NIPT Classic
from the 11th week of pregnancy
Goals
- Completely risk-free screening for chromosomal abnormalities (trisomy 13, 18, and 21) at the earliest possible stage of pregnancy
Cost of the examination
€600
NIPT (non-invasive prenatal testing) determines whether there is a risk of a chromosomal abnormality. It analyzes fragments of fetal DNA from the mother's blood. NIPT can detect 99.9% of trisomy 21 cases. The test also provides information on the risks of trisomy 18 and 13, and the chromosomal sex can be determined.
From the 11th week of pregnancy, blood collection for the NIPT (Non-Invasive Prenatal Test) can be performed at any point throughout the pregnancy. It is always recommended to combine the NIPT with an ultrasound scan.
Certainty through highest precision: The risk-free blood test for your baby
The Non-Invasive Prenatal Test (NIPT) requires only a simple blood draw, making it a completely risk-free alternative for both mother and child compared to chorionic villus sampling and amniocentesis.
The NIPT involves an examination of the mother's blood, which contains the baby's DNA. An analysis of these fragments of fetal genetic material is used to determine the risk of a genetic abnormality in the unborn child. With a high reliability of more than 99 percent, the results indicate whether Down syndrome (trisomy 21) is present. The detection rate is 92 percent for trisomy 13 (Patau syndrome) and 96 percent for trisomy 18 (Edwards syndrome). The high precision of the NIPT significantly reduces the likelihood that further clarification by invasive procedures will be recommended due to a false-positive result. The false-positive rate is less than 0.1 percent.
The NIPT is recommended in combination with the first-trimester ultrasound scan, including pre-eclampsia screening. This early screening examination can detect or rule out up to 65 percent of malformations that do not have a direct genetic cause. These cannot be detected with the NIPT.
The Non-Invasive Prenatal Test is also offered as a 2-part examination. It can be performed as early as the 11th week of pregnancy and therefore usually means early reassurance for parents. If the NIPT is carried out early (11th week of pregnancy), we recommend performing the first-trimester ultrasound, including pre-eclampsia screening, between the 12th and 14th week of pregnancy.
For twin pregnancies and pregnancies with donor eggs, a NIPT Classic is possible.
- The findings will be available 7-10 working days after the examination.
Investigation Timeline
Our prenatal center is equipped with its own laboratory. This makes it possible to carry out examinations entirely in our facility and to inform you of the results very quickly.
Book an appointment
Our prenatal center is equipped with its own laboratory. This allows us to perform all examinations entirely in-house.
Cost of the examination
€600Q&A
The NIPT is currently the best risk-free test for determining the probability of chromosomal disorders. In principle, any pregnant woman can opt for this test. The NIPT is recommended for those with an intermediate risk between 1:300 and 1:1,000 after the Combined Test, or as a primary test in cases of higher background risk.
During NIPT (Non-invasive Prenatal Testing), fetal DNA fragments that can be detected in the maternal blood are analyzed using molecular biological methods. These are detectable from gestational week 10 +0.
There are various non-invasive prenatal tests (NIPTs) that vary in their scope. The recommended NIPT used at the Prenatal Center at the Wien screens for trisomy 21, trisomy 18 and 13, as well as the baby's chromosomal sex. In addition, the child's Rhesus factor, triploidies, cystic fibrosis, and other diseases can be tested with varying detection rates.
The costs for the NIPT (non-invasive prenatal test) depend on the scope of the test. We offer 5 different test packages – please refer to our price list for the corresponding prices.
The NIPT (non-invasive prenatal test) is the most reliable non-invasive test for determining the risk of Down syndrome. The detection rate is over 99% for trisomy 21.