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Double Maker Test - Maternal Screen, 1st Trimester

  • Sample Type : Blood
  • Parameters : 2
  • Report Time : 24/48 Hrs
  • Home Collection: Yes
OFFER PRICE:  ₹2200 ₹2800 30% off

 

double marker test in pregnancy
16+ booked in last 3 days

DOUBLE MAKER TEST - MATERNAL SCREEN, 1ST TRIMESTER (2 TESTS INCLUDED)

  • Free Beta Hcg
  • Pregnancy Associated Plasma Protein A
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The double marker test (First Trimester Screening Test) is a vital component of prenatal care that involves the analysis of two key substances present in the mother's blood: pregnancy-associated plasma protein-A (PAPP-A) and free beta-human chorionic gonadotropin (β-hCG). By measuring the levels of the two substances, your healthcare professional can gain valuable insights into the probability of genetic disorders like Down Syndrome.

The double marker test provides crucial information for expecting mothers and aids in determining the appropriate course of action, such as the need for further diagnostic tests or genetic counseling. The double marker test in pregnancy not only assists in early detection but also offers peace of mind to parents-to-be.

Learn everything about the double marker test before you book your test online.

Why Is Double Marker Test In Pregnancy Recommended?

The double marker test in pregnancy is conducted to assess the risk of chromosomal abnormalities in the developing fetus. It involves analyzing the levels of pregnancy-associated plasma protein-A (PAPP-A) and free beta-human chorionic gonadotropin (β-hCG) in the mother's blood. This dual marker test provides valuable insights into the probability of genetic disorders such as Down syndrome. By evaluating these markers, healthcare professionals can determine the need for further diagnostic tests or genetic counseling. The double marker test plays a crucial role in early detection, allowing for timely intervention and appropriate medical management.

When Does Pregnancy Demand Dual Marker Test?

The Dual Marker Test in pregnancy is required during the first-trimester screening to assess the risk of chromosomal abnormalities in the developing fetus. It involves analyzing the levels of pregnancy-associated plasma protein-A (PAPP-A) and free beta-human chorionic gonadotropin (β-hCG) in the mother's blood. This double marker test provides valuable insights into the probability of genetic disorders like Down syndrome. The test is recommended for all pregnant women, especially those with advanced maternal age or a family history of genetic conditions. It aids in early detection, allowing for timely intervention and appropriate medical management if necessary.

How To Prepare For Dual Marker Blood Test?

There are no special preparations needed when getting a dual marker blood test. In certain cases, the healthcare provider might want you to fast (not consume any food for a few hours) before the test. Fasting for 8 to 12 hours before the test might be required.

Should you call for the blood test at home to check your dual marker blood test levels, or get it done at your nearest clinic? Let us help you figure it out. 

Can I Take Maternal Serum Screening At Home?

Yes, the maternal serum screening blood test can be taken at home. HealthcareOnTime’s at-home lab testing service, in association with Thyrocare, provides a convenient and efficient way to get important medical tests done from the comfort of your place without the need for a doctor's visit or a trip to a lab. It is always preferable to consult with a healthcare provider about any concerns regarding your test results.

How Much Does Double Marker Test Price In India?

The double marker test cost varies depending on various factors, such as where you live, the healthcare provider or a laboratory that performs the test, and whether or not you have health insurance coverage. You can check the double marker test price on our website. We offer this test at INR 2200. Our prices are lower than the average test prices without compromising on quality. 

You received your double marker blood test results but still need help determining if they fall under the normal range. Read this section to know if your double marker test report falls within the double marker test normal range.

What Does Double Marker Test Results Mean?

Test Result

Result Meaning

Low-Risk

Low probability of your baby having chromosomal abnormalities

Moderate-Risk

You would be suggested to consult with a Genetic Counselor

High-Risk

You will be suggested to go more for invasive tests 

What Is Normal Range For Double Marker Test In Pregnancy?

A double marker test typically gives you a low-risk, moderate-risk & high-risk test range, but for a layman, the reference normal range to look at is 25,700 to 2,88,000 mIU per mL.

Double Marker Test Normal Value

25,700 - 2,88,000 mIU per mL

What If Double Marker Test Is Positive?

If your screening comes back as moderate- or high-risk (“screen-positive”) for abnormalities, you may be suggested to understand your result with a genetic counselor.

Your double marker test results can be confirmed with more definitive and or invasive tests, such as noninvasive prenatal testing (NIPT), amniocentesis, or chorionic villous sampling. While some of these tests carry some risk to your pregnancy, they provide a much more definitive result.

Since the double marker test is done early on in your pregnancy, knowing about the risk may also help you prepare for the scenario that you’ll have a child with special needs. It'll also allow you to look for the support you’ll need.

What If Double Marker Test Is Negative?

Low-risk (screen-negative) is considered a “normal” result, which means that there’s a very low probability of your baby having chromosomal abnormalities. Hence, you will not be suggested to go for further screening, but if you have a known family or genetic history, it is recommended to go for further testing.

What Are The Potential Benefits Of Undergoing  Double Marker Test In Pregnancy?

  • A double marker test is one of the tests for pregnancy, suggested for early detection of any chromosomal abnormalities. 
  • It is a useful pregnancy screening test to determine the healthy development of the fetus 
  • Identification of high-risk pregnancies, enabling closer monitoring and specialized care.

What Are The potential risks Associated With Double Marker Test In Pregnancy?

  • Possibility of false-positive or false-negative results, leading to unnecessary anxiety or potential missed diagnosis.
  • As a double marker test is a non-invasive blood test, there are no risks associated with it. But one should be sure to follow the doctor's instructions and immediately contact the healthcare provider if there are any concerns regarding the tests or pregnancy.

If you find it difficult to schedule medical appointments and tests, HealthcareOnTime- Best diagnostic center in India is here to help. You can conveniently and affordably avail of our home testing facilities to conduct the double marker test at a time and date that works best for you. 

One of the main benefits of using HealthcareOnTime at-home lab testing is its convenience. Instead of scheduling a visit to a medical facility or clinic, you can order medical tests online and perform them at home. This is especially helpful for people with busy schedules, limited mobility, or transportation issues. HealthcareOnTime at-home lab testing offers competitive pricing, making them an affordable option for those needing medical testing services.

Exclusive Service and Reporting managed by our Partner Diagnostic Centre:

Thyrocare Technologies Limited - India's first and most advanced Totally Automated NABL/ICMR/CAP/ISO certified Laboratory providing accurate reports with top-rated quality service since 1995. Book your test immediately as we have kept the Double Marker Test price very reasonable for all our clients.

Disclaimer: Although we have endeavored to provide accurate information on this page, we strongly recommend that you seek advice from your doctor before relying on any of the test ranges or lab-test recommendations mentioned herein.

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FAQs Around Double Marker Test In Pregnancy

The dual marker test is highly accurate in assessing the risk of chromosomal abnormalities in pregnancy. It relies on the analysis of pregnancy-associated plasma protein-A (PAPP-A) and free beta-human chorionic gonadotropin (??-hCG) levels, providing reliable results for early detection and intervention.

The double marker test is typically performed during the first trimester of pregnancy, which falls between the eleventh and thirteenth week. It is part of the first-trimester screening to assess the risk of chromosomal abnormalities in the developing fetus.

The double marker test is typically conducted during the first trimester of pregnancy. It is an essential component of first trimester screening to evaluate the risk of chromosomal abnormalities in the fetus. This test can be conducted at any time of the day.

If the double marker test is missed during pregnancy, it is important to consult with your healthcare provider. They can provide guidance on alternative screening options to assess the risk of chromosomal abnormalities in the fetus.

The NIPT (Non-Invasive Prenatal Test) and Double Marker Test are different screening tests used during pregnancy. While both assess the risk of chromosomal abnormalities, NIPT is more advanced and accurate, analyzing fetal DNA from the mother's blood.

The Double Marker Test and NT (Nuchal Translucency) scan are both prenatal screening tests, but they assess different aspects of the fetus's development. While the Double Marker Test measures certain hormones in the mother's blood to evaluate the risk of chromosomal abnormalities, the NT scan uses ultrasound to measure the thickness of the baby's neck to screen for Down syndrome and other conditions.

The Double Marker Test detects chromosomal abnormalities such as Down syndrome (Trisomy 21) and Edwards syndrome (Trisomy 18) by assessing specific hormones in the mother's blood. It helps identify potential risks during pregnancy.

The double marker test is not mandatory, but it is highly recommended for pregnant women, especially those at higher risk or with a family history of genetic disorders.

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  • Disclaimer: HealthcareOnTime offers extensively researched information, including laboratory testing for health screening. However, we must emphasize that this content is not intended as a substitute for professional medical advice or diagnosis. Always prioritize consulting your healthcare provider for accurate medical guidance and personalized treatment. Remember, your health is of paramount importance, and only a qualified medical professional can make precise determinations regarding your well-being.
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