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Nuchal thickness screening is used
as an alternative to biochemical screening for Down Syndrome. The same principles
apply.
Nuchal thickness screening is carried out by a 10 minute ultrasound examination of the baby
between 11 and 14 weeks of pregnancy. The amount of fluid behind the baby's neck is measured
in millimeters and a computer used to take this, your age and the baby's size and heart rate
into account. The computer programme will tell you what your risks are of having a chromosomally
abnormal baby. The risks will be expressed in the form 1 in so many pregnancies. The
Consultant will explain the result to you.
The sensitivity of the test is about
85%. That means that if the baby has got Down Syndrome there is an 85% chance that the test will
show you to have a risk of 1 in 300 or worse (and further testing advised). If the baby is normal
there is still a 5% chance that the computer will produce a high risk figure for your pregnancy.
The equivalent figures for most biochemical screening are 55-60% and 5%.
Patient information leaflet:
Nuchal thickness screening can tell you how
likely you are to have a baby with Down Syndrome. Nuchal thickness screening can not diagnose
Down Syndrome. Invasive testing (amniocentesis or CVS) is needed to be 100% certain that a baby
has or hasn't got Down Syndrome. In nuchal thickness screening the family history,
mother's age and appearance of the baby are taken into account.
Family history: if you have an aunt, uncle, brother or sister with Down
Syndrome or if
you have a child with Down Syndrome, it might make your chances bigger of having a baby with
Down Syndrome
Mother's age: older mothers are more likely to have babies with Down Syndrome
than
younger mothers.
The baby’s appearance: all babies have some fluid at the back of their
neck. The more fluid there is the more likely the baby has Down Syndrome.
The test
To arrange a test, or consultation, please contact the hospital.
Thank you.
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