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Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”

Occlusion of the renal arteries can threaten the viability of the kidney when severe, in addition to accelerating hypertension and circulatory congestion. Renal artery stenting procedures have evolved from a treatment mainly for renovascular hypertension to a maneuver capable of recovering threatene...

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Autores principales: Textor, Stephen C., Misra, Sanjay, Oderich, Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532568/
https://www.ncbi.nlm.nih.gov/pubmed/23151953
http://dx.doi.org/10.1038/ki.2012.363
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author Textor, Stephen C.
Misra, Sanjay
Oderich, Gustavo
author_facet Textor, Stephen C.
Misra, Sanjay
Oderich, Gustavo
author_sort Textor, Stephen C.
collection PubMed
description Occlusion of the renal arteries can threaten the viability of the kidney when severe, in addition to accelerating hypertension and circulatory congestion. Renal artery stenting procedures have evolved from a treatment mainly for renovascular hypertension to a maneuver capable of recovering threatened renal function in patients with “ischemic nephropathy” and improving management of congestive heart failure. Improved catheter design and techniques have reduced, but not eliminated hazards associated with renovascular stenting. Expanded use of endovascular stent grafts to treat abdominal aortic aneurysms has introduced a new indication for renal artery stenting to protect the renal circulation when grafts cross the origins of the renal arteries. Although controversial, prospective randomized trials to evaluate the added benefit of revascularization to current medical therapy for atherosclerotic renal artery stenosis until now have failed to identify major benefits regarding either renal function or blood pressure control. These studies have been limited by selection bias and have been harshly criticized. While studies of tissue oxygenation using blood oxygen level dependent (BOLD) MR establish that kidneys can adapt to reduced blood flow to some degree, more severe occlusive disease leads to cortical hypoxia associated with microvascular rarefication, inflammatory injury and fibrosis. Current research is directed toward identifying pathways of irreversible kidney injury due to vascular occlusion and to increase the potential for renal repair after restoring renal artery patency. The role of nephrologists likely will focus upon recognizing the limits of renal adaptation to vascular disease and identifying kidneys truly at risk for ischemic injury at a time point when renal revascularization can still be of benefit to recovering kidney function.
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spelling pubmed-35325682013-07-01 Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future” Textor, Stephen C. Misra, Sanjay Oderich, Gustavo Kidney Int Article Occlusion of the renal arteries can threaten the viability of the kidney when severe, in addition to accelerating hypertension and circulatory congestion. Renal artery stenting procedures have evolved from a treatment mainly for renovascular hypertension to a maneuver capable of recovering threatened renal function in patients with “ischemic nephropathy” and improving management of congestive heart failure. Improved catheter design and techniques have reduced, but not eliminated hazards associated with renovascular stenting. Expanded use of endovascular stent grafts to treat abdominal aortic aneurysms has introduced a new indication for renal artery stenting to protect the renal circulation when grafts cross the origins of the renal arteries. Although controversial, prospective randomized trials to evaluate the added benefit of revascularization to current medical therapy for atherosclerotic renal artery stenosis until now have failed to identify major benefits regarding either renal function or blood pressure control. These studies have been limited by selection bias and have been harshly criticized. While studies of tissue oxygenation using blood oxygen level dependent (BOLD) MR establish that kidneys can adapt to reduced blood flow to some degree, more severe occlusive disease leads to cortical hypoxia associated with microvascular rarefication, inflammatory injury and fibrosis. Current research is directed toward identifying pathways of irreversible kidney injury due to vascular occlusion and to increase the potential for renal repair after restoring renal artery patency. The role of nephrologists likely will focus upon recognizing the limits of renal adaptation to vascular disease and identifying kidneys truly at risk for ischemic injury at a time point when renal revascularization can still be of benefit to recovering kidney function. 2012-11-14 2013-01 /pmc/articles/PMC3532568/ /pubmed/23151953 http://dx.doi.org/10.1038/ki.2012.363 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Textor, Stephen C.
Misra, Sanjay
Oderich, Gustavo
Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”
title Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”
title_full Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”
title_fullStr Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”
title_full_unstemmed Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”
title_short Invited Review: “Percutaneous revascularization for ischemic nephropathy: Past, Present and Future”
title_sort invited review: “percutaneous revascularization for ischemic nephropathy: past, present and future”
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532568/
https://www.ncbi.nlm.nih.gov/pubmed/23151953
http://dx.doi.org/10.1038/ki.2012.363
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