Effect of the preparation method of control samples on external quality assessment results of PSA testing
Language English Country Greece Media print
Document type Journal Article
PubMed
12680253
Knihovny.cz E-resources
- MeSH
- Electrochemistry MeSH
- Immunoassay methods standards MeSH
- Immunoenzyme Techniques methods standards MeSH
- Humans MeSH
- Luminescent Measurements MeSH
- Prostate-Specific Antigen analysis blood metabolism MeSH
- Radioimmunoassay methods standards MeSH
- Reference Standards MeSH
- Reproducibility of Results MeSH
- Quality Control MeSH
- Semen chemistry metabolism MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Prostate-Specific Antigen MeSH
BACKGROUND: The control of PSA tests is included in most systems of External Quality Assessment (EQA). As part of the preparation of control samples, seminal fluid is sometimes used to increase the level of PSA. MATERIAL AND METHODS: In two separate studies, the effect of the method of preparation of control samples was evaluated. The first study, carried out under the conditions of EQA of PSA examination, assessed the results of the analysis of samples prepared using seminal fluid and samples prepared using the addition of human serum. The second study analysed two groups of samples (sera and control samples to which seminal fluid was added) using two systems (IRMA and IMMULITE). RESULTS: The fPSA/tPSA ratio in the control samples prepared using the seminal fluid is very high (over 60%) and does not correspond to the usual values. The use of these samples resulted, when compared with the samples prepared using the addition of serum, in a substantial deterioration of inter-laboratory reproducibility of the results in EQA. The differences were most obvious when the results of individual analytical systems were compared, particularly for the examination of fPSA. CONCLUSION: The use of seminal fluid for the preparation of control samples is not appropriate.