CardiomyopathyWhat is cardiomyopathy?
Cardiomyopathy is any disease of the heart muscle in which the heart loses
its ability to pump blood effectively. In some instances, heart rhythm is
disturbed, leading to irregular heartbeats, or arrhythmias. There may be
multiple causes of cardiomyopathy, including viral infections. Sometimes,
the exact cause of the muscle disease is never found.
How does cardiomyopathy differ from other heart
disorders?
Cardiomyopathy differs from many of the other disorders of the heart in
several ways, including the following:
- Cardiomyopathy can, and often does, occur in the young.
- The condition is fairly uncommon, affecting only about 50,000
Americans (adults and children).
- Cardiomyopathy is a leading cause for heart transplantation.
- The condition tends to be progressive and sometimes worsens fairly
quickly.
- It may be associated with diseases involving other organs, as well
as the heart.
Why is cardiomyopathy a concern?Cardiomyopathy prevents the heart muscle from pumping enough
blood to meet the body's needs.
What causes cardiomyopathy?Viral infections that infect the heart are a major cause of
cardiomyopathy. In some instances, cardiomyopathy is a result of another
disease or its treatment, such as complex congenital (present at birth)
heart disease, nutritional deficiencies, uncontrollable, fast heart
rhythms, or certain types of chemotherapy for childhood cancers.
Sometimes, cardiomyopathy can be linked to a genetic abnormality. Other
times, the cause is unknown.
What types of cardiomyopathy commonly affect
children?
The following types of cardiomyopathy commonly affect children:
- dilated (congestive) cardiomyopathy
This is the most common form of cardiomyopathy. The heart muscle is
enlarged and stretched (dilated), causing the heart to become weak and
pump inefficiently. Other problems that may occur with dilated cardiomyopathy
include the following:
- irregular heart rhythms
- risk of blood clots
- congestive heart failure
Various infections (including viral) which lead to an inflammation
of the heart muscle (myocarditis) can cause this type of cardiomyopathy.
Contact with toxins or very powerful therapeutic drugs, such as certain
types of chemotherapy given to fight cancer, have been known to cause
dilated cardiomyopathy. Heredity can also be a factor. Twenty percent
of people with dilated cardiomyopathy have a parent or sibling with
the disease. In many cases, a specific cause for this type of the
disease is never identified.
Because the heart muscle is weak and unable to pump enough blood
to meet the body's demands, the body tries to preserve blood flow
to essential organs such as the brain and kidneys by reducing blood
flow to other areas of the body, such as the skin and muscles.
The following are the most common symptoms of dilated cardiomyopathy.
However, each child may experience symptoms differently. Symptoms
may include:
- pale or ashen skin color
- cool, sweaty skin
- rapid heart rate
- rapid breathing rate
- shortness of breath
- fatigue
- irritability
- chest pain
- poor appetite
- slow growth
Specific treatment for dilated cardiomyopathy will be determined
by your child's physician based on:
- your child's age, overall health, and medical history
- extent of the disease
- your child's tolerance for specific medications, procedures, or
therapies
- expectations for the course of the disease
- your opinion or preference
Your child's physician may recommend medications to accomplish the
following:
- help the heart beat more effectively
- decrease the workload of the heart
- decrease the oxygen requirements of the heart
- prevent clots from forming
- decrease inflammation of the heart
- regulate irregular heartbeats
In some cases, d ilated cardiomyopathy due to viral causes improves.
In other cases, the condition worsens and transplantation of the heart
may be considered. Consult your child's physician for more information
regarding the specific outlook for your child.
- hypertrophic cardiomyopathy (Also known as hypertrophic
obstructive cardiomyopathy, HOCM; asymmetric septal hypertrophy, ASH; or
idiopathic hypertrophic subaortic stenosis, IHSS.)
In this type of cardiomyopathy, the muscle mass of the left ventricle of
the heart is larger than normal, or the wall between the two ventricles
(septum) becomes enlarged. These abnormalities obstruct the blood flow
from the left ventricle.
The thickened muscle or septal wall can also affect one of the leaflets
of the mitral valve, which separates the left atrium and the left ventricle.
The valve leaflet becomes leaky, allowing blood to move backwards from
the left ventricle into the left atrium, instead of forward to the body.
Hypertrophic cardiomyopathy is often hereditary. One-half of children
with the disease have a parent or sibling with varying degrees of left
ventricular muscle or ventricular wall enlargement, although relatives
may or may not have symptoms.
Children with hypertrophic cardiomyopathy may have symptoms that increase
with exertion or symptoms may be unpredictable.
The following are the most common symptoms of hypertrophic cardiomyopathy.
However, each child may experience symptoms differently. Symptoms may
include:
- shortness of breath on exertion
- dizziness
- fainting
- chest pain
- abnormal heart rhythms
Specific treatment for hypertrophic cardiomyopathy will be determined
by your child's physician based on:
- your child's age, overall health, and medical history
- extent of the disease
- your child's tolerance for specific medications, procedures, or
therapies
- expectations for the course of the disease
- your opinion or preference
Your child's physician may recommend medications to accomplish the
following:
- decrease the workload of the heart
- decrease the oxygen requirements of the heart
- regulate irregular heartbeats
Surgical treatment may include:
- removal of part of the enlarged muscle
- artificial pacemaker
- heart transplantation
Consult your child's physician for more information regarding the specific
outlook for your child.
More Information
Schneider Children's
Hospital Division of Cardiology
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