Urine cytology screening for polyoma virus infection following renal transplantation: the Oxford experience

Objective: To review the first year of a monthly urine cytology screening service, introduced to identify renal transplant patients at risk of polyoma virus nephropathy (PVN), at an early, potentially treatable, stage. Methods and results: Monthly urine samples (n = 392) were received from 97/108 tr...

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Published inJournal of clinical pathology Vol. 60; no. 8; pp. 927 - 930
Main Authors Thamboo, Thomas P, Jeffery, Katie J M, Friend, Peter J, Turner, Gareth D H, Roberts, Ian S D
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and Association of Clinical Pathologists 01.08.2007
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Summary:Objective: To review the first year of a monthly urine cytology screening service, introduced to identify renal transplant patients at risk of polyoma virus nephropathy (PVN), at an early, potentially treatable, stage. Methods and results: Monthly urine samples (n = 392) were received from 97/108 transplant recipients in 2005. Of 56 patients with follow-up >6 months, 20% and 9% had significant (>10 decoy cells/cytospin) and non-significant positive cytology, respectively. The first positive urine samples occurred most commonly in the second and third month post-transplantation and patients with significantly positive samples had higher 3-month and 6-month serum creatinine levels than patients with negative urine cytology (p<0.01). Four patients with positive urine cytology had a subsequent positive plasma BK virus PCR; 3/97 patients had biopsy-proven PVN, all in the third month, 1–6 weeks after first positive urine samples. Conclusions: Significant PV viruria is common following renal transplantation with onset usually within the first 3 months. Viruria is associated with worse graft function at 3 and 6 months. The time between urine positivity and clinical PVN is short. More frequent early urine screening would be required to achieve clinical benefit.
Bibliography:local:0600927
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ark:/67375/NVC-5RJC0DFG-Q
PMID:17158638
href:jclinpath-60-927.pdf
Correspondence to:
 Ian S D Roberts
 Department of Cellular Pathology, John Radcliffe Hospital, Oxford OX3 9DU, UK; ian.roberts@orh.nhs.uk
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ISSN:0021-9746
1472-4146
DOI:10.1136/jcp.2006.042507