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Intervention: Chorionic villus sampling
Model of human embryo 1.3 mm. long. (Villi of chorion labeled at lower right.)
ICD-10 code:	16603-00
ICD-9 code:	75.33
Other codes:

Chorionic villus sampling (CVS) is a form of prenatal diagnosis to determine chromosomal or genetic disorders in the fetus. It entails getting a sample of the chorionic villus ( placental tissue) and testing it. The advantage of CVS is that it can be carried out 10-13 weeks after the last period, earlier than amniocentesis (which is carried out at 15-18 weeks).

Possible reasons for having a CVS can include:

• Mother's age of 35 years or greater
• Abnormal first trimester screen results
• Increased nuchal translucency or other abnormal ultrasound findings
• Family history of a chromosomal abnormality or other genetic disorder
• Parents are known carriers for a genetic disorder

CVS is similar to amniocentesis in terms of fetal mortality (0.2 to 0.3%)^[1]. Apart from a risk of miscarriage, there is a risk of infection and amniotic fluid leakage. The resulting amniotic fluid leak can develop into a condition known as oligohydramnios which is low amniotic fluid Level. If the resulting olighydramnios is not treated and the amniotic fluid continues to leak it can result in the baby developing what is called hypoplastic lungs (underdeveloped lungs). If the baby develops hypoplastic lungs the lungs do not have a chance to mature, and the baby can die shortly after birth.^{[citation needed]}

It is extremely important after having a CVS that the OB/GYN follow the patient closely to ensure the patient does not develop infection. The OB/GYN should also measure the patient's fundal height with a tape measure (this should be done on every prenatal visit) and routinely ultrasound the patient to ensure the baby has sufficient amniotic fluid.^{[citation needed]}

A small percentage (1-2%) of pregnancies will have confined placental mosaicism, where some but not all of the placental cells tested in the CVS will be abnormal, even though the pregnancy is unaffected.^[2] Cells from the mother can be mixed in with the placental cells obtained from the CVS procedure. Occasionally if these maternal cells are not completely separated from the placental sample, this can lead to discrepencies with the results. This phenomenon is called Maternal Cell Contamination (MCC).^[2] CVS can not detect all birth defects. Only chromosomal abnormalities are standardly tested for, or other specific genetic disorders if there is family history or other reason to test.

• Amniocentesis
• Percutaneous umbilical cord blood sampling
• Prenatal diagnosis

• March of Dimes
• MedlinePlus Encyclopedia 003406
• Cleveland Clinic

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