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Management of BK-virus infection - Swedish recommendations
Tina Dalianis1, Britt-Marie Eriksson2, Marie Felldin3
1a Department of Oncology-Pathology , Karolinska Institutet , Stockholm , Sweden.
Insights
BK-virus (BKV) associated nephropathy and haemorrhagic cystitis are serious complications in transplant patients. Management strategies focus on monitoring BKV DNA for nephropathy and awareness for cystitis, with immunosuppression reduction being key for nephropathy.
Area of Science:
- Nephrology
- Virology
- Transplantation Immunology
Background:
- BK-virus (BKV) reactivation causes nephropathy (BKVAN) in kidney transplant recipients and haemorrhagic cystitis (HC) in stem cell transplant patients.
- Management guidelines for BKVAN and BKV-HC were developed by the Swedish Reference Group for Antiviral Therapy (RAV).
Purpose of the Study:
- To provide consensus-based recommendations for the management of BKVAN and BKV-HC.
- To outline diagnostic and therapeutic strategies for BKV complications in transplant patients.
Main Methods:
- Consensus discussions among experts following individual contributions.
- Review of existing literature and clinical experience.
- Development of evidence-based recommendations.
Main Results:
- High BKV serum levels indicate increased risk for BKVAN and graft failure; renal biopsy is mandatory for diagnosis.
- Monitoring BKV DNA is recommended post-kidney transplant and with unexplained creatinine rise; reducing immunosuppression is advised for BKVAN.
- BKV monitoring is not recommended for BKV-HC; awareness of risk factors (myeloablative conditioning, specific donor types) and symptomatic treatment are suggested.
Conclusions:
- Tailored immunosuppression reduction is the primary strategy for BKVAN.
- No specific therapy exists for BKVAN or BKV-HC; management relies on monitoring, risk factor awareness, and supportive care.
Abstract:
BK-virus (BKV) associated nephropathy (BKVAN) and BKV associated haemorrhagic cystitis (HC) are complications of BKV infection/reactivation in renal and allogeneic haematopoietic stem cell transplantation (HSCT) patients, respectively. The task of how to manage these diseases was given to the chair by the Swedish Reference Group for Antiviral Therapy (RAV). After individual contributions by members of the working group, consensus discussions were held in a meeting on 23 January 2018 arranged by RAV. Thereafter, the recommendations were published in Swedish on November 2018. The current translation to English has been approved by all co-authors. High BKV serum levels suggest an increased risk for BKVAN and potential graft failure. For detection of BKVAN, careful monitoring of BKV DNA levels in serum or plasma is recommended the first year after renal transplantation and when increased creatinine serum levels of unknown cause are observed. Notably, a renal biopsy is mandatory for diagnosis. To reduce the risk for progression of BKVAN, there is no specific treatment, and tailored individual decrease of immunosuppression is recommended. For BKV-HC, BKV monitoring is not recommended, since BK-viruria frequently occurs in HSCT patients and the predictive value of BKV in plasma/serum has not been determined. However, the risk for BKV-HC is higher for patients undergoing myeloablative conditioning, having an unrelated, HLA-mismatched, or a cord blood donor, and awareness of the increased risk and early intervention may benefit the patients. Also for BKV-HC, no specific therapy is available. Symptomatic treatment, e.g. forced diuresis and analgesics could be of use.
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