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Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes

BACKGROUND: While Urinary tract infections are the most common infections in kidney transplant recipients, the impact of late acute graft pyelonephritis (AGPN) on graft outcomes remains unknown. Our study was performed to more precisely evaluate the long-term impact of AGPN. METHODS: We included 905...

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Autores principales: Pacaud, Margaux, Colas, Luc, Kerleau, Clarisse, Le Borgne, Florent, Giral, Magali, Brouard, Sophie, Dantal, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998071/
https://www.ncbi.nlm.nih.gov/pubmed/35418982
http://dx.doi.org/10.3389/fimmu.2022.824425
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author Pacaud, Margaux
Colas, Luc
Kerleau, Clarisse
Le Borgne, Florent
Giral, Magali
Brouard, Sophie
Dantal, Jacques
author_facet Pacaud, Margaux
Colas, Luc
Kerleau, Clarisse
Le Borgne, Florent
Giral, Magali
Brouard, Sophie
Dantal, Jacques
author_sort Pacaud, Margaux
collection PubMed
description BACKGROUND: While Urinary tract infections are the most common infections in kidney transplant recipients, the impact of late acute graft pyelonephritis (AGPN) on graft outcomes remains unknown. Our study was performed to more precisely evaluate the long-term impact of AGPN. METHODS: We included 9052 kidney and combined kidney-pancreas recipients who underwent transplantation between 2008 and 2018 from a French multicenter cohort. The relationships between AGPN and patient and graft survival were analyzed with a time-dependent multivariate Cox model. RESULTS: The cumulative incidence of AGPN was 20.9%. A first episode of early AGPN is associated with a non-significant increase in the risk of graft failure (hazard ratio [HR], 1.27; 95% confidence interval [95% CI], 0.90 to 1.79). Though, cumulative number of AGPN episodes (HR = 1.51; 95% CI, 0.89 to 2.57 for two episodes and HR = 2.08; 95% CI, 1.17 to 3.69 for three or more episodes) is associated with an increased risk of graft failure. In contrast, when the first episode of AGPN occurred late (i.e., 6 months post transplantation), the risk of graft failure is significantly increased (HR = 2.25; 95% CI, 1.65 to 3.07), and this risk remains relatively stable with the recurrence of late AGPN episodes. The onset of late AGPN were also associated with a higher risk of patient death. CONCLUSION: This analysis shows that late AGPN and recurrent AGPN are both risk factors for a poor long-term graft outcome and mortality. Late AGPN should not be considered benign infections in post-transplantation follow-up.
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spelling pubmed-89980712022-04-12 Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes Pacaud, Margaux Colas, Luc Kerleau, Clarisse Le Borgne, Florent Giral, Magali Brouard, Sophie Dantal, Jacques Front Immunol Immunology BACKGROUND: While Urinary tract infections are the most common infections in kidney transplant recipients, the impact of late acute graft pyelonephritis (AGPN) on graft outcomes remains unknown. Our study was performed to more precisely evaluate the long-term impact of AGPN. METHODS: We included 9052 kidney and combined kidney-pancreas recipients who underwent transplantation between 2008 and 2018 from a French multicenter cohort. The relationships between AGPN and patient and graft survival were analyzed with a time-dependent multivariate Cox model. RESULTS: The cumulative incidence of AGPN was 20.9%. A first episode of early AGPN is associated with a non-significant increase in the risk of graft failure (hazard ratio [HR], 1.27; 95% confidence interval [95% CI], 0.90 to 1.79). Though, cumulative number of AGPN episodes (HR = 1.51; 95% CI, 0.89 to 2.57 for two episodes and HR = 2.08; 95% CI, 1.17 to 3.69 for three or more episodes) is associated with an increased risk of graft failure. In contrast, when the first episode of AGPN occurred late (i.e., 6 months post transplantation), the risk of graft failure is significantly increased (HR = 2.25; 95% CI, 1.65 to 3.07), and this risk remains relatively stable with the recurrence of late AGPN episodes. The onset of late AGPN were also associated with a higher risk of patient death. CONCLUSION: This analysis shows that late AGPN and recurrent AGPN are both risk factors for a poor long-term graft outcome and mortality. Late AGPN should not be considered benign infections in post-transplantation follow-up. Frontiers Media S.A. 2022-03-02 /pmc/articles/PMC8998071/ /pubmed/35418982 http://dx.doi.org/10.3389/fimmu.2022.824425 Text en Copyright © 2022 Pacaud, Colas, Kerleau, Le Borgne, Giral, Brouard and Dantal https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Pacaud, Margaux
Colas, Luc
Kerleau, Clarisse
Le Borgne, Florent
Giral, Magali
Brouard, Sophie
Dantal, Jacques
Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes
title Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes
title_full Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes
title_fullStr Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes
title_full_unstemmed Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes
title_short Impact of Late and Recurrent Acute Graft Pyelonephritis on Long-Term Kidney Graft Outcomes
title_sort impact of late and recurrent acute graft pyelonephritis on long-term kidney graft outcomes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998071/
https://www.ncbi.nlm.nih.gov/pubmed/35418982
http://dx.doi.org/10.3389/fimmu.2022.824425
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