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Acheamnimp

Published: August 9, 2026Updated: August 16, 2026

This test measures acetylcholinesterase enzyme levels in amniotic fluid to help detect certain fetal birth defects.

Quick summary

{"Measures an enzyme in the fluid surrounding the baby during pregnancy","Helps detect neural tube defects like spina bifida","Performed on a sample of amniotic fluid collected during amniocentesis","Results help doctors assess fetal development and plan appropriate care","Abnormal results may indicate the need for additional testing"}

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
76479-5
Short code
AChE Amn-Imp
Synonyms
AChE Amn-Imp
Category
chemistry
Sample
fluid
Container
Sterile tube
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Specimen volume
2-5 mL
Stability
Room temperature: 2h, Refrigerated: 24h
Hemolysis max
300
TAT
4–24 hours
Order
routine

What is this test?

The amniotic fluid acetylcholinesterase test measures the level of an enzyme called acetylcholinesterase in the amniotic fluid. Acetylcholinesterase is normally present in small amounts in amniotic fluid, but higher levels may indicate certain fetal abnormalities, particularly neural tube defects such as spina bifida (open spine) or anencephaly (absence of a major portion of the brain).

How is the test performed?

This test requires a sample of amniotic fluid, which is collected during a procedure called amniocentesis. During amniocentesis, a thin needle is inserted through the abdomen into the uterus to withdraw a small amount of amniotic fluid. The fluid sample is then sent to a laboratory for analysis. The test specifically looks at whether acetylcholinesterase is present and in what amounts.

What do the results mean?

Results are typically reported as positive or negative for the presence of acetylcholinesterase. A positive result (detecting the enzyme) may suggest an increased risk of neural tube defects, though it does not confirm a specific diagnosis. A negative result (no enzyme detected) suggests a lower risk. Your healthcare provider will interpret these results along with other test findings, ultrasound results, and your medical history to give you a complete picture.

What are the risks of the test?

The main risk of this test comes from the amniocentesis procedure used to collect the fluid sample. These risks include a small chance of infection, bleeding, cramping, or in very rare cases, miscarriage. The procedure is generally considered safe when performed by experienced healthcare providers. Discuss any concerns with your doctor before undergoing the procedure.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings2

Frequently asked questions

Why is this test done?
This test is done to help detect neural tube defects (like spina bifida) and other serious birth defects during pregnancy. It provides important information about fetal development that can help guide medical care and allow families to prepare for the needs of a baby with special requirements.
Is the test painful?
The amniocentesis procedure used to collect the fluid may cause some discomfort, similar to menstrual cramps. A local anesthetic is often used to numb the area. Most women report only mild discomfort during the procedure.
How long does it take to get results?
Results are usually available within a few days to a week, depending on the laboratory. Your healthcare provider will contact you with the results and explain what they mean for your pregnancy.
What happens if my results are abnormal?
If results show elevated acetylcholinesterase, your doctor will likely recommend additional testing, such as a detailed ultrasound (Level II ultrasound) to examine the baby's spine and brain more closely. You may also be referred to a maternal-fetal medicine specialist for further evaluation and counseling.
Can this test tell me the exact birth defect my baby has?
No, this test indicates an increased risk but cannot determine the exact type or severity of a birth defect. Further diagnostic testing, particularly detailed ultrasound imaging, is needed to confirm and characterize any abnormality.
Is this test required?
No, this test is not required. It is an optional test that your healthcare provider may recommend based on your specific situation, such as family history, previous pregnancy complications, or other risk factors. You should discuss the benefits and limitations with your doctor to decide if it's right for you.
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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 16, 2026. · Read our editorial policy