Prenatal Testing

Nuchal Translucency

The Nuchal Translucency scan (NT) is an ultrasound performed between 11 weeks 3 days and 13 weeks 6 days in conjunction with a blood test.  However, we try to organise your appointment for between 12 weeks 4 days and 13 weeks 2 days. This means that should your baby measure a little small for dates, you do not have to come back to have the scan repeated. Alternatively, if your baby is big for dates, we can still undertake the assessment. It is important to note that the NT scan is a screening test, not a diagnostic test. The nuchal translucency is a fluid filled collection located at the back of the fetus’ neck. All fetuses have this fluid collection and it is well visualised towards the end of the first trimester. We know that a fetus with Down syndrome will usually have a much larger fluid collection  than a fetus that does not have Down syndrome.

 

When a woman is pregnant, there are two hormones she produces that may vary if a baby has Down syndrome.  The levels of these hormones are measured ideally between 10 and 11 weeks gestation, prior to the ultrasound being performed (if possible). If they are found to be in the normal range, this decreases the chance of the baby having Downs syndrome. The hormones that we test are PAPP-A and free beta HCG. The level of PAPP-A tends to decrease when the baby has Down syndrome, while the level of free beta HCG tends to increase.

Once the nuchal translucency is measured and the scan is complete, the sonographer will enter the information from the scan and the blood test into a computer programme which will assess the risk for this particular fetus.

The results would be given to you as a chance of the fetus having a chromosome anomaly. Please see chart below. 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


If you have missed the opportunity or choose not to have a Nuchal Translucency Screening scan a first trimester scan can still provide an opportunity to check the baby for many fundamental abnormalities such as limb defect, major heart defects etc.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Patient attends NT screening

test at 12- 13 ½ weeks

Moderate risk aneuploidy   1:100 – 1:1000

Low risk aneuploidy

Better than 1:1000

High risk aneuploidy

1:2 – 1:100

Amniocentesis or CVS

Fetal DNA testing

Morphology scan

at 19 – 20 weeks

Low Risk

High Risk

Morphology Scan at

19 - 20 weeks

Confirm with

Amniocentesis

Wesley Fetal Medicine Unit

Suite 12
Level 1
Wesley Medical Centre
40 Chasely Street
AUCHENFLOWER  QLD  4066

 

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Greenslopes Fetal Medicine Unit

Suite 7.106
Level 7
Nicholson Street Specialist Centre
83 Nicholson Street
GREENSLOPES QLD 4120

 

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