Acetylcholinesterase and Fetal Hemoglobin, Amniotic Fluid
Also known as: ACETYL AF
Use
This test is used following an abnormal amniotic fluid alpha fetoprotein (AFP) result to evaluate the possibility of a fetal open neural tube defect. The presence of acetylcholinesterase and fetal hemoglobin in amniotic fluid may indicate contamination of the sample with fetal blood, which is associated with a higher risk of neural tube defects. However, a negative result typically indicates a low risk of such defects. The test aids in prenatal diagnosis and helps in medical management by providing additional information alongside clinical findings and high-resolution ultrasound imaging to detect fetal anomalies.
Special Instructions
Not provided.
Limitations
The test is a Laboratory Developed Test (LDT) performed in a CLIA-certified laboratory and has not been cleared or approved by the US FDA. Therefore, its use and performance characteristics are determined by ARUP Laboratories. Interpretation should rely on a comprehensive evaluation of clinical findings, and the presence of acetylcholinesterase might be due to fetal blood contamination, which can affect the diagnostic outcome.
Methodology
Other
Biomarkers
LOINC Codes
- 30106-9 - AChE Amn Ql
- 28067-7 - Hgb F Amn Ql
- 48767-8 - Annotation comment Imp
Result Turnaround Time
3-11 days
Related Documents
For more information, please review the documents below
Specimen
Amniotic Fluid
Volume
2 mL
Minimum Volume
1 mL
Container
ARUP standard transport tube
Storage Instructions
Ambient.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 2 months |
| Refrigerated | 4 months |
| Frozen | 3 years |
Other tests from different labs that may be relevant
