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FAQ
Q: How are heart conditions
in kids diagnosed?
Q: My baby has congenital
heart disease. What could have caused this?
Q: My child was born
with a congenital heart defect. Does that mean he should not participate
in sports or other physical activities?
Q: How can I help my
child emotionally adjust to living with a heart defect?
Q: My child has a pacemaker.
What precautions should be taken for her safety?
Q: Should my child
be seen by a physician after fainting?
Q: How is my child
placed on the transplant waiting list for a new heart?
Q: After my child's
heart transplant, what is done to prevent rejection of the new
heart?
Q: Where can I find
more information on the Internet related to cardiovascular disease
and children?
Q: How are heart conditions in children
diagnosed?
A: Diagnosing and evaluating heart
disease in children can be complex and requires clinical care
by a physician or other healthcare professional. <For
more information on diagnosing and evaluating heart disease in
children>
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Q: My baby has congenital heart disease.
What could have caused this?
A: The vast majority of congenital
heart defects have no known cause. Mothers will often wonder if
something they did during the pregnancy caused the heart problem.
In most cases, nothing can be attributed to the heart defect.
Some heart problems do occur more often in families, so there
may be a genetic link to some heart defects. Some heart problems
are likely to occur if the mother had a disease while pregnant
and was taking medications, such as anti-seizure medicines. However,
most of the time, there is no identifiable reason as to why the
heart defect occurred. <For
an overview of congenital heart disease> <For
more information on the factors that contribute to congenital
heart disease>
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Q: My child was born with a congenital
heart defect. Does that mean he should not participate in sports
or other physical activities?
A: Many children with congenital
heart disease can play and participate in activities with friends,
but may tire faster and will naturally stop when they are tired.
For others, it may be necessary to actually place limits on physical
activity. Some children can play sports and participate in physical
education in school, but cannot participate in competitive or
contact sports. Always consult your child's physician as to what
type of activities are appropriate for your child. <For
more information on living with congenital heart disease>
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Q: How can I help my child emotionally
adjust to living with a heart defect?
A: Many factors influence how a
child feels about having congenital (present at birth) heart disease,
and how it affects him/her mentally and emotionally. Family, friends,
and community resources can help. <For
more information on the emotional and family issues surrounding
congenital heart disease>
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Q: My child has a pacemaker. What precautions
should be taken for her safety?
A: Your child should wear a medical
identification bracelet or necklace to let others know about the
pacemaker in case of emergency. When she is old enough to have a
wallet, it is a good idea to also carry an ID card that states she
has a pacemaker. <For
more information on living with a pacemaker>
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Q: Should my child be seen by a physician
after fainting?
A: Some types of syncope are caused
by a serious problem, so it is recommended that your child be
seen by a physician to determine the reason of all fainting spells.
<For more information
on syncope (fainting)>
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Q: How is my child placed on the transplant
waiting list for a new heart?
A: An extensive evaluation must
be completed before your child can be placed on the transplant
list. Testing includes: blood tests, diagnostic tests, and psychological
and social evaluation of the child (if old enough) and the family.
Tests are done to gather information that will help determine
how urgent it is that your child is placed on the transplant list,
as well as ensure the child receives a donor organ that is a good
match. <For more
information on heart transplant>
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Q: After my child's heart transplant, what
is done to prevent rejection of the new heart?
A: Medications must be given for
t he rest of your child's life to fight rejection. Each child
is unique, and each transplant team has preferences for different
medications. <For
more information on heart transplant>
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Q: Where can I find more information on
the Internet related to cardiovascular disease and children?
A: Information on the Internet should never substitute
the medical advice you receive from your child's physician. We
have provided here links to other World Wide Web sites with information
about cardiovascular diseases in children. We hope you find these
sites helpful, but please remember we do not control or endorse
the information presented on these Web sites, nor do these sites
endorse the information contained here. <For
additional Online Resources>
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