Filed under: Heart & Vascular
Dilated cardiomyopathy is a disease of the heart muscle, primarily affecting your heart's main pumping chamber (left ventricle). The left ventricle becomes enlarged (dilated) and can't pump blood to your body with as much force as a healthy heart can.
Dilated cardiomyopathy doesn't necessarily cause symptoms, but for some people the disease is life-threatening. Dilated cardiomyopathy is a common cause of heart failure, the inability of the heart to supply the body's tissue and organs with enough blood. Dilated cardiomyopathy may also cause irregular heartbeats (arrhythmia), blood clots or sudden death.
Dilated cardiomyopathy may affect people of all ages, including infants and children, but it's most often diagnosed in middle age.
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If you have dilated cardiomyopathy, you're likely to have signs and symptoms when the disease has caused heart failure or arrhythmias. Dilated cardiomyopathy symptoms include:
When to see a doctor
If you experience shortness of breath or other symptoms of dilated cardiomyopathy, see your doctor. Call 911 or your local emergency number if you feel chest pain that lasts more than a few minutes or have severe difficulty breathing.
If a member of your family has been diagnosed with dilated cardiomyopathy, talk to your doctor about having you or other family members screened for dilated cardiomyopathy. Early detection may benefit people with inherited forms of dilated cardiomyopathy who have no apparent signs or symptoms.
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
Dilated cardiomyopathy occurs when your heart's main pumping chamber, the left ventricle, doesn't pump as efficiently as a healthy heart. The muscles of the left ventricle stretch and become thinner (dilate). Dilating causes the heart muscle to weaken, and over time, the condition can cause heart failure.
Causes of cardiomyopathy are often unknown
In many cases, the cause of dilated cardiomyopathy can't be determined. Such cases are usually called idiopathic dilated cardiomyopathy.
Researchers have found several genes that are linked to dilated cardiomyopathy and continue to search for more.
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
Many factors can change and enlarge your heart's main pumping chamber (left ventricle). The risk factors for dilated cardiomyopathy include:
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
Enlargement of the left ventricle and its inability to pump blood efficiently can cause any of the following complications:
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
If you think you may have dilated cardiomyopathy, or are worried about your risk because of a family history, make an appointment with your family doctor. If dilated cardiomyopathy is found early, your treatment may be easier and more effective. Eventually, however, you may be referred to a heart specialist (cardiologist).
Because appointments can be brief, and because there's often a lot of ground to cover, it's a good idea to be prepared for your appointment. Here's some information to help you get ready for your appointment, and what to expect from your doctor.
What you can do
Your time with your doctor is limited, so preparing a list of questions will help you make the most of your time together. List your questions from most important to least important in case time runs out. For dilated cardiomyopathy, some basic questions to ask your doctor include:
What to expect from your doctor
Your doctor is likely to ask you a number of questions. Being ready to answer them may reserve time to go over any points you want to spend more time on. Your doctor may ask:
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
If you have symptoms associated with heart failure or arrhythmia — such as shortness of breath or fatigue — your doctor will order tests to check your heart's function, identify possible causes of your illness and decide on treatment. For some of the exams, your doctor may refer you to a heart specialist (cardiologist) or specialized technicians.
The results of some tests may help your doctor decide what additional tests to order.
Physical examination. Your doctor reviews your lifestyle habits (such as exercise, diet, smoking history and alcohol use), recent changes in weight, any signs and symptoms you've observed, and the history of heart disease and other medical conditions in your family.
Your doctor will also check for signs such as irregular heartbeats, abnormal heart sounds (heart murmurs), the accumulation of fluids in the lungs, swelling in the legs or feet, or coolness in the limbs due to poor blood circulation.
Echocardiography. An echocardiogram uses sound waves to produce images of the heart. This common test lets your doctor see your ventricles squeezing and relaxing and valves opening and closing in rhythm with your heartbeat.
The echocardiogram is the primary tool for diagnosing dilated cardiomyopathy. If you have dilated cardiomyopathy, your doctor will be able to observe enlargement of the left ventricle. An echocardiogram can also reveal how much blood is ejected from the heart with each beat and whether blood is flowing in the right direction.
Genetic screening or counseling. If your doctor can't identify the cause of dilated cardiomyopathy, he or she may suggest screening of other family members to see if the disease is inherited in your family.
No single test can determine if you carry a disease-related gene mutation. However, a thorough and detailed family history may reveal who's most at risk of dilated cardiomyopathy or whether there's evidence of other conditions that may contribute to the disease. Genetic testing is performed in some situations, usually as part of a research study.
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
The goals of treatment for dilated cardiomyopathy are to treat an underlying cause if it's known, improve blood flow, reduce symptoms and prevent further heart damage.
Medications
Doctors usually treat dilated cardiomyopathy with a combination of medications. Depending on your symptoms, you might need two or more of these drugs. Several types of drugs have proved useful in the treatment of heart failure and dilated cardiomyopathy. These medications include:
Angiotensin-converting enzyme (ACE) inhibitors. These drugs help people with dilated cardiomyopathy live longer and feel better. ACE inhibitors are a type of vasodilator, a drug that widens or dilates blood vessels to lower blood pressure, improve blood flow and decrease the workload on the heart. Examples include enalapril (Vasotec), lisinopril (Prinivil, Zestril) and captopril (Capoten).
ACE inhibitors cause an irritating cough in some people. It may be best to put up with the cough, if you can. Discuss this side effect with your doctor. Switching to another ACE inhibitor or an angiotensin II receptor blocker may relieve the cough.
Diuretics. Often called water pills, diuretics make you urinate more frequently and keep fluid from collecting in your body. The drugs also decrease fluid in your lungs, so you can breathe more easily. Commonly prescribed diuretics for heart failure include bumetanide (Bumex) and furosemide (Lasix).
Because some diuretics make your body lose potassium and magnesium, your doctor may also prescribe supplements of these minerals. If you're taking a diuretic, your doctor will likely monitor levels of potassium and magnesium in your blood through regular blood tests.
Devices
Implantable devices that may correct irregular heartbeats include:
Heart transplant
You may be a candidate for a heart transplant if medications and other treatments are no longer effective.
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
If you have dilated cardiomyopathy, these self-care strategies may help:
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.
If you eliminate lifestyle habits that can contribute to dilated cardiomyopathy, you may prevent or minimize effects of the disease:
©1998-2009 Mayo Foundation for Medical Education and Research (MFMER). Terms of use.


