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Heart Care |
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Atrial Special defect |
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An atrial septal defect
(ASD) — sometimes referred to as a hole in the
heart — is a type of congenital
heart
defect in which there is an abnormal opening
in the dividing wall between the upper filling
chambers of the heart (the atria). In most cases
ASDs are diagnosed and treated successfully with few
or no complications.
What Is an Atrial Septal
Defect?
To understand this defect, it
first helps to review some basics about the way a
healthy heart typically works.
The heart
has four chambers: The two lower pumping chambers
are called the ventricles, and the two upper filling
chambers are the atria.
In a healthy
heart, blood that returns from the body to the
right-sided filling chamber (right atrium) is low in
oxygen. This blood passes to the right-sided pumping
chamber (right ventricle), and then to the lungs to
receive oxygen. The blood that has been enriched
with oxygen returns to the left atrium, and then to
the left ventricle. It's then pumped out to the body
through the aorta, a large blood vessel that carries
the blood to the smaller blood vessels in the body.
The right and left filling chambers are separated by
a thin shared wall, called the atrial septum.
Kids with an atrial septal defect (ASD) have
an opening in the wall (septum) between the atria.
As a result, some oxygenated blood from the left
atrium flows through the hole in the septum into the
right atrium, where it mixes with oxygen-poor blood
and increases the total amount of blood that flows
toward the lungs. The increased blood flow to the
lungs creates a swishing sound, known as a
heart murmur. This heart murmur, along with other
specific heart sounds that can be detected by a
cardiologist, may be clues that a child has an ASD.
ASDs can be located in different places on the
atrial septum, and they can be different sizes. The
symptoms and medical treatment of the defect will
depend on those factors. In some rare cases, ASDs
are part of more complex types of congenital heart
disease. It's not clear why, but ASDs are more
common in girls than in boys.
What Causes an ASD?
ASDs occur during fetal development of the heart and
are present at birth. During the first weeks after
conception, the heart develops. If a problem occurs
during this process, a hole in the atrial septum may
result.
In some cases, the tendency to
develop a ASD may be genetic. There can be genetic
syndromes that cause extra or missing pieces of
chromosomes that can be associated with ASD. For the
vast majority of children with a defect, however,
there's no clear cause of the ASD.
Signs and Symptoms of an ASD
The size of an ASD and its location in the
heart will determine what kinds of symptoms a child
experiences. Most children who have ASDs seem
healthy and appear to have no symptoms. Generally,
kids with an ASD feel well and grow and gain weight
normally. Infants and children with larger, more
severe ASDs, however, may possibly show some of the
following signs or symptoms:
- Poor appetite
- Poor growth
- Fatigue
- Shortness of breath
- Lung problems and infections, such as
pneumonia
If an ASD is not treated, health problems can
develop later, including an abnormal heart rhythm
(known as an atrial arrhythmia) and problems in
how well the heart pumps blood. As kids with ASDs
get older, they may also be at an increased risk
for stroke, since a blood clot that develops can
pass through the hole in the wall between the
atria and travel to the brain. Pulmonary
hypertension (high blood pressure in the lungs)
may also develop over time in older patients with
larger untreated ASDs.
Fortunately,
most kids with ASD are diagnosed and treated long
before the heart defect causes physical symptoms.
Because of the complications that ASDs can cause
later in life, pediatric cardiologists often
recommend closing ASDs early in childhood.
Diagnosing an ASD
Generally, a child's doctor hears the heart
murmur caused by ASD during a routine checkup or
physical examination. ASDs are not always
diagnosed as early in life as other types of heart
problems, such as
ventricular
septal defect (a hole in the wall between
the two ventricles). The murmur caused by an ASD
is not as loud and may be more difficult to hear
than other types of heart murmurs, so it may be
diagnosed any time between infancy and adolescence
(or even as late as adulthood).
If a
doctor hears a murmur and suspects a heart defect,
the child may be referred to a pediatric
cardiologist, a doctor who specializes in
diagnosing and treating childhood heart
conditions. If an ASD is suspected, the
cardiologist may order one or more of the
following tests:
- Chest X-ray, which produces an image of the
heart and surrounding organs
- electrocardiogram
(EKG), which records the electrical
activity of the heart and can indicate volume
overload of the right side of the heart
Echocardiogram (echo), which uses sound waves to
produce a picture of the heart and to visualize
blood flow through the heart chambers. This is
often the primary tool used to diagnose ASD.
Treating an ASD
Once an ASD is diagnosed, treatment will
depend on the child's age and the size, location,
and severity of the defect. In kids with very
small ASDs, the defect may close on its own.
Larger ASDs usually won't close, and must be
treated medically. Most of these can be closed in
a cardiac catheterization lab, although some ASDs
will require open-heart surgery.
A
child with a small defect that causes no symptoms
may simply need to visit a pediatric cardiologist
regularly to ensure that there are no problems,
often, small defects will close spontaneously
without any treatment during the first years of
life. In general, a child with a small ASD won't
require restrictions on his or her physical
activity.
In most children with ASD,
though, doctors must close the defect if it has
not closed on its own by the time a child is old
enough to start school.
Depending on
the position of the defect, many children with ASD
can have it corrected with a cardiac
catheterization. In this procedure, a thin,
flexible tube called a catheter is inserted into a
blood vessel in the leg that leads to the heart. A
cardiologist guides the tube into the heart to
make measurements of blood flow, pressure, and
oxygen levels in the heart chambers. A special
implant can be positioned into the hole in the
septum. The device is designed to flatten against
the septum on both sides to close and permanently
seal the ASD. In the beginning, the natural
pressure in the heart holds the device in place.
Over time, the normal tissue of the heart grows
over the device and covers it entirely. This
non-surgical technique for closing an ASD
eliminates the scar on the chest needed for the
surgical approach, and has a shorter recovery
time, usually just an overnight stay in the
hospital.
Because there is a small risk
of blood clots forming on the closure device while
new tissue heals over it, children who undergo
device closure of an ASD may need to be on
medications for several months after the procedure
to prevent clots from forming.
If
surgical repair for ASD is necessary, a child will
undergo open-heart surgery. In this procedure, a
surgeon makes a cut in the chest and a heart-lung
machine is used to do the work of the circulation
while the heart surgeon closes the hole. The ASD
may be closed directly with stitches or by sewing
a patch of surgical material over the defect.
Eventually, the tissue of the heart heals
over the patch or stitches, and by 6 months after
the surgery, the hole will be completely covered
with tissue.
For 6 months following
catheterization or surgical closure of an ASD,
antibiotics are recommended before routine dental
work or surgical procedures to prevent infective
endocarditis. Once the tissue of the heart has
healed over the closed ASD most people who have
had their ASDs corrected no longer need to worry
about having a higher risk of infective
endocarditis.
Your doctor will discuss
other possible risks and complications with you
prior to the procedure. Typically, after repair
and adequate time for healing, children with ASD
rarely experience further symptoms or disease.
Caring for a
Child With an ASD
Kids who undergo
cardiac catheterization to close an ASD usually
spend the night in the hospital after the
procedure. Those who have had a catheterization
procedure should also be kept out of gym class or
sports practice for a week; after a week, they can
usually return to their normal physical
activities, with their doctor's OK.
Kids who undergo surgery for their ASDs usually go
home after a few days in the hospital if there are
no complications. After surgical ASD repair, the
main medical concern is the healing of the chest
incision. In general, the younger patients are
when they have their surgical repairs, the less
pain they will have during recovery. The child
will be watched closely for signs or symptoms that
may indicate a problem. If your child has trouble
breathing, is not eating, has fever, or redness or
pus oozing from the incision, get medical
treatment right away. In most cases, kids who have
had ASD surgery recover quickly and without
problems.
In the weeks following
surgery or cardiac catheterization, your doctor
will check on your child's progress. Your child
may undergo another echocardiogram to make sure
that the heart defect has closed completely. Kids
who have undergone ASD repair will continue to
have follow-up visits with the cardiologist.
Most children who undergo treatment for ASDs
recover quickly — you may even notice that
within a few weeks of treatment, your child is
eating more and is more active than before
surgery. However, some signs and symptoms may
indicate a problem. If your child is having
trouble breathing, call the doctor or take your
child to the emergency department immediately.
Other symptoms that may indicate a problem
include:
- A bluish tinge or color (cyanosis) to the
skin around the mouth or on the lips and tongue
- Poor appetite or difficulty feeding
- Failure to gain weight or weight loss
- Listlessness or decreased activity level
- Prolonged or unexplained fever
- Increasing pain, tenderness, or pus oozing
from the incision
Call your doctor if you notice any of these
signs in your child after closure of the ASD.
Any time a child is diagnosed with a heart
condition, it can be scary. But the good news is
that your pediatric cardiologist will be very
familiar with this condition and how to best manage
it. Most kids who've had an ASD corrected have a
normal life expectancy and go on to live healthy,
active lives.
Special
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