Amniocentesis gets a small sample of the fluid around the baby in the womb. Doctors use a thin needle through the mother’s belly to collect a small amount of amniotic fluid. This fluid contains cells from the developing baby which can be tested.
What is Amniocentesis?
Amniocentesis is a prenatal test where doctors collect a small sample of the amniotic fluid surrounding the baby for testing.
When is it done?
Amniocentesis is typically performed after 15 weeks of pregnancy when there is enough amniotic fluid available for testing.
Why is it advised?
It may be recommended if:
– Prenatal screening tests showed an increased risk of chromosomal issues
– An ultrasound found potential issues
– The parents are at higher genetic risk due to family history
– A past pregnancy resulted in a genetic or chromosomal abnormality
The amniotic fluid sample is then tested for possible chromosomal or genetic conditions.
Is there a risk to my pregnancy?
While amniocentesis is generally safe, there is a small risk of miscarriage or early delivery in about 1 in 1000 procedures.
What happens during the Amniocentesis Procedure?
The doctor uses ultrasound to find the best spot for the thin needle. A small amount of local anesthesia numbs the area. The needle is gently inserted through your abdomen into the amniotic sac. About 20ml of amniotic fluid is taken carefully to avoid touching the baby. Then the needle comes out, and a small bandage goes on.
What happens after the Amniocentesis procedure?
The fluid is tested in a lab for things like chromosomes, genetic disorders, or neural tube defects. This can provide important information about your baby’s health. Results usually take 4-15 days. After the procedure, you rest for a bit and may get an injection. The risks are very small but your doctor will monitor you and baby.
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To book a blood test, or an online blood collection or to enquire about our services,
call +91-9900811118 or visit our website