PATIENT HISTORY FOR NON INVASIVE PRENATAL TESTING 2025

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  1. Click ‘Get Form’ to open it in the editor.
  2. Begin by entering the 'Patient Name' and 'Date of Birth' in the designated fields. This information is crucial for identifying the patient.
  3. Fill in the 'Ordering Provider' details, including their NPI number and contact information. Ensure accuracy for seamless communication.
  4. Indicate the 'Gestational age at draw' along with the patient's current weight and height. Use the provided options for units (lb/kg, in/cm).
  5. For fetal sex, select from Male, Female, Ambiguous, or Unknown based on ultrasound results.
  6. If applicable, check all relevant boxes under 'Indication for testing'. This section helps clarify the reasons for testing.
  7. Finally, review all entries for accuracy before submitting your completed form with any required documents.

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NIPT stands for noninvasive prenatal testing. Its a screening test offered during pregnancy to see if the fetus is at risk for having a chromosomal disorder like Down syndrome (trisomy 21), trisomy 18 (Edwards syndrome) and trisomy 13 (Patau syndrome). The test can also determine the sex of the fetus.
The NIPT test does not require any special preparation before the test. Its a simple blood draw similar to any other blood test you might experience during your pregnancy. However, there are a few things you can do to make the overall experience smoother: Fasting- You can eat and drink normally before the test.
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.
Noninvasive prenatal testing (NIPT), sometimes called noninvasive prenatal screening (NIPS), is a method of determining the risk that the fetus will be born with certain genetic abnormalities. This testing analyzes small fragments of DNA that are circulating in a pregnant womans blood.
This screening test is available to all people at least 10 weeks pregnant. A normal screening result can be reassuring, but it does not guarantee a healthy baby. Not all birth defects or genetic conditions are identified by NIPT.
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Advantages There is no need to take a sample from inside the (in contrast with invasive prenatal diagnosis using amniotic fluid or chorionic villus sampling). This removes the small chance of miscarriage associated with invasive procedures. It is available for twin pregnancies.

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