Order Code LABAFPPT Alpha-Fetoprotein (AFP), Peritoneal Fluid
Additional Codes
Mayo Test Code: AFPPT
Reporting Name
AFP, Peritoneal FluidUseful For
An adjunct to cytology to differentiate between malignancy-related ascites and benign causes of ascites formation
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen Type
PeritonealSpecimen Required
Container/Tube: Plain, plastic, screw-top tube
Specimen Volume: 2 mL
Specimen Minimum Volume
0.5 mL (Samples <0.5 mL may be rejected)
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Peritoneal | Frozen (preferred) | 90 days | |
Ambient | 7 days | ||
Refrigerated | 7 days |
Reference Values
An interpretive report will be provided.
Day(s) Performed
Monday through Saturday
CPT Code Information
86316
Method Description
The instrument used is the Beckman Coulter UniCel DxI 800. The Beckman Coulter Access alpha-fetoprotein (AFP) immunoassay is a 2-site immunoenzymatic sandwich assay. A specimen is added to a reaction vessel with mouse monoclonal anti-AFP alkaline phosphatase conjugate, and paramagnetic particles coated with a second mouse monoclonal anti-AFP antibody. The AFP in the specimen binds to the immobilized monoclonal anti-AFP on the solid phase while, at the same time, the monoclonal anti-AFP-alkaline phosphatase conjugate reacts with different antigenic sites on the specimen AFP. After incubation in a reaction vessel, materials bound by the solid phase are held in a magnetic field while unbound materials are washed away. A chemiluminescent substrate is added to the reaction vessel, and light generated by the reaction is measured with a luminometer. The light production is directly proportional to the amount of AFP in the specimen. The amount of analyte in the specimen is determined by means of a stored multipoint calibration curve.(Package insert: Access AFP assay, Beckman Coulter Inc; 2020)
For all samples with AFP concentrations greater than 6 ng/mL, a dilution series is performed. A linear dilution excludes hooking and most major interferences. Samples that contain AFP concentrations less than or equal to 6 ng/mL are spiked with exogenous AFP to identify possible interferences that may cause a false-low result.
Reject Due To
Gross hemolysis | Reject |
Gross icterus | OK |
Method Name
Immunoenzymatic Assay
Forms
If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.