Exams and Tests
In years past, women often had no
idea that they were carrying twins until the end of pregnancy or the actual
childbirth. Since the development of better tests, most
multiple pregnancies are now identified during the
first or second
trimester.
A
fetal ultrasound can show whether there is more than
one fetus in the uterus. If you have more than one fetus, you will have an
ultrasound several times during the pregnancy to monitor fetal growth and
amniotic fluid.
Sometimes, the first sign
of a multiple pregnancy is from a test that was done for another reason. For
example, a very high level of
human chorionic gonadotropin (hCG), the “pregnancy
test” hormone, can be a sign of multiple pregnancy.
Tests used to check for genetic disorders and birth defects
Fetuses in multiple pregnancies have an increased risk of
genetic disorders and birth defects.
Test
options include:
-
Chorionic villus sampling (CVS). It uses a tiny piece
of the
placenta, taken by passing a thin tube through your
vagina and cervix and into the uterus. The sampling and genetic testing are
done between 10 and 12 weeks of pregnancy.
-
Amniocentesis, which uses a small amount of amniotic
fluid, taken by inserting a needle into your abdomen and uterus. The sampling
and genetic testing are usually done between 15 and 20 weeks of pregnancy.
(Amniocentesis is also sometimes used in the last trimester to see whether the
fetuses' lungs are mature enough to breathe well after delivery.)
CVS and amniocentesis have the same slight
miscarriage risk when used to test a multiple
pregnancy. You may
want earlier CVS results if you have to make decisions about treating or
continuing a pregnancy.
Tests used to monitor the fetuses and mother during a multiple pregnancy