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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2014
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.
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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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