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Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management

Cytomegalovirus (CMV) and BK Polyomavirus (BKPyV) are the most common opportunistic pathogens following kidney transplantation. We evaluated 102 patients with a median age of 63 at Edward Hines VA Hospital from November 2020 to December 2022. Our primary interest was the incidence of CMV and BKPyV i...

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Autores principales: Thorndyke, Anne, Joyce, Cara, Samra, Manpreet, Cotiguala, Laura, Trotter, Christine, Aguirre, Oswaldo, Chon, W. James, Sodhi, Rupinder, Lopez-Soler, Reynold I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669083/
https://www.ncbi.nlm.nih.gov/pubmed/38002060
http://dx.doi.org/10.3390/biomedicines11113060
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author Thorndyke, Anne
Joyce, Cara
Samra, Manpreet
Cotiguala, Laura
Trotter, Christine
Aguirre, Oswaldo
Chon, W. James
Sodhi, Rupinder
Lopez-Soler, Reynold I.
author_facet Thorndyke, Anne
Joyce, Cara
Samra, Manpreet
Cotiguala, Laura
Trotter, Christine
Aguirre, Oswaldo
Chon, W. James
Sodhi, Rupinder
Lopez-Soler, Reynold I.
author_sort Thorndyke, Anne
collection PubMed
description Cytomegalovirus (CMV) and BK Polyomavirus (BKPyV) are the most common opportunistic pathogens following kidney transplantation. We evaluated 102 patients with a median age of 63 at Edward Hines VA Hospital from November 2020 to December 2022. Our primary interest was the incidence of CMV and BKPyV infections, as well as CMV and BKPyV coinfection. Secondary interests included time to infection, rejection, and graft and patient survival. There were no statistically significant differences in patient age, donor age, race, transplant type, incidence of delayed graft function, or induction in both cohorts (any infection (N = 46) vs. those without (N = 56)). There was a 36% (37/102) incidence of CMV, a 17.6% (18/102) of BKPyV and an 8.8% (9/102) incidence of coinfection. There was a decreased incidence of CMV infection in Basiliximab induction versus antithymocyte globulin (21% and 43%). CMV risk status had no effect on the incidence of CMV infection following transplant. African American recipients had a lower incidence of BKPyV infection (12% vs. 39%), yet a higher incidence was observed in those with high cPRA (50% vs. 14%). Most CMV and/or BKPyV infections occurred within the first six months post-transplant (54%). Immunosuppression management of the elderly should continually be evaluated to reduce opportunistic infections post-transplant.
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spelling pubmed-106690832023-11-15 Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management Thorndyke, Anne Joyce, Cara Samra, Manpreet Cotiguala, Laura Trotter, Christine Aguirre, Oswaldo Chon, W. James Sodhi, Rupinder Lopez-Soler, Reynold I. Biomedicines Article Cytomegalovirus (CMV) and BK Polyomavirus (BKPyV) are the most common opportunistic pathogens following kidney transplantation. We evaluated 102 patients with a median age of 63 at Edward Hines VA Hospital from November 2020 to December 2022. Our primary interest was the incidence of CMV and BKPyV infections, as well as CMV and BKPyV coinfection. Secondary interests included time to infection, rejection, and graft and patient survival. There were no statistically significant differences in patient age, donor age, race, transplant type, incidence of delayed graft function, or induction in both cohorts (any infection (N = 46) vs. those without (N = 56)). There was a 36% (37/102) incidence of CMV, a 17.6% (18/102) of BKPyV and an 8.8% (9/102) incidence of coinfection. There was a decreased incidence of CMV infection in Basiliximab induction versus antithymocyte globulin (21% and 43%). CMV risk status had no effect on the incidence of CMV infection following transplant. African American recipients had a lower incidence of BKPyV infection (12% vs. 39%), yet a higher incidence was observed in those with high cPRA (50% vs. 14%). Most CMV and/or BKPyV infections occurred within the first six months post-transplant (54%). Immunosuppression management of the elderly should continually be evaluated to reduce opportunistic infections post-transplant. MDPI 2023-11-15 /pmc/articles/PMC10669083/ /pubmed/38002060 http://dx.doi.org/10.3390/biomedicines11113060 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Thorndyke, Anne
Joyce, Cara
Samra, Manpreet
Cotiguala, Laura
Trotter, Christine
Aguirre, Oswaldo
Chon, W. James
Sodhi, Rupinder
Lopez-Soler, Reynold I.
Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management
title Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management
title_full Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management
title_fullStr Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management
title_full_unstemmed Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management
title_short Risk Factors for CMV and BK Infections in an Elderly Veteran Population Following Kidney Transplantation: Implications for Immunosuppression Induction and Management
title_sort risk factors for cmv and bk infections in an elderly veteran population following kidney transplantation: implications for immunosuppression induction and management
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669083/
https://www.ncbi.nlm.nih.gov/pubmed/38002060
http://dx.doi.org/10.3390/biomedicines11113060
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