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Reviewed 2004
Iowa Expanded MSAFP/Quad Screen
The Iowa Expanded AFP/Quad Screen will provide information about
your baby before it is born. It is a test available to all women between
fifteen and twenty weeks of pregnancy. A negative screen provides
reassurance that the risk for certain birth defects and pregnancy
problems has been reduced.
Even though most babies will be healthy, the period of testing is
a stressful time. If a problem is detected you will need support and
guidance.
The AFP/Quad screen is scheduled during the 15th to 20th week of
your pregnancy. Ask your doctor, midwife or nurse if this is the right
time to have this blood test done.
Read this information with your partner and discuss any questions
with your doctor or nurse. In addition you may call 319-356-8892.
An AFP nurse will return your call.
Seeing your doctor early to begin prenatal care is an important part
of preparing for the birth of your baby. There are tests designed
to provide you and your doctor or midwife with information about your
pregnancy and your developing fetus.
Although most babies are born healthy, about three to four percent
are born with a birth defect. Frequently this happens without warning,
and families and doctors are not prepared for this difficult experience.
The Iowa Expanded MSAFP/Quad Screen is a test available to all women
early in pregnancy. This test can identify a woman with an increased
risk to have a fetus with certain kinds of birth defects or to develop
a problem later in pregnancy.
The Iowa Expanded AFP/Quad Screen is a single blood test drawn between
weeks 15 and 20 of pregnancy to measure the amount of AFP and three
other markers in the mother's bloodstream.
All of the markers are made by the fetus and placenta. The levels
of these markers may be altered in a predictable way when a fetus
has certain birth defects such as an open neural tube defect, an abdominal
wall defect, or a chromosome problem such as Down syndrome or trisomy
18.
For most women the results of this screen will be negative and no
further tests are ordered. This is reassuring, but does not guarantee
the fetus is normal.
The MSAFP/Quad screen is the first test in a series of tests that
may be done. It cannot directly diagnose birth defects, but can help
you and your doctor decide when other tests such as an ultrasound
and amniocentesis may be of value.
What causes the Iowa Expanded MSAFP/Quad Screen to be positive?
A screen is called positive if the hormone levels are too high or
too low compared to the normal levels for that week of pregnancy.
What are the reasons for a positive Iowa Expanded MSAFP/Quad Screen?
- You may be earlier or later in your pregnancy than you thought.
The levels of hormones normally change with each week of pregnancy.
After ultrasound, the result of the screen can be refigured if the
corrected fetal age was between 15 and 20 weeks at the time the
initial sample was drawn.
- You may be carrying twins.
- The hormone levels are altered, but the fetus is normal. Remember
this is a screening test and some women with a normal fetus will
have a screen that is positive.
- The fetus may be normal, but the placenta may not be functioning
properly.
- The fetus may have a neural tube defect or abdominal wall defect.
Any opening in the body of the fetus will allow higher levels of
AFP to pass into the amniotic fluid and from there into your blood
stream.
- The fetus may have Down syndrome or trisomy 18.
- The fetus may have Smith Lemli-Opitz Syndrome.
What if the Iowa Expanded AFP/Quad Screen is positive showing
a risk for Down syndrome?
An ultrasound is done. If the ultrasound changes your due date the
result of the screen may now be normal. The blood test is only repeated
if the initial sample was drawn before 15 weeks.
After ultrasound, about four percent of women will have a screen
that remains positive. They will be offered amniocentesis due to an
increased risk for Down syndrome in the fetus. The factors used to
figure the risk for chromosome problems include maternal age and weight,
fetal age (week of pregnancy), and the levels of AFP, UE3, hCG and
Inhibin A in the maternal blood.
What if the AFP Portion of the MSAFP Quad Screen is elevated?
An ultrasound is done. The blood test is repeated if the result remains
elevated after ultrasound confirms or corrects the fetal age. About
40 percent of the repeated tests will be normal and no further testing
will be needed.
What if the second MSAFP Screen remains elevated?
Those with an MSAFP Screen that remains elevated will go on to have
a more detailed ultrasound and possible an amniocentesis. About one
in 30 of these women will have a fetus with a potentially serious
birth defect. About half of these will be neural tube defects.
If the amniocentesis results are positive (abnormal) another ultrasound
will be done to identify the extent and location of the defect. This
information will be needed to provide you with accurate counseling
about the problems the fetus may have as a result of the defect.
If the ultrasound and amniocentesis (if done) are normal, but the
second MSAFP Screen remains elevated, you may have an increased risk
for problems later in the pregnancy. These problems are related to
the function of the placenta and include early labor, a smaller than
average baby and some other pregnancy problems. Most women with high
MSAFP levels will still have healthy babies, but you should discuss
your care with your doctor so you will know what to do if a problem
occurs.
Are there other conditions that may be detected because of abnormal
levels of these pregnancy markers?
Yes, it has been found that a very low estriol (UE3) may indicate
a condition called Smith-Lemli-Opitz Syndrome. Less than one half
of one percent of women screened will be positive for this condition.
What is Smith-Lemli-Opitz Syndrome?
Smith-Lemli-Opitz Syndrome is a genetic condition that results in
multiple physical and mental problems in the affected individual.
There may be a cleft palate, unusual fingers and toes, and cataracts.
Malformations of other organ systems including the brain, kidneys,
heart and lungs have also been reported. Women with lower levels of
estriol will be offered counseling and diagnosis for this condition
What can be done if a birth defect
is discovered?
It is a shock to learn that your fetus has a birth defect. You will
need information about the specific condition and any treatment that
is available. There are two primary options to consider: You may begin
to plan for the birth of a baby who may need intensive care at birth
or you may elect to end the pregnancy. Any available prenatal treatment
options for an affected fetus will be discussed at the time of the
evaluation.
What is Ultrasound?
Ultrasound (sonogram) uses sound waves to create pictures of the
fetus. Careful measurements help to determine the age of the fetus,
whether there is more than one fetus, and in some cases may reveal
a birth defect.
What is amniocentesis?
Amniocentesis involves using a thin needle to withdraw fluid from
around the fetus for testing. The fetal cells and AFP in this fluid
are studied to diagnose birth defects such as neural tube defects
and chromosome problems such as Down syndrome or trisomy 18.
What is AFP?
Alpha-fetoprotein is a substance produced by every fetus as it grows.
This substance is passed into the amniotic fluid that surrounds the
fetus and from there into the mother's bloodstream. Nothing the mother
does alters the level of the protein. It is not related to the protein
in the mother's diet, but comes directly from the fetus.
What if I am carrying twins?
Risk for neural tube defects can be evaluated but we do not provide
Down syndrome screening for twins. We do not provide screening for
pregnancies with more than two fetuses.
What are neural tube defects?
In the first weeks of pregnancy when the fetus is less than one inch
long, the brain and spinal cord begin to form a structure along the
fetal back known as the neural tube. The top of this tube develops
into the head and brain; the rest becomes the spinal cord. Neural
tube defects occur when the neural tube does not close properly around
the brain or spinal cord.
The two major types of neural tube defects are spina bifida and anencephaly.
About one in 1,000 pregnancies in Iowa results in the birth of an
infant with a neural tube defect. Half of these have spina bifida
and half have anencephaly.
The effects from spina bifida (open spine) may range from mild to
severe. The severity of the problem depends upon where the defect
in the spinal cord is located. The problems may range from weakness
of the leg muscles to actual paralysis. A higher defect on the spine
will result in more paralysis in the legs. Because the nerves that
direct bowel and bladder functions are at the base of the spinal cord,
there may be problems with bowel and bladder control. Over 80 percent
of newborns with spina bifida have hydrocephalus (water on the brain).
Corrective surgery and physical therapy can help lessen the disability
in these children so that some may lead relatively normal lives. In
severe cases the baby is stillborn or dies soon after birth.
Anencephaly (open brain) occurs when the head and brain do not develop
normally. Babies born with this condition are almost always stillborn
or die soon after birth.
If the defect is in the spinal cord itself, but is covered by skin,
the AFP will not leak into the amniotic fluid. These defects will
not be detected by the blood test and the effects tend to be less
severe.
What is Down syndrome?
Down syndrome is a birth defect caused by an extra number 21 chromosome
in every cell of the body. Individuals with Down syndrome are mentally
retarded and may have other physical problems such as heart defects.
Any woman can have a fetus with
Down syndrome, but it is known that Down syndrome and other chromosome problems
happen more often as women get older.
What is Trisomy 18?
Trisomy 18 is a chromosome problem that is caused by having three
#18 chromosomes in all the cells of the body. Serious problems with
growth and development are present before birth and physical problems
such as an open spine or heart defect may be present.
What are the risks involved in the screening process?
Anxiety: Waiting for the results of a repeated test is a very anxious
time for women who have had the Screening test. It is natural to be
afraid when considering the possibility of a problem with your baby.
The results of all repeated blood tests are telephoned to the doctor's
office the day they are complete. Fortunately, most women with a positive
Screen will have healthy babies.
Pregnancy Loss: If the screening process leads to amniocentesis there
is a small but real risk of pregnancy loss associated with this procedure.
Ask the doctor who does your amniocentesis to discuss that possibility
with you.
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