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Advanced pulmonary arterial hypertension: mechanical support and lung transplantation

The development of targeted therapies has transformed the outlook for patients with pulmonary arterial hypertension (PAH); however, some patients fail to achieve an adequate clinical response despite receiving maximal treatment. For these patients, lung transplantation remains an important therapeut...

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Detalles Bibliográficos
Autores principales: Bartolome, Sonja, Hoeper, Marius M., Klepetko, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488526/
https://www.ncbi.nlm.nih.gov/pubmed/29263172
http://dx.doi.org/10.1183/16000617.0089-2017
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author Bartolome, Sonja
Hoeper, Marius M.
Klepetko, Walter
author_facet Bartolome, Sonja
Hoeper, Marius M.
Klepetko, Walter
author_sort Bartolome, Sonja
collection PubMed
description The development of targeted therapies has transformed the outlook for patients with pulmonary arterial hypertension (PAH); however, some patients fail to achieve an adequate clinical response despite receiving maximal treatment. For these patients, lung transplantation remains an important therapeutic option, and recommendations for transplantation are included in the current European Society of Cardiology/European Respiratory Society guidelines for the diagnosis and treatment of pulmonary hypertension. Although lung transplantation is not without risk, overall long-term survival rates are good and substantial improvements in quality of life have been reported for lung transplant recipients. In this review, we describe the important considerations prior to, during and after transplantation, including the role of mechanical support, in patients with advanced PAH.
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spelling pubmed-94885262022-11-14 Advanced pulmonary arterial hypertension: mechanical support and lung transplantation Bartolome, Sonja Hoeper, Marius M. Klepetko, Walter Eur Respir Rev Review The development of targeted therapies has transformed the outlook for patients with pulmonary arterial hypertension (PAH); however, some patients fail to achieve an adequate clinical response despite receiving maximal treatment. For these patients, lung transplantation remains an important therapeutic option, and recommendations for transplantation are included in the current European Society of Cardiology/European Respiratory Society guidelines for the diagnosis and treatment of pulmonary hypertension. Although lung transplantation is not without risk, overall long-term survival rates are good and substantial improvements in quality of life have been reported for lung transplant recipients. In this review, we describe the important considerations prior to, during and after transplantation, including the role of mechanical support, in patients with advanced PAH. European Respiratory Society 2017-12-20 /pmc/articles/PMC9488526/ /pubmed/29263172 http://dx.doi.org/10.1183/16000617.0089-2017 Text en Copyright ©ERS 2017. https://creativecommons.org/licenses/by-nc/4.0/ERR articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle Review
Bartolome, Sonja
Hoeper, Marius M.
Klepetko, Walter
Advanced pulmonary arterial hypertension: mechanical support and lung transplantation
title Advanced pulmonary arterial hypertension: mechanical support and lung transplantation
title_full Advanced pulmonary arterial hypertension: mechanical support and lung transplantation
title_fullStr Advanced pulmonary arterial hypertension: mechanical support and lung transplantation
title_full_unstemmed Advanced pulmonary arterial hypertension: mechanical support and lung transplantation
title_short Advanced pulmonary arterial hypertension: mechanical support and lung transplantation
title_sort advanced pulmonary arterial hypertension: mechanical support and lung transplantation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9488526/
https://www.ncbi.nlm.nih.gov/pubmed/29263172
http://dx.doi.org/10.1183/16000617.0089-2017
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