Introducing the Generation® screen
Non-invasive prenatal testing (NIPT) is a revolutionary advance in prenatal screening.
A simple and highly accurate blood test, NIPT screens for common chromosomal abnormalities from as early as the 10th week of pregnancy, for both singleton and twin pregnancies.
NIPT can also be exclusively bundled with other advanced scientific services including, cord blood stem cell banking for your baby at birth.
Your guide to a Generation® screen.
- A single tube of blood is drawn
- You can have an NIPT blood test as early as 10 weeks
- 99% Accuracy for Trisomy 21, 18 & 13 - Down syndrome, Edwards syndrome and Patau syndrome.
- All screens are analysed in an accredited Australian* laboratory
- The lowest reported test failure rate of any NIPT
- Doctors will receive results within 5-7 days
* If a Generation® Plus test is requested, your sample will be sent to an accredited laboratory in California. Results will be available in 9-14 days due to shipping times.
This website contains only general education information. For professional advice on all prenatal screening matters, please consult your medical practitioner.
NB: Prices are correct at time of publishing and are subject to change without notice.
A simple and highly accurate blood test, Generation® is advanced prenatal screening which can detect genetic material (DNA) from the placenta in a blood test from the mother. In the past, testing DNA from the foetus required much more invasive methods such as amniocentesis or placental biopsies, which can pose risks to mothers and their babies. The Generation® screens for the most common chromosomal abnormalities that can affect your baby’s future health. The Generation® NIPT is available from as early as the 10th week of pregnancy, for both singleton and twin pregnancies.
During pregnancy, some of the baby’s DNA from the placenta crosses into your bloodstream. After your blood test, the Generation® NIPT tests this DNA to identify certain chromosome conditions in your pregnancy. The Generation® test takes a deeper approach to the science, using an advanced technology called “Massively Parallel Sequencing” to analyse millions of DNA fragments per sample and accurately count the number of chromosomes present to determine if there are too many or too few copies of the tested chromosomes in your baby.
Simply because it can be used to obtain important and accurate information about the health of your developing baby in the first trimester (at 10 weeks), with little or no risk to the pregnancy. This screening test may be an option for you if:
- You will be 35 years or older at the time of delivery (32 years or older for a twin pregnancy)
- You have an abnormal or “positive” serum screen
- Your ultrasound has revealed concerns or abnormalities with foetal growth and / or development
- You have a personal or family history suggestive of a chromosome disorder (e.g. Down syndrome)
What’s more, clinical best practice guidelines from Australian and international medical societies recommend that all pregnant women, regardless of risk status, be given the opportunity to take an NIPT and other available prenatal screening and diagnostic tests.
Chromosomes normally come in pairs. Most people have 23 pairs of chromosomes, with one pair which determines sex. Men normally have an XY pair of sex chromosomes, and women normally have an XX pair of sex chromosomes. Any more or less can lead to mental or physical disabilities, with different levels of severity.
The Generation® NIPT looks for two few (missing) or too many (extra) copies of chromosomes, which are often associated with these disabilities. The most commonly seen and tested for include:
- An extra copy of chromosome 21 (Down syndrome)
- An extra copy of chromosome 18 (Edwards syndrome)
- Chromosome 13 abnormality (Patau syndrome)
- Or sex chromosome aneuploidies (singleton only)
All of these can be accurately detected with the Generation® test. If it’s requested by your doctor, more rarely occurring microdeletion genetic syndromes are also tested for. These microdeletion syndromes are caused by the loss of a small piece of a chromosome and testing might be recommended by your doctor for a number of clinical reasons. The Generation® Plus test cannot be performed on twins.
Your test will include one of two possible results for chromosomes 21, 18 and 13.
- No Aneuploidy Detected means the expected number of chromosomes was found.
- Aneuploidy Detected means too many or too few copies of one of the chromosomes have been identified. A diagnostic test for confirmation of the result is recommended and should be discussed with your doctor.
The Generation® prenatal test is a highly accurate advanced screening test that is non-invasive. No test, however, can guarantee a baby will not have any medical issues.
The Generation® test only addresses aneuploidies of chromosomes 21, 18, 13, and sex chromosomes†. It doesn’t test for genetic and non-genetic problems that may be present in a baby or report on them.
†Sex chromosome aneuploidy testing is available for singleton pregnancies only.
The Generation® test was chosen for development by Genomic Diagnostics based on a careful evaluation of its quality and proven scientific performance.
The performance of this prenatal test has been evaluated and published in numerous major studies, including clinical experience in over 34,000 patients from over 60 leading US medical research and teaching institutions.
Those findings have been replicated in other studies which includes the New England Journal of Medicine, one of the most prestigious international medical journals. These studies have found that the test performed substantially better than conventional tests under regular clinical conditions, with 1 in 4,000 false negative results, 1 in 500 false positive results, and the lowest test failure rate of any non-invasive prenatal test.
- Make an appointment to see your medical practitioner and discuss the Generation® NIPT.
- Complete the request form with your doctor - go to www.generationNIPT.com.au.
- Pay and find a convenient collection location for your Generation® test online or contact Customer Care on 1800 822 999
- Bring the request form to your appointment. Your blood sample will be taken and sent to the lab for testing.
- Your Generation® NIPT is performed.
Your results are delivered to your medical practitioner.
The Generation® prenatal test does not qualify for a Medicare rebate. The total out-of-pocket cost to the patient for the standard test for chromosomes 13, 18, 21 and sex chromosomes is $395* which is payable prior to sample collection by calling our Customer Care Team on 1800 822 999. They can also let you know the pricing of Generation® Plus when you call.
*Prices are subject to change.