NIPT (Non-Invasive Prenatal Testing) is a screening test done during pregnancy using a sample of the mother's blood. It analyses small pieces of the baby's DNA that circulate in the mother's blood to check for certain chromosome conditions. This test screens for changes in the number of chromosomes across all chromosome pairs, including conditions such as Down syndrome. It is a screening test, so it estimates the chance of a condition rather than giving a final diagnosis.

Before the Test

Remember this is a screening test, not a final diagnosis. A higher chance result usually needs confirmation with further tests.

Tell your doctor about twin or multiple pregnancy, as this can affect testing.

Fasting is not required.

During the Test

A trained Orange Health Labs professional will collect your sample during the visit.

Follow the instructions given to you at the time of collection.

The sample is labelled and sent to the laboratory for testing.

Let the collection team know if you feel unwell during the procedure.

It is recommended:

To screen for common chromosome conditions in the baby such as Down syndrome.

To offer a safe option that needs only a blood sample from the mother.

To help decide whether further diagnostic tests are needed.

To give reassurance on early information in pregnancy.

Usually done from about 10 weeks of pregnancy onwards, as your doctor advises. A single blood sample from the mother is enough.