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What are the results of non invasive prenatal testing NIPT?

NIPT is a blood test that is more accurate than the first pregnancy screening test. Its offered to women who are carrying a baby identified from previous screening tests as having a higher chance of having either Downs syndrome, Edwards syndrome, or Pataus syndrome. No screening test is 100% accurate.

What is the cut off for NIPT testing?

Quantitative differences in chromosome fragments in maternal blood can be used to distinguish fetuses affected with trisomy 21, and a tew other fetal aneu- plodies, from those that are not affected. Testing can be done any time ater 10 weeks; typically i1is done between 10-22 weeks.

Is NIPT non invasive?

NIPT is considered noninvasive because it requires drawing blood only from the pregnant woman and does not pose any risk to the fetus.

Does insurance cover the NIPT test?

Prenatal genetic test The NIPT genetic test is typically covered by insurance when its considered medically necessary by a doctor and you meet the coverage criteria set by the insurance plan.

What is the NIPT test code for insurance?

In general, the codes for NIPT testing are: 81420: Fetal chromosomal aneuploidy (e.g., trisomy 21, monosomy X) genomic sequence analysis panel, circulating cell-free fetal DNA in maternal blood, must include analysis of chromosomes 13, 18, and 21.

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When is NIPT recommended?

When is NIPT done in pregnancy? NIPT can be performed any time after 9 weeks into your pregnancy earlier than any other prenatal screening or diagnostic test.

What is considered a medical necessity for NIPT?

NIPT is considered medically necessary in the following circumstances: Maternal age or oocyte age of 35 years or older at delivery; or. Fetal ultrasound findings indicating an increased risk of aneuploidy; or. History of a prior pregnancy with a trisomy; or.

What is the CPT code for NIPT non invasive prenatal testing?

In general, the codes for NIPT testing are: 81420: Fetal chromosomal aneuploidy (e.g., trisomy 21, monosomy X) genomic sequence analysis panel, circulating cell-free fetal DNA in maternal blood, must include analysis of chromosomes 13, 18, and 21.

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When is NIPT recommended?

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