatation of the cusp of mitral and tricuspid valves

Functional mitral regurgitation


  • Trans thoracic echocardiography
  • Cardiac MRI
  • Chest x-ray- increased cardio thoracic ratio and pulmonary edema


  • Implantable cardioverter defibrillator
  • Cardiac resynchronization therapy

Peripartum Cardiomyopathy

This type of cardiomyopathy mainly takes place from the last month of pregnancy up to 5 months of postpartum. In this we can find conditions such as Pregnancy induced hypertension, valvular diseases. Recovery is possible in peripartum cardiomyopathy.

Takotsubo Cardiomyopathy

This cardiomyopathy occurs due to catecholamine surge. In this case recovery is possible.