Skip navigation
MedlinePlus Trusted Health Information for You U.S. National Library of MedicineNational Institutes of Health
Contact Us FAQs Site Map About MedlinePlus
español Home Health Topics Drug Information Medical Encyclopedia Dictionary News Directories Other Resources

 

Medical Encyclopedia

Other encyclopedia topics:  A-Ag  Ah-Ap  Aq-Az  B-Bk  Bl-Bz  C-Cg  Ch-Co  Cp-Cz  D-Di  Dj-Dz  E-Ep  Eq-Ez  F  G  H-Hf  Hg-Hz  I-In  Io-Iz  J  K  L-Ln  Lo-Lz  M-Mf  Mg-Mz  N  O  P-Pl  Pm-Pz  Q  R  S-Sh  Si-Sp  Sq-Sz  T-Tn  To-Tz  U  V  W  X  Y  Z  0-9 

Chorionic villus sampling

Printer-friendly versionEmail this page to a friend
Contents of this page:

Illustrations

Chorionic villus sampling
Chorionic villus sampling
Chorionic villus sampling - series
Chorionic villus sampling - series

Definition    Return to top

Chorionic villus sampling (CVS) is a procedure for taking a small piece of placental tissue (chorionic villi) from the uterus in the early stages of pregnancy to check for the presence of genetic defects in the fetus.

How the test is performed    Return to top

Depending on where the placenta is located, CVS can be performed through the cervix (transcervical) or through the abdomen (transabdominal). The techniques are thought to be equally safe and effective for obtaining samples. Both the transcervical and the transabdominal CVS are performed with ultrasound guidance.

An abdominal ultrasound is performed to determine the position of the uterus, the size of the gestational sac, and the position of the placenta within the uterus. Your vulva, vagina, and cervix are then cleansed with an antiseptic such as Betadine. For the transabdominal procedure, the abdomen is also cleansed.

The transcervical procedure is performed by inserting a thin plastic tube through the vagina and cervix to reach the placenta. Ultrasound is used to help guide the tube into the appropriate area and a small sample of chorionic villus tissue is withdrawn.

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 laboratory.

How to prepare for the test    Return to top

Your health care provider will explain the procedure, its risks, and alternative procedures such as amniocentesis. Genetic counseling is recommended prior to the procedure. This will allow you to make an unhurried, informed decision regarding options for prenatal diagnosis.

You will be asked to sign a consent form before this procedure, and 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 to fill your bladder, which allows adequate visualization so the sample may be taken.

How the test will feel    Return to top

The ultrasound is not uncomfortable. A clear, water-based conducting gel is applied to the skin to help with the transmission of the sound waves. A handheld probe called a transducer is then moved over the area. In addition, your health care provider may apply pressure on your abdomen in an attempt to manually locate the position of your uterus.

The antiseptic cleansing solution will feel cold initially and may irritate your skin if it is not removed after the procedure. Some people are allergic to Betadine. Notify your health care provider if you are allergic to Betadine or if you have any other allergies.

Patients report that the actual sampling feels similar to a Pap smear, where there is some discomfort and a feeling of pressure. There may be a small amount of bleeding following the procedure.

An obstetrician can perform this procedure in about 5 minutes, after the preparation.

Why the test is performed    Return to top

This test is a way of detecting congenital (present from before birth) defects. The sample is used to study the DNA, chromosomes, and enzymes of the fetus and can be done earlier than amniocentesis, about 10 to 12 weeks after your last menstrual period.

Test results from a CVS are obtained within 1 to 2 weeks, whereas amniocentesis results may take as long as a month. Earlier diagnosis of congenital defects may relieve some of the concerns of your family, especially if a therapeutic abortion is under consideration.

Chorionic villus sampling does not detect neural tube defects. If neural tube defects or Rh incompatibility are a concern, an amniocentesis will be performed.

Normal Values    Return to top

Normal values would indicate an absence of congenital defects.

What abnormal results mean    Return to top

Analysis of the biopsy may indicate any of more than 200 disorders, including the following:

What the risks are    Return to top

The risks of CVS are only slightly higher than those of an amniocentesis. Fetal loss occurs about 2% of the time.

Possible complications include the following:

Special considerations    Return to top

Report any signs that there may be complications of the procedure to your health care provider:

Update Date: 7/8/2004

Updated by: Bryan R. Hecht, M.D., Department of Obstetrics and Gynecology, Northeastern Ohio Universities College of Medicine, Rootstown, OH. Review provided by VeriMed Healthcare Network.

adam.com logo

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 2002 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.