BK virus: Difference between revisions
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==Diagnosis== |
==Diagnosis== |
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=== Nephropathy === |
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* Nephropathy: screening with urine or blood PCR followed by biopsy if concurrent renal dysfunction to confirm the diagnosis |
* Nephropathy: screening with urine or blood PCR followed by biopsy if concurrent renal dysfunction to confirm the diagnosis |
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* BKV Transplantation Associated Virus Infections Working Group developed a consensus definition<ref>Hannah Imlay, Paul Baum, Daniel C Brennan, Kimberly E Hanson, Michael R Hodges, Aimee C Hodowanec, Takashi E Komatsu, Per Ljungman, Veronica Miller, Yoichiro Natori, Volker Nickeleit, Jules O’Rear, Andreas Pikis, Parmjeet S Randhawa, Deirdre Sawinski, Harsharan K Singh, Gabriel Westman, Ajit P Limaye, BK Disease Definitions Working Group of the Transplantation Associated Virus Infection Forum With the Forum for Collaborative Research, Consensus Definitions of BK Polyomavirus Nephropathy in Renal Transplant Recipients for Clinical Trials, ''Clinical Infectious Diseases'', Volume 75, Issue 7, 1 October 2022, Pages 1210–1216, <nowiki>https://doi.org/10.1093/cid/ciac071</nowiki></ref> |
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** Proven: demonstration of active BKV within renal tissue by IHC for SV40 or ISH |
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** Probable: requires all of the following: |
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*** Renal biopsy not performed or inadequate specimen |
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*** Renal transplant recipient receiving immunosuppression |
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*** Renal allograft dysfunction (≥20% rise in serum creatinine from baseline) |
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*** No likely alternative process |
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*** Significant BKPyV DNAemia in plasma on repeated measurement |
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**** For well-validated assays, >4 log<sub>10</sub> copies/mL corresponds to biopsy-confirmed disease |
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=== Other === |
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* Hemorrhagic cystitis: urine PCR is relatively non-specific, although a high viral load may be supportive |
* Hemorrhagic cystitis: urine PCR is relatively non-specific, although a high viral load may be supportive |
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* Urine cytology may show decoy cells, though they are also seen in CMV and adenovirus |
* Urine cytology may show decoy cells, though they are also seen in CMV and adenovirus |
Revision as of 01:51, 7 October 2022
Background
Microbiology
- Double-stranded DNA virus in the Polyomaviridae family
Epidemiology
- Very high seroprevalence with asymptomatic infection ocurring in childhood
- Disease is seen in immunosuppressed patients, especially renal transplant recipients
- BKV nephropathy is seen in 1 to 10% of renal transplant recipients
- BKV ureteric stenosis is seen in about 3% of renal transplant recipients
- Hemorrhagic cystitis is seen in 10 to 25% of hematopoietic stem cell transplantation recipients
Clinical Manifestations
Nephropathy
- Typically a cause of nephropathy in renal transplant patients
- Onset is 10 to 13 months post-transplant, with a wide range of 6 days to 5 years
- Presents with slowly increasing creatinine levels
- Occasional hematuria and fever
Ureteral Stenosis
- Causes urinary obstruction and AKI in the donor kidney, usually without pain since it is not innervated
Hemorrhagic Cystitis
- Complicates 10 to 25% of hematopoietic stem cell transplantations, most commonly in the context of GVHD
- Symptoms include hematuria, dysuria, urinary urgency and frequency, and suprapubic pain
- Clotting hematuria can cause urinary obstruction and renal failure
Other Syndromes
- Very rarely causes encephalitis and pneumonitis
Diagnosis
Nephropathy
- Nephropathy: screening with urine or blood PCR followed by biopsy if concurrent renal dysfunction to confirm the diagnosis
- BKV Transplantation Associated Virus Infections Working Group developed a consensus definition[1]
- Proven: demonstration of active BKV within renal tissue by IHC for SV40 or ISH
- Probable: requires all of the following:
- Renal biopsy not performed or inadequate specimen
- Renal transplant recipient receiving immunosuppression
- Renal allograft dysfunction (≥20% rise in serum creatinine from baseline)
- No likely alternative process
- Significant BKPyV DNAemia in plasma on repeated measurement
- For well-validated assays, >4 log10 copies/mL corresponds to biopsy-confirmed disease
Other
- Hemorrhagic cystitis: urine PCR is relatively non-specific, although a high viral load may be supportive
- Urine cytology may show decoy cells, though they are also seen in CMV and adenovirus
Management
- There is no directed therapy
- Nephropathy is typically managed by decreasing immunosuppression, monitoring viremia for response
- Ureteral stenosis is similarly managed, but may require surgical intervention
- Hemorrhagic cystitis is managed supportively, with continuous bladder irrigation, analgesia, hydration, and transfusion of platelets or erythrocytes as needed
- Target for platelets is >50k
Prevention
- In renal transplant patients, monitor for viremia monthly after transplant, decreasing immunosuppression if positive
- ↑ Hannah Imlay, Paul Baum, Daniel C Brennan, Kimberly E Hanson, Michael R Hodges, Aimee C Hodowanec, Takashi E Komatsu, Per Ljungman, Veronica Miller, Yoichiro Natori, Volker Nickeleit, Jules O’Rear, Andreas Pikis, Parmjeet S Randhawa, Deirdre Sawinski, Harsharan K Singh, Gabriel Westman, Ajit P Limaye, BK Disease Definitions Working Group of the Transplantation Associated Virus Infection Forum With the Forum for Collaborative Research, Consensus Definitions of BK Polyomavirus Nephropathy in Renal Transplant Recipients for Clinical Trials, Clinical Infectious Diseases, Volume 75, Issue 7, 1 October 2022, Pages 1210–1216, https://doi.org/10.1093/cid/ciac071
References
- ^ Hannah Imlay, Paul Baum, Daniel C Brennan, Kimberly E Hanson, Michael R Hodges, Aimee C Hodowanec, Takashi E Komatsu, Per Ljungman, Veronica Miller, Yoichiro Natori, Volker Nickeleit, Jules O’Rear, Andreas Pikis, Parmjeet S Randhawa, Deirdre Sawinski, Harsharan K Singh, Gabriel Westman, Ajit P Limaye. Consensus Definitions of BK Polyomavirus Nephropathy in Renal Transplant Recipients for Clinical Trials. Clinical Infectious Diseases. 2022;75(7):1210-1216. doi:10.1093/cid/ciac071.