NON-INVASIVE PRENATAL TESTING (Nipt)
The Ultrasound Suite along with the Bray Women’s Health Centre are now offering Harmony and Panorama non-invasive prenatal testing. Please call 012761522 to chat to one of our receptionists in the Bray Women’s Health Centre.
Non-invasive prenatal testing (Nipt) analyses cell-free fetal DNA circulating in the mother’s blood. It is a new screening test for Down syndrome (trisomy 21) and other conditions such as Edward’s syndrome and Patau syndrome (trisomies 18 and 13), as well as X and Y chromosome conditions. This simple blood test must be performed in conjunction with a dating ultrasound.
NIPT has a high accuracy for assessing fetal trisomy risk. It identifies more than 99% of fetuses with trisomy 21, 98% of fetuses with trisomy 18, 80% of fetuses with trisomy 13, and 96% of fetuses with Turner Syndrome in singleton pregnancies.
In addition to this the fetus’s sex can be determined with >99% accuracy. Accuracy for detecting other sex chromosome anomalies varies by condition. More importantly, the number of women who are required to have invasive testing (amniocentesis or CVS) after undergoing NIPT is <1%.
Please note that if the results of the test show high risk for one of the conditions it does not mean that the fetus definitely has the condition, although it is highly likely. So in the event of a high risk result we strongly recommend amniocentesis or CVS. Please also note that these tests are specific for the above mentioned conditions and they do not rule out all fetal and other pregnancy related abnormalities.
A basic scan is performed in conjunction with the blood test to confirm viability, gestational dating and number of fetuses. Please note this is a simple diagnostic scan just to obtain the above information. You will get a report, 2 pictures as well as a short video clip (a few seconds) of the scan in your take-home package. The scan must be performed at least 2 weeks before the blood test, ideally on the same day.
(€435 Bloods +€80 Scan)
Can be done from 10 weeks onward
Results available within 5 working days
Screens for Downs syndrome, Edwards syndrome, Patau syndrome, fetal sex (optional), Turner syndrome, Klinefelter syndrome, Triple X syndrome, XYY syndrome, and XXYY syndrome
Can be performed on twins, IVF donor egg and IVF donor egg twinsFind out more at www.ariosadx.com
(Basic €370 + €80 Scan)
(with 22q11.2 Deletion €420 + €80 Scan)
(Full Extended Panel €560 + €80 Scan)
Can be done from 9 weeks onward
Results available within 10 working days
Screens for Downs syndrome, Edwards syndrome, Patau syndrome, fetal sex (optional), Turner syndrome, Klinefelter syndrome, Triple X syndrome, XYY syndrome, XXYY syndrome, Triploidy, 22q11.2 deletion (DiGeorge), Prader-Willi, Cri-du-chat, and 1p36 deletion
Cannot be performed on twins, IVF donor egg and IVF donor egg twinsFind out more at - www.panoramatest.com/en