What instructions should be given to a client scheduled for an amniocentesis?

You had an amniocentesis. This is a prenatal test. It helps you learn whether a fetus has health problems. The test is most often done between the 15th and 20th week of pregnancy. It is also done to check the condition of the lungs of a baby who will be delivered several weeks early.

Home care

  • Limit your activity for 24 to 48 hours after the procedure.

  • Know the risks involved with amniocentesis. This can help you recognize if you are having complications. Make sure you understand the following risks:

    Amniocentesis is a prenatal test that can detect chromosomal differences, such as those that cause Down syndrome, as well as extra or missing pieces of chromosomes, called copy number variants, some of which are associated with certain conditions. This test, which is typically performed at 16 to 22 weeks of pregnancy, can also be used in at-risk fetuses to identify some genetic diseases caused by a difference in a single gene, including cystic fibrosis, sickle cell disease and Tay-Sachs disease. In addition, amniocentesis can be used to screen for neural tube defects, which are birth defects of the brain and spine, such as spina bifida.

    The doctors, nurses and other members of the UCSF Prenatal Diagnostic Center bring a wealth of expertise and experience to your care and have performed more than 40,000 amniocentesis procedures over the past 25 years.

    Why choose amniocentesis over chronic villus sampling (CVS)?

    Although performed later in a pregnancy than CVS, amniocentesis has the advantage of screening for neural tube defects, such as spina bifida. (Those who opt for CVS need to have a blood test later during pregnancy to screen for neural tube defects.) Therefore amniocentesis is recommended if you have a child with a neural tube defect, if you have one of these conditions yourself, or if the other biological parent does. Also, there is a slightly higher risk of miscarriage from CVS compared with amniocentesis.

    What happens before and during the procedure?

    First you'll meet with a genetic counselor, who will assess your pregnancy history and family history, explain options for prenatal screening and testing, and answer any questions or concerns you have. This appointment may happen in person at the UCSF Prenatal Diagnostic Center or via a video visit.

    You'll then have an ultrasound to assess the location of the fetus and placenta and to evaluate fetal growth. During the amniocentesis itself, which is performed under ultrasound guidance, a needle is inserted through the abdomen to remove a small amount of amniotic fluid. Most patients don't find the procedure painful, although some experience cramping or other minor discomfort.

    The sample is sent to the lab for testing. Most results are available within two weeks, although certain tests may take up to a month.

    Are there risks associated with the test?

    There is a small risk of miscarriage as a result of an amniocentesis. It is approximately 1 in 900.

    What are the possible results from amniocentesis?

    • Normal – A normal result indicates that the test did not identify evidence of the conditions it was checking for.
    • Abnormal – An abnormal result indicates that the test identified a genetic difference in the pregnancy. If this occurs, you'll discuss the results and your options with a genetic counselor and other health care providers at our center, as well as your own doctor. For any decision you make, we offer referrals and support resources.
    • Uncertain – An uncertain result indicates that a genetic difference was identified but its impact on the pregnancy is unclear. If this occurs, you'll discuss the results and your options with a genetic counselor and other health care providers at our center, as well as your own doctor. Additional testing may be recommended.

    Will my insurance cover the cost?

    Most insurance plans cover amniocentesis, chorionic villus sampling and other prenatal tests, especially for pregnant people over 35. You may need a referral from your primary care doctor or an authorization from your health plan to ensure coverage. Our office staff is available to assist you with insurance questions.

    Amniocentesis is a prenatal test that can diagnose genetic disorders (such as Down syndrome and spina bifida) and other health issues in a fetus. A provider uses a needle to remove a small amount of amniotic fluid from inside your uterus, and then a lab tests the sample for specific conditions.

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    Overview

    What instructions should be given to a client scheduled for an amniocentesis?
    Amniocentesis is a prenatal test that diagnoses certain congenital disorders during pregnancy.

    What is amniocentesis?

    Amniocentesis is a prenatal testing procedure usually performed during the second or third trimester of pregnancy. It can diagnose certain chromosomal conditions (such as Down syndrome) or genetic conditions (such as cystic fibrosis). During amniocentesis, your healthcare provider uses a thin needle to remove a small amount of amniotic fluid from the sac surrounding the fetus. This fluid sample then gets tested in a laboratory.

    During pregnancy, the fetus grows inside the amniotic sac. Amniotic fluid surrounds and protects the fetus inside the amniotic sac. It also contains some of the fetus's cells. These cells contain genetic information that helps diagnose genetic conditions.

    Who gets amniocentesis?

    Your healthcare provider may recommend amniocentesis during pregnancy when:

    • Ultrasound testing detects a fetal abnormality.
    • A prenatal screening test detects an increased risk for a chromosome disorder.
    • Certain genetic disorders (such as sickle cell disease or cystic fibrosis) run in your family or you test positive as a carrier of a genetic disorder.
    • You’re older than 35 at the time of delivery. This is because individuals over 35 have a higher chance of having a baby with a chromosomal disorder.

    What does amniocentesis test for?

    An amniocentesis test can detect chromosomal, genetic disorders or congenital disabilities (sometimes called birth defects) such as:

    • Down syndrome.
    • Tay-Sachs disease.
    • Neural tube defects such as spina bifida or anencephaly.

    This test can also evaluate:

    • Fetal lung development: This is helpful if you need to give birth sooner than expected to protect the health of you or the fetus.
    • Rh disease: This is a potentially serious condition where you and the fetus have different blood Rh types.

    Amniocentesis is sometimes used to treat polyhydramnios (when you have too much amniotic fluid). Providers use amniocentesis to remove excess fluid.

    When is amniocentesis performed?

    Most amniocentesis procedures happen between 15 and 20 weeks of gestation (during the second trimester of pregnancy). Having an amniocentesis earlier in pregnancy poses more risks, such as miscarriage.

    In some cases, healthcare providers perform amniocentesis tests later in pregnancy. If your provider recommends this test to check fetal lung development or treat polyhydramnios, it will likely happen during the third trimester.

    Can I choose not to have amniocentesis?

    Yes. If your provider recommends you have an amniocentesis, they will explain why. Your provider (or a genetic counselor) will review the test’s risks and benefits. In the end, whether or not to have this test is up to you.

    Test Details

    How should I prepare for an amniocentesis?

    Your healthcare provider may provide specific instructions to you for the hours or days leading up to amniocentesis. Generally, there aren’t restrictions on diet or activity. Tell your provider what medications you’re taking so they can let you know if you should stop taking them before your test. Follow any other instructions provided to you.

    If you need an amniocentesis test, it’s normal to have questions. Some questions for your provider could include:

    • Why do you recommend I have amniocentesis?
    • What does amniocentesis mean for the health of the fetus and me?
    • What are the potential risks?
    • What should I do to prepare for my test?
    • When should I expect to get test results?
    • Is genetic counseling available to help me?

    What are the risks of amniocentesis?

    Most amniocentesis procedures are safe. But amniocentesis does present small but serious risks for both you and the fetus.

    Some complications of amniocentesis are:

    • Cramping.
    • Bleeding or leaking amniotic fluid.
    • Injury or infection.
    • Loss of the pregnancy.
    • Premature labor.

    Complications from amniocentesis are rare. In less than 1% of cases, amniocentesis leads to miscarriage or early delivery. About 2% of people have spotting or camping after amniocentesis.

    Your provider can answer your questions and help you make a decision that’s best for you.

    Why is there a risk of miscarriage with amniocentesis?

    Miscarriage after amniocentesis is very uncommon. Possible causes could be damage to the amniotic sac or amniotic membranes, losing amniotic fluid, bleeding or infection. Discuss your risk of miscarriage with your healthcare provider before the test.

    How do doctors perform amniocentesis?

    Your obstetrician or perinatologist performs amniocentesis. First, you’ll lie on your back with your stomach showing. During this procedure, your healthcare provider:

    • Cleans a small area on your belly with an antiseptic (to kill germs).
    • Applies a special gel on your belly.
    • Moves a wand-like device over the gel to capture ultrasound images of the fetus on a nearby monitor.
    • Inserts a thin, hollow needle through your abdomen and uterus (into the amniotic sac but away from the fetus).
    • Removes a small amount of fluid through the needle.
    • Removes the needle from your abdomen.
    • Monitors the fetal heartbeat and movement on the ultrasound to ensure they weren’t affected by the procedure.

    After the procedure, your healthcare provider sends the amniotic fluid sample to a lab. The lab separates the fetal cells from the amniotic fluid then analyzes the cells. The cells grow for several days in the lab before being tested for genetic conditions or neural tube defects. You should have complete test results in about two weeks.

    How long does an amniocentesis take?

    An amniocentesis procedure may take around 30 minutes from start to finish. But the actual sampling process (when the needle is inside your uterus) takes only a minute or two.

    How painful is amniocentesis?

    You may be uncomfortable or feel a sting when your healthcare provider inserts the needle through your skin. You may also have minor menstrual-like cramping during the procedure. Cramps can last for a few hours afterward.

    How accurate is an amniocentesis test?

    The accuracy of amniocentesis is about 99% in detecting abnormalities. However, it doesn’t measure the severity of the condition.

    In some cases, certain factors (such as not collecting enough fluid during the test) may mean the lab can’t analyze the amniotic fluid as expected. This is not common.

    Can amniocentesis cause autism?

    No, there aren’t any studies that link autism spectrum disorder to amniocentesis.

    Results and Follow-Up

    When will I receive the amniocentesis results?

    The time it takes to receive your results will depend on what tests the lab needs to conduct on the amniotic fluid. You may hear some information from your provider as soon as three or four days after your test. Some test results may take two weeks or longer. Genetic counseling may be available to help you understand what the results mean for your pregnancy and what your options are moving forward.

    What do the results of an amniocentesis test mean?

    If amniocentesis shows that the fetus has a specific health condition, your healthcare provider may refer you to a neonatologist. Remember, amniocentesis doesn’t tell you the severity of the condition, only that a condition is present. Based on the diagnosis, a neonatologist can discuss specific treatments, surgeries, or medications. You may want to discuss what kind of care your baby needs during the first days, months or years of its life.

    Can I resume my usual activities after an amniocentesis test?

    After an amniocentesis test, you should go home and relax for the rest of the day. You can take acetaminophen for discomfort. Avoid any activity that takes a lot of physical effort, like exercise or sex. You should feel ready to get back to your routine one or two days after the procedure.

    When should I call my healthcare provider?

    After an amniocentesis, call your provider if you develop:

    • Fever.
    • Vaginal bleeding.
    • Vaginal discharge or leakage of fluid.
    • Moderate to severe abdominal pain (anything worse than mild cramps).
    • Swelling or redness where your provider inserted the needle.

    Additional Details

    Is amniocentesis worth the risk?

    Only you can determine if amniocentesis is worth the risk. Like most medical procedures, there is a small chance of complications. Your risk of complications depends on several factors. Talk with your healthcare provider about the risk amniocentesis poses to your pregnancy.

    Having amniocentesis may help you:

    • Determine the best treatment for your child as early as possible.
    • Begin planning for a child with special needs.
    • Prepare for any lifestyle changes or modifications to your home.
    • Identify support groups and resources.

    Some people decide against amniocentesis because the test results have no bearing on their decision about the pregnancy, or they don’t want to take any risks in harming the fetus.

    What is the cost of an amniocentesis test?

    The cost of amniocentesis varies and is dependent on whether or not you have health insurance. Talk to your insurance provider before the test to make sure you understand the out-of-pocket costs and what they are willing to cover. If you don’t have insurance or your plan doesn’t cover amniocentesis, you’ll have to pay for it yourself.

    What’s the difference between amniocentesis and chorionic villus sampling?

    Chorionic villus sampling (CVS) is another test to diagnose genetic conditions during pregnancy. CVS testing takes a small sample of cells from the placenta (the organ that supplies the fetus with food and oxygen). A CVS is performed earlier in pregnancy, at 10 to 13 weeks. Amniocentesis happens after 15 weeks. Additionally, amniocentesis can test for neural tube defects, but CVS can’t detect these conditions.

    Is there a less invasive test available?

    Cell-free fetal DNA testing (using the pregnant person’s blood) can detect some chromosomal abnormalities such as Down syndrome. However, genetic conditions such as cystic fibrosis can’t be diagnosed through this blood test. Amniocentesis is still the gold standard for the diagnosis of chromosomal and genetic disorders.

    A note from Cleveland Clinic

    Healthcare providers perform amniocentesis tests for different reasons. Providers typically recommend amniocentesis when they believe the potential benefits of testing outweigh the small but real risks to you and your baby. This test can provide valuable information about fetal health. But you get to make the final decision on whether having an amniocentesis test is right for you. Don’t be afraid to talk to your healthcare provider about your concerns. There is no wrong answer.

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    Last reviewed by a Cleveland Clinic medical professional on 04/01/2022.

    References

    • American Pregnancy Association. Amniocentesis. (https://americanpregnancy.org/prenatal-testing/amniocentesis/) Accessed 4/5/2022.
    • March of Dimes. Amniocentesis. (https://www.marchofdimes.org/pregnancy/amniocentesis.aspx) Accessed 4/5/2022.
    • Merck Manuals. Prenatal Diagnostic Testing. (https://www.merckmanuals.com/home/women-s-health-issues/detection-of-genetic-disorders/prenatal-diagnostic-testing#v45388368) Accessed 4/5/2022.
    • National Health Service. What happens: amniocentesis. (https://www.nhs.uk/conditions/amniocentesis/what-happens/) Accessed 4/5/2022.
    • National Library of Medicine. Amniocentesis (amniotic fluid test). (https://medlineplus.gov/lab-tests/amniocentesis-amniotic-fluid-test/) Accessed 4/5/2022.
    • Planned Parenthood. What’s amniocentesis?. (https://www.plannedparenthood.org/learn/pregnancy/prenatal-care/whats-amniocentesis) Accessed 4/5/2022.

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    What precautions should be taken after amniocentesis?

    After the test, rest at home and avoid strenuous activities for at least 24 hours, or as directed by your healthcare provider. Tell your healthcare provider if you have any of the following: Any bleeding or leaking of amniotic fluid from the needle puncture site or the vagina. Fever or chills.

    What is amniocentesis and when should a woman go in to have the procedure done?

    Amniocentesis is a prenatal procedure that your doctor may recommend you have during pregnancy. The test checks for fetal abnormalities (birth defects) such as Down syndrome, cystic fibrosis or spina bifida. In most cases, the results are normal. Amniocentesis is performed between 16 and 20 weeks into the pregnancy.

    How is the procedure of amniocentesis performed?

    During the test, a long, thin needle is inserted through your abdominal wall, guided by an ultrasound image. The needle is passed into the amniotic sac that surrounds your baby and a small sample of amniotic fluid is removed for analysis.

    What approach is used for amniocentesis?

    Amniocentesis is a diagnostic technique for withdrawing amniotic fluid from the uterine cavity using a needle via a transabdominal approach.