Incidence of BK polyomavirus infection after kidney transplantation is independent of type of immunosuppressive therapy
Autor: | E. Achilles, S Scheidat, Nina Dietze, Bjoern Nashan, Lutz Fischer, Jun Li, Josephine Radtke, Friedrich Thaiss, Martina Koch |
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Rok vydání: | 2015 |
Předmět: |
Male
Basiliximab medicine.medical_treatment 030232 urology & nephrology 030230 surgery medicine.disease_cause Gastroenterology 0302 clinical medicine Risk Factors Germany Kidney transplantation Incidence Antibodies Monoclonal Immunosuppression Induction Chemotherapy Middle Aged BK virus Infectious Diseases Female Kidney Diseases Immunosuppressive Agents medicine.drug Adult medicine.medical_specialty Recombinant Fusion Proteins Calcineurin Inhibitors Viremia Nephropathy Maintenance Chemotherapy 03 medical and health sciences Internal medicine medicine Humans Transplantation Homologous Everolimus Aged Retrospective Studies Immunosuppression Therapy Transplantation Polyomavirus Infections business.industry Mycophenolic Acid medicine.disease Kidney Transplantation Calcineurin Tumor Virus Infections BK Virus Immunology business |
Zdroj: | Transplant infectious disease : an official journal of the Transplantation Society. 18(6) |
ISSN: | 1399-3062 |
Popis: | Background BK polyomavirus (BKV) infection and BKV nephropathy (BKVN) are risk factors for allograft function and survival. Methods We retrospectively analyzed BK viremia and BKVN in 348 patients who received a kidney transplantation donated after brain death (n = 232) or living donation (n = 116) between 2008 and 2013. 266 patients were treated with standard immunosuppression consisting of basiliximab induction, calcineurin inhibitor (CNI), and mycophenolate (MPA, n = 219) or everolimus (n = 47). 82 patients received more intense immunosuppression with lymphocyte depletion, CNI and MPA (n = 38) or everolimus (n = 44). Results BK viremia occurred in 33 (9.5%) patients in the first year and in 7 (2.0%) recipients in the second year after transplantation. BKVN occurred in 4 (1.1%) patients in the first year. Donor and recipient age, diabetes, previous transplantation, and type of transplantation (donated after brain death vs. living donation) were no risk factors (P>0.05). BK incidence did not differ depending on induction or maintenance immunosuppression. Conclusion Incidence of BK viremia is independent of recipient characteristics, type of transplantation as well as induction and maintenance immunosuppression. This article is protected by copyright. All rights reserved. |
Databáze: | OpenAIRE |
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