NIPT Advanced (4th Generation) Test Cost 7 Procedure

Non invasive prenatal testing (nipt): what is it? There are several non-invasive prenatal test kinds, including Harmony, Generation, and Panorama (NIPT). They examine the mother's blood and check for the baby's DNA (analyses maternal serum for fetal DNA).

It offers only a limited amount of chromosome 21, 13, 18, and/or XY screening (sex chromosomes).

NIPT pinpoints

• Ninety-nine percent of trisomy 21 fetuses (Down syndrome)
• Trisomy 18 affects 97% of fetuses (Edwards syndrome)
• Trisomy 13 affects 92% of fetuses (Patau syndrome)

An advanced screening test rather than a diagnostic test should be considered when using NIPT with Harmony, Generation, or Panorama. Not all cases of trisomy 21, 18, or 13 are caught by it.

In comparison to combined first trimester screening, NIPT has a decreased rate of false positive results. As a result, fewer women will need an amniocentesis or chorionic villus sampling to confirm a high risk result if their unaffected baby is indeed healthy and unaffected by a chromosome abnormality. Since both chorionic villus sampling and amniocentesis are linked to a risk of miscarriage owing to the operation, this exposes fewer women to that risk

The fetus is not at risk during NIPT, a straightforward blood test.

When can I bring an NIPT?

NIPT is often carried out 10 to 12 weeks following conception. It can be utilized in IVF gestations as well as singleton and twin incubations.

NIPT can be carried out at any point after 10 weeks of pregnancy, especially if concerns are raised following your morphological ultrasound at 18 to 20 weeks that indicate an increased risk for trisomy 21, trisomy 18, or trisomy 13.

There are 2 paths that NIPT is normally utilized

• As a foremost line of examination. This implies that you must first experience NIPT and then return for the nuchal transparency ultrasound / first trimester screening at 13 weeks of incubation.
• As a contingency check. This implies that you first do the nuchal translucency ultrasound/first trimester screening and then, based on your recalculated risks, determine whether further testing is necessary. Afterward, you can decide whether to do NIPT or prenatal diagnostic testing with CVS/amniocentesis, based on how much extra knowledge about the baby's chromosomes you want

Where can I find my NIPT Results?

Once the NIPT conclusions are in, our medic will get in tinge with you personally. Generally, this brings one to two weeks.

Your initial blood sample might not always produce a result. This frequently has to do with technical issues, therefore your baby is not necessarily at fault. It is more likely to happen if you are further along in your pregnancy

For example, if you are 10 weeks along rather than 13 weeks or for other reasons, like an increase in maternal weight. If this happens, we will contact you to organize for the unrestricted exhibition of another specimen of your blood. The majority of patients will receive a result from this repeat sample.