AMNIOCENTESIS & TRIPLE TEST


Amniocentesis

An amniocentesis is a test in which a small sample of fluid from the womb is taken . It involves passing a needle through the skin of the mother, through the wall of the womb and on to the fluid without touching the baby. Approximately 20 ml of the fluid is taken. This amount is small compared to the amount of fluid in the womb. It is done under the guidance of ultrasound.
Laboratory tests are carried out.
A test is carried out on the cells which are present in the fluid. It involves culture of the cells and study the chromosomes from the nucleus of the cells. It is possible to find out if the baby has
Downs syndrome (mongolism), or any of the other less common chromosome problems. Also by looking at the chromosomes, the sex of the baby can be determined.

Who should have the test?

  1. Women of 35 years and over at the time of delivery.
  2. Women who have already had a child with a problem such as Down?s syndrome or spina bifia.
  3. Other reasons like parents who are known to have a chromosomal abnormality themselves or who are known to be at risk of having a baby with one of a number of rare metabolic disorders.

The reason for advising women over 35 years of age to have amniocentesis is as the age of the women increases, the chance of her having a baby with a chromosomal abnormality also increases. The commonest chromosome abnormality is Down?s syndrome. It does not matter if the women had previous normal deliveries. The chance is there with advancing age.

Chromosomal abnormality

Maternal age

% chromosomal abnormality

35

1.25

36

1.41

37

1.50

38

1.65

39

2.10

40

2.36

42

4.01

45

7.28


When to carry out amniocentesis?

It is considered safer for the fetus to wait till at least 16 weeks when the pregnancy is stable and the fluid is adequate for the sampling. The procedure can be done in the clinic. It not much discomfort and the procedure takes about less than a minute to insert the needle and aspirate the fluid from the womb. Most patient inform us that they experienced far less discomfort from the test than they had expected. Any discomfort that is felt is usually very minor. After a short rest of half an hour, patient can return home. It is advisable to take it quietly for the rest of the day and possibly the next day although there is no reason to stay in bed all the time.

Complications

The complication of miscarriage quoted for the procedure is 0.5%. Apart from the very slight risk of a miscarriage the amniocentesis test does not appear to be associated with any other complications to the baby or to the pregnancy. The test, like any other, may fail either because no specimen is obtained from the sampling or because the laboratory cannot produce a result. However, this situation is very rare.

I usually ask the patient to return in a week for a check up. Patients were told to return earlier should there be any loss of blood or water from the vagina or any other pains after the amniocentesis.

Results

The chromosome test for Down?s syndrome takes 2 to 3 weeks because of the requirement to grow the cells in the laboratory. The laboratory will send the results directly to the clinic. Recently there is improvement in the examination technique that the results may be obtained at an earlier date.

When the result showed that there is abnormality, it is still possible to perform a termination of the pregnancy before 24 weeks.

Triple test

For patients who do not wish to have an amniocentesis or patients with ages less than 35, the next best is to do a blood test called the triple test. The test involves taking 5 ml of blood to measure 3 hormones – fetoprotein (AFP), gonadotropin (HCG) and unconjugated estriol (UE3). The results with the age of the mother will be computed to give a risk factor. It is a screening test and not actual study of cells like in amniocentesis. It cannot pinpoint which fetus is actually affected. Women with abnormal results indicated by higher risk than normal are advised to have further testing. On the other hand, an abnormal result does not mean that the baby definitely has a birth defect. It is a prenatal statistic risk assessment only.

Even though the triple test suggests that the risk is low, it cannot guarantee a normal baby or be certain that everything is all right with the baby. It is a screening test and will detect 85% of all open neural tube defects, about 75% of ventral wall defects, and approximately 60% of babies affected with Down syndrome. There are other kinds of problems the Triple Test cannot detect.

The best time for the Triple Test to be performed is between the 15th and 18th week since the last menstrual period. The result can be known in a couple of days.

Being a prenatal risk assessment, the decision of accepting the risk or not is very much dependent on the patient.

[Copyright 2005]
Lien Clinic for Women
Mount Elizabeth Medical Centre, 3 Mount Elizabeth #05-03, Singapore 228510
Telephone: (65) 6736 3331, Facsimile: (65) 6736 3332, E-mail: lien@lienclinic.com