Triple Marker Test in Hyderabad
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How to Book A Triple Marker Test in Hyderabad?
What is the Triple Marker Test used for?
A triple marker screen test analyses a blood sample for the presence of AFP, HCG, and estriol.
- AFP is a protein made by the fetus. High levels of this protein may signal potential abnormalities such as neural tube malformations or the inability of the fetus’s abdomen to close.
- The placenta produces HCG, which is a hormone. Low levels may suggest an issue with the pregnancy, such as a miscarriage or an ectopic pregnancy. A molar pregnancy, or multiple pregnancies with two or more children, might be indicated by high HCG levels.
- Estriol is an estrogen produced by both the fetus and the placenta. Low estriol levels, especially when combined with low AFP and high HCG levels, may suggest a higher risk of conceiving a baby with Down syndrome.
What is included in the Triple Marker Test?
For many years, pregnant women have had access to the Triple Test, which can offer you and your doctor vital information about your pregnancy. When used in conjunction with diagnostic methods such as ultrasonography and amniocentesis (examination of amniotic fluid which is a bag of water surrounding the baby), MSAFP (Maternal serum AFP) can detect up to 85 percent of open neural tube abnormalities. Abnormal Triple Test findings, followed by ultrasound and amniocentesis, may detect 60 to 70% of Down syndrome pregnancies and many Trisomy 18 pregnancies. In addition to providing information about potential neural tube defects, Down syndrome, and Trisomy 18, the Triple Test may help to identify twins, detect additional abnormalities, and warn your doctor of elevated risks for other pregnancy issues.
Procedure for Triple Marker Test
The triple marker screen test is performed in a hospital, clinic, doctor’s office, or laboratory. The procedure is comparable to that of any other blood test.
Step 1: The technician will first instruct you to extend your arm and make a fist. This will aid him in locating your vein.
Step 2: The doctor will next wrap a strap over the patient’s arm and firmly secure this area.
Step 3: The technician will next use an antibacterial and antiseptic wipe to clean the area.
Step 4: A needle attached to a vial used for blood storage will then be inserted.
Step 5: Once the vial is full, the technician will remove it and wipe the region with an antiseptic and antibacterial swab.
Step 6: The blood sample will then be submitted to a facility for analysis, where a biochemist will assess it.
Step 7: The results will then be entered into the software and transmitted to the doctor. The doctor will then inform you of the outcome.
The triple marker screen tests have no negative effects. You may feel some discomfort as a result of the needle used to draw blood, but this will pass rapidly.
How to prepare for the Triple Marker Test?
The triple pregnancy test is a risk-free test. This test does not necessitate any particular eating, drinking, or other preparation on the part of the female subject prior to the procedure hour.
Things to consider after the Triple Marker Test is complete
Additional screening tests may be used by certain parents in order to better comprehend the diagnosis or to obtain a second opinion. Prenatal ultrasounds, for example, can assist parents to confirm a diagnosis. Consult your primary care physician for a list of other tests to help you decide which test is best for you based on your needs.
Being prepared is the greatest method to deal with potential problems. Knowing whether or not your kid is healthy is the first step in preparing for your life together. The triple marker test will assist you in preparing for and ruling out potential difficulties impacting your child’s health and wellbeing. So plan ahead of time for this and another required testing, and enjoy a safe pregnancy!
What conditions can the Triple Marker Test detect?
This test can aid in the detection of genetic abnormalities like Down syndrome, Trisomy 18 syndrome and neural tube defects, prenatal/fetal infections or multiple pregnancies. If your AFP levels are high, your doctor will most likely conduct a thorough ultrasound to look for neural tube problems in the fetal skull and spine.
How much does the Triple Marker Test cost?*
The triple marker test is predicted to cost between INR 1250 and 4200.
*Disclaimer: The value varies based on location, time, and your preferred lab partner.
How long does it take to get the results for the Triple Marker Test?
You can expect to get the results for the Triple Marker Test test within 24 to 48 hours after the sample is collected. However, in certain cases, depending on the location, medical advice, and preferred lab partner, it may take longer.
What do abnormal Triple Marker Test results indicate?
An abnormal test may indicate the presence of multiple pregnancies or certain genetic anomalies in the baby like Down syndrome, Trisomy 18 or neural tube defects. If the index of suspicion is high, your doctor will most likely order additional testing or refer you to a specialist. An ultrasound exam is frequently the initial step. This examination helps determine the baby’s age and examine the brain, spinal cord, kidneys, and heart for any issues. Amniocentesis is another test that you could have. This test examines the fluid surrounding the infant. The findings of these tests will assist your doctor in determining whether or not your baby has a condition.
Disclaimer: Please consult with your doctor for interpreting the test reports.
Is Triple Marker a definitive test?
The triple marker test is not a definitive step as its main purpose is screening. It is critical to understand what a screening test is in order to feel at ease while taking one. A screening test is not used to make a diagnosis. It examines a number of data, such as age, ethnicity, blood test results, and so on, before indicating a risk factor for the presence of specific anomalies. A screening test is not conclusive in terms of pinpointing a specific problem; rather, it only aids in determining whether additional tests are required to determine a specific ailment or problem.
How to read the Triple Marker Test report?
The triple marker test is just a predictor or estimate of the likelihood of various genetic illnesses. The test can also be used to identify and recognize multiple birth scenarios. It indicates whether additional and deeper testing is required.
If the test results are good, the doctor will recommend additional amniocentesis and ultrasound testing for a more in-depth probe. The test results may or may not be accurate.
The AFP count from the amniocentesis result is taken into account. If the count remains low, you will be asked to undergo uterine ultrasound testing. Through fetal spine and skull examination, this test provides the gynecologist with an indication of possible genetic problems. Ultrasound can also detect the presence of numerous fetuses as well as their ages.
Greater AFP levels in the triple marker test suggest the probability of brain abnormalities. The typical AFP levels observed in women under the age of 35 range from 1.38 to 187.00 IU/ml. According to studies, the levels of beta-hCG range from 1.06 to 315 ng/ml.
The usual level for unconjugated estriol (uE3) ranges from 0.25 to 28.5.
Why to book a Triple Marker Test?
A triple marker test can detect pregnancy problems and the existence of multiple fetuses. A triple marker screen test is especially effective for women over the age of 35. The main advantage of this test is that it detects birth problems in the infant and allows a pregnant woman to plan ahead of time for them. Among these genetic illnesses and anomalies are:
- Trisomy 18, often known as Edward’s syndrome, is a chromosomal anomaly.
- Down syndrome is a condition in which there is extra genetic material from chromosome 21 in the cell.
- Neural tube defects are congenital disorders that affect the brain, spine, and spinal cord.
Triple Marker Test at home – how does it work?
The Triple Marker Test is just like any other blood test. A lab technician visits your home when you book your tests through the MFine app. The lab technician first cleans the arm and then inserts a syringe into a vein. The required amount of blood is then taken into a vial. The lab technician then removes the needle and places cotton wool or a bandage over the prick.
Are there any risks involved with the Triple Marker Test?
This test has no known adverse effects. Because the amount of blood drawn is so small, even the loss of blood is insignificant in terms of the mother’s health.
What can affect the results for the Triple Marker Test?
The triple marker test findings indicate the chance of a newborn having a genetic disease. The outcomes, however, are determined by the following factors:
- The pregnant woman’s age
- Weight of a pregnant woman
- Whether she is expecting a single child or multiple children
- How far along in her pregnancy she is
After you have this test, your OB/GYN will review the results and let you know whether they are negative or positive. If the results of this test are false positive or she does not find a normal number for the triple marker test, your doctor may recommend additional tests.
Why Book the Triple Marker Test in Hyderabad?
- The Triple marker test is meant for women who are in their second trimester (usually between 15-20 weeks of pregnancy). It analyzes how likely an unborn child could have genetic disorders. To prevent any unwanted abnormalities or disability in a prospective child, one must get the test done as per the medical advice. Moreover, doctors can also prescribe tests for evaluation as factors like mother s’ weight, ethnicity, age, co-morbidities, and the likelihood of twin pregnancy can also alter values and thus, suspect any abnormality. It also helps to detect neural tube defects in the fetus.
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What does the Triple Marker Test measure?
What Preparation is Needed for the Triple Marker Test ?
- A blood sample is collected for screening of the levels of HCG, AFP, and estriol (known as triple marker test). The patient needs to note that the test is valid between 14-22 weeks of gestation. However, the ideal time is between 15-20 weeks of gestation
- The patient must have an ultrasound report, not older than 5 days before the sample collection. It is advised to give a blood sample within 48 hours of the ultrasound.
- The person may be asked about the medical history for the test as it provides clear tracking and insight into the record.
- It is always suggested to inform the doctor about the medications that the person is taking before undergoing the Triple marker test
What Happens to Your Test Sample?
What do Abnormal Results Indicate?
Frequently Asked Questions | FAQs
Can I avail at-home sample collection in Hyderabad?
Yes, you can avail at-home sample collection anywhere in India. Our lab technician will arrive at your doorstep at a chosen time slot and will collect your blood sample. Post this the lab will connect with you(call/mail). You will be asked to provide your medical history on-call/mail for the test.
What is the cost of a Triple marker test in Hyderabad?
The range for testing in Hyderabad varies from lab to lab, with the majority charging Rs 2448 per test which is the average price in Hyderabad to less than Rs 1600 in some government medical facilities
I stay in Andhra Pradesh. Can I book a Triple marker test for my wife staying in Hyderabad?
You can book the lab test for your relative staying anywhere in India.
How can I reschedule my appointment for the triple marker test?
You can reschedule a scheduled appointment for a triple marker test through the ‘Rescheduling Appointments’ page on your account. All you need is your login credentials and phone number to access this page.
Is the lab technician coming for Blood sample collection for the Triple marker test vaccinated?
Yes. Our lab technicians are fully vaccinated. Further, they also ensure safety throughout by wearing a mask and using sanitiser and gloves during sample collection
When is the Triple marker test recommended?
A doctor may recommend a Triple marker test as this test is a part of prenatal screening during the pregnancy. It involves multiple factor screening to identify a genetic abnormality in the developing baby. It is usually recommended in between 15-20 weeks of gestation.
Is a prescription required to book a Triple marker test?
Yes, a prescription is required to book a triple marker test as it involves a complete investigation such as medical history, ultrasound, not 5 days or older before sample collection.
Does MFine provide result interpretation along with the reports?
Yes. MFine provides result interpretation along with the reports. Also, you will be able to avail a free doctor consultation after the lab test to understand your reports accurately. Our doctor will also advise and prescribe medicines if required based on the results.
Is the Triple marker test definitive?
This particular test is not a definitive test to confirm whether the prospective child will have a genetic disorder as many factors may affect the levels of the HCG, AFP, and estriol such as age, ethnicity or comorbidities such as diabetes, hypertension and anaemia, mediations, and the type of pregnancy such as twin or triplet pregnancy. To confirm the results, the doctor may suggest an ultrasound to see the fetus’s spine and brain.
What other tests are usually recommended along with the Triple marker test?
Tests that are recommended along with triple marker test for proper diagnosis are:
- Fetal Ultrasound.
- Amniocentesis (this test checks fluid around the baby)
- Test for hormone inhibin A
What diseases can be detected through the Triple marker test?
Triple marker test detects the genetic and chromosomal abnormalities that can be reported after birth. This test is part of prenatal screening as it helps in screening for neural tube defects. Moreover, chromosomal anomalies that it detects are Klinefelter’s’ disease, down syndrome (responsible for the growth and developmental delays), and turner s’ syndrome.
How can I download a Triple marker test report?
- Login to MFine
- Go to your profile
- Click Attachment and Reports
- Click Lab Report and download the same.