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Alpha-Fetoprotein, Amniotic Fluid and Reflex to AchE and Fetal Hgb (NY)
Test Code17850
CPT Codes
82106<br><strong>This test code is for New York patient testing. For non-New York patient testing, use test code 232.</strong>
Includes
If the AFP MoM is >1.99, Acetylcholinesterase and Fetal Hemoglobin will be performed at an additional charge (CPT code(s): 82664, 83033).
Preferred Specimen
3 mL random amniotic fluid collected in a sterile leak-proof container
Minimum Volume
1.5 mL
Instructions
Avoid contaminating the fluid with blood.
This test is automatically performed on all Alpha-Fetoprotein amniotic fluids when the MoM is greater than 1.99.
Note: Sample may be received frozen for AFP. Once frozen, however, a chromosome study cannot be added.
This test is automatically performed on all Alpha-Fetoprotein amniotic fluids when the MoM is greater than 1.99.
Note: Sample may be received frozen for AFP. Once frozen, however, a chromosome study cannot be added.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 14 days
Refrigerated: 21 days
Frozen: 1 year
Refrigerated: 21 days
Frozen: 1 year
Methodology
Gel Electrophoresis • Radial Immunodiffusion (RID)
AFP: Chemiluminescent
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Mon-Sat; Report available: 4 days
Reference Range
See Laboratory Report
Clinical Significance
Elevated AFP concentrations in amniotic fluid provide laboratory support for the diagnosis of neural tube lesion in the fetus.