Antenatal testing describes procedures performed during pregnancy to detect health problems in the growing fetus; establish characteristics such as fetal age, sex, or weight; or diagnose any material conditions that may affect fetal development.
Antenatal tests and exams are important tools for protecting the health of a pregnant woman and her developing child. Various tests are administered over the course of pregnancy to determine if the mother has any health conditions that may interfere with normal development of the fetus or if the fetus has any health conditions that may affect the baby's quality of life. Often, families will use information provided by the tests to prepare for the baby's birth and make arrangements for special care if needed or make the decision to terminate the pregnancy. Physicians also use antenatal tests to determine various characteristics of the fetus, such as gestational age, size, and position in the uterus, or to verify the presence of multiple fetuses.
Women who become pregnant may undergo tests at any stage in their pregnancy: during the first trimester (weeks one through 12), second trimester (weeks 13–26), or third trimester (weeks 27–40+). What tests are ordered depends on the stage of pregnancy, the age and health of the mother, the medical history of both parents, and the family's background or ethnicity. There are two distinct types of antenatal tests:
- Screening tests tend to be less invasive and indicate the possibility of a certain genetic disorder or birth defect but do not determine with certainty that the abnormality exists.
- Diagnostic tests tend to more invasive but are able to determine with more certainty that a fetus will be born with a certain condition.
Blood and urine tests
In the early stages of pregnancy, physicians may order blood or urine tests to screen for possible disorders or infections that could affect the growing fetus. The tests may also be ordered in later stages if the pregnant woman comes in contact with an infectious agent or develops symptoms of infection. In many cases, complications can be avoided if early diagnosis is made and treatment initiated. Examples of conditions that are commonly screened for with blood and/or urine tests include:
- Rh factor: About 15 percent of people lack a certain blood protein called Rh factor and are called Rh negative. Complications may arise if an Rh-negative mother is carrying an Rh-positive child. These can be avoided if the mother is given a substance called Rh immune globulin (RhIg) at approximately 28 weeks into the pregnancy and again within 72 hours after the baby is born.
- Anemia: If there is too little of a substance called hemoglobin in a pregnant woman's red blood cells, a condition called anemia may result. If a blood test reveals low hemoglobin, supplementation with iron may be recommended.
- Human immunodeficiency virus: HIV can be transmitted from mother to child, although treatment of the disease during pregnancy can greatly reduce the risk of transmission. Because it is possible for individuals to be infected without exhibiting symptoms and because unprotected sex is a major risk factor for contracting the virus, the American Academy of Pediatrics recommended in 1999 that a screening test for HIV be routinely offered. A second test later in pregnancy may be recommended if the pregnant woman is considered to be at high risk of becoming infected with HIV.
- Syphilis: If transmitted from mother to child during pregnancy, syphilis leads to death of the fetus or newborn in approximately 40 percent of cases. The goal of syphilis screening is to diagnose and treat infections before transmission occurs. Syphilis is treated with antibiotics.
- Rubella (German measles ): Although the majority of women in the United States are immune to rubella because of prior immunization or infection, serious complications to the fetus (such as deafness, blindness, or heart defects) can arise if a woman becomes infected during pregnancy. If a woman is found to not have immunity, it will be recommended that she avoid contact with infected individuals during her pregnancy and receive a vaccination against rubella after she gives birth.
- Group beta strep (GBS): GBS is a type of bacteria commonly found in the vagina and rectum. GBS can be present in a person's body without causing any symptoms, so many women do not realize they are infected with it. Newborns who are exposed to GBS, however, can develop serious complications such as meningitis, pneumonia , blindness, deafness, and death is possible. Doctors test for the presence of GBS in urine or in samples collected from the vagina or rectum. This test is usually performed late in pregnancy, at 35 to 37 weeks of gestation. If a woman is found to be infected with GBS, physicians generally administer antibiotics to the mother so the baby is not born with the infection.
A multiple marker test or triple screen is used to determine if a fetus is at an increased risk of having certain congenital abnormalities. The test has a high rate of false-positives; as few as 10 percent of women with abnormal results go on to have babies with congenital defects. The purpose of the test is to determine if further testing (such as ultrasound or amniocentesis ) is warranted. The test requires a sample of maternal blood, typically taken during the fifteenth and twentieth week of pregnancy, and measures the level of certain pregnancy hormones.
Ultrasound is a device that records sound waves as they bounce off the developing fetus and create an image that is projected onto a large computer screen. A physician may order an ultrasound scan to listen for a fetal heartbeat, determine a woman's precise due date, or check for twins , among other uses. Also known as a sonogram, the procedure takes only a few minutes, is safe and painless, and usually is covered by health insurance.
During the procedure, an ultrasound technician asks the pregnant woman to remove her clothes and change into a gown. The technician may rub some gel on the woman's fundus (lower abdomen), which helps the hand-held device pick up sound waves. In certain cases, the technician may insert a plastic probe into the woman's vaginal canal to get a clearer picture of the fetus. Early in pregnancy, the test may need to be done with a full bladder.
Pregnant women will often have their first ultrasound between eight and 12 weeks of gestation. In normal cases, the technician is able to identify a fetal heartbeat, which appears as a flashing light on the screen. Closer to the due date, physicians use ultrasound to make sure the fetus is in the correct head-first position to exit the birth canal, to assess the fetus for certain birth defects, and to determine the sex of the fetus if the parents desire.
Between ten and 14 weeks of gestation, ultrasonography may be used to measure a small collection of fluid beneath the skin at the back of the neck. Called nuchal translucency, the measurement tends to be larger in fetuses with genetic abnormalities such as Down syndrome , trisomy 13, trisomy 18, Turner syndrome , and triploidy. A particular neck measurement combined with maternal age as an indicator (e.g. the incidence of the disorder increases in proportion to the age of the mother) has been shown to correctly diagnose Down syndrome in 75 to 80 percent of cases; this number increases to 90 percent if the procedure is combined with the multiple marker test.
Amniocentesis is a more invasive test that carries a higher risk of complications than blood tests or ultrasonography, but is able to determine more precisely the presence of certain birth defects. It is also used to determine the level of maturity of the baby's lungs, of particular interest if the baby will be delivered prematurely. During amniocentesis, a doctor inserts a thin needle through a woman's abdomen and into the uterus. Using ultrasound as a guide, the doctor uses the needle to withdraw a sample of fluid from the amniotic sac. Afterward, tiny cells shed by the fetus can be studied in the laboratory; scientists can analyze the samples to determine if the fetus has certain genetic conditions. Amniocentesis is typically performed during the second trimester of pregnancy and particularly in mothers over the age of 40.
Chorionic villus sampling
Chorionic villus sampling (CVS) is a procedure that allows for prenatal diagnosis during the first trimester (generally between ten and 12 weeks of gestation, during the embryonic stage of development). The test involves taking a small sample of cells from the placenta with a needle through the abdominal wall or a small tube (catheter) through the cervix. The procedure is guided by ultrasound. The cells are then analyzed in a laboratory for the presence of genetic abnormalities.
The risks associated with antenatal testing depend on the specific procedure being performed:
- Blood tests: The risks associated with blood testing are minimal and include discomfort, bleeding from the puncture site, hematoma (collection of blood under the skin), and infection.
- Ultrasound: As of 2004 there is no recognized risk for ultrasonography.
- Amniocentesis: The risk of miscarriage associated with amniocenteses performed between 15 and 20 weeks is less than 0.5 percent. The other risks are maternal infection, injuries to the fetus, and premature labor.
- Chorionic villus sampling: The risk of miscarriage associated with CVS performed between nine and 11 weeks is less than 2 percent. The risks are similar to those associated with amniocentesis.
Impending parenthood is often accompanied by concerns that the baby may be born with defects or other health problems that would affect the quality of life of the baby and the family . That worry is often weighed against the anxiety associated with antenatal tests and their risks. Parents should be encouraged to educate themselves on the benefits and risks associated with the various antenatal screening procedures and work with their obstetrician to formulate an individualized prenatal care plan.
Alpha fetoprotein test —A screening blood test that can be done after the sixteenth week of pregnancy to evaluate the possibility of spina bifida and other neural tube defects in the fetus.
Amniocentesis —A procedure performed at 16–18 weeks of pregnancy in which a needle is inserted through a woman's abdomen into her uterus to draw out a small sample of the amniotic fluid from around the baby for analysis. Either the fluid itself or cells from the fluid can be used for a variety of tests to obtain information about genetic disorders and other medical conditions in the fetus.
Breech position —The foot-down or bottom-down position of a fetus just before delivery.
Group B streptococcus —A serotype of streptococcus, Streptococcus agalactiae, which is beta hemolytic and can cause neonatal sepsis, pneumonia, or meningitis if present in the birth canal at the time of delivery especially when the delivery is difficult.
Hemoglobin —An iron-containing pigment of red blood cells composed of four amino acid chains (alpha, beta, gamma, delta) that delivers oxygen from the lungs to the cells of the body and carries carbon dioxide from the cells to the lungs.
Meningitis —An infection or inflammation of the membranes that cover the brain and spinal cord. It is usually caused by bacteria or a virus.
Ultrasonography —A medical test in which sound waves are directed against internal structures in the body. As sound waves bounce off the internal structure, they create an image on a video screen. Ultrasonography is often used to diagnose fetal abnormalities, gallstones, heart defects, and tumors. Also called ultrasound imaging.
Seashore, Margretta R. "Genetic Counseling." In Cecil Textbook of Medicine. Edited by Lee Goldman and J. Claude Bennett. Philadelphia: Saunders, 2000.
Simpson, Joe Leigh. "Diagnostic Procedures for Prenatal Genetic Diagnosis." In Obstetrics: Normal and Problem Pregnancies. Edited by Steve G. Gabbe et al. New York: Churchill Livingstone, 2002.
Andrews, Janet I., Daniel J. Diekema, and Jerome Yankowitz. "Prenatal Testing for Infectious Disease." Clinics in Laboratory Medicine 23, no. 2 (June 2003): 295–315.
Bubb, Jennifer A., and Anne L. Matthews. "What's New in Prenatal Screening and Diagnosis?" Primary Care 31, no. 3 (September 2002): 561.
American College of Obstetricians and Gynecologists. 409 12th St., SW, PO Box 96920, Washington, DC 20090–6920. Web site: <www.acog.org>.
March of Dimes Birth Defects Foundation. 275 Mamaroneck Ave., White Plains, NY 10605. Web site: <www.modimes.org>.
Singh, Daljit, Jai Rup Singh, and Vanita Kumar. "Prenatal Diagnosis for Congenital Malformations and Genetic Disorders." eMedicine, July 29, 2004. Available online at <www.emedicine.com/oph/topic485.htm> (accessed December 23, 2004).
Stephanie Dionne Sherk Melissa Knopper
"Antenatal Testing." Gale Encyclopedia of Children's Health: Infancy through Adolescence. . Encyclopedia.com. (December 9, 2017). http://www.encyclopedia.com/medicine/encyclopedias-almanacs-transcripts-and-maps/antenatal-testing-0
"Antenatal Testing." Gale Encyclopedia of Children's Health: Infancy through Adolescence. . Retrieved December 09, 2017 from Encyclopedia.com: http://www.encyclopedia.com/medicine/encyclopedias-almanacs-transcripts-and-maps/antenatal-testing-0
Antenatal testing includes any diagnostic procedures performed before the birth of a baby.
These tests and exams are essential for protecting the health of a pregnant woman and her developing child.
Some tests, such as amniocentisis, carry a small risk of a miscarriage or other complications that could harm the mother or baby.
Women who become pregnant undergo a wide variety of tests throughout the nine months before delivery. In the early stages, physicians order blood tests to screen for possible disorders or infections, such as human immunodeficiency virus (HIV), which can pass from the mother to the fetus. Later, the focus shifts to checking on fetal well-being with a variety of technological tools such as ultrasound scans. Descriptions of the most common tests and procedures used during pregnancy are listed below.
When a woman first learns she is pregnant, her physician will run a series of routine urine and blood tests to determine her blood type, check for anemia and gestational diabetes, make sure she is immune to rubella (German measles ) and check for infectious diseases like HIV, hepatitis, chlamydia or syphilis. Physicians also usually do pelvic exam to screen for cervical cancer and check the patient's blood pressure. As the pregnancy progresses, more tests will follow.
Ultrasound is a device that records sound waves as they bounce off the developing fetus to create an image, which is projected onto a large computer screen. Physicians order an ultrasound scan to listen for a fetal heartbeat, determine a woman's precise due date and check for twins, among other uses. An ultrasound scan also is known as a sonogram. The procedure takes a few minutes, is painless and usually is covered by health insurance.
Ultrasound— A device that records sound waves as they bounce off a developing fetus to create an image, which is projected onto a large computer screen
Breech position— When a child is oriented feet first in the mother's uterus just before delivery.
Alpha fetoprotein screen— A test that measures the level of alpha fetoprotein, a substance produced by a fetus with birth defects, in the mother's blood.
Amniocentesis— An invasive procedure that allows physicians to check for birth defects by collecting a sample of fetal cells from inside the amniotic sac.
GBS— Group B streptococci are a type of bacteria that, if passed to a can cause inflammation of the brain, spinal cord, blood or lungs. In some cases, it can result in infant death
The ultrasound technician will ask the pregnant woman to remove her clothes and change into a gown. The technician may rub some gel on the woman's stomach, which helps the hand-held device pick up sound waves better. In certain cases, the technician may insert a plastic probe into the woman's vaginal canal to get a clearer picture of the fetus. Early in pregnancy, the test may need to be done with a full bladder.
Unlike x rays, ultrasound is safe to use during pregnancy. It does not cause any known side-effects that would harm the mother or baby.
Pregnant women usually will have their first ultrasound anytime between 8 and 12 weeks of gestation. In normal cases, the technician is able to identify a fetal heartbeat, which appears as a flashing light on the screen. Closer to the due date, physicians use ultrasound to make sure the fetus is in the correct position to exit the birth canal head first.
Sometimes an ultrasound will show that a fetus has stopped growing, or a gestational sac has formed without a fetus, and a miscarriage has occurred. Later in pregnancy, it also may show that the child is in a breech position, oriented feet first, which can cause a difficult labor.
Tests for birth defects
Most obstetricians offer parents a variety of ways to find out if their developing child might have birth defects such as spina bifida and Down Syndrome. An alpha fetoprotein screen can be done through a simple blood test in the doctor's office between the 16th and 18th week of gestation. It tells the odds that their child will have a severe congenital anomaly. The test works by measuring the level of alpha fetoprotein, a substance produced by a fetus with birth defects. Low levels of alpha fetoprotein in the mother's blood may indicate Down's Syndrome. In that case, the next step for most couples is amniocentesis because the alpha fetoprotein test can give false-positive results. Amniocentesis is a more accurate test, but it also has higher risks of complications.
This procedure typically is used to diagnose Down syndrome while a developing child is still in the womb, at 15-28 weeks.
During amniocentesis, a doctor inserts a needle through a woman's vaginal canal and inside her cervix. Using ultrasound as a guide, the doctor pierces the uterus to withdraw a sample of fluid from the amniotic sac. Afterwards, tiny cells shed by the fetus can be studied in the laboratory. Scientists can analyze DNA samples to determine if the fetus has Down syndrome or other genetic conditions. Amniocentesis also can determine the sex of the fetus.
Women who have a history of recurring miscarriages may not want to have this procedure.
Amniocentesis is usually performed in a doctor's office on an outpatient basis.
Common side effects include cramping and bleeding.
In about one out of every 1,000 cases, amniocentesis causes a needle to puncture the uterine wall, which could result in miscarriage.
In most cases, couples find out their baby does not have a birth defect.
If the results come back positive for Down's Syndrome or other serious conditions, the couple must decide if they want to end the pregnancy. Others use the knowledge to plan and prepare any special care needed for their future child.
Group B Strep
This test is for Group B streptococci (GBS) infection.
By testing for GBS, physicians can determine if a woman is at risk of passing this infection along to her child.
Women who have had a prior child with GBS, or who have a fever or prolonged or premature rupture of the amniotic sac may be at higher risk for this type of infection.
GBS is a type of bacteria commonly found in the vagina and rectum. Unlike regular strep throat, GBS can be present in a person's body without causing any symptoms, so many women do not realize they are infected with it.
To test for the presence of GBS, doctors may take a urine sample. They also may collect samples from the vagina or rectum, which are then analyzed in a lab. This test is usually performed late in pregnancy, at 35-37 weeks of gestation.
This is a routine urine test or pelvic exam with no side effects.
In many cases, doctors do not find any evidence of this type of infection.
If a woman is found to be infected with Group B strep, physicians usually wait to treat it until just before labor begins. At that time, they may give the mother antibiotics so the baby is not born with the infection. Newborns who are exposed to Group B strep can have inflammation of the brain, spinal cord, blood or lungs. In some cases, this serious complication can result in infant death.
Planning your Pregnancy and Birth. Washington, DC: The American College of Obstetricians and Gynecologists, 2000.
Parkey, Paula. "Birth Defects: Is Prenatal Screening Advisable?" CBS HealthWatch April, 2000. 〈http://www.cbshealthwatch.com/cx/viewarticle/214798〉.
American College of Obstetricians and Gynecologists. 409 12th St., S.W., P.O. Box 96920, Washington, DC 20090-6920. 〈http://www.acog.org〉.
March of Dimes Birth Defects Foundation. 275 Mamaroneck Avenue, White Plains, NY 10605. (888) 663-4637. 〈http://www.modimes.org〉.
"Antenatal Testing." Gale Encyclopedia of Medicine, 3rd ed.. . Encyclopedia.com. (December 9, 2017). http://www.encyclopedia.com/medicine/encyclopedias-almanacs-transcripts-and-maps/antenatal-testing
"Antenatal Testing." Gale Encyclopedia of Medicine, 3rd ed.. . Retrieved December 09, 2017 from Encyclopedia.com: http://www.encyclopedia.com/medicine/encyclopedias-almanacs-transcripts-and-maps/antenatal-testing