1. What is a First Trimester Screening Test?
The First Trimester Screening Test is a prenatal test that combines a blood test and an ultrasound to evaluate the baby’s risk for chromosomal abnormalities such as Down syndrome, trisomy 18, and other genetic issues.
2. Why is a First Trimester Screening Test Done?
This test helps identify the chance of chromosomal problems early in pregnancy. It provides valuable information about the baby’s development and can guide further testing or decisions about managing the pregnancy.
3. How is the First Trimester Screening Test Done?
The test includes a blood sample from the mother and an ultrasound (nuchal translucency scan) to measure fluid at the back of the baby’s neck. Results are analyzed together for accurate risk assessment.
4. Who Should Get a First Trimester Screening Test?
This test is recommended for all pregnant women, especially those over 35 or with a family history of genetic disorders. It’s part of standard prenatal care to monitor early fetal development and risk levels.
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5. Why is the First Trimester Screening Test Needed?
The test offers early insight into the baby’s health and helps identify risks for genetic conditions. Knowing these risks early allows for better pregnancy planning, further testing, and timely medical care if needed.
6. How the First Trimester Screening Test is Done?
It involves two steps: a blood test to measure pregnancy-related proteins and an ultrasound to assess fetal development. Both results are combined to evaluate the baby’s risk for chromosomal abnormalities.
7. For Whom First Trimester Screening Test is Suitable?
This test is suitable for all expectant mothers in their first trimester, particularly those at higher risk due to age, medical history, or previous pregnancies with complications or genetic abnormalities.
8. Which Symptoms or Conditions Require First Trimester Screening Test Monitoring?
Although not symptom-based, the test is important if there’s advanced maternal age, abnormal ultrasound findings, or a family history of chromosomal disorders. It aids early detection of potential genetic conditions in the fetus.
Need for the First Trimester Screening Test
This screening helps detect genetic risks in the fetus early in pregnancy, improving care decisions and planning.
1. Early Detection of Chromosomal Disorders :- Identifies risks of conditions like Down syndrome and trisomy 18, enabling further diagnostic tests and early medical intervention if needed.
2. Non-Invasive and Safe for Mother and Baby :- The test is done with a simple blood draw and ultrasound, posing no harm to the baby and offering peace of mind for expectant parents.
3. Supports Informed Pregnancy Decisions :- Results allow doctors and parents to decide if further testing, such as chorionic villus sampling (CVS), is necessary to confirm any concerns.
4. Monitors Fetal Development in Early Pregnancy :- The ultrasound portion checks for physical abnormalities and fetal growth patterns that might signal underlying health issues or developmental concerns.
5. Recommended for High-Risk Pregnancies :- Especially helpful for women over 35, those with previous abnormal pregnancies, or a family history of genetic disorders, allowing for early risk assessment.
Why Choose mediSuggest for First Trimester Screening Test?
Compassionate prenatal testing with top-rated labs, expert care, and reliable results at your fingertips.
1. Access to Accredited Diagnostic Centers :- We partner with NABL and ISO-certified labs that follow precise standards for prenatal testing, ensuring you receive accurate, trustworthy screening results.
2. Ultrasound with Expert Fetal Imaging Specialists :- Our ultrasound services are conducted by trained radiologists specializing in prenatal care, offering detailed insight into your baby’s development.
3. End-to-End Pregnancy Testing Support :- From test booking to post-result consultation, we support you at every step, helping you feel confident in your early pregnancy journey.
4. Fast Result Delivery with Expert Interpretation :- Get your test results within 24–48 hours along with an interpretation by a certified gynecologist or genetic counselor, available through mediSuggest.
5. Convenient Online Test Booking Platform :- Book your appointment online, choose from top diagnostic centers near you, and receive reminders and reports directly on your phone.
Frequently Asked Questions
Is there any risk to the baby?
No, the test is non-invasive. The blood test is taken from the mother, and the ultrasound is completely safe for both mother and baby.
How accurate is the First Trimester Screening Test?
It is not diagnostic but provides a risk estimate. It is over 85% effective at identifying pregnancies that may be at risk for certain genetic issues.
What week should I take the test?
The test is done between 11 and 14 weeks of pregnancy to ensure accurate results from both the ultrasound and blood analysis.
Is the test mandatory for all pregnant women?
While not mandatory, it is strongly recommended as part of routine prenatal care to help identify any early risks to the baby’s development.
What does the First Trimester Screening Test check for?
It checks for the risk of chromosomal abnormalities such as Down syndrome (trisomy 21) and trisomy 18, using a blood test and an ultrasound scan.