Double Marker Test

All About Double Marker Test (Dual marker test) | Shree IVF Clinic - Dr. Jay Mehta

What is Double Marker Test?

The double marker test or the dual marker test is actually a maternal serum screening test. Doctors perform this test in the 1st trimester of the gestation period. It helps to scan the amount of b-human Chorionic Gonadotropin (a pregnancy hormone) & Pregnancy Associated Plasma Protein in erythrocytes.

Doctors advise this for females who are above the age of 35 because they fall at risk of delivering a baby with Down’s syndrome. A dual marker test in correspondence with another test is the nuchal translucency (NT). It confirms the diagnosis of any genetic abnormalities.

Everything You Need to Know About Double Marker Test

Advantages | Preparation | When recommended | Uses | Procedure | Results | Normal Range  | Cost

Advantages of double marker test

  • It helps to find out the trisomy of chromosome number 13. It is responsible for causing mental retardation of the infant and severe birth defects.
  • Most importantly, it is helpful to detect chromosomal aberration of 21 resulting in Down’s syndrome.
  • It helps to detect high-risk factors about the pregnancy. It also helps to determine whether it would be detrimental to the health of the mother also.
  • This test has good detection rates
  • If the mother is positive after the test for this abnormality, it gives time to the couples to analyze the entire situation. And it also helps to consider whether they are willing to go for further tests to determine the accuracy of the results. Or, whether they are going towards MTP.

How to prepare for this Double Marker Test?

Doctors perform this test by a blood sample as well as performing an ultrasound scan. The sterilization of the apparatus and the machines should be ready beforehand. Maternal screen details like in vitro fertilization reports and details of body weight and diabetic status of the patient should be made ready before the test commences.

This test is ideal if the pregnant female is above the age of 35 years.  If they show any elevated signs of genetic aberrations it can be determined by studying their pedigree chart.

Double marker test uses

  • To detect and prevent down’s syndrome in the newborn child
  • To detect whether there would be a loss of muscle mass, short neck, excess growth of skin at the back of the neck of the infants.
  • For the well-being of the mother and to ascertain upward slanting of eyes, stunted growth, flattened facial appearance in the newborns, and extreme mental and physical handicaps.
  • Ascertain the trisomy of chromosome number 18, which would otherwise lead to clenched fists, and deformities of the heart, lungs, stomach, intestines, and various essential organs required for the proper metabolism and functioning of the body.
  • To detect a disorder, ‘rocker bottom feet’ which leads to feet deformation, and thereby it gets a shape like the bottom of the rocking chair.
  • Detect microcephaly (small and deformed head), micrognathia (abnormal shape of jaws and the mouth), scrunched fists, arched spine, and abnormally shaped chest.
  • To detect short sternum and delays in neurological functions of the brain.
  • Distinguish umbilical hernia in case of the mother carrying the child.

How is this Double Marker Test Performed?

This test is quite easy to perform since we only require the blood sample of the pregnant mother. Some other steps followed are:

  • A syringe helps to take the blood sample from the arteries.
  • The health care provider will then tie an elastic band on the arms thereby causing swelling of the blood vessels.
  • Once the arteries are clearly visible, an antiseptic helps to clean off the particular area under observation.
  • The insertion of the needle takes place finely into the blood vessel with a pinprick. The sample collection takes place first and preservation happens and then for testing.

There is no such risk with this test. In very rare cases, a female might experience increased bleeding, hematoma formation, bruising, or infection at the site of needle prick.

How are the test results interpreted?

The result of the above test can fall under two categories – screen positive and screen negative. The test however does not merely depend on the blood samples. It also depends on two other factors – the age of the mother and the age of the child. It also depends on the period of time when the test takes place during the 9 months of the gestation period using an ultrasound.

The results are thereby present in the reports in the form of ratios. A ratio of 1:10 to 1:250 is termed as ‘screen positive’ results. They are highly dangerous for both the mother and the developing embryos.

A ratio of 1:1000 or above is a safe result and poses fewer threats or risks. A 1:10 ratio implies that 1 out of 10 pregnancies have a chance of developing a disease which is quite high.  A 1:1000 ratio would thereby suggest that 1 out of 1000 pregnancies has a high-risk development factor. This is quite negligible.

If the test results are positive, the doctor may suggest further diagnostic tests like amniocentesis, etc. If the results of the tests are positive and if the parents still want to continue with the pregnancy, there are high chances. That can also be the death of the baby during parturition.

Result of dual test normal range

A Free-beta Human Chorionic Gonadotropin range for all age groups should be between 25,700 to 2,88,000 mIU per ml. This is the normal range for this above-concerned test.

Double marker test cost

The cost of the Dual marker test varies depending on the reputation of the institution. It also depends upon the accuracy of the test results, and the sensitiveness of the instruments, and the requirements of the machines. On an average basis, it ranges somewhat between Rs 2,500 to Rs 4,000.

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Dr. Jay Sir is a very intelligent and wise person. He is an all-rounder with excellent mentoring capabilities, meaning he not only works but also guides, teaches, gives first-hand observations, gives opportunities to learn and grow as a doctor, with live hands-on surgical demonstrations. He proves a literal meaning of the term "Doctors are messengers of God", I have observed his unbiased views and respect towards all other pathies👌

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We have been married since 12 years and have done multiple procedures for fertility treatment. We were referred here by a doctor friend of ours. We became pregnant with IVF. The best thing about this place is that Dr Jay is really hands on and very very very honest. From the first part of ultrasounds till the part of delivery and in between all procedures is all handled in one place. This is one of the rare 24 Hour open Ivf clinic. It's doing many other cancer and laparoscopy surgery also. It's very very busy almost all the time but the staff is superb here. Very transparency. We are blessed with a baby boy here and even if it was a Sunday Dr jay came from his holiday just to do my wife delivery. It's so much high commitment that I really am impressed. He is such a big doctor but so Humble.

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Dr. Jay Mehta is a very professional, knowledgeable, and God-Gifted Obstetrician-Gynecologist-Fetologist who believes in genuineness and ethical ways to help families for a noble cause. He is "Saving generations". Another interesting, sincere and quite a responsible effort by Dr. Jay is online gynecology and obstetrics guidance lectures for practicing family physicians from all over India. Rather, he loves and enjoys sharing his utmost experiences. May God bless him forever...!

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Dr. Jay Mehta Fertility and IVF Specialist In Mumbai

Dr. Jay Mehta

Fertility and IVF Specialist

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Dr. Jay Mehta is the Scientific Director of Shree IVF Clinic. He is a well-known Fertility and IVF Specialist and also among few doctors in the country who specializes in Embryology and Andrology.

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