Non Invasive Prenatal Testing (NIPT) - PrenatalSAFE 3

Understanding Non Invasive Prenatal Testing (NIPT) What is NIPT? The Non Invasive Prenatal Testing (NIPT) is a revolutionary screening tool that allows parents to assess the risk of certain genetic conditions in their unborn child without... Read more

Understanding Non Invasive Prenatal Testing (NIPT)

What is NIPT?

The Non Invasive Prenatal Testing (NIPT) is a revolutionary screening tool that allows parents to assess the risk of certain genetic conditions in their unborn child without invasive procedures. Unlike traditional methods, NIPT analyses small fragments of fetal DNA found in the mother's bloodstream. This means that it's safer for both mother and baby because it eliminates the risk of miscarriage associated with invasive tests such as amniocentesis or chorionic villus sampling. As a result, many expectant parents are choosing NIPT for peace of mind during their pregnancy.

How Does it Work?

During the NIPT process, a blood sample is taken from the mother, which is then sent to a specialized lab for analysis. Using advanced technology, the lab can detect genetic anomalies such as Down syndrome, Trisomy 18, and Trisomy 13. The accuracy of NIPT is one of its greatest advantages, boasting detection rates of over 99% for certain conditions. This high level of accuracy provides parents with reliable information early in the pregnancy, helping them make informed decisions about their prenatal care.

Benefits of Choosing PrenatalSAFE 3 NIPT

Choosing the PrenatalSAFE 3 NIPT Blood Test comes with numerous benefits. First and foremost, it is non-invasive, thus avoiding the risks associated with more invasive genetic testing procedures. Parents also appreciate the confidentiality and ease of the process, as results are typically available within days. Additionally, the test can be performed as early as the 10th week of pregnancy, allowing early detection of potential issues. This proactive approach helps ensure that parents have the support they need throughout their pregnancy journey.

This prenatal blood test checks traces of the baby’s DNA in your blood for:

Down Syndrome (Trisomy 21)
Edwards Syndrome (Trisomy 18)
Patau Syndrome (Trisomy 13)
Gender Identification – find out the gender of your baby or babies (identical twins and single babies only)

These tests are typically available on the NHS only for high-risk mothers, but with a private test they can be taken by any expectant mother for complete peace of mind. Suitable from 10 weeks pregnancy onwards.

Free post-test genetic counselling is provided for any results which show a positive chance of a condition affecting your baby or babies.

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From 10 Weeks Pregnancy
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Results in 5-7 working days

Organise my own blood collection Collection Method £315 Suitable if you know a doctor or nurse who can take your blood

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Blood taken by a professional in-clinic Collection Method £335 Visit one of our clinics to have blood taken from your arm from a healthcare professional

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Book a home nurse visit to have your blood sample taken Collection Method £355 Choose 3 preferred dates for a Nurse to come to your location at your convenience

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What biomarkers do we test?

More Information

The PrenatalSAFE 3 NIPT blood test will assess the sample to identify the number of copies for chromosomes 13, 18 and 21 (aneuploidies). This detects whether the baby, or babies, have the genetic conditions Down Syndrome, Edwards Syndrome or Patau Syndrome. It can also tell you the gender of your baby or babies (identical twins and single babies only).

If you receive a high risk result, you will be offered support from a professional Genetic Counsellor at no extra cost. Unlike other providers, our genetic counselling service is included in the price of the test.

This is the basic NIPT test that is equivalent to the current NHS offering for high risk patients.

Analysed in a leading UK laboratory, the test is suitable for all pregnant women from 10 weeks of pregnancy onwards, with single or multiple foetuses and conceived naturally or using IVF/Donor Eggs. You do not have to be considered high risk, and can be of any age to take this test.

Based on an internal study from Eurofins Genoma, the test is highly accurate, with positive predictive values (the likelihood of the result being correct and not a false-positive) of:

Trisomy 21 (Down Syndrome) – 99.32%
Trisomy 18 (Edwards Syndrome) – 98.94%
Trisomy 13 (Patau Syndrome) – 82.22%

Unlike an invasive test such as an Amniocentesis, this simple blood test does not pose any risks to a pregnant woman or her unborn child. It is the safest way to detect genetic health conditions before birth.

When will I get the results?

The results will be sent to you directly in 5-7 days of the sample being received at the laboratory. The results report will clearly state whether the conditions have been detected so you can take this information to your GP for further discussion and investigation if needed.

Free post-test genetic counselling is provided for any results which show a positive chance of a condition affecting your baby or babies.

Important information

To qualify for this test you must:

be at least 10 weeks pregnant
have completed your first scan (private or NHS)

Goodbody will provide a specialised testing kit to be used by a qualified professional only.

Not sure if this test
is right for you?

Enquire via the form and a member of our team will get back to you, they are more than happy to help answer your questions and talk through the best option for you.

Contact us if you aren't sure, we'd be happy to help!

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AFTER YOUR TEST

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We promise to deliver affordable testing to everybody.

When you’re worried about your health, life can feel very stressful, especially if you don’t have the answers you need. We believe that health testing should be available to all, giving you answers when and where you need them.

That’s why we’ve partnered with Splitit, Dopple and Clearpay so you can pay for your tests in interest-free instalments, if you prefer.