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Test Request and Patient Consent Form NonInvasive Prenatal Testing Location Code (internal use only): Doctor code (internal use only): PLEASE USE BLOCK CAPITAL LETTERS TO FILL IN THE FORMRequesting
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How to fill out non-invasive prenatal screening test
How to fill out non-invasive prenatal screening test
01
Schedule an appointment with your healthcare provider to discuss the option of non-invasive prenatal screening test.
02
Provide a blood sample which will be used to analyze cell-free fetal DNA.
03
Wait for the results to be processed and reviewed by your healthcare provider.
04
Discuss the results with your healthcare provider to understand the implications for your pregnancy.
Who needs non-invasive prenatal screening test?
01
Non-invasive prenatal screening test is recommended for pregnant women who are at increased risk for having a baby with genetic conditions, such as women over the age of 35 or those with a family history of genetic disorders.
02
It may also be recommended for women who have had an abnormal ultrasound or screening test results.
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What is non-invasive prenatal screening test?
Non-invasive prenatal screening test is a screening test that analyzes cell-free DNA from the mother's blood to detect genetic conditions in a fetus.
Who is required to file non-invasive prenatal screening test?
Pregnant women or individuals seeking information about the genetic health of their fetus may opt to undergo non-invasive prenatal screening test.
How to fill out non-invasive prenatal screening test?
The test involves a simple blood draw from the pregnant woman, which is then analyzed in a laboratory to detect any genetic abnormalities.
What is the purpose of non-invasive prenatal screening test?
The purpose of the test is to provide information about the genetic health of the fetus, allowing healthcare providers and parents to make informed decisions about the pregnancy.
What information must be reported on non-invasive prenatal screening test?
The test results typically report on the presence or absence of certain genetic conditions in the fetus, such as Down syndrome.
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