Ten common tests you can expect during pregnancy are…
1.
Nuchal Translucency.
Nuchal translucency is a screening ultrasound examination obtained between weeks 11 and
14 of pregnancy.
Because it is a screening test, nuchal translucency can't determine for sure if a baby has a
birth defect.
A positive screening
test requires follow-up with a diagnostic test to definitively diagnose a birth defect.
It measures the amount of fluid at the base, or nuchal fold, of a fetus' neck.
The timing of a nuchal translucency screen is crucial due to the fact that the nuchal
fold is still transparent during weeks 11 through 14 of fetal development.
The nuchal fold becomes less transparent beyond week 14 of fetal
development.
If the amount of fluid at the nuchal fold is increased, the likelihood of a birth defect
is increased.
Nuchal translucency may be used as a screening test for Down syndrome, congenital heart defects,
and other genetic
disorders.
There are no risks associated with nuchal translucency screening.
2.
Pregnancy-Associated Plasma Protein A. Pregnancy-associated plasma protein A (PAPP-A),
also known as Pappalysin-1, is a protein produced by the placenta during pregnancy.
Levels of PAPP-A can be determined using a blood test and can be used to screen for aneuploidy,
which
is an abnormal number of chromosomes in a cell.
Aneuploidy can be seen with Down syndrome or other chromosomal abnormalities.
Pappalysin-1 is also associated with complications of pregnancy such as small size for gestational
age
(SGA), preterm labor, preeclampsia, spontaneous abortion, and stillbirth.
The screening blood test for pregnancy-associated plasma protein A (PAPP-A) is typically obtained
between weeks 11 and 14 of pregnancy.
Abnormally low levels of PAPP-A are associated with aneuploidy and certain complications
of
pregnancy.
A positive screening test requires follow-up with a diagnostic test to definitively diagnose
the kind of aneuploidy or specific pregnancy complication.
Down syndrome, or trisomy 21, is the most common cause of aneuploidy.
3.
Human Chorionic Gonadotropin (hCG).
Human chorionic gonadotropin (hCG) is a hormone produced by the placenta during pregnancy.
The presence of hCG in both the urine and blood is detected in pregnancy tests.
Some cancerous tumors also produce hCG.
Levels of hCG can be
determined using a blood test and can be used along with other blood markers to screen for
certain birth defects such as Down syndrome, spina bifida, or anencephaly.
Anencephaly is a condition in which the fetus is born with a
partially formed brain and spinal cord.
A blood test to measure hCG is usually performed between weeks 15 and 20 of pregnancy.
It is usually drawn as part of the maternal triple or quadruple screening test.
The maternal triple screening test consists of hCG, alpha-
fetoprotein (AFP), and estriol (E3).
The maternal quadruple screening test consists of substances measured in the triple screening
plus the hormone inhibin A. Elevated levels of hCG may be seen in a multiple pregnancy
(twins or
triplets) or a molar pregnancy.
Decreased levels of hCG may be seen in an ectopic (outside of the uterus) pregnancy.
4.
Alpha-Fetoprotein.
Alpha-fetoprotein (AFP) is a blood protein manufactured by the fetal liver and can be
found in amniotic fluid surrounding the fetus.
It is the most abundant blood protein found in the fetus.
AFP also crosses the placenta and can be
measured in maternal blood.
As a result, maternal serum AFP can be used as a screening tool to assess the probability
of potential genetic disorders or birth defects.
A blood test to measure AFP is generally done between 15 and 20 weeks of pregnancy, with
the most accurate results obtained between weeks 16 and 18.
It is typically drawn as part of the maternal triple (hCG, AFP, and E3) or quadruple
(hCG, AFP, E3, and inhibin A) screening test.
High levels of AFP may be associated with the presence of a neural tube defect (such
as spina bifida or anencephaly), an omphalocele (failure of closure of the abdomen), or a
multiple
pregnancy.
The most common cause of an elevated AFP level is a miscalculated due date.
Low levels of AFP may suggest chromosomal abnormalities such as Down (trisomy 21) or
Edward (trisomy 18) syndromes.
5.
Estriol.
Estriol (E3) is one of the three forms of the hormone estrogen and is produced by the
placenta.
As a result, it is only produced in significant amounts during pregnancy and becomes the dominant
estrogen during pregnancy.
The other two
forms of estrogen include estrone (E1) and estradiol (E2).
A blood test to measure estriol is usually performed between weeks 15 and 20 of pregnancy.
It is usually drawn as part of the maternal triple (hCG, AFP, and E3) or quadruple (hCG,
AFP, E3, and inhibin A) screening test.
Low levels of
E3 may be associated with a neural tube defect such as spina bifida or anencephaly.
Low levels of E3 may also be associated with pregnancy loss (fetal demise).
6.
Inhibin A. Inhibin A is a hormone produced primarily
by the placenta.
Small amounts of inhibin A are also synthesized in the ovaries of females.
Inhibin A was added to the maternal triple screening (making it the quadruple screening
test) in
1998.
The quadruple screening test has since been quickly adopted to replace the maternal triple
screen as the panel of choice for the screening of neural tube defects and chromosomal abnormalities.
A blood test to measure inhibin A is usually performed between weeks 15 and 20 of pregnancy.
It is part of the maternal quadruple screening test, which measures hCG, AFP, and E3.
High levels of the hormone inhibin A may be associated
with chromosomal abnormalities such as Down syndrome.
The quadruple screening test along with other factors such as maternal age, race/ethnicity,
and weight are used to calculate the chances of a neural tube defect or chromosomal
abnormality affecting a pregnancy.
7.
Chorionic Villus Sampling (CVS).
Chorionic villus sampling (CVS) is performed as a prenatal diagnostic test.
It involves removing a small sample of chorionic villi from the placenta.
The sample can be obtained through the cervix (transcervical) or the abdominal wall
(transabdominal).
The chorionic villi share the same genetic makeup as the fetus.
Reasons for CVS include increased nuchal translucency, abnormal first trimester screening results,
previous pregnancy or family history of chromosomal
or genetic disorder, advanced maternal age (age > 35 years), and parents being known
carriers of a genetic disorder.
Chorionic villus sampling is typically carried out between weeks 10 and 12 of pregnancy.
It can be used to diagnose chromosomal abnormalities (such as Down syndrome) or other genetic disorders
(such as cystic fibrosis).
CVS cannot
diagnose neural tube defects.
Complications of CVS may include miscarriage (0.7 percent) or uterine infection (rarely).
8.
Amniocentesis.
Amniocentesis refers to surgical puncture to remove fluid from the amnion, or sac surrounding
the fetus.
It is a prenatal diagnostic test.
Practitioners use ultrasound guidance to safely remove amniotic fluid from the amnion.
The
amniotic fluid furnishes cells shed by the fetus for analysis.
The most common reason for amniocentesis is an abnormal maternal triple or quadruple screening
test in the second trimester of pregnancy.
Amniocentesis is typically performed between weeks 15 and 20 of pregnancy.
The procedure can diagnose chromosomal abnormalities, neural tube defects, and genetic disorders
in upwards of 99-percent of cases.
Down syndrome is the most
common chromosomal abnormality.
The most common neural tube defect is spina bifida.
Amniocentesis has a small risk for miscarriage, which occurs with a frequency ranging from
1 in 400 to 1 in 200 procedures.
Other side effects may
include abdominal or pelvic cramping and leakage of amniotic fluid.
9.
Oral Glucose Tolerance Test.
The oral glucose tolerance test (OGTT) is used to screen for the possibility of diabetes
occurring with pregnancy (gestational diabetes).
Factors that increase the risk of gestational diabetes include history of gestational diabetes
with a previous pregnancy, giving birth to an infant weighing more than 9-pounds, age
younger than 25, and being overweight before becoming pregnant.
The OGTT is performed between weeks 24 and 28 of pregnancy.
It consists of drawing a fasting blood glucose followed by ingestion of a 75-gram load of
glucose.
Blood samples for glucose levels are taken and recorded every hour for two
consecutive hours.
Normal results for OGTT are fasting levels less than 92 mg/dL, one-hour levels less than
180 mg/dL, and two-hour levels less than 153 mg/dL.
Pregnancy-related complications of gestational diabetes may include
excessive birth weight (macrosomia), preeclampsia, and increased risk of developing type 2 diabetes.
10.
Group B Streptococcus Culture.
Group B streptococcus (GBS) is a bacterium that can colonize the lower genital tract
of women.
The event causes no problem in non-pregnant women, but has the potential to cause serious
illness in a mother and her newborn.
The presence
of GBS can lead to a severe infection of the placenta (chorioamnionitis), urinary tract
infections (UTIs), preterm labor/birth, kidney infection (pyelonephritis), or sepsis (a severe
bacterial blood infection).
Pregnant women should be screened for the presence of GBS via vaginal and rectal swabs
sent for culture between weeks 35 and 37 of pregnancy.
The GBS infection may be spread to newborns as they pass through the birth canal.
It is one
of the most common causes of life-threatening infections in newborns, including meningitis
and pneumonia.
Mothers should be treated with antibiotics to reduce the transmission of GBS to their
newborns.
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