Culture - amniotic fluid; Culture - amniotic cells; Alpha-fetoprotein - amniocentesis
Amniocentesis is a test that can be done during pregnancy to look for certain problems in the developing baby. These problems include:
Amniocentesis removes a small amount of fluid from the sac around the baby in the womb (uterus). It is most often done in a doctor's office or medical center. You do not need to stay in the hospital.
You will have a pregnancy ultrasound first. This helps your health care provider see where the baby is in your womb.
Numbing medicine is then rubbed onto part of your belly. Sometimes, the medicine is given through a shot in the skin on the belly area. The skin is cleaned with a disinfecting liquid.
Your provider inserts a long, thin needle through your belly and into your womb. A small amount of fluid (about 4 teaspoons or 20 milliliters) is removed from the sac surrounding the baby. In most cases, the baby is watched by ultrasound during the procedure.
The fluid is sent to a laboratory. Testing may include:
Results of genetic testing usually take about 2 weeks. Other test results come back in 1 to 3 days.
Sometimes amniocentesis is also used later in pregnancy to:
Your bladder may need to be full for the ultrasound. Check with your provider about this.
Before the test, blood may be taken to find out your blood type and Rh factor. You may get a shot of medicine called Rho(D) Immune Globulin (RhoGAM and other brands) if you are Rh negative.
Amniocentesis is usually offered to women who are at increased risk of having a child with birth defects. This includes women who:
Genetic counseling is recommended before the procedure. This will allow you to:
Amniocentesis can be used to diagnose many different gene and chromosome problems in the baby, including:
A normal result means:
Note: Amniocentesis typically is the most accurate test for genetic conditions and malformation, Although rare, a baby may still have genetic or other types of birth defects, even if amniocentesis results are normal.
An abnormal result may mean your baby has:
Talk to your provider about the meaning of your specific test results. Ask your provider:
Risks are minimal, but may include:
Driscoll DA, Simpson JL, Holzgreve W, Otano L. Genetic screening and prenatal genetic diagnosis. In: Gabbe SG, Niebyl JR, Simpson JL, et al, eds. Obstetrics: Normal and Problem Pregnancies. 7th ed. Philadelphia, PA: Elsevier; 2017:chap 10.
Patterson DA, Andazola JJ. Amniocentesis. In: Fowler GC, eds. Pfenninger and Fowler's Procedures for Primary Care. 4th ed. Philadelphia, PA: Elsevier; 2020:chap 144.
Wapner RJ, Dugoff L. Prenatal diagnosis of congenital disorders. In: Resnik R, Lockwood CJ, Moore TR, Greene MF, Copel JA, Silver RM, eds. Creasy and Resnik's Maternal-Fetal Medicine: Principles and Practice. 8th ed. Philadelphia, PA: Elsevier; 2019:chap 32.BACK TO TOP
Review Date: 6/30/2019
Reviewed By: John D. Jacobson, MD, Professor of Obstetrics and Gynecology, Loma Linda University School of Medicine, Loma Linda Center for Fertility, Loma Linda, CA. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.
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