Triple Marker Test- Beckman (Benetech) in Mandi

Triple Marker Test in Mandi

Overview

Pregnancy is the most beautiful phase of one’s life, which comes with happy moments and a bundle of responsibilities. During pregnancy, several genes pass on from parent to child, which can be good or bad. Doctors recommend several tests and scans to detect abnormalities and chromosomal defects to avoid possible complications. One among the other tests is a Triple Marker Test. Also known as Triple Test, Multiple Marker Test, and Multiple Marker Screening, Triple Marker Test helps physicians understand your pregnancy.

It is a simple investigation advised to pregnant women to identify any genetic or chromosomal disorders in the fetus. Triple Marker Test In Pregnancy predicts developmental disorders and helps find any risk of Down syndrome to the fetus. The triple screening of substances in the placenta, including alpha-fetoprotein, human chorionic gonadotropin, and estriol involved in the test. Therefore, it is as comfortable as other blood test procedures..

Standard Benefits Associated With Triple Marker Tests:

• Help parents prepare for birth.
• Detect any genetic or congenital disabilities in the fetus at a very early stage.
• Help to find any health hazards or possible complications to the unborn baby.
• Also, identify multiple pregnancies.
• Diagnose all possible pregnancy complications that further make mom-to-be and baby accessible for early treatment.

Triple Marker Test Is Recommended For Women Meeting The Following Conditions:

• Are over the age of 35 years and more.
• Have a family history of genetic defects.
• Suffering from diabetes and other severe prenatal viral infections.
• Have been exposed to radiation.
• On-medication with significant side effects.

Interpretation Of The Test Results:

It is indeed helpful in diagnosing any genetic disorders in the fetus, yet the results or Triple Marker Test Normal Values largely depend on several factors, including:

• Age: After each menstrual cycle, women lose eggs present in their bodies from birth and may have abnormal chromosomes that can cause genetic disorders in babies.
• Body Weight: If the mother is overweight, it can cause complications during pregnancy and could be risky to mother and baby both.
• Diabetes Or Other Health Disorders: This could also be why one needs to be extra conscious and careful during pregnancy.

Other than the above, ethnicity, pregnancy period or multiple pregnancies are a few common factors that can affect the results.

Cost Of Triple Marker Test:

The test is gaining popularity because it detects and treats birth defects in children at an early stage. Triple Marker Test Cost or Triple Marker Test Price varies from center to center depending on different factors. However, with Redcliffe Labs, you can Book Triple Marker Test at Rs. 2799. The cost is very much reasonable, so get it done today to avoid any possible complications in your pregnancy tomorrow.

Triple Marker Test Price in Mandi

Triple Marker Test Cost in Different Cities - Redcliffe Labs

Note: We also offer Triple Marker Test PAN India. Please call the number 8988988787 to check the availability of our services in your area.

Purpose of the Triple Marker Test

The Triple Marker Test is crucial in identifying the risk of certain genetic conditions in the developing fetus, making it a vital part of prenatal care. 

• Screening for Chromosomal Abnormalities—The test helps to identify the risk of chromosomal abnormalities, including Down syndrome (Trisomy 21) and Trisomy 18. Abnormal AFP, hCG, and estriol may indicate a higher risk of these conditions.
• Detects Neural Tube Defects—High levels of AFP suggest the presence of neural tube defects, such as spina bifida or anencephaly, in which the fetal spine or brain does not develop properly. 
• Assess Pregnancy Complications- The Triple Marker Test in Pregnancy can also provide insights into potential complications like preeclampsia, gestational diabetes, or placental issues.

When is the Triple Marker test needed?

The Triple Marker blood test in Mandi is recommended during pregnancy under specific conditions when there is a need to assess the risk of genetic abnormalities or congenital disabilities. Here are the primary scenarios when the test is considered necessary:

• The people above 35 years
• had a child with any congenital disability previously 
• Have a family history of genetic disorders
• Conceive using IVF
• Have pre-existing health issues like diabetes or high blood pressure
• Routine testing
• Family history of genetic disorders
• Abnormal Ultrasound tests
• Multiple Pregnancies (Twins or More)

Preparation for the Triple Marker Test 

There is no such preparation is required-

• Timing of the Test—The triple marker blood test in Mandi is performed between the 15th and 20th weeks of pregnancy. 
• No Special Fasting Required—You are not required to fast before the test. You can eat and drink as usual.
• Inform Your Healthcare Provider—Consult your doctor about your condition, including gestational age, weight, and any relevant medical history. It is also important to inform your healthcare provider if you're taking any medicines or supplements, as some substances may affect the test results.

The procedure of the Triple Marker Test

The procedure for the Triple Marker Test is straightforward and involves the following simple steps:

• The healthcare provider will clean the arm area with an antiseptic solution and tie a tourniquet to the arm.
• Next, the healthcare provider will use a sterile needle to draw a small amount of blood from the vein of your arm. 
• The blood is collected into a vial or test tube. Once the blood sample is collected, the phlebotomist removes the needle and applies gentle pressure to the puncture site to stop bleeding. Then, he puts a bandage over the site.
• The sample will then be sent to a lab, where it will be analyzed to measure the levels of three specific markers.
• The laboratory uses these measurements and information about your gestational age, weight, and other factors to identify the risk of chromosomal abnormalities (such as Down syndrome) and neural tube defects.
• The results of the triple marker test in Mandi will be available within three days of sample collection. 

After the blood draw, you can return to your regular activities. There is typically no need for special care, but if you experience any discomfort or bruising at the blood draw site, applying a cold compress can help alleviate symptoms.

What do the Triple Marker Test reports indicate?

The Triple Marker Test report provides an assessment of the risk of certain genetic conditions and congenital disabilities based on the levels of three specific markers in the mother's blood: Alpha-fetoprotein (AFP), Human chorionic gonadotropin (hCG), and Estriol. Here’s how the results are typically interpreted:

Alpha-fetoprotein (AFP):

The normal levels of AFP indicate a low risk of neural tube defects and other chromosomal abnormalities.

• The high levels of AFP indicate neural tube defects such as spina bifida or anencephaly.
•  Abdominal wall defects in the fetus, such as gastroschisis.
•  Multiple pregnancies (e.g., twins), as more AFP is produced.

Low AFP levels indicate Down syndrome, Trisomy 18, incorrect estimated date, where the pregnancy is earlier than believed.

Human Chorionic Gonadotropin (hCG)

• The normal levels of hCG mean a risk of chromosomal abnormalities
• The high levels of hCG indicate Down syndrome (Trisomy 21), molar pregnancy (a rare complication involving abnormal growth of the placenta), and multiple pregnancies.
• The low hcg levels indicate trisomy 18, ectopic pregnancy, and potential miscarriages. 

uE3- Estriol Unconjugated

The normal estriol level is an estrogen produced by the placenta and the fetus. Normal levels are generally reassuring, indicating a lower risk of chromosomal abnormalities.

The low levels of estriol levels may indicate Down syndrome, trisomy, adrenal gland problems in the fetus, and placental insufficiency. 

The test results are interpreted as a combination of these three markers and factors like the mother's age, weight, ethnicity, and gestational age.

If the results suggest an elevated risk, your medical professional may recommend additional tests, such as amniocentesis, chorionic villus sampling (CVS), or a detailed ultrasound, to provide more definitive information.

 Overall, the Triple Marker test in Mandi helps identify pregnancies at higher risk for certain conditions, allowing for timely follow-up and informed decision-making.

Things You Should Know Before Triple Marker Test:

• Triple Marker Screening Test is just like a blood test that analyzes any genetic disorders in the unborn baby.
• For the test, your healthcare provider takes a blood specimen to detect the level of AFP, HCG, and estriol.
• Apart from the discomfort that comes with a needle, there is no specific complication associated with the test.
• The test is totally risk-free for the mother and unborn baby as well and can be done at a reasonable Triple Marker Test Cost.

Characteristics That Make Redcliffe Labs A Reliable Center For Triple Marker Tests:

• Have a highly qualified and trained team.
• Provide multiple testing and scans, adhering to quality and safety standards.
• A home sample pick-up facility is available to offer maximum convenience to patients.
• Keep patient information and reports confidential.
• Use ultra-modern techniques to offer exceptional services.
• Provide affordable and cost-effective testing and treatment.

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

Book Your Test Today!

Don’t put your baby at risk! Get the test done to detect any genetic disorders, if any, to begin the treatment at the earliest. Book Your Home Triple Marker Test In Pregnancy with Redcliffe Labs via the website or call. Our tests are available at reasonable rates.