Tetralogy of Fallot
What is tetralogy of Fallot?
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Tetralogy of Fallot (TOF or "TET") is a complex condition
of several congenital (present at birth) defects that occur due
to abnormal development of the fetal heart during the first 8 weeks
of pregnancy. These problems include the following:
- ventricular septal defect (VSD) - an opening in the
ventricular septum, or dividing wall between the two lower chambers
of the heart known as the right and left ventricles.
- pulmonary (or right ventricular outflow tract) obstruction
- a muscular obstruction in the right ventricle, just below
the pulmonary valve, that decreases the normal flow of blood.
The pulmonary valve may also be small.
- overriding aorta - the aorta is shifted towards the
right side of the heart so that it sits over the ventricular
septal defect.
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"Tetralogy" refers to four heart problems. The fourth
problem is that the right ventricle becomes enlarged as it tries
to pump blood past the obstruction into the pulmonary artery.
Normally, oxygen-poor (blue) blood returns to the right atrium
from the body, travels to the right ventricle, then is pumped
through the pulmonary artery into the lungs where it receives
oxygen. Oxygen-rich (red) blood returns to the left atrium from
the lungs, passes into the left ventricle, and then is pumped
through the aorta out to the body.
In tetralogy of Fallot, blood flow within the heart varies, and
is largely dependent on the size of the ventricular septal defect,
and how severe the obstruction in the right ventricle is.
- With mild right ventricle obstruction, the pressure in the
right ventricle can be slightly higher than the left. Some of
the oxygen-poor (blue) blood in the right ventricle will pass
through the VSD to the left ventricle, mix with the oxygen-rich
(red) blood there, and then flow into the aorta. The rest of
the oxygen-poor (blue) blood will go its normal route to the
lungs. These children may have slightly lower oxygen levels
than usual, but may not appear blue.
- With more serious obstruction in the right ventricle, it is
harder for oxygen-poor (blue) blood to flow into the pulmonary
artery, so more of it passes through the VSD into the left ventricle,
mixing with oxygen-rich (red) blood, and then moving on out
to the body. These children will have lower than normal oxygen
levels in the bloodstream, and may appear blue, especially whenever
the pressure in the right ventricle is very high and large amounts
of oxygen-poor (blue) blood passes through the VSD to the left
side of the heart.
Tetralogy of Fallot occurs in about two out of every 10,000 live
births. It makes up about 8 percent of all cases of congenital
heart disease. Tetralogy of Fallot occurs equally in boys and
in girls.
What causes tetralogy of Fallot?
Some congenital heart defects may have a genetic link, either occurring
due to a defect in a gene, a chromosome abnormality, or environmental
exposure, causing heart problems to occur more often in certain
families.
Maternal abuse of alcohol during pregnancy, leading to fetal
alcohol syndrome (FAS), is linked to tetralogy of Fallot. Mothers
who take medications to control seizures and mothers with phenylketonuria
(PKU) are also more likely to have a baby with tetralogy of Fallot.
Most of the time, this heart defect occurs sporadically (by chance),
with no clear reason evident for its development.
Why is tetralogy of Fallot a concern?
The amount of oxygen-poor (blue) blood that passes through the VSD
to the left side of the heart varies. If the right ventricle obstruction
is severe, or if the pressure in the lungs is high, a large amount
of oxygen-poor (blue) blood passes through the VSD, mixes with the
oxygen-rich (red) blood in the left ventricle, and is pumped to
the body. The more blood that goes through the VSD, the less blood
that goes through the pulmonary artery to the lungs, and the less
oxygen-rich (red) blood that returns to the right side of the heart.
Soon, nearly all the blood in the left ventricle is oxygen-poor
(blue). This is an emergency situation, as the body will not have
enough oxygen to meet its needs.
Some situations, such as crying, increase the pressure in the
lungs temporarily, and increasing blueness might be noted as a
baby with tetralogy of Fallot cries. In other situations, the
pathway from the right ventricle to the pulmonary artery becomes
tighter, preventing much blood from passing that way, and allowing
oxygen-poor (blue) blood to flow through the VSD into the left
heart circulation. Both of these situations are nicknamed "TET
spells." Sometimes, steps can be taken to lessen the pressure
or the obstruction, and allow more blood to flow into the lungs
and less through the VSD. These steps, however, are not always
effective.
What are the symptoms of tetralogy of Fallot?
The following are the most common symptoms of tetralogy of Fallot.
However, each child may experience symptoms differently. Symptoms
may include:
- Because large amounts of oxygen-poor (blue) blood can flow
to the body under certain circumstances, one of the indications
of tetralogy of Fallot is blueness (blue color of the skin,
lips, and nail beds) that occurs with such activity as crying
or feeding, and quickly becomes more obvious.
- Some babies do not have noticeable cyanosis (blue color of
the skin, lips, and nailbeds), but may instead be very irritable
or lethargic due to a decreasing amount of oxygen available
in the bloodstream.
- Some children become pale or ashen in color, and may have
cool, clammy skin.
Any of these can be symptoms of tetralogy of Fallot. The symptoms
of tetralogy of Fallot may resemble other medical conditions or
heart problems. Always consult your child's physician for a diagnosis.
How is tetralogy of Fallot diagnosed?
Your child's physician may have heard a heart murmur during a physical
examination, and referred your child to a pediatric cardiologist
for a diagnosis. A heart murmur is simply a noise caused by the
turbulence of blood flowing through the obstruction from the right
ventricle to the pulmonary artery. Symptoms your child exhibits
will also help with the diagnosis.
A pediatric cardiologist specializes in the diagnosis and medical
management of congenital heart defects, as well as heart problems
that may develop later in childhood. The cardiologist will perform
a physical examination, listening to the heart and lungs, and
make other observations that help in the diagnosis. The location
within the chest that the murmur is heard best, as well as the
loudness and quality of the murmur (harsh, blowing, etc.) will
give the cardiologist an initial idea of which heart problem your
child may have. However, other tests are needed to help with the
diagnosis, and may include the following:
- chest x-ray - a diagnostic test which uses invisible
electromagnetic energy beams to produce images of internal tissues,
bones, and organs onto film.
- electrocardiogram (ECG or EKG) - a test that records
the electrical activity of the heart, shows abnormal rhythms
(arrhythmias or dysrhythmias), and detects heart muscle stress.
- echocardiogram (echo) - a procedure that evaluates
the structure and function of the heart by using sound waves
recorded on an electronic sensor that produce a moving picture
of the heart and heart valves.
- cardiac catheterization - a cardiac catheterization
is an invasive procedure that gives very detailed information
about the structures inside the heart. Under sedation, a small,
thin, flexible tube (catheter) is inserted into a blood vessel
in the groin, and guided to the inside of the heart. Blood pressure
and oxygen measurements are taken in the four chambers of the
heart, as well as the pulmonary artery and aorta. Contrast dye
is also injected to more clearly visualize the structures inside
the heart.
Treatment for tetralogy of Fallot treated:
Specific treatment for tetralogy of Fallot will be determined by
your child's physician based on:
- your child's age, overall health, and medical history
- extent of the condition
- your child's tolerance for specific medications, procedures,
or therapies
- expectations for the course of the condition
- your opinion or preference
Tetralogy of Fallot is treated by surgical repair of the defects.
A team of cardiac surgeons performs the surgery, usually before
an infant is 1 year old. In many cases, the repair is made at
around 6 months of age, or even a little earlier. Repairing the
heart defects will allow oxygen-poor (blue) blood to travel its
normal route through the pulmonary artery to receive oxygen.
The operation is performed under general anesthesia, and involves
the following:
- The ventricular septal defect is closed with a patch.
- The obstructed pathway between the right ventricle and the
pulmonary artery is opened and enlarged with a patch. If the
pulmonary valve is small, it may be opened as well.
Postoperative care for your child:
Children will spend time in the intensive care unit (ICU) after
tetralogy of Fallot repair. During the first several hours after
surgery, your child will be very drowsy from the anesthesia that
was used during the operation, and from medications given to relax
him/her and to help with pain. As time goes by, your child will
become more alert.
While your child is in the ICU, special equipment will be used
to help him/her recover, and may include the following:
- ventilator - a machine that helps your child breathe
while he/she is under anesthesia during the operation. A small,
plastic tube is guided into the windpipe and attached to the
ventilator, which breathes for your child while he/she is too
sleepy to breathe effectively on his/her own. After a truncus
repair, children will benefit from remaining on the ventilator
overnight or even longer so they can rest.
- intravenous (IV) catheters - small, plastic tubes inserted
through the skin into blood vessels to provide IV fluids and
important medicines that help your child recover from the operation.
- arterial line - a specialized IV placed in the wrist
or other area of the body where a pulse can be felt, that measures
blood pressure continuously during surgery and while your child
is in the ICU.
- nasogastric (NG) tube - a small, flexible tube that
keeps the stomach drained of acid and gas bubbles that may build
up during surgery.
- urinary catheter - a small, flexible tube that allows
urine to drain out of the bladder and accurately measures how
much urine the body makes, which helps determine how well the
heart is functioning. After surgery, the heart will be a little
weaker than it was before, and, therefore, the body may start
to hold onto fluid, causing swelling and puffiness. Diuretics
may be given to help the kidneys to remove excess fluid from
the body.
- chest tube - a drainage tube may be inserted to keep
the chest free of blood that would otherwise accumulate after
the incision is closed. Bleeding may occur for several hours,
or even a few days after surgery.
- heart monitor - a machine that constantly displays
a picture of your child's heart rhythm, and monitors heart rate,
arterial blood pressure, and other values.
Your child may need other equipment not mentioned here to provide
support while in the ICU, or afterwards. The hospital staff will
explain all of the necessary equipment to you.
Your child will be kept as comfortable as possible with several
different medications; some which relieve pain, and some which
relieve anxiety. The staff will also be asking for your input
as to how best to soothe and comfort your child.
After discharged from the ICU, your child will recuperate on
another hospital unit for a few days before going home. You will
learn how to care for your child at home before your child is
discharged. Your child may need to take medications for a while
at home, and these will be explained to you. The staff will give
you instructions regarding medications, activity limitations,
and follow-up appointments before your child is discharged.
Caring for your child at home following tetralogy of Fallot
repair:
Pain medications, such as acetaminophen or ibuprofen, may be recommended
to keep your child comfortable at home. Your child's physician will
discuss pain control before your child is discharged from the hospital.
After surgery, older children usually have a fair tolerance for
activity. Your child may become tired easily, and sleep more right
after surgery, but, within a few weeks, your child should be fully
recovered.
Long-term outlook after tetralogy of Fallot surgical repair:
Most children who have had a tetralogy of Fallot surgical repair
will live healthy lives. Activity levels, appetite, and growth will
eventually return to normal in most children. Your child's cardiologist
may recommend that antibiotics be given to prevent bacterial endocarditis
after discharge from the hospital.
Consult your child's physicians regarding the specific outlook
for your child.
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