Formal Name
First Trimester Screen [Pregnancy-associated plasma protein-A (PAPP-A), free beta human chorionic gonadotropin (hCG) as either free beta subunit or total hCG, and nuchal translucency (NT) ultrasound]
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This article waslast modified on 25 October 2018.
At a Glance
Why Get Tested?

To assess the risk of a foetus having a chromosomal abnormality, such as Down’s syndrome (trisomy 21).

When To Get Tested?

Usually between 11 and 14 weeks of pregnancy

Sample Required?

A blood sample taken from a vein in your arm. Measurement of nuchal translucency (NT) requires a special ultrasound examination to be performed.

Test Preparation Needed?

You may be requested to have a full bladder when having the nuchal translucency ultrasound performed. Having a full bladder when you attend for your scan usually makes it easier to see the baby clearly and measure the nuchal translucency.

On average it takes 7 working days for the blood test results to come back from the hospital, depending on the exact tests requested. Some specialist test results may take longer, if samples have to be sent to a reference (specialist) laboratory. The X-ray & scan results may take longer. If you are registered to use the online services of your local practice, you may be able to access your results online. Your GP practice will be able to provide specific details.

If the doctor wants to see you about the result(s), you will be offered an appointment. If you are concerned about your test results, you will need to arrange an appointment with your doctor so that all relevant information including age, ethnicity, health history, signs and symptoms, laboratory and other procedures (radiology, endoscopy, etc.), can be considered.

Lab Tests Online-UK is an educational website designed to provide patients and carers with information on laboratory tests used in medical care. We are not a laboratory and are unable to comment on an individual's health and treatment.

Reference ranges are dependent on many factors, including patient age, sex, sample population, and test method, and numeric test results can have different meanings in different laboratories.

For these reasons, you will not find reference ranges for the majority of tests described on this web site. The lab report containing your test results should include the relevant reference range for your test(s). Please consult your doctor or the laboratory that performed the test(s) to obtain the reference range if you do not have the lab report.

For more information on reference ranges, please read Reference Ranges and What They Mean.

What is being tested?

The first trimester screen is a combination of two blood tests and a special ultrasound scan that are used to assess a pregnant woman's risk of carrying a baby with Down’s syndrome (trisomy 21) or other rarer fetal anomalies like Edward’s syndrome (Trisomy 18) or Patau’s syndrome (Trisomy 13). Analysing biochemical markers together, along with the woman's age, increases both the sensitivity and specificity of the screening results.

  • Pregnancy-associated plasma protein A (PAPP-A) is a protein produced first by the outer layer of the developing pregnancy (trophoblast) and then by the growing placenta. During a normal pregnancy, levels of this protein increase in the pregnant woman's blood until delivery.
  • Human chorionic gonadotropin (hCG) is a hormone produced by the developing pregnancy and then produced in large quantities by the placenta. The Free beta subunit is used in first trimester screening. Levels usually rise rapidly in the pregnant woman's circulation for the first 8 to 10 weeks, then decrease and stabilise at a lower level for the remainder of the pregnancy.
  • Nuchal translucency is a measurement made during the ultrasound scan. The ultrasonagrapher measures the fluid collection between the spine and the skin at the nape of the foetus's neck. It is a procedure that requires a specially trained sonographer, proper alignment of the foetus, and careful measurement.

If the results of first trimester screening give cause for concern, diagnostic tests (e.g.amniocentesis or chorionic villus sampling (CVS) will be recommended.

How is the sample collected for testing?

Blood is taken from a vein in the woman's arm. The nuchal translucency ultrasound scan may be performed from outside the abdomen (transabdominally) or the probe may be inserted into the vagina (transvaginally).

Is any test preparation needed to ensure the quality of the sample?

You may be requested to have a full bladder when having the nuchal translucency ultrasound scan performed. Having a full bladder when you attend for your scan usually makes it easier to see the baby clearly and measure the nuchal translucency.

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Common Questions
  • How is it used?

    The combination of tests for PAPP-A, free beta hCG and nuchal translucency that are included in the first trimester screen are used to assess the risk that the fetus a pregnant woman is carrying has Down’s syndrome (trisomy 21), or another fetal anomaly, such Edward’s syndrome or Patau’s syndrome.

  • When is it requested?

    The test must be performed between 11 and 14 weeks of pregnancy. For women who miss this window there is the option of second trimester screening.

  • What does the test result mean?

    A mathematical calculation using the results obtained from the PAPP-A and free beta hCG blood tests, and the nuchal translucency measurement is used to determine a numeric risk of Down’s Syndrome, or other fetal anomaly, in the fetus. This risk is compared with a nationally agreed cut-off. If the risk is higher than the cut-off value (e.g., risk of 1 in 150 or higher), then it is considered that the woman may be at increased risk for having a baby with a fetal anomaly.

    In pregnancies with a Down’s syndrome fetal PAPP-A levels tend to be lower, HCG levels are tend to be high and the NT measurement is likely to be high.

    In pregnancies with an Edward’s or Pataussyndrome fetal PAPP-A and HCG levels both tend to be low and the NT measurement is likely to be high.The interpretation of these results should be provided by a healthcare professional who can explain the meaning of the results and offer choices about further testing and follow up. It is important to remember that screening tests are not diagnostic of fetal abnormalities and that screening will not detect all cases of Down’s syndrome, Edward’s syndrome or Patau’s syndrome.

    For example: while the first trimester screen can correctly identify approximately 85% of women carrying a foetus with Down’s syndrome, about 2-3% of normal pregnancies will have a false-positive result (the test result is positive, but the fetus does not have Down’s syndrome).

    If a screening test is high risk, more definitive tests are needed to confirm a diagnosis. These may include a diagnostic test such as chorionic villus sampling (CVS) in the first trimester or amniocentesis in the second trimester. While these two procedures give a definite result, they are also invasive and carry a small risk of miscarriage and a rare risk of injury to the fetus.

    Another option for further testing is Non-Invasive Prenatal Testing (NIPT), which is now widely available although not currently via the NHS.

  • Is there anything else I should know?

    Test results are very dependent on nuchal translucency techniques and the accurate determination of the gestational age of the foetus. If the gestational age of the fetus has not been accurately determined, the results may be either falsely high or low.

    In twin pregnancies it is still possible to perform first trimester combined screening using PAPP-A and hCG, although the accuracy of the test is lower.

    In triplet pregnancies it is not possible to use combined screening and risk has to be calculated using ultrasound measurements alone.

  • What is Down’s syndrome?

    About 1 in 700 babies are born with Down’s syndrome (trisomy 21) each year. The condition causes mild to moderate mental retardation and developmental problems and is associated with congenital heart defects, respiratory and hearing problems, leukaemia, and thyroid disorders. Many of the complications of Down’s syndrome can be treated and the lifespan of those affected has greatly increased in recent years. The risk of having a child with Down’s syndrome or other chromosomal abnormality increases with the age of the mother. Although the risk of having an affected baby is significantly greater in those older than 35, the majority of Down’s syndrome babies (about 80%) are born to those under 35 because this age group has the greatest number of children. For this reason, it is recommended that all pregnant women be offered a screening test for Down’s syndrome.

    See the NHS choices links below for more information on Edward’s and Patau’s syndrome.

  • Are there other non-invasive screening tests for these disorders?

    There is a newer test called Non-Invasive Prenatal Testing (NIPT) which involves analysis of cell-free fetal DNA (cffDNA) from the mothers blood..

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