| What is amniocentesis?
Amniocentesis is one of several diagnostic tests that can
be carried out during pregnancy. It is used to detect any
possible chromosome abnormalities in the unborn child that
may cause Down's syndrome or other congenital problems.
In amniocentesis, a sample of the amniotic fluid that surrounds
the foetus is removed and analysed. This test is performed
from week 15 of the pregnancy onwards.
When is amniocentesis offered?
Amniocentesis is offered during pregnancy when:
a woman is considered at high risk because of a serum screening
test (blood test), which measures the levels of pregnancy
hormones in her blood. By combining these results with the
mother's age, it is possible to calculate the risk of the
child having Down's syndrome.
a woman is considered at high risk because she has previously
had a pregnancy affected by a chromosomal or genetic disorder.
an ultrasound examination has detected features or abnormalities
indicating an increased risk of a chromosome abnormality.
a woman requests it because she is concerned that her baby
may have a chromosome abnormality.
amniocentesis is occasionally required in the investigation
and management of other conditions in pregnancy such as
rhesus diseases. In these circumstances, the amniotic fluid
is analysed for substances in the fluid itself and not specifically
to look at the baby's chromosomes.
How is amniocentesis carried out?
Using ultrasound to guide the way, a fine needle is inserted
through the mother's abdomen and into the fluid surrounding
the foetus. About 20ml of the amniotic fluid is removed
and sent to a laboratory for analysis. The procedure usually
takes 5 to 10 minutes and the mother will feel only slight
discomfort. The foetus will be unaware of the procedure.
After the procedure, the mother should rest for the day.
She may feel slight cramping. Bleeding and leaking of fluid
from the vagina is not normal and she should contact the
hospital if this happens.
If her blood group is rhesus-negative (one in eight women
have this blood group), she will be given an injection of
Anti-D immunoglobulin into a muscle of her arm or leg. Anti-D
immunoglobulin is a substance administered to rhesus-negative
women when they have been potentially exposed to rhesus-positive
blood cells, for example after giving birth, a threatened
miscarriage, or amniocentesis. Its purpose is to prevent
the mother developing antibodies against the foetal blood
cells, which can cause severe jaundice or even foetal death.
The use of Anti-D immunoglobulin has been one of the success
stories of the last 20 years.
How long will it take to know the result?
A preliminary result may be available within 48 hours and
the final result will be known in two to three weeks.
Is amniocentesis safe for the mother and baby?
Amniocentesis is not risk-free and carries a slight risk
of causing a miscarriage. Between 1 in every 100 and 1 in
every 200 amniocentesis procedures will cause a miscarriage,
usually within three weeks of the procedure.
Before deciding upon screening and diagnostic tests the
mother should discuss any concerns she may have with her
obstetrician. Having information about the baby's chromosomes
has to be balanced against the small but real risk of losing
the pregnancy.
How reliable is the result from an amniocentesis?
Very few things in life are guaranteed 100 per cent reliable.
Amniocentesis comes very close, with a certainty of 99.9
per cent in identifying chromosome abnormalities.
What happens if the test shows abnormalities?
There is no treatment for chromosome abnormalities. If
a diagnosis is made before birth, and depending on the nature
of the abnormality that has been detected, the woman will
usually be offered a termination of pregnancy. The decision
whether or not to continue with the pregnancy always rests
with the parents and some parents may decide to continue.
Before an amniocentesis test is carried out, it is therefore
important for the expectant parents to consider what difference
an abnormal result would make to their wish to continue
with the pregnancy.
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