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This document serves as a request form for the maternal serum screening test, which assesses the risk of Down syndrome, neural tube defects, and other pregnancy-related pathologies. It includes patient details, clinical information, and guidelines for specimen collection.
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How to fill out maternal serum screening test

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How to fill out maternal serum screening test

01
Obtain the maternal serum screening test kit from your healthcare provider or laboratory.
02
Ensure that the patient is aware of the purpose of the test and when it should be taken.
03
Collect a blood sample, typically between the 15th and 20th week of pregnancy, as advised.
04
Label the sample accurately with the patient's information and the date of collection.
05
Follow any specific handling and transport instructions provided to preserve sample integrity.
06
Submit the sample to the designated laboratory for analysis.
07
Wait for results, which usually take a few days to a week, and arrange for a follow-up appointment to discuss.

Who needs maternal serum screening test?

01
Pregnant women, especially those between 15 and 20 weeks gestation.
02
Women with a family history of genetic disorders or complications.
03
Women over the age of 35 at the time of delivery.
04
Women who have had abnormal results in previous screenings or tests.
05
Women concerned about their baby's risk of certain birth defects.
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The maternal serum screening test is a blood test performed during pregnancy to assess the risk of certain genetic conditions in the fetus, such as Down syndrome and neural tube defects.
Pregnant women, typically between the 15th and 20th weeks of gestation, are required to undergo maternal serum screening test as part of routine prenatal care.
To fill out the maternal serum screening test, the healthcare provider will collect a blood sample and the patient may need to provide personal and medical history information. The specific details will be documented in the provided laboratory requisition form.
The purpose of maternal serum screening test is to detect the likelihood of fetal abnormalities and conditions early in pregnancy, allowing for further testing or monitoring if necessary.
The information that must be reported includes the patient's demographic details, gestational age, prenatal history, blood sample results, and risk assessment outcomes.
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