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Understanding Your Medical Test: What Patients Should Know About Testing, Results, and Follow-Up Care

Published: August 9, 2026Updated: August 17, 2026

A blood test done during pregnancy to screen for potential genetic and developmental conditions in the fetus.

Quick summary

{"Screens for chromosomal conditions like Down syndrome and Edwards syndrome","Checks for neural tube defects and abdominal wall defects in the baby","Performed between 15-20 weeks of pregnancy","Results indicate risk level, not a definitive diagnosis","Often combined with first trimester screening for greater accuracy"}

Medically reviewed by WellAlly Editorial TeamLast reviewed August 17, 2026Editorial policy

Key facts at a glance

LOINC
49032-6
Short code
2nd trimester 5 screen SerPl-Imp
Synonyms
2nd trimester 5 screen SerPl-Imp
Category
chemistry
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Ref low
0
Ref high
17
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Specimen volume
5 mL
Stability
Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
4–24 hours
Order
routine

This test is a medical examination that your healthcare provider may order to gather important information about your health. It can help detect a medical condition, confirm or rule out a diagnosis, or measure how well a part of your body is working. Knowing the purpose of the test can help you feel more prepared and confident on the day of your appointment.

The Second Trimester Penta Maternal Screen is a blood test that measures five substances (markers) in a pregnant woman's blood: alpha-fetoprotein (AFP), human chorionic gonadotropin (hCG), estriol (uE3), inhibin A, and sometimes pregnancy-associated plasma protein-A (PAPP-A). These markers are produced by the placenta and the baby and can indicate whether there may be certain developmental or genetic conditions.

Your doctor may recommend this test for several reasons. It can be used to investigate symptoms you have been experiencing, such as pain, fatigue, or unexplained changes in your body. It may also be part of a routine screening to catch problems early, or a way to monitor an ongoing condition and check whether your current treatment plan is working as expected.

This screening test helps identify pregnancies at higher risk for: Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), neural tube defects (such as spina bifida), and abdominal wall defects. It does not diagnose these conditions but shows if further testing is recommended.

The exact procedure depends on the type of test being done, but most tests are quick and well tolerated. A trained healthcare professional will explain each step before starting. You may be asked to give a small sample, such as blood or urine, or to lie still while imaging equipment takes pictures. You might feel brief discomfort, such as a quick pinch, but serious pain is uncommon.

A healthcare provider will draw a small blood sample from your arm. The sample is sent to a laboratory for analysis. The test is typically done between 15 and 20 weeks of pregnancy. Results are usually available within a few days.

Your results will be compared with standard reference ranges that show what is typical for healthy people. A result within the normal range is generally reassuring, while an abnormal value does not automatically mean you are seriously ill. Many factors, including medications, diet, and stress, can affect the numbers, so your healthcare provider will review the full picture and explain what your specific results mean.

Results are reported as a risk assessment (such as 1 in 1,000 or 1 in 100). A 'screen positive' result means there is a higher risk, but does not confirm a problem. A 'screen negative' result means the risk is low, but does not guarantee a healthy baby. Your healthcare provider will explain what your specific results mean for your pregnancy.

After the test is complete, you can usually return to your normal activities right away, unless your provider gives you different instructions. The sample or images will be analyzed, and the results are typically sent to your doctor within a few days. If anything needs further attention, the office will contact you to schedule a follow-up visit or discuss the next steps in your care.

If results show increased risk, your doctor may recommend additional testing such as a detailed ultrasound, amniocentesis, or cell-free DNA testing for more definitive answers. The decision to pursue further testing is personal and should be discussed with your healthcare provider.

Reference range

NCBI: NSE 0-17 ng/mLN/A

Specimen: serum

No special preparation usually required. Stay well hydrated. Inform your healthcare provider of all medications and supplements you are taking.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Frequently asked questions

Does a positive result mean my baby definitely has a problem?
No. A positive screening result means your baby has a higher risk of certain conditions, but it does not provide a definitive diagnosis. Only about 1 in 50 women with a positive screen actually have an affected pregnancy. Further diagnostic testing is needed to confirm.
Can I eat or drink before this test?
Yes, you can eat and drink normally before this test. No special preparation is required.
How accurate is this test?
The detection rate varies by condition: approximately 80% for neural tube defects, 60-80% for Down syndrome, and 60-70% for Edwards syndrome. The false positive rate is around 5%. Accuracy improves when combined with first trimester screening results.
Is this test safe for my baby?
Yes, this is a simple blood test with no risk to the pregnancy. It only requires a small blood sample from the mother.
What if I don't want to know the results?
Screening is optional. You have the right to decline any testing. Discuss your preferences with your healthcare provider to make an informed decision that aligns with your values and beliefs.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 17, 2026. · Read our editorial policy