Triple Marker Test - Price, Range, Procedure, Results - 2024

27993500

Includes 3 Parameters

20% off for a limited period

Home Sample Collection in 2 hours*
FastingNot Required
Get reports in3 days
Home Sample Collection in 2 hours*

Additional Instructions

Mandatory - Submission of Maternal History Form & Latest copy of Ultrasound report during sample collection. The recommended period is 15-22 weeks.

What is it for ?

During pregnancy AFP, hCG, and estriol levels are measured to find genetic disorders like Down Syndrome.

Also known as: Triple Screen, 2nd Trimester Screening, Maternal Screening

Sample Type

Blood

test Instructions

  • Age Group: 21-45 Years

Benefits

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Smart Reports In 24 hours*
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Free Reports Consultation
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Most Affordable Pricing
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On-time Sample Collection
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NABL Certified Labs
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Presence In 220+ Cities

Included Tests

Package includes following parameters

Triple Marker (3)

  • AFP- Alpha Feto Protein Maternal Marker
  • Beta HCG Total
  • uE3- Estriol Unconjugated

Q&A

Helps you know your test better

Q. What Is A Triple Marker Test?

A. It’s a simple test available at a nominal Triple Marker Test Price and is recommended for pregnant women to determine any genetic or chromosomal disorders developed during the prenatal phase.

Q. What Happens During Triple Marker Screening?

A. It is like any other blood test and requires no special preparation or fasting. During the examination, your healthcare provider will clean the skin, ask you to make a fist to make the vein more accessible, insert the needle to draw some blood specimens, and collect them in a vial to send to the lab for analysis.

Q. What Do The Triple Marker Test Indicate?

A. It’s a screening test and not a diagnostic test and can only predict any possible abnormalities or genetic disorders in a baby. There are chances of false results. Therefore, doctors can prescribe several other scans or diagnose if required for better clarity or accuracy.

Q. What Are The Disorders That Can Be Screened With Triple Marker Test?

A. It can detect Trisomy 18, Down syndrome, Neural tube defects, and other Chromosomal abnormalities in a fetus to begin the treatment as soon as possible.

Q. Is There Any Risk To Baby During The Test?

A. Blood is drawn from the mother only. Therefore, no such risk to the baby is involved in the procedure.

Table of Content

Introduction to Triple Marker Test

Becoming parents is a blessing but never easy, as it comes with several responsibilities. Throughout your pregnancy journey, your doctor may suggest different tests to monitor the baby's growth inside and ensure the safety of both the unborn baby and the mother-to-be. Each test suggested during pregnancy as a part of Prenatal screening is significant for monitoring pregnancy, detecting abnormalities (if any), and initiating preventive measures or treatment while there is still time. Among all the parental screening tests, a Triple Marker Test is mostly suggested to screen pregnant women for congenital disabilities. It helps assess the risk of fetal chromosomal abnormalities and genetic disorders.

Doctors often suggest a Triple Marker Test as a part of a Prenatal screening test between the 15th & 20th week of pregnancy. However, the time may vary, depending on the individual's circumstances. Redcliffe Labs is the name to recall if you are looking for a reliable diagnostic service provider for a Triple Marker Test in Pregnancy. With a wide network of labs and collection centers spread nationwide, we bring diagnostic care to every individual. So, worry not, and book your Triple Marker Test at home with us now.

Triple Marker Test Details In Brief:

Also Known As Triple Screen, 2nd Trimester Screening, Maternal Screening
Purpose Screen for the possibility of chromosomal defects in the developing fetus.
Preparation Do not take any over-the-counter medicine without confirming with your doctor
Fasting No Fasting Required
Get Reports Within 3 Days
Cost INR 2799

Triple Marker Test Details

Reasons You May Need A Triple Marker Test:

A healthcare practitioner often suggests a Triple Marker Blood Test to pregnant women as part of routine prenatal screening, especially with high-risk factors. Here are some of the circumstances your doctor may suggest Triple Marker Screening:

  • Maternal Age: Pregnancy at 35 or older is more likely to cause complications and increases one's risk of having babies with Down Syndrome and other chromosomal abnormalities. The test helps assess their risk of developing such problems at the early stage possible.
  • Previous Pregnancy Complications: Pregnant women with previous pregnancies with chromosomal abnormalities are always suggested to go for a Triple Test to monitor the current pregnancy while assessing the risks closely.
  • Family History: You may need a Triple Screen Test if you have a history of giving birth to babies with genetic disorders or congenital disabilities to evaluate the current pregnancy and associated risks.
  • Abnormal Ultrasound Findings: If your routine ultrasound or screening indicates some abnormalities that could be linked with chromosomal abnormalities, a Triple Screen Blood Test is often advised as a follow-up screening.

While there are multiple reasons a doctor may suggest a Triple Marker Test, also called 2nd Trimester Screening, it is not a definitive test and only a screening test. It can only indicate one's risk of having babies with chromosomal abnormalities. If the results are positive and show higher risks, your doctors may suggest additional tests to clarify and confirm the presence of any chromosomal or genetic disorders. Getting tested may give you better insight into your pregnancy and help you make informed decisions.

Conditions That Can Be Screened With A Triple Marker Test:

The primary objective of this Triple Test is to monitor pregnancy and assess the likelihood of the different conditions in the fetus, including:

  • Down Syndrome: As a genetic disorder, Trisomy 21, also called Down Syndrome, occurs due to an extra chromosome 21, leading to distinct facial appearance, intellectual disabilities, & developmental delays. A triple screen test helps look for markers indicating the risk of babies with this problem.
  • Edwards syndrome: Also called Trisomy 18, is another chromosomal defect causing developmental delays and leading to premature death. And A triple screening test helps assess fetal risk with Trisomy 18 or Edwards syndrome.
  • Neural tube defects (NTDs): Moreover, a Triple Screening Testing screen for one's likelihood of developing congenital disabilities, which can lead to severe disabilities or other life-threatening conditions.

It is critical to understand none of the conditions mentioned above can be diagnosed with a Triple Marker Test; rather, it indicates the risk levels of these conditions.

Triple Marker Tests List:

A Triple Marker Blood Test usually evaluates three major substances in the maternal blood to assess the risks of having a baby with chromosomal disabilities. Such substances are:

  • Alpha-fetoprotein (AFP): Alpha-fetoprotein is a protein secreted by the developing fetus. If its levels are too much in your blood, it indicates a higher risk of neural tube defects or certain chromosomal abnormalities.
  • Human chorionic gonadotropin (hCG): Another substance this blood test measures is hCG, a hormone produced by the placenta. Low hCG levels usually indicate potential pregnancy complications, like ectopic pregnancy or higher chances of miscarriage. On the contrary, elevated hCG levels indicate multiple or molar pregnancies.
  • Estriol: Lastly, Estriol is an estrogen hormone that can be measured through this triple marker test, as its abnormal levels are usually associated with a higher risk of certain chromosomal disorders.

The test doesn't confirm any chromosomal abnormality or genetic disorder but indicates the risk of developing one. Your healthcare provider may suggest additional tests and other preventive measures depending on the test results.

Benefits Of A Triple Marker Screen Test:

  • While monitoring pregnancy or the unborn baby's development, the test helps detect the risk of congenital disabilities in the early stage.
  • Besides, the test helps assess the risks of other possible pregnancy complications early, making it easier to manage them better.
  • Early diagnosing may help one make genetic counseling or other informed pregnancy-related decisions that benefit both the mother and baby.

Remember, a Triple Marker Screen Test is highly advisable to help you avoid several pregnancy-related complications.

Preparations Required For A Triple Marker Test:

Typically, no preparations are required for A Triple Screening Test. It is a non-invasive blood test that can be performed without fasting. However, some guidelines to be followed for accurate reports are:

  • Generally, a Triple Marker Test is often suggested between the 15th to 20th week of pregnancy. However, the appropriate time for the test can vary, depending on the individual's circumstances. Therefore, it should be discussed before the test for better clarity.
  • It is a simple test that requires no fasting. However, if you are on some medications or a special diet plan, share this with your doctor before the test. Also, follow their instructions on stopping or continuing to take them before the test.
  • Relax and be comfortable; your anxiety or stress can influence your hormones or test results. If you have known allergies, fear of needles, or other queries, discuss them with the phlebotomists so that they can guide you better.

In general, no preparations are necessary. However, depending on your condition or any other factor, if special instructions are advised, follow them to avoid discrepancies in the test results.

Procedure Of A Triple Marker Test:

It is a non-invasive procedure that involves the following steps:

  • A phlebotomist will tie a tourniquet (a band) on the upper arm during the process.
  • Then they may ask you to make a fist so the vein can be found easily.
  • Once the vein is found, they will disinfect the area using a disinfectant.
  • Then, a needle will be inserted on the clean site to collect blood samples for processing.
  • Once the sample is collected, the punctured site will be covered using a cotton ball, and the collected sample will then be transferred to the vial for sending to the laboratory.
  • A phlebotomist will then put a bandage on the punctured site to prevent the infection.

The procedure is simple and safe and poses no risks to your pregnancy. However, during the blood drawing procedure, you may experience slight discomfort, pain, or a little bruise at the punctured site, which will be resolved soon. If you experience something unusual or the symptoms are not fading, seek medical assistance immediately.

Procedure Of A Triple Marker Test

Triple Marker Test Normal Range:

The approximate normal range for a Triple Marker Pregnancy Test is:

Parameters

Normal Value

Alpha-fetoprotein (AFP)

1.38 -187.00 IU/ml

Human chorionic gonadotropin (hCG)

1.06 - 315 ng/ml

Estriol

0.25 -28.5 nmol/l

This range may vary from lab to lab for several reasons, like technology or processing methods.

Triple Marker Test Result Interpretation:

The outcome will be positive or negative depending on the normal values of the Triple Marker Test. While positive test results indicate higher than average possibilities of having a baby with chromosomal abnormalities, negative test result exhibits very low or no risks of developing congenital disabilities in the fetus.

Remember, abnormal or positive triple marker test results don’t always indicate a birth defect. Similarly, negative triple-screen test results don’t always rule out pregnancy risks. Depending on the test results or other factors like medical history, age, and more, you may be advised to undergo additional tests for better clarity and a more accurate diagnosis.

Triple Marker Test Price @ Redcliffe Labs!

We create all our health tests and packages, keeping customers' different needs and budgets. Therefore, you can book different tests with us at highly competitive rates. With Redcliffe Labs, Triple Marker Test Price is just Rs 2799. You can book the test to get screened from the comfort of your home. So, what are you waiting for? We also provide Express Slots, which help you get your sample picked within 45 minutes. Book now!

Triple Marker Test Price

Pregnancy-Related Tests/Packages That You Can Book with Redcliffe Labs

Tests/Packages Offer Price in INR
HCG Test ₹499
HCG Tumor Marker (Cancer) Test ₹650
Alpha Fetoprotein (AFP), Maternal Marker Test ₹900
Pregnancy Associated Plasma Protein-A(PAPP-A) Test ₹1000
Double Marker Test- Auto-Delfia ₹2500
Double Marker Test ₹2400
Double Marker Test + PLGF- Roche ₹3200
Quadruple Marker Test ₹3600

So, Don’t Put Your Baby’s Health On Guess. Take A Triple Marker Test!

As part of your prenatal screening, a triple marker pregnancy test is highly advisable to detect and manage the problem while there is still time. Redcliffe Labs is your trusted diagnostic partner from where you can book a Triple Marker Test at home. We are committed to precision and provide accurate test results within a stipulated timeframe. So, delay no more and get yourself tested in time.

Frequently Asked Questions

What is the Triple Marker Test?
Also known as Triple Test or Triple Screen Test, Triple Marker Test is a prenatal screening test that helps assess the risk for certain chromosomal abnormalities & genetic disorders by measuring three major substances, including AFP, hCG, and Estoril.
    What is the Triple Marker Test during pregnancy?
    The test is often suggested during pregnancy to thoroughly screen pregnant women and assess their risks of having babies with chromosomal abnormalities.
      Is the Triple Marker Test necessary after the Double Marker Test?
      The triple marker screening test is only sometimes necessary, and doctors may suggest this test, depending on individual factors. If Double Marker Test presents a higher risk or additional risk factors, your healthcare provider may recommend this test for further evaluation.
        What is the cost of a Triple Marker Test?
        The Triple Marker Test Cost may vary depending on the location, lab, and additional tests (if any). With Redcliffe Labs, we keep our costs and charges to the nominal possible, and hence, you can book a Triple Marker Test at Rs 2799 with us.
          When is the Triple Marker Test done?
          Doctors often suggest a Triple Marker Test between the 15th & 20th week of pregnancy to ensure early detection of potential abnormalities (if any).
            Is the Triple Marker Test mandatory?
            No! Triple Marker Test is not compulsory for all pregnancies. Doctors decide whether the test is required depending on maternal age, medical history, previous test results, and other risk factors.
              How accurate is the Triple Marker Test?
              Since it is not a definitive test but a screening test that helps screen for your risks of having a baby with chromosomal abnormalities. So, the accuracy can vary, and false-positive or false-negative results may occur. Depending on the test results, your healthcare practitioner may suggest additional tests.
                How is the Triple Marker Test done?
                It is a simple blood test. During the procedure, a phlebotomist will draw blood from the vein of a pregnant woman and send it to the laboratory for analysis.
                  Why is the Triple Marker Test done?
                  It is done to screen for fetal chromosomal abnormalities, neural tube defects, and genetic disorders. Moreover, it helps identify pregnancies at higher risk for these conditions so doctors can suggest further action accordingly.

                    20% off for a limited period

                    Frequently Asked Questions

                    What is the Triple Marker Test?
                    Also known as Triple Test or Triple Screen Test, Triple Marker Test is a prenatal screening test that helps assess the risk for certain chromosomal abnormalities & genetic disorders by measuring three major substances, including AFP, hCG, and Estoril.
                      What is the Triple Marker Test during pregnancy?
                      The test is often suggested during pregnancy to thoroughly screen pregnant women and assess their risks of having babies with chromosomal abnormalities.
                        Is the Triple Marker Test necessary after the Double Marker Test?
                        The triple marker screening test is only sometimes necessary, and doctors may suggest this test, depending on individual factors. If Double Marker Test presents a higher risk or additional risk factors, your healthcare provider may recommend this test for further evaluation.
                          What is the cost of a Triple Marker Test?
                          The Triple Marker Test Cost may vary depending on the location, lab, and additional tests (if any). With Redcliffe Labs, we keep our costs and charges to the nominal possible, and hence, you can book a Triple Marker Test at Rs 2799 with us.
                            When is the Triple Marker Test done?
                            Doctors often suggest a Triple Marker Test between the 15th & 20th week of pregnancy to ensure early detection of potential abnormalities (if any).
                              Is the Triple Marker Test mandatory?
                              No! Triple Marker Test is not compulsory for all pregnancies. Doctors decide whether the test is required depending on maternal age, medical history, previous test results, and other risk factors.
                                How accurate is the Triple Marker Test?
                                Since it is not a definitive test but a screening test that helps screen for your risks of having a baby with chromosomal abnormalities. So, the accuracy can vary, and false-positive or false-negative results may occur. Depending on the test results, your healthcare practitioner may suggest additional tests.
                                  How is the Triple Marker Test done?
                                  It is a simple blood test. During the procedure, a phlebotomist will draw blood from the vein of a pregnant woman and send it to the laboratory for analysis.
                                    Why is the Triple Marker Test done?
                                    It is done to screen for fetal chromosomal abnormalities, neural tube defects, and genetic disorders. Moreover, it helps identify pregnancies at higher risk for these conditions so doctors can suggest further action accordingly.