Original Article
Prostate Cancer and Prostatic Diseases (2007) 10, 270–273; doi:10.1038/sj.pcan.4500962; published online 13 March 2007
Point-of-care PSA testing: an evaluation of PSAwatch
O Karim1,2, A Rao1, M Emberton2,3, D Cochrane2, M Partridge2, P Edwards2, I Walker4 and I Davidson2
- 1Department of Urology, Wexham Park Hospital, Slough, UK
- 2Mediwatch Plc, Swift House, Rugby, UK
- 3Department of Urology, The Institute of Urology, University College London, London, UK
- 4Department of Biochemistry, Wexham Park Hospital, Slough, UK
Correspondence: Mr O Karim, Department of Urology, Wexham Park Hospital, Wexham Street, Slough, Berkshire SL2 4HL, UK. E-mail: omer.karim@mac.com
Received 13 October 2006; Revised 11 January 2007; Accepted 4 February 2007; Published online 13 March 2007.
Abstract
We present a new quantitative prostate-specific antigen (PSA) assay using a portable, point-of-care test (PSAwatch) and reader system (BioScan) for measuring PSA concentrations in the range from 0.5 to
25
g/l. Blood samples from patients (n=199) were submitted for laboratory PSA and also evaluated using PSAwatch and the BioScan system. PSA concentrations in 188 men were
25
g/l and studied. Correlation between the two methods was good (R2=0.88) with a standard error of 1.588. The regression line had a bias of -0.02 at the concentration of 4.00
g/l. This is the first report of a quantitative, portable, point-of-care PSA test and reader system. PSAwatch may reduce the number of hospital visits for patients with prostate disease.
Keywords:
PSA, point-of-care, assay, immunochromatography, quantitative
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Point-of-care PSA testing: an evaluation of PSAwatch
Prostate Cancer and Prostatic Diseases Original Article
