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Mod.PR 11.H3ENG Rev. 05PATIENT CONSENT FORM PrenatalSafe NonInvasive Prenatal Test (NIPT) This blood test is designed to measure the combined maternal and fetal DNA present in maternal blood, and
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How to fill out non-invasive prenatal testing nipt

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How to fill out non-invasive prenatal testing nipt

01
Contact a healthcare provider to discuss the option of non-invasive prenatal testing (NIPT).
02
Schedule an appointment for the NIPT test.
03
Provide a blood sample for the NIPT test.
04
Wait for the test results to be analyzed by a genetic counselor or healthcare provider.

Who needs non-invasive prenatal testing nipt?

01
Pregnant women who are at high risk for chromosomal abnormalities in the fetus.
02
Women with a family history of genetic disorders.
03
Women who have had abnormal results from other prenatal screenings.
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Non-invasive prenatal testing (NIPT) is a genetic screening test used to assess the risk of certain genetic conditions in a fetus by analyzing small fragments of fetal DNA circulating in a pregnant woman's blood.
Non-invasive prenatal testing is typically recommended for pregnant individuals who are at higher risk of having a baby with genetic conditions, such as those over a certain age, with a family history of genetic disorders, or with abnormal ultrasound results.
To fill out non-invasive prenatal testing, patients should consult with their healthcare provider, who will provide the necessary forms and instructions to complete the test order, including personal health information and relevant medical history.
The purpose of non-invasive prenatal testing is to identify the risk of certain genetic abnormalities, such as Down syndrome, trisomy 18, and trisomy 13, allowing for earlier informed decisions about further testing or pregnancy management.
The report from non-invasive prenatal testing typically includes the likelihood of the fetus having certain genetic conditions, the percentage risk associated with those conditions, and any recommendations for follow-up testing.
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