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Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis
Prediction of the risk of cardiovascular events (CVE's) is important to optimize outcomes after kidney transplantation. Aortoiliac stenosis is frequently observed during pre‐transplant screening. We hypothesized that these patients are at higher risk of post‐transplant CVE's due to the joi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285727/ https://www.ncbi.nlm.nih.gov/pubmed/34674329 http://dx.doi.org/10.1111/ctr.14515 |
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author | Babakry, Shabnam Rijkse, Elsaline Roodnat, Joke I. Bijdevaate, Diederik C. IJzermans, Jan N.M. Minnee, Robert C. |
author_facet | Babakry, Shabnam Rijkse, Elsaline Roodnat, Joke I. Bijdevaate, Diederik C. IJzermans, Jan N.M. Minnee, Robert C. |
author_sort | Babakry, Shabnam |
collection | PubMed |
description | Prediction of the risk of cardiovascular events (CVE's) is important to optimize outcomes after kidney transplantation. Aortoiliac stenosis is frequently observed during pre‐transplant screening. We hypothesized that these patients are at higher risk of post‐transplant CVE's due to the joint underlying atherosclerotic disease. Therefore, we aimed to assess whether aortoiliac stenosis was associated with post‐transplant CVE's. This retrospective, single‐center cohort study included adult kidney transplant recipients, transplanted between 2000 and 2016, with contrast‐enhanced imaging available. Aortoiliac stenosis was classified according to the Trans‐Atlantic Inter‐Society Consensus (TASC) II classification and was defined as significant in case of ≥50% lumen narrowing. The primary outcome was CVE‐free survival. Eighty‐nine of 367 patients had significant aortoiliac stenosis and were found to have worse CVE‐free survival (median CVE‐free survival: stenosis 4.5 years (95% confidence interval (CI) 2.8–6.2), controls 8.9 years (95% CI 6.8–11.0); log‐rank test P < .001). TASC II C and D lesions were independent risk factors for a post‐transplant CVE with a hazard ratio of 2.15 (95% CI 1.05–4.38) and 6.56 (95% CI 2.74–15.70), respectively. Thus, kidney transplant recipients with TASC II C and D aortoiliac stenosis require extensive cardiovascular risk management pre‐, peri,‐ and post‐transplantation. |
format | Online Article Text |
id | pubmed-9285727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92857272022-07-18 Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis Babakry, Shabnam Rijkse, Elsaline Roodnat, Joke I. Bijdevaate, Diederik C. IJzermans, Jan N.M. Minnee, Robert C. Clin Transplant Original Articles Prediction of the risk of cardiovascular events (CVE's) is important to optimize outcomes after kidney transplantation. Aortoiliac stenosis is frequently observed during pre‐transplant screening. We hypothesized that these patients are at higher risk of post‐transplant CVE's due to the joint underlying atherosclerotic disease. Therefore, we aimed to assess whether aortoiliac stenosis was associated with post‐transplant CVE's. This retrospective, single‐center cohort study included adult kidney transplant recipients, transplanted between 2000 and 2016, with contrast‐enhanced imaging available. Aortoiliac stenosis was classified according to the Trans‐Atlantic Inter‐Society Consensus (TASC) II classification and was defined as significant in case of ≥50% lumen narrowing. The primary outcome was CVE‐free survival. Eighty‐nine of 367 patients had significant aortoiliac stenosis and were found to have worse CVE‐free survival (median CVE‐free survival: stenosis 4.5 years (95% confidence interval (CI) 2.8–6.2), controls 8.9 years (95% CI 6.8–11.0); log‐rank test P < .001). TASC II C and D lesions were independent risk factors for a post‐transplant CVE with a hazard ratio of 2.15 (95% CI 1.05–4.38) and 6.56 (95% CI 2.74–15.70), respectively. Thus, kidney transplant recipients with TASC II C and D aortoiliac stenosis require extensive cardiovascular risk management pre‐, peri,‐ and post‐transplantation. John Wiley and Sons Inc. 2021-11-09 2022-01 /pmc/articles/PMC9285727/ /pubmed/34674329 http://dx.doi.org/10.1111/ctr.14515 Text en © 2021 The Authors. Clinical Transplantation published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Babakry, Shabnam Rijkse, Elsaline Roodnat, Joke I. Bijdevaate, Diederik C. IJzermans, Jan N.M. Minnee, Robert C. Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
title | Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
title_full | Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
title_fullStr | Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
title_full_unstemmed | Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
title_short | Risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
title_sort | risk of post‐transplant cardiovascular events in kidney transplant recipients with preexisting aortoiliac stenosis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285727/ https://www.ncbi.nlm.nih.gov/pubmed/34674329 http://dx.doi.org/10.1111/ctr.14515 |
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