What Do You Need To Know About The Newborn Screening Test

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What Do You Need To Know About The Newborn Screening Test

Newborn screening is a pathology test that incorporates screening a newborn child for specific disorders and conditions. If they go undetected, they may hinder the baby’s normal development. Usually, this procedure takes place right before the mother leaves the hospital with her baby. Some of the conditions uncovered during newborn screening can cause severe health problems during infancy or childhood. Trutest Laboratories can offer Newborn Screening by TMS. If you wish to learn more about this test, you should continue reading.

1. About the program: As mentioned above, newborn screening is primarily a preventive healthcare program. Through this test, it’s possible to uncover more than forty severe disorders. Some of them are common while others aren’t. As this test takes place before the symptoms become observable, it becomes possible for doctors to treat the conditions early. Just remember that the screening method won’t rule out one or more diseases or confirm them.

2. IEM: Among all the conditions tested using this method, the first one is IEM. It stands for Inborn Errors of Metabolism. In reality, it’s a combination of several disorders caused by chemicals produced naturally by the body. Things tend to take a turn for the worst when the body of the child fails to expel these chemicals. Fortunately, it’s possible to detect these conditions using his technique.

3. Types of problems screened: The Newborn Screen Test by Tandem Mass Spectrometry (TMS) cost isn’t high. However, it checks for more than forty different disorders in babies. Most of these problems are metabolic by nature. The pathologist conducting the test will draw a small sample of blood to look for chemical imbalances. Usually, these imbalances pass on to the child from the parents.

4. Chances: So, what’s the possibility that your newborn child will suffer from these conditions? In developed nations, the infant mortality rate remains between 5 and 10 in every 1000 newborns. Unfortunately, the infant mortality rate in the subcontinent is about 10 times more than that of developed nations. Naturally, the chance of a baby dying within a year or two after birth will always be there. That’s why it’s of the utmost importance that you don’t skip this test.

5. Treatment: You shouldn’t worry about treatment because the conditions detected by this test are treatable. However, you need to get your baby diagnosed at the earliest. With early detection, you can get your baby treated. Rest assured, if you take your baby to a competent pediatrician, the specialist will mitigate all symptoms and effects of the conditions. Some of the conditions are simple enough to treat just by controlling the child’s diet.

Final considerations

Generally, it’s best to get registered for the Newborn Screening Test during pregnancy. Screening test kits are always available. Even if you miss your chance to register during pregnancy, you can do it immediately after delivery. The hospital you’ll get admitted it can also offer relevant tests. The screening takes place between 48 hours after childbirth and 13 days. Sometimes, medical experts suggest screening a child at the age of 2.