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

  1. 1Department of Urology, Wexham Park Hospital, Slough, UK
  2. 2Mediwatch Plc, Swift House, Rugby, UK
  3. 3Department of Urology, The Institute of Urology, University College London, London, UK
  4. 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.

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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 less than or equal to25 mug/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 less than or equal to25 mug/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 mug/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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