Chorionic villus sampling
Chorionic villus sampling (CVS) is a test some pregnant women have to screen their baby for genetic problems.
CVS; Pregnancy - CVS; Genetic counseling - CVS
How the Test is Performed
CVS can be done through the cervix (transcervical) or through the belly (transabdominal). Miscarriage rates are slightly higher when the test is done through the cervix.
The transcervical procedure is performed by inserting a thin plastic tube through the vagina and cervix to reach the placenta. Your health care provider uses ultrasound images to help guide the tube into the best area for sampling. A small sample of chorionic villus (placental) tissue is then removed.
The transabdominal procedure is performed by inserting a needle through the abdomen and uterus and into the placenta. Ultrasound is used to help guide the needle, and a small amount of tissue is drawn into the syringe.
The sample is placed in a dish and evaluated in a lab. Test results take about 2 weeks.
How to Prepare for the Test
Your provider will explain the procedure, its risks, and alternative procedures such as
You will be asked to sign a consent form before this procedure. You may be asked to wear a hospital gown.
The morning of the procedure, you may be asked to drink fluids and refrain from urinating. Doing so fills your bladder, which helps your provider see where to best guide the needle.
Tell your provider if you are allergic to iodine or shellfish, or if you have any other allergies.
How the Test will Feel
The ultrasound does not hurt. A clear, water-based gel is applied to your skin to help with the transmission of the sound waves. A hand-held probe called a transducer is then moved over your belly area. In addition, your provider may apply pressure on your abdomen to find the position of your uterus.
The gel will feel cold at first and may irritate your skin if not washed off after the procedure.
Some women say the vaginal approach feels like a
An obstetrician can perform this procedure in about 5 minutes, after preparation.
Why the Test is Performed
The test is used to identify any genetic disease in your unborn baby. It is very accurate, and it can be done very early in a pregnancy.
Genetic problems can occur in any pregnancy. However, the following factors increase the risk:
- An older mother
- Past pregnancies with genetic problems
- Family history of genetic disorders
CVS can be done sooner in pregnancy than amniocentesis, most often at about 10 to 12 weeks.
CVS does not detect:
- Neural tube defects (these involve the spinal column or brain)
Rh incompatibility(this occurs when a pregnant woman has Rh-negative blood and her unborn baby has Rh-positive blood)
- Birth defects
- Issues related to brain function, such as autism and intellectual disability
A normal result means there are no signs of genetic defects in the developing baby. Even though the test results are very accurate, no test is 100% accurate at testing for genetic problems in a pregnancy.
What Abnormal Results Mean
This test can help detect hundreds of genetic disorders. Abnormal results may be due to many different genetic conditions, including:
Down syndrome Hemoglobinopathies Tay-Sachs disease
Talk to your provider about the meaning of your specific test results. Ask your provider:
- How the condition or defect may be treated either during or after the pregnancy
- What special needs your child may have after birth
- What other options you have about maintaining or ending your pregnancy
The risks of CVS are only slightly higher than those of amniocentesis.
Possible complications include:
- Miscarriage (in up to 1 in 100 women)
- Rh incompatibility in the mother
- Rupture of membranes which may lead to miscarriage
If your blood is Rh negative, you may receive a medicine called Rho(D) immune globulin (RhoGAM and other brands) to prevent Rh incompatibility.
You will receive a follow-up ultrasound 2 to 4 days after the procedure to make sure your pregnancy is proceeding normally.
Cheng EY. Prenatal diagnosis. In: Gleason CA, Juul SE, eds. Avery's Diseases of the Newborn. 10th ed. Philadelphia, PA: Elsevier; 2018:chap 18.
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.
Wapner RJ, Dugoff L. Prental 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.
Review Date: 09/25/2018
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