Wednesday, January 26, 2022

                                                                Cardiomyopathy


 


Overview

Cardiomyopathy (kahr-dee-o-my-OP-uh-thee) is a disease of the heart muscle that makes it harder for your heart to pump blood to the rest of your body. Cardiomyopathy can lead to heart failure.

 

The main types of cardiomyopathy include dilated, hypertrophic and restrictive cardiomyopathy. Treatment — which might include medications, surgically implanted devices, heart surgery, or in severe cases, a heart transplant — depends on which type of cardiomyopathy you have and how serious it is.

 

Types

Dilated cardiomyopathy

Hypertrophic cardiomyopathy

Symptoms

There might be no signs or symptoms in the initial stages of cardiomyopathy. But as the condition advances, signs and symptoms usually appear, including:

 

Breathlessness with activity or even at rest

Swelling of the legs, ankles, and feet

Bloating of the abdomen due to fluid buildup

Cough while lying down

Difficulty lying flat to sleep

Fatigue

Heartbeats that feel rapid, pounding or fluttering

Chest discomfort or pressure

Dizziness, lightheadedness, and fainting

Signs and symptoms tend to get worse unless treated. In some people, the condition worsens quickly; in others, it might not worsen for a long time.

 

When to see a doctor

See your doctor if you have one or more signs or symptoms associated with cardiomyopathy. Call 911 or your local emergency number if you have severe difficulty breathing, fainting or chest pain that lasts for more than a few minutes.

 

Some types of cardiomyopathies can be passed down through families (inherited). If you have the condition, your doctor might recommend that your family members be checked.


 






Causes

Often the cause of the cardiomyopathy is unknown. In some people, however, it is the result of another condition (acquired) or passed on from a parent (inherited).

 

Certain health conditions or behaviors that can lead to acquired cardiomyopathy include:

 

Long-term high blood pressure

Heart tissue damage from a heart attack

Long-term rapid heart rate

Heart valve problems

COVID-19 infection

Certain other infections, especially those that cause inflammation of the heart

Metabolic disorders, such as obesity, thyroid disease, or diabetes

Lack of essential vitamins or minerals in your diet, such as thiamin (vitamin B-1)

Pregnancy complications

Iron buildup in your heart muscle (hemochromatosis)

The growth of tiny lumps of inflammatory cells (granulomas) in any part of your body, including your heart and lungs (sarcoidosis)

The buildup of abnormal proteins in the organs (amyloidosis)

Connective tissue disorders

Drinking too much alcohol over many years

Use of cocaine, amphetamines, or anabolic steroids

Use of some chemotherapy drugs and radiation to treat cancer

 

Types of cardiomyopathies include:


 




Dilated cardiomyopathy. In this type of cardiomyopathy, the pumping ability of your heart's main pumping chamber — the left ventricle — becomes enlarged (dilated) and cannot effectively pump blood out of the heart.

 

Although this type can affect people of all ages, it occurs most often in middle-aged people and is more likely to affect men. The most common cause is coronary artery disease or heart attack. However, it can also be caused by genetic defects.

 

Hypertrophic cardiomyopathy. This type involves abnormal thickening of your heart muscle, which makes it harder for the heart to work. It mostly affects the muscle of your heart's main pumping chamber (left ventricle).

 

Hypertrophic cardiomyopathy can develop at any age, but the condition tends to be more severe if it occurs during childhood. Most people with this type of cardiomyopathy have a family history of the disease. Some genetic mutations have been linked to hypertrophic cardiomyopathy.

 

Restrictive cardiomyopathy. In this type, the heart muscle becomes stiff and less flexible, so it cannot expand and fill with blood between heartbeats. This least common type of cardiomyopathy can occur at any age, but it most often affects older people.

 

Restrictive cardiomyopathy can occur for no known reason (idiopathic), or it can by caused by a disease elsewhere in the body that affects the heart, such as amyloidosis.

 

Arrhythmogenic right ventricular dysplasia. In this rare type of cardiomyopathy, the muscle in the lower right heart chamber (right ventricle) is replaced by scar tissue, which can lead to heart rhythm problems. It is often caused by genetic mutations.

Unclassified cardiomyopathy. Other types of cardiomyopathies fall into this category.

 

Risk factors

There are a number of things that can increase your risk of cardiomyopathy, including:

 

Family history of cardiomyopathy, heart failure and sudden cardiac arrest

Long-term high blood pressure

Conditions that affect the heart, including a past heart attack, coronary artery disease or an infection in the heart (ischemic cardiomyopathy)

Obesity, which makes the heart work harder

Long-term alcohol misuse

Illicit drug use, such as cocaine, amphetamines, and anabolic steroids

Treatment with certain chemotherapy drugs and radiation for cancer

Many diseases also raise your risk of cardiomyopathy, including:

 

Diabetes

Thyroid disease

Storage of excess iron in the body (hemochromatosis)

Amyloidosis

Sarcoidosis

Connective tissue disorders

 

Complications

An enlarged heart

Cardiomyopathy can lead to serious complications, including:

 

Heart failure. Your heart cannot pump enough blood to meet your body's needs. Untreated, heart failure can be life-threatening.

Blood clots. Because your heart cannot pump effectively, blood clots might form in your heart. If clots enter your bloodstream, they can block the blood flow to other organs, including your heart and brain.

Heart valve problems. Because cardiomyopathy causes the heart to enlarge, the heart valves might not close properly. This can cause blood to flow backward in the valve.

Cardiac arrest and sudden death. Cardiomyopathy can trigger abnormal heart rhythms that cause fainting or, in some cases, sudden death if your heart stops beating effectively.

In many cases, you cannot prevent cardiomyopathy. Let your doctor know if you have a family history of the condition.

 

You can help reduce your risk of cardiomyopathy and other types of heart disease by living a heart-healthy lifestyle and making lifestyle choices such as:

 

Avoiding the use of alcohol or cocaine

Controlling high blood pressure, high cholesterol, and diabetes

Eating a healthy diet

Getting regular exercise

Getting enough sleep

Reducing your stress

 

 

Many patients suggest to their physicians that the quality of their interactions, our mindfulness and the efficiency of their visits mean health care like they have never experienced.

Cardiomyopathy is a medical term for a number of genetic and nongenetic diseases involving the heart muscle that adversely affect the heart's mechanical pumping function and its electrical system. It can occur in people of all ages, races, or genders, and it is a frequent cause of sudden cardiac arrest and sudden cardiac death.





Jan Rick Jennings, MHA, LFACHE

Senior Consultant

Senior Management Resources, LLC

JanJennings@EagleTalons.net

JanJennings@Blog.Blogspot.com

 

 

412.913.0636 Cell

724.733.0509 Office

                  

January 26, 2022                                                                         

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