What is Triple Marker Test?

The triple marker screen test is also known as the triple test, multiple marker test, multiple marker screening, and AFP Plus. It analyzes how likely an unborn baby is to have certain genetic disorders. The exam measures the levels of three important substances in the placenta: alpha-fetoprotein (AFP).

Why take Triple Marker Test?

Triple marker tests identify pregnancies that have a high risk of babies having the following abnormalities:

• Trisomy 21 (Down’s syndrome)
• Trisomy 18 (Edward syndrome)
• Neural tube defects

These tests are NOT diagnostic tests. Your doctor will order a confirmatory test when the screening test is positive (high risk)

Are there any special precautions to be taken before a triple marker test in Jhansi?

Yes, there are certain precautions that need to be taken before a triple marker test in Jhansi. Here are some of them:

1. Consult a doctor: Before taking the test, it is important to consult a doctor to understand the procedure and its implications.

2. Fasting: It is advisable to fast for at least 8 hours before taking the test. This ensures that the results are accurate.

3. Avoid medication: If you are taking any medication, it is important to inform your doctor before the test. Some medications can interfere with the test results.

4. Avoid smoking and alcohol: Smoking and alcohol consumption should be avoided for at least 24 hours before the test. These substances can also interfere with the results.

5. Wear comfortable clothing: Wear comfortable and loose-fitting clothes to the test. This makes it easier for the technician to take your blood sample.

6. Relax: It is natural to feel anxious before the test, but it is important to relax and stay calm. Stress can affect the test results.

7. Drink plenty of water: Drinking plenty of water before the test helps to keep you hydrated and also makes it easier to take the blood sample.

In conclusion, taking the necessary precautions before a triple marker test in Jhansi can help to ensure accurate results and a hassle-free experience.

How long does it take to get the results of a triple marker test in Jhansi?

The triple marker test is a prenatal test that is usually performed between the 15th and 20th week of pregnancy. The test is designed to screen for Down syndrome, neural tube defects, and other chromosomal abnormalities in the developing fetus.

In Jhansi, the results of the triple marker test usually take around 3-5 days to come back. However, the exact turnaround time can vary depending on the laboratory where the test is performed, as well as other factors such as the volume of tests being processed at the time.

It's important to note that the triple marker test is not a diagnostic test, but rather a screening test. This means that a positive result does not necessarily mean that the fetus has a chromosomal abnormality or neural tube defect. Instead, it indicates that further testing may be necessary to confirm the diagnosis.

If you're considering getting a triple marker test in Jhansi, it's a good idea to speak with your healthcare provider to learn more about the test, what it involves, and what to expect from the results. Your healthcare provider can also help you interpret the results and determine what further testing, if any, may be necessary.

Are there any risks associated with a triple marker test in Jhansi?

The triple marker test, also known as the triple screen test, is a prenatal test that screens for the risk of chromosomal abnormalities in the fetus, such as Down syndrome, neural tube defects, and certain genetic disorders. While the test is generally considered safe and effective, there are some risks associated with it in Jhansi, just as there are with any medical procedure.

One of the main risks associated with the triple marker test in Jhansi is the possibility of false positives. This means that the test may show that there is a higher risk of a chromosomal abnormality than there actually is. This can lead to unnecessary anxiety and stress for expectant parents, and may also result in more invasive tests, such as amniocentesis, which carries its own risks.

Another risk associated with the triple marker test is the possibility of false negatives. This means that the test may show that there is a low risk of a chromosomal abnormality when there actually is one. This can lead to a false sense of security for expectant parents, who may opt out of further testing or prenatal care.

In addition to these risks, there may be other factors that affect the accuracy of the triple marker test in Jhansi. For example, variations in laboratory procedures or equipment may impact the results, as can differences in the population being tested. It is important for expectant parents to discuss these risks and any concerns with their healthcare provider before deciding to undergo the triple marker test.

Overall, while the triple marker test can provide valuable information about the health of a fetus, it is important to weigh the potential risks and benefits before deciding to undergo the test. Expectant parents should have a clear understanding of what the test involves, what the results may mean, and what further testing may be necessary. They should also discuss any concerns or questions with their healthcare provider.

In conclusion, the triple marker test is a prenatal screening tool that can help identify the risk of chromosomal abnormalities in a developing fetus. While the test is generally safe and effective, there are potential risks associated with it, including false positives and false negatives. Expectant parents should speak with their healthcare provider to learn more about the test and its risks and benefits before deciding whether to undergo the triple marker test. By making an informed decision, expectant parents can take an active role in ensuring the health and well-being of their growing family.

What is the procedure for a triple marker test in Jhansi?

The triple marker test, also known as the multiple marker test, is a prenatal screening test that analyzes the blood of pregnant women to assess the risk of their developing fetus of having certain genetic disorders or birth defects. This test is usually recommended to pregnant women between 15 and 20 weeks of gestation.

If you are in Jhansi and want to undergo the triple marker test, you can follow these steps:

1. Consult a gynecologist or a prenatal care specialist: The first step is to find a doctor who specializes in prenatal care and can guide you through the process of the triple marker test. You can ask for referrals from your family doctor or friends who have undergone this test.

2. Schedule an appointment: Once you have found a doctor, schedule an appointment with them. Make sure to inform them about your pregnancy and the stage of gestation.

3. Blood sample collection: On the day of the test, you will be asked to provide a blood sample for analysis. This can be done at the doctor's clinic or at a lab recommended by them.

4. Wait for the results: The results of the triple marker test usually take a week or two to come back. Your doctor will discuss the results with you and recommend further tests or treatments, if required.

It is important to note that the triple marker test is only a screening test and not a diagnostic test. If the results of the test indicate a high risk of genetic disorders or birth defects, your doctor may recommend further diagnostic tests such as amniocentesis or chorionic villus sampling to confirm the diagnosis. It is crucial for expectant parents to understand that the triple marker test is just one tool in the assessment of their baby's health and well-being.

In conclusion, the triple marker test is a valuable prenatal screening tool that can help identify the risk of certain genetic disorders and birth defects in a developing fetus. However, it is essential to remember that it is not a definitive diagnosis and may have false positives and false negatives. Expectant parents should discuss the test and its risks and benefits with their healthcare provider before deciding whether to undergo the test. By doing so, they can make an informed decision and take an active role in ensuring the health and well-being of their growing family.

What is the cost of a triple marker test in Jhansi?

The cost of a triple marker test in Jhansi can vary depending on the laboratory and the location. On average, the cost of the test ranges from Rs. 2,000 to Rs. 4,000.

The triple marker test is a prenatal screening test that measures the levels of three substances in a pregnant woman's blood - alpha-fetoprotein (AFP), human chorionic gonadotropin (hCG), and estriol. The test is typically done between 15 and 20 weeks of pregnancy and is used to identify if the baby is at risk of certain birth defects or chromosomal abnormalities.

It is important to note that the cost of the test may vary based on the type of laboratory or hospital where the test is being conducted. Some laboratories may charge more than others, and fees may also vary based on the location of the laboratory.

It is advisable to research and compare prices of different laboratories before undergoing the triple marker test. Additionally, it is important to consult with a medical professional before taking any medical tests.

Is this test for you?

This test is conducted between the 14th and 18th weeks of pregnancy.
The test is often most recommended under the following scenarios

• Age of the pregnant woman is above 35
• Dual Marker tests were abnormal
• Birth defects in the family
• The pregnant woman is diabetic and under insulin medication
• If it is suspected that the pregnant woman was exposed to a high dose of radiation
• A viral infection during pregnancy

More about Triple Marker Test?

AFP (Alpha-fetoprotein) AFP or alpha fetoprotein is made by the foetal liver and some amount of this substance gets into the mother’s blood. Higher levels of AFP are seen in Neural tube defects and levels are decreased in Down syndrome and Edward syndrome. What if I am a man and have high AFP level? What if I am a non-pregnant woman and have high AFP level? In men, non-pregnant women, and children, AFP in the blood can mean certain types of cancer, especially cancer of the testicles, ovaries, stomach, pancreas, or liver are present. uE3 (Unconjugated Estriol) Estriol is a hormone produced by the placenta, using ingredients made by the fetal liver and adrenal glands. In pregnancies with Down Syndrome or Edward Syndrome, it is observed that the Estriol levels are reduced.

Your doctor will help you interpret your report basis your test results
Increased risk for HCG uE3 AFP Inhibin A
Open spina bifida Normal Normal High Not Applicable
Anencephaly Low Low High Not Applicable
Down syndrome High Low Low High
Edwards syndrome Low Low Variable Not Applicable

In pregnancies with Down Syndrome, high levels of HCG and Inhibin A are observed
In pregnancies with Edwards Syndrome, HCG and Estriol levels are low
Open Neural Tube defect is suspected when AFP levels are high. Opening in the spine may lead to more AFP leaking into the mother’s blood

TRIPLE MARKER TEST

The triple marker screen test is also known as the triple marker test time, multiple marker test, multiple marker screening, and AFP Plus. It analyzes how likely an unborn baby is to have certain genetic disorders. 

The exam measures the levels of three important substances in the placenta:

• Alpha-fetoprotein (AFP)
• Human chorionic gonadotropin (HCG)
• Estriol

Triple marker test in pregnancy. It’s used for women who are between 15 and 20 weeks pregnant. An alternative to this test is the quadruple marker screen test, which also looks at a substance called inhibin A.

What does a triple marker screen test do?

A triple marker screen test takes a sample of blood and detects the levels of AFP, HCG, and estriol in it.

• AFP: A protein produced by the fetus. High levels of this protein can indicate certain potential defects, such as neural tube defects or failure of the fetus’s abdomen to close.
• HGC: A hormone produced by the placenta. Low levels may indicate potential problems with the pregnancy, including possible miscarriage or ectopic pregnancy. High levels of HGC can indicate a molar pregnancy or multiple pregnancies with two or more children.
• Estriol: An estrogen that comes from both the fetus and the placenta. Low estriol levels may indicate a risk of having a baby with Down syndrome, especially when paired with low AFP levels and high HGC levels.

Who benefits from the triple marker screen test?

Triple marker screen tests help prospective parents prepare and assess options. They also alert doctors to watch a fetus more closely for other signs of complications.

The test is often most recommended for women who:

• Are 35 years old or older
• Have a family history of birth defects
• Have diabetes and use insulin
• Have been exposed to high levels of radiation
• Had a viral infection during pregnancy

What are the benefits of a triple marker screen test?

A triple marker screen test can indicate potential complications with a pregnancy, as well as the presence of multiple fetuses. This helps parents prepare for birth. If all the test results are normal, parents know that they are less likely to have a child with a genetic disorder.

You can book an online appointment for a triple marker screen test in Jhansi and choose the home sample collection option. Our phlebotomist crew is fully licensed, trained, and certified to collect blood samples from home. The triple marker test price may differ from city to city. The cost of a  triple marker screen test in Jhansi @CNCPathlab is very affordable. When making an online appointment for a triple marker screen test with CNC Pathlab, one has the option of selecting home sample collection. The triple marker screen test results will be made available online within 24 hours of sample collection, at which point anyone can consult their doctor and decide on the best course of treatment depending on their results.