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Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events
Pirfenidone is currently the only approved therapy for idiopathic pulmonary fibrosis, following studies demonstrating that treatment reduces the decline in lung function and improves progression-free survival. Although generally well tolerated, a minority of patients discontinue therapy due to gastr...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003341/ https://www.ncbi.nlm.nih.gov/pubmed/24639005 http://dx.doi.org/10.1007/s12325-014-0112-1 |
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author | Costabel, Ulrich Bendstrup, Elisabeth Cottin, Vincent Dewint, Pieter Egan, Jim J. J. Ferguson, James Groves, Richard Hellström, Per M. Kreuter, Michael Maher, Toby M. Molina-Molina, Maria Nordlind, Klas Sarafidis, Alexandre Vancheri, Carlo |
author_facet | Costabel, Ulrich Bendstrup, Elisabeth Cottin, Vincent Dewint, Pieter Egan, Jim J. J. Ferguson, James Groves, Richard Hellström, Per M. Kreuter, Michael Maher, Toby M. Molina-Molina, Maria Nordlind, Klas Sarafidis, Alexandre Vancheri, Carlo |
author_sort | Costabel, Ulrich |
collection | PubMed |
description | Pirfenidone is currently the only approved therapy for idiopathic pulmonary fibrosis, following studies demonstrating that treatment reduces the decline in lung function and improves progression-free survival. Although generally well tolerated, a minority of patients discontinue therapy due to gastrointestinal and skin-related adverse events (AEs). This review summarizes recommendations based on existing guidelines, research evidence, and consensus opinions of expert authors, with the aim of providing practicing physicians with the specific clinical information needed to educate the patient and better manage pirfenidone-related AEs with continued pirfenidone treatment. The main recommendations to help prevent and/or mitigate gastrointestinal and skin-related AEs include taking pirfenidone during (or after) a meal, avoiding sun exposure, wearing protective clothing, and applying a broad-spectrum sunscreen with high ultraviolet (UV) A and UVB protection. These measures can help optimize AE management, which is key to maintaining patients on an optimal treatment dose. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12325-014-0112-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4003341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-40033412014-04-30 Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events Costabel, Ulrich Bendstrup, Elisabeth Cottin, Vincent Dewint, Pieter Egan, Jim J. J. Ferguson, James Groves, Richard Hellström, Per M. Kreuter, Michael Maher, Toby M. Molina-Molina, Maria Nordlind, Klas Sarafidis, Alexandre Vancheri, Carlo Adv Ther Review Pirfenidone is currently the only approved therapy for idiopathic pulmonary fibrosis, following studies demonstrating that treatment reduces the decline in lung function and improves progression-free survival. Although generally well tolerated, a minority of patients discontinue therapy due to gastrointestinal and skin-related adverse events (AEs). This review summarizes recommendations based on existing guidelines, research evidence, and consensus opinions of expert authors, with the aim of providing practicing physicians with the specific clinical information needed to educate the patient and better manage pirfenidone-related AEs with continued pirfenidone treatment. The main recommendations to help prevent and/or mitigate gastrointestinal and skin-related AEs include taking pirfenidone during (or after) a meal, avoiding sun exposure, wearing protective clothing, and applying a broad-spectrum sunscreen with high ultraviolet (UV) A and UVB protection. These measures can help optimize AE management, which is key to maintaining patients on an optimal treatment dose. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12325-014-0112-1) contains supplementary material, which is available to authorized users. Springer Healthcare 2014-03-18 2014 /pmc/articles/PMC4003341/ /pubmed/24639005 http://dx.doi.org/10.1007/s12325-014-0112-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Review Costabel, Ulrich Bendstrup, Elisabeth Cottin, Vincent Dewint, Pieter Egan, Jim J. J. Ferguson, James Groves, Richard Hellström, Per M. Kreuter, Michael Maher, Toby M. Molina-Molina, Maria Nordlind, Klas Sarafidis, Alexandre Vancheri, Carlo Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events |
title | Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events |
title_full | Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events |
title_fullStr | Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events |
title_full_unstemmed | Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events |
title_short | Pirfenidone in Idiopathic Pulmonary Fibrosis: Expert Panel Discussion on the Management of Drug-Related Adverse Events |
title_sort | pirfenidone in idiopathic pulmonary fibrosis: expert panel discussion on the management of drug-related adverse events |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003341/ https://www.ncbi.nlm.nih.gov/pubmed/24639005 http://dx.doi.org/10.1007/s12325-014-0112-1 |
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