What is the Double Marker Test?
The test results produce a prenatal screener determining two substances in a woman's blood: Free Beta-hCG and associated with plasma pregnancy protein A. Biochemical markers are available to assess the risk of chromosomal abnormalities in a fetus, for instance, Down syndrome (Trisomy 21) Edwards syndrome (Trisomy 18).
The journey of pregnancy is beautiful. But it is fraught with decisions and timed tests. One of these is the Double marker test, which checks on the baby’s health at a very early stage in the pregnancy. It not only looks at health, but can provide a huge amount of information about chromosomal abnormalities, which can help inform the parents and their doctors.
The Purpose of Double Marker Test is not to make a diagnosis but to definitely screen for pregnancies that may be at a higher risk for having some chromosomal anomalies. It is generally recommended to be performed in the first trimester so an intervention can be made if necessary or testing can be done such as chorionic villous sampling (CVS) or amniocentesis.
Even though they are both engaged in early pregnancy care, the double marker test does not confirm pregnancy. Early pregnancy confirmation can be done by UPT, ultrasound, or blood tests. The double marker test is done after pregnancy is confirmed to assess fetal health through risk analysis from blood biomarkers and maternal age.
It is usually done between the 11th and 14th weeks of pregnancy, and that time is very important because it is during this period that the biochemical markers are best determined. Delayed testing will lessen the effect of the test and might be offered other types of screenings.
Normal range of Double Marker Test are best understood as being complicated. They differ according to maternal age, weight, and gestational age. Results of the standard test are usually placed under the categories screen positive or screen negative. Screen negative means low-risk pregnancies and a screen positive indicates a higher risk and a probable need for further testing.
A positive result could indicate a higher chance of Down syndrome rather than a genetic disorder. It usually indicates to a doctor that it should conduct more testing to confirm or rule out the problem. Regarding your outcome, always get advice from a certified professional.
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A double marker test is an insight into the early development of your baby, and much more than just a number. While such results do not equate to a diagnosis, they may inform some risks which can be further evaluated for reassurance or prompt attention. Complications should always be checked by your trusted fertility or obstetrics specialist so that you know what your test results actually mean and what your next steps are.
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