It is natural for any mother-to-be to want her baby to be he althy. Therefore, she cares so much about the unborn baby. Therefore, there are so many tests and examinations. For every pregnant woman, doctors prescribe a special analysis - screening. It consists of an ultrasound scan and a blood test for specific proteins and hormones. It is aimed at detecting fetal chromosomal diseases at the earliest stages.
Therefore, if the doctor has prescribed a biochemical screening, there is no need to be afraid of him and be afraid that the child will have Down syndrome. The examination is aimed precisely at eliminating the risk of this and other diseases. Conduct biochemical screening in the first trimester for a period of 10-14 weeks and in the second trimester for a period of 16-18 weeks. In the third trimester, as a rule, only ultrasound screening is performed.
Most expectant mothers know that pregnancy can be determined by the presence of the hCG hormone in the blood. The same hormone indicates the correct or incorrect development of the fetus. The thing is that for each period of pregnancy there are own norms for its content in the body. Deviations from normal values canjudge the risk of any pathologies. It is the amount of hCG that determines the biochemical screening of the first trimester.
A decrease in its level may indicate a delay in the development of the fetus or its death, the risk of miscarriage. An increased amount of gonadotropin warns of the possibility of pathologies. But there is no need to immediately panic if the indicators deviate from the norm. They are not a final judgment. So far, this is only a warning that you need to contact a geneticist who can correctly interpret the results and prescribe an additional examination. Moreover, for example, indicators above the norm can mean not only fetal pathologies, but also toxicosis or diabetes in the mother, multiple pregnancy, or even simply an incorrect determination of the gestational age. Together with the level of hCG, the amount of PAPP-A protein is examined. And the value can only be interpreted in the aggregate of both indicators
Biochemical screening in the second trimester adds to the study the hormones of the placenta and liver of a growing child - free estriol and alpha-fetoprotein. According to the results obtained, one can also judge the presence of chromosomal diseases, developmental disorders due to viral diseases, intrauterine infections, and the risk of miscarriage. But we recall that only a geneticist can give a correct assessment of the situation. Even an observing obstetrician-gynecologist is not always able to draw accurate conclusions. Perhaps the deviation from the norm is caused by the condition of the expectant mother, who should pay attention to the he alth of the kidneys or liver.
In addition to pregnancy screening, newborn screening is also carried out. This analysis is mandatory for all born children and is of a preventive nature. The study helps to determine the presence of hereditary diseases. After all, early detection of the disease simplifies its treatment. Therefore, if the expectant mother doubts whether it is worth undergoing biochemical screening, there can be only one answer - definitely, it is worth it. This will help to avoid many problems and keep the nerve cells intact - after all, they will still be needed when raising a beloved child.
