Non Invasive Prenatal Testing (NIPT) - PrenatalSAFE Complete Plus
Understanding Non Invasive Prenatal Testing (NIPT) - PrenatalSAFE Complete Plus
What is Non Invasive Prenatal Testing?
Non Invasive Prenatal Testing (NIPT) - PrenatalSAFE Complete Plus is a revolutionary method designed to assess the risk of genetic conditions in your unborn child. This test is non-invasive, utilising a simple blood sample from the mother, which makes it safe for both the mother and the baby. Because it analyses small fragments of fetal DNA, it provides highly accurate results for conditions such as Down syndrome and other chromosomal abnormalities.
How Does PrenatalSAFE Work?
PrenatalSAFE Complete Plus works by examining the free-floating DNA present in a pregnant woman’s bloodstream. This DNA originates from the placenta, which shares the same genetic material as the fetus. The testing process is simple and only requires a blood draw, so it is quick and convenient. Furthermore, this non-invasive approach significantly reduces the risk compared to invasive tests like amniocentesis, which carry a slight risk of miscarriage.
The Benefits of Choosing PrenatalSAFE Complete Plus
Choosing PrenatalSAFE Complete Plus offers several benefits, including early detection and peace of mind. Many parents appreciate the detailed insights into their baby’s health provided by this testing method. Additionally, because the results are generally available within a week, parents can make informed decisions about their pregnancy sooner. Therefore, NIPT is not only a convenient option but also aligns with modern parental expectations for safe and accurate prenatal care.
This prenatal blood test, sometimes known as the Safe test, checks traces of the baby’s DNA in your blood for:
- Down Syndrome (Trisomy 21)
- Edwards Syndrome (Trisomy 18)
- Patau Syndrome (Trisomy 13)
- Turner Syndrome (Monosomy X)
- Klinefelter syndrome
- Jacobs Syndrome
- Rare Autosomal Aneuploidies
- Genetic Deletions and Duplications
- 9 different Microdeletion Syndromes including Prader-Willi, Angelman and DiGeorge Syndrome.
- 5 Inherited Genetic Diseases including Deafness, Thalassemia, Sickle Cell Anaemia and Cystic Fybrosis
- Almost 50 De Novo diseases, which develop spontaneously during conception or fertilisation
- Gender Identification – single pregnancies and identical twins
This test is significantly more extensive than the tests offered on the NHS to high risk mothers, and can be taken by any expectant mother, regardless of risk status.
Suitable from 10 weeks pregnancy onwards, and for all single pregnancies.
Free post-test genetic counselling is provided for any results which show a positive chance of a condition affecting your baby or babies.
Read lessCouldn't load pickup availability
What biomarkers do we test?
Compare NIPT tests
Find the right test for your pregnancy
All Goodbody NIPT tests use a simple, safe blood sample from 10 weeks. The right one for you depends on how much you want to know.
| Compare tests | PrenatalSAFE 3 The essentials From £315 View test | PrenatalSAFE 5 Adds sex chromosomes From £375 View test | PrenatalSAFE Karyo All 23 chromosome pairs From £645 View test | Most popularPrenatalSAFE Karyo Plus Adds 9 microdeletions From £795 View test | Most comprehensivePrenatalSAFE Complete Plus Most comprehensive From £1,545 Your selection |
|---|---|---|---|---|---|
| Conditions screened | 3 | 7 | 10 | 19 | 21+ |
| Down, Edwards & Patau syndrome Trisomy 21, 18 & 13 | |||||
| Sex chromosome disorders Turner, Klinefelter, Jacobs | |||||
| All 23 chromosome pairs Aneuploidies, deletions & duplications | |||||
| 9 microdeletion syndromes Prader-Willi, Angelman, DiGeorge & more | |||||
| 5 inherited genetic diseases Cystic fibrosis, sickle cell, thalassemia, deafness | |||||
| ~50 De Novo diseases Spontaneous mutations not inherited from parents | |||||
| Gender identification Single pregnancies & identical twins | |||||
| Twin pregnancy | |||||
| Results turnaround | 3–5 working days | 3–5 working days | 5–7 working days | 10–12 working days | Staged: 10 & 20 working days |
| From pregnancy week | 10 weeks | 10 weeks | 10 weeks | 10 weeks | 10 weeks |
| Sample collection | In-clinic or at home | In-clinic or at home | In-clinic or at home | In-clinic or at home | In-clinic or at home |
| Free post-test genetic counselling Included with every positive result | |||||
| Price (from) | £315 | £375 | £645 | £795 | £1,545 |
| Choose test | Choose | Choose | Choose | Choose | Your selection |
All prices are for in-clinic appointments. Home visits available at a small additional cost. Free post-test genetic counselling is included with every test should a positive result arise.
Meet the clinical lead
Hear Dr Roy explain how NIPT testing works
This is the safest and easiest way to find out the gender or check the genetic health of your baby during pregnancy, with FREE genetic counselling provided if you receive a positive result for any health condition. We provide a specialised testing kit to take with you to your appointment and a FREE pre-consultation on Karyo, Karyo Plus, and Complete Plus Tests.
How our NIPT tests work
Book online...
Book online, receive your kit and take to your local Goodbody clinic.
Send it back…
Send your sample in the post to be analysed at an accredited laboratory.
Get results.
Get your comprehensive detailed results report from the laboratory, with guidance from our support team.
Available testing locations
Who are prenatal
blood tests for?
Suitable for women of all ages, of at least 10 weeks of gestation (at the time of their blood draw appointment), who have had their pregnancy type (single or twin) previously confirmed by an ultrasound scan. The pregnancy can be naturally conceived or through IVF.
- Peace of Mind Early
- Trusted Accuracy
- Care That Stays With You
How do the NIPT tests work?
Our genetic health tests are called NIPT tests, or Non-Invasive Prenatal Tests. An NIPT is a blood test taken from the mother during pregnancy, using state of the art DNA technology to check whether the baby has high risks of certain chromosomal health conditions.
During pregnancy the placenta sheds cell free DNA (cfDNA) into the mother’s bloodstream. This means that the mother’s blood continues a mixture of your own DNA, and that of your baby’s placenta. By extracting and evaluating the cfDNA in your blood, we can identify the risk to your baby of a range of health conditions and diseases.
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!
Register Your Interest
FAQs
PLACING AN ORDER
Which test should I choose?
How does the service work?
When will my order arrive?
How accurate are your tests?
I've just paid, can I change my order?
Can I order a test for someone else?
Why do I need a kit for my appointment?
How often should I take my test?
ARRANGING AN APPOINTMENT
How do I book an appointment?
How is the test carried out?
Do I need to fast before my test?
I am nervous about my blood test appointment.
Do I need to take my kit to my appointment?
AFTER YOUR TEST
My blood was haemolysed - what does that mean?
Do you provide results 7 days a week?
How do I book a follow up GP consultation?
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.
