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Lung Transplantation for Idiopathic Pulmonary Fibrosis
Despite advances in the development of novel pharmaceutical agents to treat idiopathic pulmonary fibrosis (IPF), there are no medical therapies known to resolve fibrosis or improve lung function in IPF. Therefore, lung transplantation remains the only life-saving therapy available to treat patients...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121325/ http://dx.doi.org/10.1007/978-1-62703-682-5_18 |
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author | Lamas, Daniela J. Lederer, David J. |
author_facet | Lamas, Daniela J. Lederer, David J. |
author_sort | Lamas, Daniela J. |
collection | PubMed |
description | Despite advances in the development of novel pharmaceutical agents to treat idiopathic pulmonary fibrosis (IPF), there are no medical therapies known to resolve fibrosis or improve lung function in IPF. Therefore, lung transplantation remains the only life-saving therapy available to treat patients with IPF. However, a shortage of suitable donor organs limits the number of affected individuals who can undergo this procedure, and this shortage highlights the need to allocate donor lungs to those who are in the greatest need of a life-saving therapy yet ensure that those who undergo transplantation will have a reasonable expectation of long-term survival. Still, outcomes remain relatively poor for many patients after lung transplantation, although a sizable minority of patients can enjoy long-term survival after lung transplantation. |
format | Online Article Text |
id | pubmed-7121325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71213252020-04-06 Lung Transplantation for Idiopathic Pulmonary Fibrosis Lamas, Daniela J. Lederer, David J. Idiopathic Pulmonary Fibrosis Article Despite advances in the development of novel pharmaceutical agents to treat idiopathic pulmonary fibrosis (IPF), there are no medical therapies known to resolve fibrosis or improve lung function in IPF. Therefore, lung transplantation remains the only life-saving therapy available to treat patients with IPF. However, a shortage of suitable donor organs limits the number of affected individuals who can undergo this procedure, and this shortage highlights the need to allocate donor lungs to those who are in the greatest need of a life-saving therapy yet ensure that those who undergo transplantation will have a reasonable expectation of long-term survival. Still, outcomes remain relatively poor for many patients after lung transplantation, although a sizable minority of patients can enjoy long-term survival after lung transplantation. 2013-09-13 /pmc/articles/PMC7121325/ http://dx.doi.org/10.1007/978-1-62703-682-5_18 Text en © Springer Science+Business Media New York 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Lamas, Daniela J. Lederer, David J. Lung Transplantation for Idiopathic Pulmonary Fibrosis |
title | Lung Transplantation for Idiopathic Pulmonary Fibrosis |
title_full | Lung Transplantation for Idiopathic Pulmonary Fibrosis |
title_fullStr | Lung Transplantation for Idiopathic Pulmonary Fibrosis |
title_full_unstemmed | Lung Transplantation for Idiopathic Pulmonary Fibrosis |
title_short | Lung Transplantation for Idiopathic Pulmonary Fibrosis |
title_sort | lung transplantation for idiopathic pulmonary fibrosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121325/ http://dx.doi.org/10.1007/978-1-62703-682-5_18 |
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