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Non-invasive Prenatal Testing (NIPT) methods, test for fetal genetic conditions during pregnancy.
All Trimester non-invasive pre-natal screening tests are completed in laboratories based in Europe. Unlike other tests on the market, Trimester NIPT tests are not outsourced to external laboratories in the US or China.
Simple. Safe. Reliable.
The test to check the number of eggs you have left in your ovaries is known as ‘ovarian reserve’. When trying to assess your probability of conception, egg quality and quantity, your age is one of the most important factors to consider as the number of eggs constantly decreases with age and by the time you start the menopause your egg store is depleted.
All tests marked with a star * require the blood sample to be taken on Day 2- 4 of your monthly menstrual cycle. If you experience longer cycles the optimum day must be calculated*
NIPT tests are suitable for pregnant women from the 10th week of pregnancy.
We have tests that are suitable for both single and twin pregnancies (including vanishing twin). Please note the NIPT test will analyse the chance of an affected result for the pregnancy, but will not be able to provide a twin-specific chance.
The test is suitable for pregnancies achieved by IVF techniques, including gamets donation.
The test is suitable for surrogate pregnancies.
Gender determination can only report if a Y chromosome is or is not present. It will not identify which twin or if both twins are male.
Trimester NIPT’s can be performed any time after 10 weeks — this is earlier than any other antenatal screening or diagnostic test.
NHS antenatal screening;
Nuchal translucency scanning: between 11 and 13 weeks
CVS: 10 to 13 weeks
Quad screen: between 14 and 22 weeks
Amniocentesis usually performed between 16 and 18 weeks & sometimes as early as 13 or 14 weeks or as late as 23 or 24 weeks
In the event of a 'higher chance' NIPT result we make a medical referral to your local fetal medicine team who will help you to decide the next steps forward, including whether to have a fully diagnostic test like Chorionic Villus Sampling (CVS) or amniocentesis (“amnio”). Both tests analyze a baby’s own genetic material, collected from the amniotic fluid or placenta to tell with 100 percent certainty whether a baby actually has a chromosome abnormality. However, these tests are invasive, which means they slightly increase the chance of miscarriage approx 2% for Chrorionic Villus Sampling (CVS) nationally ie. approximately 1 in every 50 women, and 1% increase for Amniocentesis, which is 1 in every 100 women who have the procedure.
NIPT is not suitable if you have been diagnosed with cancer or know that you have chromosomal abnormalities including Trisomy 13, 18 and 21.
NIPT cannot be performed if you have had an organ transplant or received stem cell therapy or immunotherapy within the last 12 months.
NIPT cannot be performed if you have had a blood transfusion with the last 3 months.
High levels of biotin can skew common tests used to diagnose conditions including pregnancy, cancer, thyroid disease, heart disease, anaemia, and other hormonal-related conditions. Fortunately, often only a day without taking the supplement is required for accurate test results. It is best to undertake testing for Fertility or Menopause before commencing any form of hormone therapy such as HRT or the contraceptive pill. If in doubt check with your doctor.
The contraceptive pill/HRT can affect the results of some tests, you may need to consider taking the test when on a break from these to give more accurate results.
Food does not usually affect your blood tests for hormonal studies so it’s okay to eat.
However, if you are having your Cholesterol status checked then you must fast for at least 8 hours before, so best to book in for an AM appointment.



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