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Non-Invasive Prenatal Testing (NIP) Harmony and PanoramaPatient Information The vast majority of babies are normal. However, all women, irrespective of their age, have a small chance of delivering

How to fill out non invasive prenatal testing

How to fill out non invasive prenatal testing:

1. Find a reputable healthcare provider or genetic testing center that offers non invasive prenatal testing (NIPT). You can ask your obstetrician or genetic counselor for recommendations.
2. Schedule an appointment for the NIPT. It is typically done between 10 and 12 weeks of pregnancy, but can be done as early as 9 weeks.
3. On the day of the appointment, make sure to bring your identification documents, insurance information, and any previous prenatal test results if applicable.
4. The healthcare provider will explain the procedure and its benefits and risks to you. You will also have the opportunity to ask any questions or address any concerns you may have.
5. The actual NIPT procedure involves a simple blood draw from the mother. The healthcare provider will use a needle to draw a small sample of blood from your arm.
6. The blood sample will then be sent to a laboratory for analysis. The lab will extract and examine free-floating fetal DNA that is present in the mother's bloodstream.
7. The laboratory will analyze the DNA for specific genetic conditions, such as Down syndrome, trisomy 18, and trisomy 13. The presence or absence of these conditions will be determined.
8. The results of the NIPT usually take around 7-10 days to be available. Your healthcare provider will schedule a follow-up appointment to discuss the results with you.
9. Once you receive the results, your healthcare provider will go over them with you and explain their implications. They will discuss any further testing or necessary actions based on the results.

Who needs non invasive prenatal testing:

1. Women who are at an increased risk of having a baby with chromosomal abnormalities can benefit from non invasive prenatal testing. This includes women who are 35 years or older, have a family history of genetic disorders, have had a previous pregnancy with chromosomal abnormalities, or have received abnormal results from other prenatal screening tests.
2. Non invasive prenatal testing is also recommended for women who simply want more information about their baby's health and genetic makeup. It can provide a peace of mind and help parents prepare for any potential health concerns.
3. It is important to note that non invasive prenatal testing is not a diagnostic test and cannot provide a definitive diagnosis. In some cases, further invasive testing, such as amniocentesis or chorionic villus sampling, may be necessary for confirmation. Your healthcare provider will guide you on the next steps based on the NIPT results and your individual situation.

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