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This document outlines the protocol for the Maternal Serum Screening Program at Wake Forest University School of Medicine, which provides maternal serum alpha-fetoprotein screening to detect neural
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How to fill out maternal serum screening program

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How to fill out Maternal Serum Screening Program Protocol

01
Begin by gathering all necessary patient information, including name, date of birth, and medical history.
02
Obtain the consent form from the patient and ensure it is signed.
03
Collect the required blood sample from the patient following standard laboratory protocols.
04
Label the blood sample accurately with the patient's information.
05
Complete the Maternal Serum Screening Program Protocol form, ensuring all sections are filled out clearly.
06
Include specific details regarding the gestational age and any relevant clinical information.
07
Submit the filled-out form and blood sample to the designated laboratory for analysis.
08
Ensure to follow up with the lab for results and communicate them back to the patient as required.

Who needs Maternal Serum Screening Program Protocol?

01
Pregnant individuals, particularly those who are in their first or second trimester, who are at risk for chromosomal abnormalities.
02
Patients with a family history of genetic disorders may also benefit from the screening.
03
Healthcare providers should recommend the screening based on patient history and risk factors.
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People Also Ask about

The maternal serum screening is a blood test done during the second trimester of pregnancy. Blood will be taken from a vein in your arm with a needle and sent to a lab for testing. Your doctor may also recommend other tests.
The cut-off for a clinical pregnancy was 190 IU/L (sensitivity, 81.2; specificity, 87.1%; positive predictive value (PPV), 94%; and negative predictive value (NPP), 65.2%) and that for live birth was 213 IU/L (sensitivity, 80%; specificity, 71%; PPV, 75.7%; and NPP, 75.7%).
The laboratory has established a MoM cutoff of 2.5, which classifies each screen as either screen-positive or screen-negative. A screen-positive result indicates that the value obtained exceeds the established cutoff.
The following screening methods are available during pregnancy: Alpha-fetoprotein (AFP) test or multiple marker test. Amniocentesis. Chorionic villus sampling. Cell-free fetal DNA testing. Percutaneous umbilical blood sampling (withdrawing a small sample of the fetal blood from the umbilical cord) Ultrasound scan.
NIPT is a more accurate type of screening test for Down syndrome than maternal serum screening (MSS). NIPT also looks for a much wider range of chromosome conditions than MSS. However, NIPT is more expensive and is not covered by Medicare or private health insurance.
Understanding the cut-off The test has a cut-off of 1 in 350 for trisomy 21. If you got a "screen positive" result for trisomy 21, it is because the chance for your baby to have trisomy 21 was calculated to be higher than 1 in 350.
The second trimester maternal serum screening test can identify a pregnancy with increased chance of Down syndrome, Edward syndrome or neural tube defects. The test involves the pregnant woman having a blood test between 14 and 20 weeks + 6 days gestation.
The test has a cut-off of 1 in 350 for trisomy 21. If you got a "screen positive" result for trisomy 21, it is because the chance for your baby to have trisomy 21 was calculated to be higher than 1 in 350.

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The Maternal Serum Screening Program Protocol is a set of guidelines designed to identify potential genetic disorders and congenital abnormalities in a fetus through the analysis of specific biomarkers present in a pregnant woman's blood.
Health care providers involved in prenatal care, including obstetricians and gynecologists, are required to file the Maternal Serum Screening Program Protocol as part of their routine screenings for pregnant patients.
To fill out the Maternal Serum Screening Program Protocol, healthcare providers must complete the designated forms with patient information, test results, and any relevant medical history. The forms should ensure accuracy and comprehensiveness to facilitate proper screening.
The purpose of the Maternal Serum Screening Program Protocol is to assess the risk of fetal conditions such as Down syndrome and other chromosomal abnormalities, enabling early intervention and informed decision-making for prospective parents.
The information that must be reported includes maternal demographics, gestational age, laboratory test results including specific biomarkers, and any relevant clinical findings that could impact the results of the screening.
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