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Quadruple screen test

Quad screen; Multiple marker screening; AFP plus; Triple screen test; AFP maternal; MSAFP; 4-marker screen; Down syndrome - quadruple; Trisomy 21 - quadruple; Turner syndrome - quadruple; Spina bifida - quadruple; Tetralogy - quadruple; Duodenal atresia - quadruple; Genetic counseling - quadruple; Alpha-fetoprotein quadruple; Human chorionic gonadotropin - quadruple; hCG - quadruple; Unconjugated estriol - quadruple; uE3 - quadruple; Pregnancy - quadruple; Birth defect - quadruple; Quadruple marker test; Quad test; Quadruple marker screen

The quadruple screen test is a blood test done during pregnancy to determine whether the baby is at risk for certain birth defects.

How the Test is Performed

This test is most often done between the 15th and 22nd weeks of the pregnancy. It is most accurate between the 16th and 18th weeks.

A blood sample is taken from the pregnant woman and sent to the lab for testing.

The test measures levels of 4 pregnancy hormones:

  • Alpha-fetoprotein (AFP), a protein produced by the baby
  • Human chorionic gonadotropin (hCG), a hormone produced in the placenta
  • Unconjugated estriol (uE3), a form of the hormone estrogen produced in the fetus and the placenta
  • Inhibin A, a hormone released by the placenta

If the test does not measure levels of inhibin A, it is called the triple screen test.

To determine the chance of your baby having a birth defect, the test also factors in:

  • Your age
  • Your ethnic background
  • Your weight
  • Your baby's gestational age (measured in weeks from the day of your last period to the current date)

How to Prepare for the Test

No special steps are needed to prepare for the test. You can eat or drink normally before the test.

How the Test will Feel

You may feel slight pain or a sting when the needle is inserted. You may also feel some throbbing at the site after the blood is drawn.

Why the Test is Performed

The test is done to find out if your baby might be at risk for certain birth defects, such as Down syndrome and birth defects of the spinal column and brain (called neural tube defects). This test is a screening test, so it does not diagnose problems.

Certain women are at greater risk of having a baby with these defects, including:

  • Women who are over 35 years old during pregnancy
  • Women taking insulin to treat diabetes
  • Women with a family history of birth defects

Normal Results

Normal levels of AFP, hCG, uE3, and inhibin A.

Normal value ranges may vary slightly among different laboratories. Talk to your health care provider about the meaning of your specific test results.

What Abnormal Results Mean

An abnormal test result does NOT mean that your baby definitely has a birth defect. Often, the results can be abnormal if your baby is older or younger than your provider had thought.

If you have an abnormal result, you will have another ultrasound to check the age of the developing baby.

More tests and counseling may be recommended if the ultrasound shows a problem. However, some people choose not to have any more tests done, for personal or religious reasons. Possible next steps include:

  • Amniocentesis, which checks the AFP level in the amniotic fluid surrounding the baby. Genetic testing can be done on the amniotic fluid removed for the test.
  • Tests to check for certain birth defects (such as Down syndrome).
  • Genetic counseling.
  • Ultrasound to check the baby's brain, spinal cord, kidneys, and heart.
  • Prenatal cell-free DNA screening, which uses cell-free DNA from the placenta and the fetus in the mother's bloodstream. A normal result might help avoid needing amniocentesis.

During pregnancy, increased levels of AFP may be due to a problem with the developing baby, including:

High AFP can also mean that you are carrying more than 1 baby.

Low levels of AFP and estriol and high levels of hCG and inhibin A may be due to a problem such as:

  • Down syndrome (trisomy 21)
  • Edwards syndrome (trisomy 18)

Considerations

The quadruple screen can have false-negative and false-positive results (although it is slightly more accurate than the triple screen). More tests are needed to confirm an abnormal result.

If the test is abnormal, you may need to talk to a genetic counselor.

References

ACOG Practice Bulletin No. 162: Prenatal diagnostic testing for genetic disorders. Obstet Gynecol. 2016;127(5):e108-e122. PMID: 26938573 pubmed.ncbi.nlm.nih.gov/26938573/.

Driscoll DA, Simpson JL. Genetic screening and prenatal genetic diagnosis. In: Landon MB, Galan HL, Jauniaux ERM, et al, eds. Gabbe's Obstetrics: Normal and Problem Pregnancies. 7th ed. Philadelphia, PA: Elsevier; 2021:chap 10.

Dugoff L, Wapner RJ. Prenatal diagnosis of congenital disorders. In: Lockwood CJ, Copel JA, Dugoff L, et al, eds. Creasy and Resnik's Maternal-Fetal Medicine: Principles and Practice. 9th ed. Philadelphia, PA: Elsevier; 2023:chap 30.

Williams DE, Pridjian G. Obstetrics. In: Rakel RE, Rakel DP, eds. Textbook of Family Medicine. 9th ed. Philadelphia, PA: Elsevier; 2016:chap 20.

  • Quadruple screen

    Quadruple screen - illustration

    A blood test can be performed between the 15th and 22nd weeks of the pregnancy to determine whether the baby is at risk for certain birth defects. Blood is drawn from a vein and the sample is sent to a laboratory for testing. If the test is abnormal other tests can be performed to rule out birth defects.

    Quadruple screen

    illustration

    • Quadruple screen

      Quadruple screen - illustration

      A blood test can be performed between the 15th and 22nd weeks of the pregnancy to determine whether the baby is at risk for certain birth defects. Blood is drawn from a vein and the sample is sent to a laboratory for testing. If the test is abnormal other tests can be performed to rule out birth defects.

      Quadruple screen

      illustration

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    Review Date: 3/31/2024

    Reviewed By: LaQuita Martinez, MD, Department of Obstetrics and Gynecology, Emory Johns Creek Hospital, Alpharetta, GA. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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