What is a fetal echo?
Fetal echocardiography is
short for fetal echocardiogram, an ultrasound examination doctors use to check
for congenital heart defects. This disease affects about 1% of births each year
and covers a wide range of heart problems. The most common diagnosis of
congenital heart disease is a ventricular septal defect.
Understanding the fetal echo
The transducer used in a fetal
echocardiogram is called a transducer. It emits ultrasonic waves into the
abdomen, which create an image on the doctor's screen. These sound waves have a
frequency that travels through your skin and your baby's skin to bounce off the
structures of the heart.
This type of test does not
cause pain or harm to you or your child. It usually takes 30 minutes to 2 hours
due to the complexity of the baby's heart development and the number of things
the doctor is looking for.
A fetal echocardiogram is very
similar to other ultrasounds performed during pregnancy. It differs in that it
is only used to look at your baby's heart and no other structures.
What happens during a fetal echo?
An ultrasound technician
performs an examination and imaging. A pediatric cardiologist reads and
interprets the images like a specialist who understands the development of your
baby's heart in the womb.
Doctors do ultrasounds while
your baby is in the womb because 25% of babies with congenital heart defects
need treatment or surgery during their first year of life. Early detection
helps doctors prepare for child care and make sure they have a plan.
Preparation for fetal
echocardiography. Some ultrasounds require you to have a full bladder for best
results. A fetal echocardiogram is not required. In fact, you may prefer to
empty your bladder before the test, as this can take up to 2 hours.
As your doctor refers you to a
specialist, it is important that your technician has as much information as
possible. This may include details such as:
- Your own heart defect
- Family history of heart defects
- Medical records
- Details of your concerns
Why fetal echo is Important
Fetal echocardiography can
detect congenital heart defects that occur in the womb and can affect the
structure and function of your baby's heart. A mild congenital heart defect may
be a hole in your baby's heart, while a more severe case may be missing parts.
Types of congenital heart defects include:
- Atrialseptal defect
- Atrioventricular septal defect
- Coarctation of the aorta
- Double-outlet right ventricle
- d-transposition of the great arteries
- Ebstein anomaly
- Hypoplastic left heart syndrome
- Interrupted aortic arch
- Pulmonary atresia
- Single ventricle
- Tetralogyof fallot
- Total anomalous pulmonary venous return
- Tricuspid atresia
- Truncus arteriosus
- Ventricular septal defect
Fetal echocardiography results
The pediatric cardiologist
tells you and your doctor the results of the ultrasound. You can get the
answers you need from the test, or you can get more questions. It depends on
the child's gestational age, diagnosis, and imaging quality.
After the study is completed,
you will meet with a pediatric cardiologist to learn more about the results.
You may need to do one or more tests before the baby is born to monitor the
severity of the condition. This is true even if your first test comes back
normal.
Fetal echocardiograms are
considered reliable after 17 weeks of gestation, although they can be performed
vaginally instead of abdominally as early as 12 weeks. If a heart defect is
found, you will discover the best and worst scenarios for your child.
This will help you prepare for
what is to come after the birth. In some cases, children require observation or
surgery immediately after birth to stabilize the condition. Your doctor will
give you all the options available, talk about the possible outcomes of each,
and allow you and your partner to make the best decision.
A congenital heart defect can
increase your child's risk of developing other genetic problems, such as Down's
syndrome or DiGeorge's syndrome. Benign tumors can appear with heart problems,
which indicates tuberous sclerosis.
Other tests may include:
- High-level fetal ultrasound, more detailed ultrasound to look for other abnormal signs
- Fetal magnetic resonance imaging, which examines the development of your baby's organs.
- Genetic counseling, an assessment that determines the likelihood of a genetic disease, including the likelihood that future children will have a similar disease.
- Amniocentesis, which identifies chromosomal abnormalities, genetic disorders and some birth defects based on your baby's DNA while still in the womb
Fetal echo risks
Fetal echocardiograms are safe for both mother and child. This type of ultrasound poses no significant risk. However, not doing the recommended test can put your baby at risk after birth.