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What tests might I need during pregnancy?

时间: 2016-11-23 08:11 信息来源: LIU 点击次数:

澳门新葡京线上注册 www.lantianting.com Some tests are screening tests, others are diagnostic tests. If your health care provider orders a screening test, keep in mind that such tests do not diagnose problems. They evaluate risk. So a screening test result that comes back abnormal does not mean there is a problem with your infant. It means that more information is needed. Your health care provider can explain what the test results mean possible next steps.

The types of tests you may have during pregnancy include1:

Routine Tests

  • Glucose challenge screening. Given between 24 28 weeks of pregnancy, this screening determines your risk for gestational diabetes. You will consume a sugary drink get a blood test 1 hour later to measure your blood sugar levels.

  • Group B streptococcus (pronounced STREP-tuh-KOK-uhss) infection screening. This test is performed between 35 37 weeks of pregnancy to look for bacteria (GBS) that can cause pneumonia or other serious infections in your infant. Swabs will be used to take cells from your vagina rectum. Women who test positive for GBS will need antibiotics when in labor.

  • Ultrasound exam. You will likely have an ultrasound exam between 18 20 weeks of pregnancy to check for any problems with the developing fetus. During an ultrasound exam, gel is spread on your belly a special tool is moved over it to create a "picture" of the fetus on a monitor.

  • Urine test. At each prenatal visit, you will give a urine sample, which will be tested for signs of diabetes, urinary tract infections, preeclampsia.

Screening for Chromosomal Neural Tube Defects (NTDs) Other Conditions2

  • Nuchal translucency (pronounced NOO-kuhl trans-LOO-sen-see) screening. This screening test uses ultrasonography to measure the thickness of the back of the fetus’s neck between 11 14 weeks. This information, combined with the mother’s age the results of the serum screen, helps health care providers determine the fetus’s potential risk for chromosomal abnormalities other problems.

  • First trimester screen. Blood is drawn to test for PAPP-A free beta-hCG (or hCG) may be combined with performing a nuchal translucency ultrasound. This test will provide the risk for Down syndrome as well as other chromosomal problems.

  • Maternal serum screen (also called quad screen, triple test, triple screen, multiple marker screen, or AFP). Blood is drawn to measure the levels of certain substances that determine the risk of the fetus having chromosomal abnormalities NTDs. This screening test is done between 15 20 weeks of pregnancy.

  • Chorionic villus (pronounced KOR-ee-ON-ihk VIL-uhss) sampling (CVS). If your fetus is at risk for a chromosomal defect or other genetic disorders, your doctor may recommend this test when you are between 10 13 weeks pregnant. In this test, a needle is inserted through the cervix or the abdomen to remove a small sample of cells from the placenta.

  • Amniocentesis (pronounced AM-nee-oh-sen-TEE-sis). Given between 15 20 weeks of pregnancy, this test is used to diagnose chromosomal disorders, such as Down syndrome your infant’s risk for NTDs, such as spina bifida. After a local anesthetic is given, a thin needle is inserted into the abdomen to draw out a small amount of amniotic fluid cells from the sac surrounding the fetus. The fluid is sent to a lab for testing.

  • Cell free fetal DNA. A new, noninvasive test uses the mother’s blood to look for increased amounts of material from chromosomes 21, 18, 13. This test can be given as early as 10 weeks to women whose age, family history, or standard screening results put them at higher risk for having a child with a chromosome disorder. The test is not recommended for women who are at low risk or are carrying multiple fetuses.3

  • Carrier screening for cystic fibrosis (CF). A blood or saliva test determines if you your partner are carriers for this genetic disease that affects breathing digestion. Both parents must be a carrier for their child to get CF. About 1 in 30 Americans is a symptomless carrier of the CF gene.4

Additional Testing that Your Health Care Provider May Recommend5

  • Glucose tolerance test. If the 1-hour glucose challenge screening is above a certain cutoff, your health care provider may order this test. You will fast for at least 8 hours before the test. Your blood is drawn to test your "fasting blood glucose level." You will consume a sugary drink, your blood will be taken every hour for 3 hours to see how your body reacts to the sugar.

  • Non-stress test. This test is performed in the third trimester (28 weeks or later) to monitor the fetus’s health. A belt placed around your belly measures the fetal heart rate while the fetus is at rest while the fetus is moving or kicking. This test can determine if the fetus is getting enough oxygen.

  • Biophysical profile (BPP). This test, given in the third trimester of pregnancy, monitors the fetus’s breathing, movement, muscle tone, heart rate as well as the amount of amniotic fluid to determine fetal well-being. The BPP includes an ultrasound test a non-stress test.


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