Definition | Reasons for Procedure | Possible Complications | What to Expect | Call Your Doctor

Reasons for Procedure

Amniocentesis is most often done to see if there is an abnormality in your baby's genes (DNA). It can also be done to see if your baby is developing correctly.

Factors that indicate that you may need this procedure include:

Depending on your risk factors, cells in the amniotic fluid are tested for:

  • Chromosome abnormalities. The results are usually ready within 14 days. Missing or extra chromosomes lead to physical birth defects and intellectual disability. Down's syndrome is one example.
  • Inherited genetic diseases—Test results are usually ready in 1-5 weeks. Examples include:

Amniocentesis may also be done:

  • To determine whether the baby's lungs are mature
  • In high-risk pregnancies that may require early delivery

Possible Complications

Complications that may occur with an amniocentesis include:

  • Miscarriage—Extremely rare
  • Bleeding, cramping, and leaking fluid from the vagina
  • Infection
  • Mixing of blood if you and your baby have different blood types
  • Need for repeat testing
  • Harm to the fetus by needle—Rare

Factors that may increase your risk of complications include:

  • Maternal obesity
  • Previous abdominal surgery

Be sure to discuss these risks with your doctor before the procedure.

What to Expect

This is usually done when you are 16 weeks pregnant. It is done later in the pregnancy when checking your baby's lung maturity.

First, your doctor will do an ultrasound. This will help to choose a safe spot to insert the needle. Your abdomen will be cleaned. Next, the doctor will insert a very thin needle through your abdomen into your uterus. A few teaspoons of amniotic fluid will be taken out. After the needle is removed, the doctor will make sure that your baby's heartbeat is normal. In most cases, an ultrasound will be used throughout the procedure.