Sign in →

Test ID BLOD0198 Prostatic Acid Phosphatase, Serum

Useful For

Aiding in predicting recurrence after radical prostatectomy for clinically localized prostate cancer

 

Following response to androgen ablation therapy, when used in conjunction with prostate-specific antigen

Specimen Type

Serum


Specimen Required


Patient Preparation: For 12 hours before specimen collection, do not take multivitamins or dietary supplements containing biotin (vitamin B7), which is commonly found in hair, skin, and nail supplements and multivitamins.

Collection Container/Tube: 

Preferred: Red top

Acceptable: Serum gel

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.


Reject Due To

Gross hemolysis Reject
Gross lipemia OK

Specimen Minimum Volume

0.4 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 7 days
  Frozen  180 days

Day(s) Performed

Monday, Wednesday, Friday

Report Available

1 to 3 days

Method Name

Automated Chemiluminescent Immunometric Assay

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

84066

Reporting Name

Prostatic Acid Phosphatase, S

Reference Values

≤2.1 ng/mL

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

Secondary ID

8019
Sanford Laboratories - Sioux Falls/Rapid City Additional Information:

SANFORD LABORATORY INTERFACE BUILD INFORMATION

Result Code  Result Code Description 
3340 Prostatic Acid Phosphatase