Often considered if
You want early information. Your doctor suggests screening. You want to talk about next steps with clear results.
NIPT is a blood test in pregnancy. It estimates whether the baby may have a higher chance of some chromosome conditions. It uses only the mother’s blood (no needle into the womb).
NIPT is not ultrasound. It is a blood test. Both are common parts of pregnancy care.
The sample is mother’s blood. The lab looks for DNA pieces from the pregnancy.
NIPT means Non-Invasive Prenatal Testing.
A pregnancy blood test that shows higher or lower chance for some chromosome conditions. Not a final diagnosis.
Many pregnant people can ask their doctor about NIPT. Your doctor decides if it is right for you.
You want early information. Your doctor suggests screening. You want to talk about next steps with clear results.
The test is optional. Talk with your doctor or midwife before you decide.
Families ask because they care. Your doctor helps you choose what fits your pregnancy.
Yes for pregnancy safety as a blood test. NIPT uses only the mother’s blood. It does not put a needle into the womb. It is different from tests like amniocentesis.
Only a maternal blood draw. No needle into the womb.
Usually available from about 10 weeks of pregnancy, when enough pregnancy DNA is present.
Helps show higher or lower chance for screened chromosome conditions.
Results help your clinician decide if more counseling or testing is useful.
Talk with your doctor
1You talk with your doctor.
Blood from the arm
2Blood is taken from your arm.
Trusted lab checks DNA
3A trusted lab checks the DNA.
Your doctor explains the report
4Your doctor gets the report and explains it to you in clear words.
Performance depends on the laboratory panel and clinical context. Your doctor interprets the report.
NIPT is a highly accurate screening method for common trisomies when performed under the right conditions. It is still not a diagnostic test.
We share pathway details with your clinic. Your doctor explains performance in your specific case.
The chance of the screened conditions looks lower. Your doctor still guides your pregnancy care.
This does not mean the baby definitely has a condition. Your doctor may suggest another test to be sure.
Exact numbers and lab details are shared by your doctor and our team when your pathway is set.
Results are explained by your clinician, not by a website alone.
No. Only the mother’s blood is taken. There is no needle into the womb.
No. It is a screening test. It shows chance. Only some other tests can confirm.
Usually from about 10 weeks of pregnancy, when there is enough pregnancy DNA in the blood. Your doctor tells you the right time.
Talk with your doctor, or request information from us. We explain the process in clear words.
Request information. We answer clearly. Then you decide with your doctor.