The NFWP Comprehensive Guide to Pregnancy

Alpha-Fetoprotein Test

This presently is an optional blood test performed between the 16th and 18th weeks of pregnancy. This special blood test detects neural tube defects. Neural tube defects are abnormalities in the brain and spinal cord of the fetus.

 Defects in the central nervous system occur when the neural tube (the brain and spinal cord tissues) fail to close as the fetus develops. When the brain and spinal cord are exposed directly to the amniotic fluid which surrounds the baby, it is called an “open defect.” Sometimes the poorly developed neural tube is covered by skin or bone, referred to as a “closed defect.”

The two common neural tube defects are anencephaly and spina bifida. Babies with anencephaly are born with deformities of the head and brain and die soon after birth. Those born with spina bifida can live a long time, but may suffer paralysis in the lower body and legs. Also, there is often a lack of bladder and/or bowel control which maybe treated with surgery. 

The chance of producing a child with a neural tube defect is 1-2 for every 1,000 live births. Babies born to mothers who have had a previous child with the same problem are at greatest risk, as are those with parents or grandparents who have neural tube defects.

As with all prenatal tests, a normal test does not guarantee a normal baby at birth. About 20 percent of the infants born with neural tube defects have normal alpha-fetoprotein (AFP) levels. Most of these are closed defects which are typically less severe.

Conversely, an initial abnormal test reading does not mean the fetus has a neural tube defect. Abnormal levels of AFP are frequent, occurring in about 50 of every 1,000 women tested. Only one or two of those 50 actually have a neural tube problem. A high AFP may be due to a miscalculation of the baby’s age, or due to twins in the womb. Various other temporary fetal conditions can cause an elevated AFP reading. Second AFP tests are normal in about half of those who are retested.

If a second test also indicates an abnormal AFP, a sonogram is usually given to determine the fetal age, look for more than one fetus, or scan for neural tube defects and other abnor­mal conditions which may be responsible for the elevated test.

If the sonogram shows a single fetus at the approximate age determined by the initial due date with no fetal abnormalities, an amniocentesis is performed. An abnormally high level of AFP in the amniotic fluid indicates a 90 percent chance that a serious problem is present.

An abnormally low AFP reading may indicate that there is a chromosomal problem, such as Downs Syndrome (Mongolism). An amniocentesis can resolve this issue.

 TriScreen Test

This optional test combines the alpha-fetoprotein results with two other blood substances to give us the triscreen test. The results are obtained from a blood sample from the mother at 16-18 weeks of pregnancy. The majority of neural tube defects and two of three babies with Down’s Syndrome can be detected with this test. Further testing such as sonography and/or amniocentesis may be required with an abnormal test.

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