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Quad Screen / Triple Screen | Pregnancy Power Hour
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Prenatal Test · screening

Quad Screen / Triple Screen

Optionalweeks 15–22 (optimal 16–18)

The Quad Screen, also known as the Triple Screen, is an optional second-trimester blood test that helps estimate the risk for certain chromosomal conditions and neural tube defects.

3 min read

Quick answer

The Quad Screen, also known as the Triple Screen, is an optional second-trimester blood test that helps estimate the risk for certain chromosomal conditions and neural tube defects.

On this page
  1. What it is
  2. When and how it happens
  3. What the results mean
  4. Questions worth asking

The Quad Screen, sometimes referred to as the Triple Screen or maternal serum screening, is a second-trimester blood test that offers insights into the estimated risk for specific genetic conditions and neural tube defects. It's an optional screening tool that can provide you with more information as you navigate your pregnancy.

What it is

This screening measures the levels of four specific markers in your blood: alpha-fetoprotein (AFP), human chorionic gonadotropin (hCG), unconjugated estriol, and inhibin-A. These four markers, when analyzed together, help estimate the likelihood of your baby having certain conditions. Specifically, the Quad Screen is designed to assess the risk for Down syndrome (Trisomy 21), Trisomy 18, and neural tube defects.

While newer screening options like NIPT (Non-Invasive Prenatal Testing) have largely become the preferred method for Down syndrome screening due to their higher detection rates, the Quad Screen still plays a valuable role. It's particularly useful for screening for neural tube defects, such as spina bifida, where a high AFP level can be an indicator. For some, it might also be a more accessible option if NIPT is not covered by insurance, as it is generally less expensive.

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When and how it happens

The Quad Screen is typically performed during the second trimester of pregnancy, specifically between weeks 15 and 22, with optimal accuracy often achieved between weeks 16 and 18. It involves a simple blood draw, much like other routine prenatal labs. The most crucial factor for accurate interpretation of the results is precise dating of your pregnancy. This is why an early Dating Ultrasound is so important, as it helps ensure the test results are evaluated against the correct gestational age.

This test is a screening, not a diagnostic tool. This means it can identify pregnancies that have a higher chance of certain conditions, but it cannot definitively diagnose them. Thinking about this test, much like considering a Nuchal Translucency (NT) Scan in the first trimester, is about gathering information to help you make informed decisions about your care.

What the results mean

If your Quad Screen results indicate a higher estimated risk for one of the conditions, it doesn't mean your baby definitely has that condition. Instead, it suggests that further investigation might be helpful. An abnormal result typically leads to a recommendation for a more detailed ultrasound, often called an Anatomy Scan, to look for specific markers or physical findings. In some cases, your provider might discuss diagnostic tests like Amniocentesis, which can provide a definitive diagnosis.

It's important to remember that this test has a detection rate for Down syndrome of approximately 80%. This means it identifies about 8 out of 10 pregnancies with Down syndrome, but it also means some cases might be missed, and some elevated risks might not lead to a diagnosis. Understanding these nuances can help you approach your results with a calm and clear perspective. Your provider is your best resource for your specific situation and for interpreting your individual results.

Questions worth asking

As you consider or receive results from your Quad Screen, you get to decide what information feels most helpful for you. Asking questions can empower you to feel more confident in your choices. One option might be to ask:

  • "Given my personal history and other screenings, is the Quad Screen the most appropriate option for me, or are there others we should consider?"
  • "If my results come back as 'high risk,' what are the exact next steps we would take, and what are the pros and cons of those diagnostic options?"
  • "How does the accuracy of this test compare to other available screenings for my specific situation?"
  • "What support is available if we receive an unexpected result, and what resources can help us understand our options?"

Remember, every decision about prenatal testing is a personal one, and you have the autonomy to choose the path that feels right for you and your family.

Common questions

What is the Quad Screen?+

It's a second-trimester blood test measuring four markers (AFP, hCG, estriol, inhibin-A) to estimate risk for Down syndrome, Trisomy 18, and neural tube defects. It's an optional screening.

When is the Quad Screen performed?+

It's typically done between weeks 15 and 22 of pregnancy, with optimal results often obtained between weeks 16 and 18. Accurate dating is crucial for correct interpretation.

Brittany Nance

“Pregnancy is under-supported at every week. This is the kind of clear, calm guidance I give my one-on-one clients — and the questions worth taking back to your provider.”

Brittany Nance · Pregnancy Wellness Consultant · full-spectrum doula

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Written by Brittany Nance, Pregnancy Wellness Consultant· BADT Full Spectrum Doula · Founder, Pregnancy Power Hour
Last reviewed July 1, 2026

This is evidence-informed education from a birth-doula perspective, not medical advice. Always discuss your individual situation with your prenatal care provider.

On this page

  1. What it is
  2. When and how it happens
  3. What the results mean
  4. Questions worth asking

Keep reading

  • RelatedNuchal Translucency (NT) ScanThe Nuchal Translucency (NT) scan is an optional first-trimester ultrasound that, combined with blood tests, estimates the risk of certain chromosomal conditions and structural concerns.
  • RelatedNIPT — Cell-Free DNA ScreeningNIPT, or cell-free DNA screening, is an optional blood test available from 10 weeks of pregnancy that screens for certain chromosomal conditions and can determine fetal sex.
  • RelatedAmniocentesisAmniocentesis is an optional diagnostic test performed in the second trimester to provide definitive information about your baby's chromosomes, neural tube development, and potential infections.
  • RelatedGlucose Challenge Test (1-hour)The 1-hour glucose challenge test is a common screening in the second trimester to check for gestational diabetes, typically done between weeks 24 and 28.
  • RelatedCVS — Chorionic Villus SamplingChorionic Villus Sampling (CVS) is an optional diagnostic test performed between weeks 10 and 13 to provide definitive information about your baby's chromosomes by sampling placental tissue.
  • RelatedPreeclampsia Screening (PE Risk Assessment)Preeclampsia risk evaluation is a routine part of your prenatal care, combining blood pressure and urine checks with early assessments to identify potential risks.