Alternate Names : Culture - amniotic fluid, Culture - amniotic cells
Amniocentesis is a test during pregnancy that removes a small amount of fluid from the sac around the baby to look for birth defects and chromosome problems.
Why is the Test Performed?
The test can find chromosome problems such as:
Later on in a pregnancy, the test may be used to find problems such as:
This test is also sometimes done later in pregnancy to determine whether the baby's lungs are developed if there is a condition that requires early delivery.
How is the Test Performed?
Amniocentesis is done on an outpatient basis. You do not need to stay in the hospital.
The doctor will find the exact location of the baby, usually by performing a pregnancy ultrasound.
The health care provider will clean an area of skin on the mother's belly area. A numbing medication (anesthetic) may be applied to the skin, or a local anesthetic may be injected into the skin.
The doctor inserts a long, thin needle through the abdomen and into the womb (uterus). A small amount of fluid is taken from the fluid-filled sac that surrounds the baby.
How to Prepare for the Test?
Your bladder must be full for the ultrasound. There are no food or drink restrictions.
You may need to provide a blood sample to determine your blood type and Rh factor. You may get an injection of a medication called Rhogam if you are Rh negative.
You will need to sign a consent form before the test.
How will the Test Feel?
If an anesthetic is used, you may feel a sharp, stinging sensation for a few seconds. When the needle enters the amniotic sac, you may feel a sharp pain lasting a few seconds.
Some women feel pressure in the lower abdomen when the fluid is pulled out. After the procedure, you may have some minor cramping.
Pictures & Images
See all Pictures & Images