Pregnancy- Aneuplody Screening
Let me say at the outset this is a difficult area- emotionally, ethically, and the complexity of the choices available. I will help you as much as I can digest what the current state of play is. Please feel free to get me to clarify any uncertainty when you see me in person.
Aneuploidy screening is the term applied to the detection of chromosomal abnormalities before birth. All of these tests are optional. The main condition being sought ot is Down syndrome (an extra copy of the 21st chromosome) but other abnormailities can turn up as part of the process.
Down Syndrome (Trisomy 21) is a condition in which a baby carries an extra chromosome. Chromosomes contain the genetic blueprint that regulate growth and development. Babies with Down Syndrome have an extra chromosome and this creates various problems. Children with Down syndrome are at increased risk of abnormalities of the heart, bowel, hearing, and breathing. They are also at increased risk of developing diabetes and dementia, and intellectual disability of varying degrees.
The degree of learning disability cannot be determined prior to birth. It may be profound (10%), severe (70%), or mild (20%). About 45% of individuals with Down syndrome will survive to the age of 60.
The risk of having a baby with Down Syndrome increases with advancing maternal age but women at ANY age can conceive a baby with Down Syndrome. The approximate risk of having a baby with Down Syndrome is age dependent, set out in the table below;
Age Risk Of Down Syndrome
At Birth At 12 weeks
20 1:1500 1:1000
25 1:1350 1:900
30 1:900 1:600
32 1:660 1:440
34 1:440 1:300
35 1:350 1:240
36 1:280 1:190
37 1:200 1:150
38 1:170 1:110
40 1:100 1:65
42 1:55 1:35
44 1:30 1:20
The risk of having a baby with Down Syndrome at birth is less than the risk at 12 weeks. This is because a percentage of babies with Down Syndrome will not make it through the pregnancy. That is, in the absence of a termination, the mother would experience a miscarriage or stillbirth.
Testing may be performed (see below for the options). There would be out of pocket expenses, the amount depending on the test. A few general comments about testing;
There are lots of conditions (eg. Autism) where, at the moment, test results will be normal. That is, we cannot check for a "normal" baby, but can check for some chromosome problems.
Testing will not pick up 100% of cases of Down Syndrome. That is, it may suggest that a baby does not have Down Syndrome even though the baby does. This is called a false negative finding.
There is a small chance that the test will suggest that your baby has Down syndrome even though it does not. This is called a false positive finding. The NT+ has about a 5% false positive rate, while the cfDNA rate is about 0.1%
If you have a NT+ or cfDNA study that suggests a chromosome problem, then a CVS or amniocentesis will be offered to decide if the result was a true positive (baby has Down Syndrome) or false positive (baby has normal chromosomes). A CVS or amniocentesis (performed at 13-16) weeks has a risk of causing a miscarriage of about 0.5% (1:200).
Whether or not you have testing depends, in the main, on whether you would consider termination if the baby was affected. What do I think?. As long as you are prepared to accept that the tests (NT or cfDNA) study have false positive and false negative findings, I am more than happy to order the test.
A summary of NT and NIPT is;
Nuchal Translucency (NT). It is zero risk. An ultrasound at 12-14 weeks can be performed by certain specialised ultrasound practices and measures an area of the fluid at the babies neck called the Nuchal Translucency (NT). A thicker than normal NT in combination with an abnormal protein in your blood (PAPP-A) is associated with an increased risk of chromosome problems. In combination with a blood test the NT+ scan can detect 80-90% of cases of Down Syndrome. It returns a risk ratio. Can vary from 1:2 to about 1:20,000. A positive NT+ study is considered to be either more than 1:300, or at a risk that you judge merits further testing. If you have a positive NT+ study, then either a NIPT test (for moderate risk) or a CVS-Amniocentesis will be offered.
The NT scan may show up changes that are not associated with Down syndrome (and will not show up on the NIPT test). If those cases, it may be suggested that a CVS be performed, and the fetal sample collected be subjected to a special type of analysis called CGH.
The out of pocket cost for an NT scan ranges from $200-$300
Cell free DNA (cfDNA), Fetal free DNA (ffDNA), or Non invasive prenatal testing (NIPT). Zero risk. During pregnancy some of the fetal DNA is released into the mothers circulation. To say that the reliable detetion and analysis of this DNA is complex is a gross understatement. On the one hand it consists of a simple maternal blood test (zero risk), on the other this is an emerging technology.
There are a number technologies at the moment; ▶Genesyte (Genea), ▶Materni21 (Healthscope Pathology), ▶Harmony Verify (Douglass Pathology), ▶iGeneScreen (Laverty Pathology). These are changing technologies. Please click on each link above if you may proceed with cfDNA and want to know more about the technology. It involves a maternal blood test at about 10-13w. Takes one week to process. Generally returns either a positive result (about 1:3 chance of Down syndrome) or a negative result (depending on maternal age that ranges from 1:10,000 to 1:150,000).
The out of pocket cost for an NIPT test is about $450 (June 2016)
One, both or none?
There are various positions as to whether to have one test, both tests, or a mix.
Firstly, if you would not consider termination under any circumstances, then perhaps having no testing is the option for you.
One view is that you have an NT done, and if that risk is (say) more than 1:2000 then have an NIPT. If the NT shows some findings suspicious for other chromosome problems then have a CVS with CGH testing.
Alternatively have an NT scan and if there are no suspicious findings suggesting non Down syndrome abnormalities, then have an NIPT done for the extra reassurance it provides.
The third option is just have an NIPT alone, and accept that there are rare cases of abnormailities that will be missed by the NIPT but may have been suggested by the pathway NT->CVS->CGH.
If the tests cost $1 each, then I would suggest that do both. If you could only afford one test, then I would suggest the NIPT test.
CVS & Amniocentesis
CVS is an invasive procedure. It is performed at 13-14w. There is a less than 1:200 risk of miscarriage (and more recent studies suggest it is much lower than that). Rarely needs an amniocentesis if fails. If a termination is decided upon, can be done in theatre.
An amniocentesis is also an invasive procedure. It is performed at 15w. There is also an approximate 1:200 risk of miscarriage. If termination decided upon, usually requires a labour.
CVS and Amniocentesis are invasive procedures, which enable the chromosomes or genetic material of your baby to be examined. These tests have a small risk (about 1:200) of causing miscarriage and will therefore are usually only offered in pregnancies where there appears to be an increased risk of chromosome or genetic abnormalities.
This is a complex evolving area. What follows are some links (these positions will change over the short term!);
Society of Mateno Fetal medicine (MFM) specialists
College of GP's views
Position of the RANZCOG