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The epidemiology of early deep vein thrombosis in kidney transplant recipients

BACKGROUND: Because kidney transplant recipients may be at increased risk for deep vein thrombosis (DVT) following transplantation, we investigated the incidence, risk factors, treatments and outcomes of early DVT among kidney transplant recipients. METHODS: An observational, single-centre cohort st...

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Autores principales: Qu, Wendi, Minkovich, Michelle, Clotea, Ioana, Famure, Olusegun, Li, Yanhong, Lee, Jason Y., Selzner, Markus, Kim, S. Joseph, Ghanekar, Anand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Impact Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069415/
https://www.ncbi.nlm.nih.gov/pubmed/37001976
http://dx.doi.org/10.1503/cjs.021821
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author Qu, Wendi
Minkovich, Michelle
Clotea, Ioana
Famure, Olusegun
Li, Yanhong
Lee, Jason Y.
Selzner, Markus
Kim, S. Joseph
Ghanekar, Anand
author_facet Qu, Wendi
Minkovich, Michelle
Clotea, Ioana
Famure, Olusegun
Li, Yanhong
Lee, Jason Y.
Selzner, Markus
Kim, S. Joseph
Ghanekar, Anand
author_sort Qu, Wendi
collection PubMed
description BACKGROUND: Because kidney transplant recipients may be at increased risk for deep vein thrombosis (DVT) following transplantation, we investigated the incidence, risk factors, treatments and outcomes of early DVT among kidney transplant recipients. METHODS: An observational, single-centre cohort study was conducted among adult kidney transplant recipients from Jan. 1, 2005, to Dec. 31, 2016 with 1-year followup. Time to DVT was assessed using the Kaplan–Meier method. Cox proportional hazards and linear regression models were used to analyze risk factors for and outcomes of DVT. RESULTS: The cumulative incidence of DVT was 4.25% at 3 months after transplant. In multivariable analysis, the use of depleting induction agents (hazard ratio [HR] 2.13, 95% confidence interval [CI] 1.05–4.35]), white recipient race (HR 1.84. 95% CI 1.08–3.12), the use of kidneys from expanded criteria donors (HR 2.13, 95% CI 1.05–4.32) and lower recipient body mass index (HR 0.95, 95% CI 0.91–1.00) increased the risk for early DVT. Peritransplant DVT prophylaxis was not associated with early DVT. Early DVT was not associated with reduced graft function, death, graft failure or first hospital readmission. CONCLUSION: Risk factors for early DVT in our cohort of kidney transplant recipients included white recipient race, use of depleting agents, lower recipient body mass index and use of expanded criteria donors. As practice patterns of donor and recipient selection in kidney transplantation evolve, the results of this study may aid in perioperative risk assessments and decision-making about the use of DVT prophylaxis.
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spelling pubmed-100694152023-04-04 The epidemiology of early deep vein thrombosis in kidney transplant recipients Qu, Wendi Minkovich, Michelle Clotea, Ioana Famure, Olusegun Li, Yanhong Lee, Jason Y. Selzner, Markus Kim, S. Joseph Ghanekar, Anand Can J Surg Research BACKGROUND: Because kidney transplant recipients may be at increased risk for deep vein thrombosis (DVT) following transplantation, we investigated the incidence, risk factors, treatments and outcomes of early DVT among kidney transplant recipients. METHODS: An observational, single-centre cohort study was conducted among adult kidney transplant recipients from Jan. 1, 2005, to Dec. 31, 2016 with 1-year followup. Time to DVT was assessed using the Kaplan–Meier method. Cox proportional hazards and linear regression models were used to analyze risk factors for and outcomes of DVT. RESULTS: The cumulative incidence of DVT was 4.25% at 3 months after transplant. In multivariable analysis, the use of depleting induction agents (hazard ratio [HR] 2.13, 95% confidence interval [CI] 1.05–4.35]), white recipient race (HR 1.84. 95% CI 1.08–3.12), the use of kidneys from expanded criteria donors (HR 2.13, 95% CI 1.05–4.32) and lower recipient body mass index (HR 0.95, 95% CI 0.91–1.00) increased the risk for early DVT. Peritransplant DVT prophylaxis was not associated with early DVT. Early DVT was not associated with reduced graft function, death, graft failure or first hospital readmission. CONCLUSION: Risk factors for early DVT in our cohort of kidney transplant recipients included white recipient race, use of depleting agents, lower recipient body mass index and use of expanded criteria donors. As practice patterns of donor and recipient selection in kidney transplantation evolve, the results of this study may aid in perioperative risk assessments and decision-making about the use of DVT prophylaxis. CMA Impact Inc. 2023-03-31 /pmc/articles/PMC10069415/ /pubmed/37001976 http://dx.doi.org/10.1503/cjs.021821 Text en © 2023 CMA Impact Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Research
Qu, Wendi
Minkovich, Michelle
Clotea, Ioana
Famure, Olusegun
Li, Yanhong
Lee, Jason Y.
Selzner, Markus
Kim, S. Joseph
Ghanekar, Anand
The epidemiology of early deep vein thrombosis in kidney transplant recipients
title The epidemiology of early deep vein thrombosis in kidney transplant recipients
title_full The epidemiology of early deep vein thrombosis in kidney transplant recipients
title_fullStr The epidemiology of early deep vein thrombosis in kidney transplant recipients
title_full_unstemmed The epidemiology of early deep vein thrombosis in kidney transplant recipients
title_short The epidemiology of early deep vein thrombosis in kidney transplant recipients
title_sort epidemiology of early deep vein thrombosis in kidney transplant recipients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069415/
https://www.ncbi.nlm.nih.gov/pubmed/37001976
http://dx.doi.org/10.1503/cjs.021821
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