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What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?

Coronary artery disease in the transplanted heart, also known as cardiac allograft vasculopathy (CAV), is one of the major causes of mortality late after transplantation. It affects up to 50% of all heart transplant recipients within 5 years of surgery. The mechanisms of CAV are multifactorial and i...

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Autor principal: Kobashigawa, Jon
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC59623/
https://www.ncbi.nlm.nih.gov/pubmed/11714434
http://dx.doi.org/10.1186/cvm-1-3-166
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author Kobashigawa, Jon
author_facet Kobashigawa, Jon
author_sort Kobashigawa, Jon
collection PubMed
description Coronary artery disease in the transplanted heart, also known as cardiac allograft vasculopathy (CAV), is one of the major causes of mortality late after transplantation. It affects up to 50% of all heart transplant recipients within 5 years of surgery. The mechanisms of CAV are multifactorial and include both immune and nonimmune factors. Ischemia of the graft at the time of transplantation is one of the more important nonimmune factors, because this leads to endothelial cell injury. Immune factors involving cellular and humoral rejection can further insult the vascular endothelial cell, leading to a cascade of immunologic responses. The optimal treatment prophylaxis for CAV has not been established. The treatment approach to this major post-transplant complication includes modification of risk factors through medical therapies and strategies. The early use of diltiazem and/or pravastatin or simvastatin has been demonstrated to be effective in reducing the development of CAV, but does not completely prevent it. There are many ongoing studies involving newer immunosuppressive agents that may hold promise for the future.
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spelling pubmed-596232001-11-06 What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy? Kobashigawa, Jon Curr Control Trials Cardiovasc Med Review Coronary artery disease in the transplanted heart, also known as cardiac allograft vasculopathy (CAV), is one of the major causes of mortality late after transplantation. It affects up to 50% of all heart transplant recipients within 5 years of surgery. The mechanisms of CAV are multifactorial and include both immune and nonimmune factors. Ischemia of the graft at the time of transplantation is one of the more important nonimmune factors, because this leads to endothelial cell injury. Immune factors involving cellular and humoral rejection can further insult the vascular endothelial cell, leading to a cascade of immunologic responses. The optimal treatment prophylaxis for CAV has not been established. The treatment approach to this major post-transplant complication includes modification of risk factors through medical therapies and strategies. The early use of diltiazem and/or pravastatin or simvastatin has been demonstrated to be effective in reducing the development of CAV, but does not completely prevent it. There are many ongoing studies involving newer immunosuppressive agents that may hold promise for the future. BioMed Central 2000 2000-12-04 /pmc/articles/PMC59623/ /pubmed/11714434 http://dx.doi.org/10.1186/cvm-1-3-166 Text en Copyright © 2000 Current Controlled Trials Ltd
spellingShingle Review
Kobashigawa, Jon
What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
title What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
title_full What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
title_fullStr What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
title_full_unstemmed What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
title_short What is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
title_sort what is the optimal prophylaxis for treatment of cardiac allograft vasculopathy?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC59623/
https://www.ncbi.nlm.nih.gov/pubmed/11714434
http://dx.doi.org/10.1186/cvm-1-3-166
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