Prostate Specific Antigen (PSA)

Accreditation Status: UKAS Schedule of Accreditation
Date Scheme started: 1990
Clinical Applicability: Diagnosis and management of prostate carcinoma
Analytes:

Total PSA (SER/020), Free PSA (SER/030)

Each analyte is available separately

Units for Reporting: ug/L (total and free PSA) in relation to the WHO International Standard.
Samples Distributed: Liquid format. Normal and pathological human serum.
Number of Distributions per year: 12
Number of Samples per Distribution: 2
Frequency of Distributions: Every two months as outlined in the Distribution Schedule
Schedule of Analysis: Data entry is via the web for the submission of results. Data analysis commences 14 days after sample dispatch. Late returns are accepted and will contribute to the laboratory's cumulative performance statistics.
Data Analysis:

All Laboratory Trimmed Mean (ALTM) with truncation at 2SD, SD, and CV%.

Reports also show method specific statistics. Individual laboratory performance is expressed in terms of MRBIS, SDBIS, and MRVIS.

Chosen Coefficient of Variation for Prostate Specific Antigen is 6% Chosen Coefficient of Variation for Free Prostate Specific Antigen is 6%.

Performance Scoring: MRVIS
Criteria of Performance:

Laboratory performance for Total PSA and Free PSA is classified in terms of the MRVIS over a running analytical window of 12 Distributions (12 months)

  MRVIS
Ideal <50
Good 50-100
Adequate 101-200
Poor >200 or SDBIS > 200

 

Persistent Poor Performance:

Defined as being in the Poor Performance category for two or more successive Distributions