What is an Amniocentesis ?
Amniocentesis is a prenatal diagnostic procedure that involves the removal of a small amount of amniotic fluid from the sac surrounding a fetus to test for genetic disorders or congenital abnormalities.
Amniocentesis is an invasive procedure that can be performed in either a hospital or a doctor’s office. It typically takes place between 15 and 20 weeks of pregnancy. The amniotic fluid is removed from the sac surrounding the fetus through a needle inserted into the vagina or abdomen.
Amniocentesis has been replaced by non-invasive prenatal testing (NIPT) which does not require an invasive procedure and can be performed as early as 12 weeks into pregnancy. NIPT tests for certain genetic disorders, such as Down syndrome, trisomy 18, and trisomy 13. It also assesses for several other conditions, including neural tube defects like spina bifida, and offers the option of a non-invasive test for pregnancy complications such as blood clots. Amniocentesis is an invasive procedure that can be performed in either a hospital or a doctor’s office.

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