Preferred initial screening test for prostate cancer in conjunction with digital rectal exam. Use to monitor patients for recurrence of cancer.
Quantitative Electrochemiluminescent Immunoassay
Within 24 hours
New York DOH Approval Status
Serum Separator Tube (SST) or Plasma Separator Tube (PST). Also acceptable: Plain Red, Green (Sodium or Lithium Heparin), Lavender (EDTA), or Pink (K2EDTA).
Allow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)
Grossly hemolyzed specimens. Vaginal washings.
After separation from cells: Ambient: 24 hours; Refrigerated: 3 days; Frozen: 6 months
The Roche PSA electrochemiluminescent immunoassay is used. Results obtained with different test methods or kits cannot be used interchangeably. The Roche PSA method is approved for use as an aid in the detection of prostate cancer when used in conjunction with a digital rectal exam in men age 50 and older. The Roche PSA is also indicated for the serial measurement of PSA to aid in the prognosis and management of prostate cancer patients. Elevated PSA concentrations can only suggest the presence of prostate cancer until biopsy is performed. PSA concentrations can also be elevated in benign prostatic hyperplasia or inflammatory conditions of the prostate. PSA is generally not elevated in healthy men or men with non-prostatic carcinoma.
|Component Test Code*||Component Chart Name||LOINC|
|0070121||Prostate Specific Antigen, Total||83112-3|
- Total PSA