Cardiomyopathy

Overview

What is cardiomyopathy?

Cardiomyopathy refers to problems with your heart muscle that can make it harder for your heart to pump blood effectively. There are many types and causes of cardiomyopathy, and it can affect people of all ages. Depending on the type of cardiomyopathy that you have, your heart muscle may become thicker, stiffer or larger and weaker than normal. A weakened heart can lead to significant reductions in exercise tolerance. In more advanced cases debilitating symptoms at rest can arise due to heart failure. Patients with severe cardiomyopathies are generally at higher risk for irregular rhythms, some of which can be life-threatening and cause cardiac arrest.

There are many types of cardiomyopathies:

  • Dilated Cardiomyopathy: The heart's chambers enlarge, weakening the heart's ability to pump blood. This is often caused by heart attacks, long-term alcohol use or viral infections. In many cases, the cause is unknown, but treatments focus on improving heart function and managing symptoms. Without intervention, it can lead to heart failure.
  • Hypertrophic Cardiomyopathy: The heart muscle thickens, making it difficult for blood to flow through. This condition is usually inherited and can cause chest pain, shortness of breath or fainting, especially during physical activity. Severe cases may require surgery or procedures to reduce the thickness of the heart muscle.
  • Restrictive Cardiomyopathy: This rare condition causes the heart muscle to stiffen, preventing it from fully relaxing and filling with blood. It is often caused by diseases like amyloidosis or sarcoidosis, and treatment options are limited. Symptom management and slowing disease progression are the main goals of treatment.
  • Constrictive Cardiomyopathy: This occurs when the pericardium, the thin sac surrounding the heart, becomes thickened and rigid, restricting the heart's ability to expand and contract. It is most commonly caused by prior heart surgery or infections, and surgery to remove the thickened pericardium may be necessary in severe cases.
  • Takotsubo Cardiomyopathy (Broken Heart Syndrome): This temporary condition is triggered by extreme emotional or physical stress, causing part of the heart to weaken. It mimics the symptoms of a heart attack but usually resolves with treatment. Women, particularly post-menopausal, are more prone to this condition.
  • Arrhythmogenic Cardiomyopathy: Fat or scar tissue replaces the normal heart muscle, particularly in the right ventricle, causing dangerous arrhythmias. This genetic condition often affects young athletes and can lead to sudden cardiac death. Treatment focuses on controlling arrhythmias and reducing the risk of sudden death.
  • Left Ventricular Noncompaction: A rare genetic disorder where the heart muscle fails to develop normally, leading to structural abnormalities. Patients with this condition are at high risk for heart failure and arrhythmias, and treatment often involves medications and implanted devices to support heart function. 

What are symptoms of cardiomyopathy?

Some people with cardiomyopathy never have any symptoms. Other people may not have symptoms until the condition gets worse. Common symptoms include the following:

  • Shortness of breath
  • Chest pain, especially after physical activity or heavy meals
  • Swelling of the legs or abdomen
  • Tiredness even after resting
  • Dizziness and fainting
  • Arrhythmias (irregular heartbeats)
  • Heart murmurs (extra or unusual sounds heard during a heartbeat)
  • Babies and young children may experience vomiting, diarrhea, difficulty eating and breathing, fussiness and poor growth

Call 911 if you are having trouble with breathing, swelling or any other unusual symptoms that last for a significant period. 

What causes cardiomyopathy

Cardiomyopathies can be inherited or acquired.

  • Acquired” means that you were not born with the disease, but you developed it due to another disease or condition. Conditions that damage your heart can lead to cardiomyopathy.
  • Inherited” means that your parents passed the gene for the disease on to you. Hypertrophic cardiomyopathy and arrhythmogenic cardiomyopathy are inherited types of the disease. Mutations or changes in the genes that control how your heart is formed during fetal development. 

What risk factors can lead to cardiomyopathy

Risk factors you can control:

  • Drinking a lot of alcohol regularly (more than 2 drinks per day for men or 1 drink per day for women) places your heart at increased risk of weakening and enlarging.
  • Major health problems and risk factors that can be treated and managed and if not, can contribute to developing severe coronary artery disease and heart attacks. These include tobacco use, obesity, hypertension, diabetes, high cholesterol, sedentary lifestyle, and high stress.  
  • Very stressful situations, which can raise your risk of takotsubo cardiomyopathy, also called broken heart syndrome, especially if you have other risk factors.
  • Using cocaine or amphetamines, or exposure to other potentially harmful toxins.

Risk factors you can’t control:

  • Age: Some types of cardiomyopathies are more common in certain age groups and risk of coronary disease increases with age.
  • Genetics: Both for specific genetic cardiomyopathies as well as for developing coronary disease and heart attacks which are the leading cause of dilated cardiomyopathy. In addition, risk factors like diabetes and hypertension that lead to coronary disease and heart attacks follow familial patterns.  
  • Arrhythmogenic cardiomyopathy is more common in teens and young adults.
  • Dilated cardiomyopathy is more common in adults between 20 and 60 years old.
  • Hypertrophic cardiomyopathy due to genetic abnormalities is more common in people in their 30s.
  • Takotsubo cardiomyopathy is more common in women after menopause.
  • Family history of cardiomyopathy or other heart conditions
  • Chemotherapy or radiation treatment for cancer

Medical conditions that increase your risk factor:

  • Heart inflammation from endocarditis, myocarditis, or pericarditis
  • Infections, such as viral hepatitis and HIV
  • Obesity, diabetes or other problems with your metabolic system
  • Thyroid disease and other problems with your hormone levels
  • Rare diseases that affect how well your muscles work, such as Duchenne muscular dystrophy and those that cause abnormal substances to build up in your heart, such as sarcoidosis or amyloidosis 

How doctors diagnose cardiomyopathy

Your doctor may screen you for cardiomyopathy if a close relative has this condition or has had another serious heart condition, or if people in your family have died suddenly presumed to be a result of cardiac arrest. Your doctor may also notice signs of cardiomyopathy during a routine exam.

Cardiomyopathy diagnostic tests

To diagnose cardiomyopathy, your doctor may order one or more tests:

  • Blood tests: To check for substances that indicate heart failure or muscle damage.
  • Imaging: Echocardiograms, MRI and CT scans provide images of the heart's structure and function.
  • Cardiac catheterization: A catheter is inserted into the heart to measure pressure and obtain images of the coronary arteries.
  • Genetic testing: To diagnose inherited cardiomyopathies.

Cardiomyopathy procedures

Your doctor may order one of these medical procedures to confirm your diagnosis:

  • Echocardiography: A safe, non-invasive test using sound waves to visualize the heart’s structure and function. It’s often the first test ordered to assess heart abnormalities and can help identify the cause of cardiomyopathy.
  • Cardiac catheterization: An invasive test where a catheter is inserted into a blood vessel and threaded into the heart to take images and measure pressure. This helps determine the cause of cardiomyopathy and guide treatment strategies.
  • Coronary angiography: Performed during cardiac catheterization, this involves injecting contrast dye into the coronary arteries to detect blockages. If blockages are found, your doctor may perform angioplasty and stenting or recommend bypass surgery. While generally safe, risks include bleeding, infection or arrhythmias, especially in older patients or those with kidney disease or diabetes.
  • Heart biopsy (myocardial biopsy): Rarely performed, this involves removing a small piece of heart tissue to check for specific causes of cardiomyopathy. It is typically done during cardiac catheterization.

Advanced imaging

Other imaging techniques can provide additional information to help diagnose whether a patient has a cardiomyopathy, as well as its underlying cause. These include CT scanning, MRI (Magnetic Resonance Imaging) and PET (Positron Emission Tomography). Typically, these tests will also use contrast agents or radioactive tracers (low enough dose to be very safe) to enhance imaging and make diagnosis more feasible and accurate.

Cardiomyopathy treatment and medicine

If you have cardiomyopathy but don’t have any symptoms, you may not need treatment. Some types that occur suddenly, such as dilated cardiomyopathy, may go away without treatment.  

If your doctor recommends treatment, your treatment plan will depend on the type of cardiomyopathy you have, how serious it is, and whether you have any complications. Your doctor will discuss your treatment options with you to choose a treatment plan that works best for you. Treatment for cardiomyopathy might not cure the underlying problem with your heart. The main goals of treatment include:

  • Controlling your symptoms so that you can have a good quality of life
  • Managing any medical conditions that caused or contributed to developing the cardiomyopathy
  • Stopping the disease from getting worse
  • Preventing serious problems, such as sudden cardiac arrest

Your treatment may include medicines, procedures and devices as guided by your cardiologist.  

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Medication icon

Medication

The following medicines can help treat your symptoms. If your doctor prescribes a medicine, they have determined that the benefits outweigh the risks for your condition. The options for medication treatment continue to develop and grow in number. Most of these medications are very beneficial in patients with cardiomyopathies and congestive heart failure. Options include:

  • Diuretics: Help your body remove excess sodium and water, reducing blood volume for the heart to pump. Close monitoring is needed due to possible side effects like dehydration, low blood pressure and electrolyte imbalances.
  • ACE Inhibitors and ARBs (Angiotensin Receptor Blockers): Lower blood pressure and reduce strain on the heart, improving outcomes in heart failure and reducing complications.
  • Beta blockers: Reduce heart rate and blood pressure by blocking adrenaline, helping the heart work more efficiently and lowering the risk of complications.
  • Entresto: Combines a diuretic (sacubitril) with an ARB (valsartan) and is highly effective in improving symptoms and survival in heart failure.
  • SGLT-2 inhibitors: Originally for diabetes, these medicines now improve heart function and outcomes in heart failure. They may have side effects like kidney issues and infections.
  • Hydralazine/Isosorbide dinitrate: An alternative for those unable to take ACE inhibitors or ARBs, commonly used in African American patients. Side effects include low blood pressure and headaches.
  • Digoxin: Used to treat fast or irregular heartbeats, but it requires careful monitoring due to potential toxicity.
  • Calcium channel blockers: May be prescribed for those who can't tolerate beta blockers.
  • Isradipine: Used to increase heart rate in cases of slow heart function.
  • Electrolyte balancing medications: Necessary to correct dangerous shifts in potassium, sodium or magnesium caused by heart failure treatments.
  • Blood thinners (anticoagulants): Help prevent clots, especially in patients with atrial fibrillation, but carry a risk of bleeding. 
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Heart devices & procedures

If medications don’t relieve your symptoms, your doctor may suggest a procedure or device.

  • Implanted devices: Patients with severe dilated cardiomyopathy are at risk of sudden cardiac arrest from arrhythmias. Implantable Cardiac Defibrillators (ICDs), small devices placed under the skin, reduce this risk. In advanced heart failure, specialized defibrillators with an extra lead can improve heart function. Pacemakers may be used if heart rates are too slow due to cardiomyopathy or medication. In severe cases, Left Ventricular Assist Devices (LVADs) may be implanted to help the heart pump blood but are used in only the sickest patients.
  • Septal myectomy: For hypertrophic cardiomyopathy with severe thickening of the heart muscle, surgery may be needed to remove part of the thickened muscle, improving blood flow.
  • Alcohol septal ablation: An alternative to surgery, this catheter-based procedure uses alcohol to shrink the thickened heart muscle that blocks blood flow in hypertrophic cardiomyopathy.
  • Catheter ablation: Used to treat arrhythmias, this procedure involves inserting catheters into the heart to locate and treat abnormal heartbeats using radiofrequency waves, extreme cold or lasers. Risks include bleeding, infection, heart damage and arrhythmias. 

How to prevent cardiomyopathy

You may be able to prevent acquired cardiomyopathy or help lower your risk of problems. Make heart-healthy lifestyle changes, such as choosing heart-healthy foods, being physically active, aiming for a healthy weight, quitting smoking and managing stress. Also, do not drink too much alcohol, and avoid illegal drugs such as cocaine.

  • Get treatment for medical conditions that can cause cardiomyopathy or make your condition worse.
  • There is no way to prevent inherited cardiomyopathy. However, you can take steps to prevent it from getting worse and to prevent serious health problems. 

We understand how challenging it can be to break free from the grip of tobacco and nicotine addiction. That’s why we offer free support and resources to help you quit smoking and using other tobacco products. Learn more about our free tobacco cessation program, including our free nicotine replacement therapy.

What it's like to live with cardiomyopathy

If you have cardiomyopathy, talk to your doctor about heart-healthy lifestyle changes and routine medical care that you may need to help you manage the disease. Your doctor may ask you to make lifelong changes. These can help manage any existing problems as well as prevent future complications.

  • Aim for a healthy weight. Overweight and obesity can make your heart work harder.
  • Choose heart-healthy foods. Your doctor may suggest choosing foods that are lower in sodium (salt) and fat. Talk with your doctor about the amounts and types of fluids that are safe and healthy for you. Too much fluid can make your symptoms worse.
  • Get good-quality sleep. You may need to get tested for sleep disorders, such as sleep apnea, that can make your symptoms worse.
  • Get regular physical activity. Ask your doctor what types and amounts of exercise are safe for you. This will depend on the type of cardiomyopathy that you have and whether you have any symptoms or problems.  
  • Manage stress. Extreme stress can cause cardiomyopathy or trigger an irregular heartbeat.
  • Quit smoking. Smoking raises your risk of other heart conditions that can make your cardiomyopathy worse.
  • Limit your alcohol intake. For men, this is no more than two drinks a day, and one drink a day for women. Also, do not use illegal drugs.
  • Cardiomyopathy often runs in families. Your parents, children, or brothers and sisters may also have this condition and may need to go to their doctors to get checked.

In severe cases, cardiomyopathies can cause major high-risk health problems that can affect the heart and brain.

  • Heart failure: This serious condition happens when your heart doesn’t pump enough blood for your body’s needs.
  • Arrhythmia (irregular heartbeat): Cardiomyopathy can affect the electrical signals in your heart that control your heart rate and rhythm.
  • Heart valve disease: Cardiomyopathy can damage your heart valves, which are flaps of tissue in your heart that open and close with each heartbeat. Your heart vavles make sure that blood flows in the right direction through your heart's four chambers and to the rest of your body.  
  • Stroke: Cardiomyopathy weakens the heart, making it hard to pump blood well. Blood can pool in the chambers of your heart and cause a blood clot. If a clot breaks off and travels to your brain, it can cause a life-threatening stroke.
  • Cardiogenic shock: This is a life-threatening condition that occurs when your heart can’t pump enough blood and oxygen to your brain, kidneys, and other important organs.
  • Cardiac arrest: Cardiomyopathy can cause your heart to stop beating suddenly and unexpectedly.

Learn the warning signs of stroke and how to help someone who is in cardiac arrest.

Call 911 right away if you think you or someone else is having a stroke, is in shock or suffering a sudden cardiac arrest.  

Cardiomyopathy treatment near you

Cardiology services at Ballad Health

Our extensive network of highly trained cardiologists, surgeons and advanced practice providers are here to support you and help you navigate a heart-related diagnosis.

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CVA Heart Institute Learning Center

We understand that receiving a cardiomyopathy diagnosis can be overwhelming. Our goal is to alleviate your fears and help you to understand your condition. 

We have an informational video library, education tools and heart-related FAQs so that you have the resources you need.

Heart care patient stories

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Tony Buchanan cardiac patient
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Shelia sitting on a park bench, reading a book on a beautiful sunny day
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Portrait photo of Vic Boatman

Read our patient stories

Our patients inspire us every day, and we’re honored when they trust us with their care. They tell their stories best, so we’ve gathered a few here to share with you.

Many of these patients received life-saving care for heart conditions when they weren’t experiencing any symptoms. These experiences have changed they way they look at their individual care and helped them see the importance of regular preventive screenings.