ARUP's Laboratory Test Directory

Alpha Fetoprotein, Total & L3 Percent : 0081208

Mnemonic: AFP L3

Methodology: Liquid-Phase Binding Immunoassay
Performed: Thu
Reported: 1-8 days
Specimen Required: Collect:  One 3 mL red or serum separator tube.

Transport:  1 mL serum at 2-8°C.  Submit specimen in an ARUP Standard Transport Tube.

Pediatric Collection/Transport:  0.5 mL serum at 2-8°C.

Remarks:  Separate serum from cells ASAP.  Avoid repeated freeze/thaw cycles.

Unacceptable Conditions:  Plasma specimens.

Stability:  After separation from cells: Ambient: 8 hours; Refrigerated: 1 week; Frozen: 3 months
Reference Interval:
 
Test Number Components Reference Interval
 Alpha Fetoprotein Total 0-15 ng/mL
 Alpha Fetoprotein L3 Percent Less than 10.0%

Interpretive Data: The Wako LiBASys method is used. Results obtained with different assay methods or kits cannot be used interchangeably. The Wako AFP-L3% assay is intended as a risk assessment test for the development of hepatocellular carcinoma in patients with chronic liver diseases. Elevated AFP-L3% values have been shown to be associated with a seven-fold increase in the risk of developing hepatocellular carcinoma within the next 21 months. Patients with elevated serum AFP-L3% should be more intensely evaluated for evidence of hepatocellular carcinoma. The result is not interpretable as a tumor marker in pregnant females.
CPT Code(s): 82107
 
 

 

 

 
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