As part of your routine NHS pregnancy care, you will be asked if you’d like to have the combined screening test for Down’s, Edwards’ and Patau’s syndromes.
What are these syndromes exactly?
All 3 syndromes are genetic disorders where a baby has an extra copy (or part of a copy) of a particular chromosome, leading to particular set of disabilities or growth problems. Both Edwards’ and Patau’s syndrome are very rare – and more serious – than Down’s syndrome.
Edwards’ syndrome or Trisomy 18 (T18) causes major brain abnormalities, and can also cause heart problems, unusual head and facial features, and serious growth problems. Most babies with T18 will die before they are born, be stillborn or die shortly after birth.
Patau’s syndrome or Trisomy 13 (T13) can also cause major brain abnormalities and heart problems, as well as cleft lip and palate, growth problems, poorly formed eyes and ears, and kidney problems. Most babies with T13 will die before they are born, be stillborn or die shortly after birth.
Down’s syndrome or Trisomy 21 (T21) can cause some growth delays, mild to moderate learning disability and distinctive facial characteristics. Many babies affected by it, if carried to term, grow up to live happy, healthy and full lives – with, where it’s needed, extra medical or specialist help.
How likely is it that my baby has 1 of these syndromes?
It’s highly unlikely. It’s thought that Down’s syndrome affects 1 in every 500 pregnancies, while the much rarer Edwards’ syndrome affects 1 in every 1500 pregnancies. Patau’s syndrome is extremely rare and is diagnosed in fewer than 200 babies a year.
Will the combined screening test tell me for sure either way?
No, we’re afraid it’s a little bit more complicated than that – as this test will only tell you whether you’re high risk or low risk of having a baby with Down’s, Edwards’ or Patau’s.
If you’re told your risk is low (as the vast majority of women are), you won’t need any further testing; if you’re told your risk is high, you will probably be offered further, more accurate, tests. Some of these tests carry a (very small) risk of miscarriage.
“But be reassured that 95% of women who have the combined screening test get results which are low risk,” says Jane Fisher from the charity Antenatal Results and Choices (ARC).
Do I have to have the combined test?
No. It’s completely up to you whether you have it or not. And, if you do decide to have it, you don’t have to be screened for all 3 syndromes, if you don’t want to.
So, you can choose:
- To have the test, screening for Down’s, Edwards’ and Patau’s
- To have the test, screening for Down’s only
- To have the test, screening for Edwards’ and Patau’s only
- Not to have the test at all
Many pregnant women decide they do want to have the combined screening test because, if it did come back as high risk, they’d then want to have the other more accurate tests – and, if those came back positive, they could either make a decision about whether to continue with the pregnancy or be prepared for what’s to come.
For those who choose not to have the combined screening test, like MFM forum poster Ninja Pigeon, it’s often more of a gut decision that knowing more wouldn’t make any difference. “We didn’t have any testing, over and above the normal ultrasound scan,” she says. “We talked about it and we both agreed that we wouldn’t terminate whatever, so the tests were redundant.
“But I don’t think there’s any right or wrong here. It’s a very personal choice.”
When do I have the combined screening test?
You’ll be offered this test towards the start of your NHS antenatal care, when you’re between 11 and 14 weeks pregnant.
So what exactly does the testing involve? Why is it called ‘combined’?
“It is called the ‘combined screening test’ because it combines a nuchal translucency (NT) scan with a blood test,” says Nigel Thomson, professional officer for ultrasound at the Society and College of Radiographers. “The NT scan is done (if you consent to it) during your 1st routine ultrasound scan, often called the dating scan or 12-week scan.”
The results from the NT scan and the blood test age are then further combined with your age and the gestational age (how many weeks old your baby appears to be, according how long he or she measure, head to bottom, during your scan).
You may have the scan and the blood test on the same day, or they may be done separately.
The blood test is the usual needle-in-the-arm job and may be done by your midwife or a phlebotomist (someone who specialises in taking blood sample). It’s common for the blood sample needed for the combined screening test to be taken at the same time as blood is taken for the routine pregnancy blood tests (to check your blood type and so on) – to save jabbing you in the arm twice.
“During the NT scan,” says Nigel, “the fluid in the space at the back of your baby’s neck is measured by the sonographer who’s conducting your ultrasound scan.” (Babies with abnormalities tend to accumulate more fluid in this space than average at this stage of pregnancy.)
Occasionally, and usually because of the way your baby is lying, it’s not possible for the sonographer to get an NT measurement. If this is the case for you, you should be offered a 2nd scan. If it’s still not possible to get a measurement then, you may then be referred for a quadruple test (a different blood test that screens for Down’s but not Edwards’ or Patau’s) or, if your hospital offers it, a NIPT (a newer blood test that screens for dozens of conditions).
When will I get the results?
You may be told the NT test result on the day you have your scan. But the length of time it take to give you your final combined test results varies and, obviously, often depends on whether you have the 2 tests done on separate days, and how long your hospital takes to process all the information gathered by the tests.
Generally speaking, you should hear between 1 to 3 weeks.
What do the results mean?
If you’re given the NT test result separately, you’ll be told the fluid measurement in millimetres: a measurement of 3.5mm or more suggests your baby could be at increased risk of Down’s, Edwards’ and Patau’s.
But the result that really matters is the combined result, and that’s the 1 that comes as a risk score. Well, 2 risk scores: 1 for Down’s and 1 for Edwards’ and Patau’s combined.
“If you are told your risk is between 1 in 2 and 1 in 150, then you are considered higher risk,” says Jane Fisher. But that doesn’t mean your baby definitely has any of the 3 syndromes; it just means you may be offered other, more accurate tests.
Anything over 1 in 501 is considered low risk. “If you are low risk,” says Jane, “it is important to remember that this does not mean your baby definitely does not have a syndrome.” It just means it is extremely unlikely – so unlikely, there’s no need for further testing.”
How accurate are the results? The combined screening test picks up more than 4 out of 5 (85 to 90%) of babies with Down’s syndrome, Edwards’ syndrome and Patau’s syndrome.
But in 2 out of every 100 tests, the result may indicate that your baby has 1 of the syndromes, when he or she doesn’t: a ‘false positive’.
If I’m told I’m high risk, what happens next?
If your result is considered higher risk, you will be offered an appointment with a midwife to discuss going on to have a further, more accurate tests. You don’t have to have them if you don’t want to.
You may be offered a new screening test called NIPT (also known as cffDNA), which is a blood test that offers a higher degree of accuracy in detecting Down’s, Edwards’ and Patau’s. Some NHS hospitals offer NIPT but others don’t yet offer it – although there are plans to starting offering it at all hospitals from 2018. You may be able to have a NIPT at your hospital if you’re prepared to pay; alternatively, you could pay for it at one of the many private clinics that now offer it.
If you don’t have NIPT, or if the NIPT result is positive, you are likely to be offered either amniocentesis or CVS – both of which are called ‘diagnostic’ tests because the results are so accurate (99%) that, if it’s positive for Down’s, Edwards’ or Patau’s, doctors will view it as a diagnosis. Both amniocentesis and CVS carry with them a small risk of miscarriage, so you’ll have the difficult task of weighing up if it’s worth taking that small risk to find out for (almost completely) sure.
Just be reassured that there will be lots of advice and support offered to you along the way. And you may find it helpful to express your feelings on our Chat forum.