Dr Quek Swee Chong
Obstetrician & Gynaecologist
Congratulations! Now that you have a bun in the oven, you will be seeing your doctor frequently – and even more so during the final trimester – to ensure your pregnancy is a healthy one.
There are a series of prenatal tests and scans available to check on the well-being of both mother and baby during pregnancy but not all tests are necessary. Your doctor will be able to advise you on the ones you need.
Apart from the routine tests that are carried out at every antenatal visit such as blood pressure, weight, and urine dipstick for sugar and protein, the following tests are also performed if your doctor considers them necessary.
Other blood tests may also be done depending on the mother's ethnic background and medical history. These include screening for infections like toxoplasmosis, a parasitic disease, and cytomegalovirus, a common virus related to those that cause chickenpox and herpes simplex; and screening for carrier status of genetic disorders like cystic fibrosis, sickle cell disease and Tay-Sachs disease. Results for blood tests may take up to a week.
An early viability ultrasound scan from about 6 – 8 weeks of gestation can confirm that the pregnancy is developing normally and will identify the foetal heartbeat.
From about 8 – 10 weeks, dating the pregnancy can be performed by ultrasound and is accurate to within a week. This can ensure the most accurate calculation of the expected due date (EDD).
These tests are not compulsory but all pregnant women should be offered them regardless of age. Several options for this type of screening are available. Note that screening tests are not diagnostic – this means that while they are mostly accurate, an 'abnormal' result will need to be confirmed by more invasive methods of testing (see section below on CVS and amniocentesis).
This consists of 2 tests. First, a certified operator will perform an ultrasound scan to assess the thickness of skin in the neck of the foetus. This is known as a nuchal translucency. Next a blood sample is taken from the mother. The combined results are analysed with a proprietary computer algorithm software and a resultant 'risk score' is calculated. The test is performed between 11 and 14 weeks, and is about 90% accurate. Test results are typically available within the same day.
This refers to a group of tests that detect foetal DNA (also known as cell free DNA) in a sample of blood taken from the mother. In actual fact, this DNA arises from the placenta and not actually from the foetus itself. There is therefore a small chance that the results may not be 100% accurate.
These tests can be done from 9 weeks onwards and they all screen for the common chromosomal disorders: Trisomy 21 for Down Syndrome, Trisomy 18 for Edwards Syndrome and Trisomy 13 for Patau Syndrome. In addition, they can also determine gender and other genetic disorders like triploidy and microdeletions. While they cannot detect every genetic disorder, they are highly accurate, between 97 – 99%, for the most common ones like Down Syndrome.
There are several companies that offer the test, and each one offers slightly different screening panels for the various genetic disorders. The companies include Harmony, MaterniT21 Plus, Panorama, EasyDNA and iGene.
These are invasive tests and are usually indicated for the following:
CVS can be performed earlier, at 11 – 12 weeks, and involves inserting a biopsy needle through the mother’s abdomen under ultrasound guidance into the placenta to withdraw a small amount of placental tissue for testing. The whole procedure takes a few minutes and is relatively painless. Results typically take 2 – 3 weeks.
Amniocentesis is usually performed later, between 16 – 20 weeks and also involves inserting a hollow bore needle through the abdomen under ultrasound guidance. The needle is directed into a pool of amniotic fluid surrounding the foetus and a small amount of amniotic fluid is removed for testing. Results are available after 2 – 3 weeks.
Both CVS and Amniocentesis are invasive tests and carry a small risk of causing miscarriage (CVS 0.5 – 1%; Amniocentesis 0.25 – 0.5%).
This is usually performed between 19 – 22 weeks. This test looks for structural anomalies in the foetus that can occur even though there are no genetic abnormalities detected. In particular, the scan checks for any abnormal heart structures, facial clefts, head, abdomen and limb size, placental position, doppler blood flow, cervical length, and the amount of amniotic fluid present.
This test, which screens for gestational diabetes, is usually performed between 24 – 28 weeks. Gestational diabetes is a type of diabetes that affects some women during pregnancy. While most cases will resolve after delivery, women with gestational diabetes are at higher risk of developing Type 2 diabetes later in life.
It involves 3 blood tests. You will begin the test in a fasting state, and drink a 75g glucose drink. This is followed by 2 more blood tests 1 and 2 hours later. Results are usually available within 1 – 3 days.
From late in the second trimester and going into the third trimester, some women may be required to undergo repeat ultrasound scans to monitor the growth of the foetus. This usually also includes Doppler ultrasound scans that check the flow in the blood vessels supplying blood to the foetus.
This is a group of bacteria that is normally present in the genital area of around 30% of women. GBS generally does not cause any problems, but can affect the baby as it passes through the birth canal during delivery. A vaginal swab is taken, usually around 35 weeks, and if it is positive for GBS, antibiotics are usually prescribed.
This is a routine test performed during labour to continuously monitor baby's heartbeat as well as the frequency and intensity of any uterine contractions. In the third trimester, a CTG may also be ordered by the doctor to monitor the well-being of the baby.