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NonInvasive Prenatal Testing Test Request Form DXPDS389 V1.0 Issue May 2021 Please enter all mandatory information marked with asterisk (*) clearly, in BLOCK CAPITALS. Illegible forms may cause test
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How to fill out non-invasive prenatal testing

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How to fill out non-invasive prenatal testing

01
To fill out non-invasive prenatal testing, follow these steps:
02
Begin by scheduling an appointment with a healthcare provider who offers non-invasive prenatal testing.
03
During the appointment, the healthcare provider will explain the procedure and ensure that you understand the benefits and risks involved.
04
You will have a blood sample taken, usually from your arm, which will be sent to a laboratory for analysis.
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The laboratory will analyze the DNA in your blood to look for specific genetic conditions or abnormalities in the fetus.
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The results of the test will be communicated to you by your healthcare provider, who will explain the findings and any necessary follow-up actions.
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It is important to keep in mind that non-invasive prenatal testing does not provide a definitive diagnosis, but rather assesses the risk of certain conditions.
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Discuss the results with your healthcare provider and make any necessary decisions regarding further testing or medical interventions based on the findings.
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Remember to ask any questions you may have during the process to ensure you are well-informed and comfortable with the procedure.

Who needs non-invasive prenatal testing?

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Non-invasive prenatal testing is recommended for:
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- Pregnant women who are at higher risk for certain genetic conditions or chromosomal abnormalities, such as advanced maternal age (35 years or older), previous pregnancies with chromosomal abnormalities, or a family history of genetic disorders.
03
- Women with abnormal ultrasound findings or abnormal prenatal screening test results, indicating a higher risk for genetic conditions.
04
- Couples who have previously had a child with a genetic condition or chromosomal abnormality.
05
- Women who desire additional information about their pregnancy and want to assess the risk of certain conditions in the fetus.
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However, it is important to note that the decision to undergo non-invasive prenatal testing should be made in consultation with a healthcare provider who can provide personalized guidance based on your individual circumstances.
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Non-invasive prenatal testing (NIPT) is a screening test that analyzes cell-free fetal DNA in the mother's blood to detect genetic conditions in the fetus.
Pregnant women who are seeking information about the genetic health of their fetus are required to undergo non-invasive prenatal testing.
To fill out non-invasive prenatal testing, a blood sample is taken from the pregnant woman and sent to a laboratory for analysis.
The purpose of non-invasive prenatal testing is to identify genetic conditions in the fetus, such as Down syndrome, trisomy 18, and trisomy 13.
The results of non-invasive prenatal testing include the likelihood of the fetus having certain genetic conditions.
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