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Effect of pirfenidone on wound healing in lung transplant patients
BACKGROUND: The drug pirfenidone has been shown to slow the progression and decrease mortality of idiopathic pulmonary fibrosis (IPF). Its exact mechanism is unknown, but it likely inhibits pro-fibrotic cytokine transforming growth factor beta, a known contributor to wound healing. We evaluated whet...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001132/ https://www.ncbi.nlm.nih.gov/pubmed/29946463 http://dx.doi.org/10.1186/s40248-018-0129-4 |
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author | Mortensen, Amber Cherrier, Lauren Walia, Rajat |
author_facet | Mortensen, Amber Cherrier, Lauren Walia, Rajat |
author_sort | Mortensen, Amber |
collection | PubMed |
description | BACKGROUND: The drug pirfenidone has been shown to slow the progression and decrease mortality of idiopathic pulmonary fibrosis (IPF). Its exact mechanism is unknown, but it likely inhibits pro-fibrotic cytokine transforming growth factor beta, a known contributor to wound healing. We evaluated whether patients taking pirfenidone until lung transplantation had increased risk of impaired wound healing post-transplant. This information could determine whether pirfenidone should be discontinued prior to listing to allow for a wash-out period. METHODS: We retrospectively reviewed patients who underwent lung transplantation for pulmonary fibrosis at Norton Thoracic Institute in Phoenix, Arizona, from January 2014 to December 2015. RESULTS: We describe 18 patients who took pirfenidone up to a month before transplant. Aside from one patient who experienced sternal dehiscence due to a surgical issue, all remaining patients did well with no evidence of airway dehiscence. Each of these 17 patients had been on pirfenidone for at least 30 days; nine patients had been on pirfenidone for over 90 days. Baseline characteristics including age, sex, body mass index, renal function, liver function, glucose level, pre-transplant corticosteroid use, and post-transplant immunosuppressant therapy were similar. CONCLUSIONS: In our experience, pirfenidone may be safely continued until lung transplantation. Only one patient in our series experienced impaired wound healing related to a surgical issue, even when pirfenidone was continued until lung transplantation. We found no evidence of impaired wound healing or airway complications after lung transplantation in patients who were treated with pirfenidone before lung transplantation. |
format | Online Article Text |
id | pubmed-6001132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60011322018-06-26 Effect of pirfenidone on wound healing in lung transplant patients Mortensen, Amber Cherrier, Lauren Walia, Rajat Multidiscip Respir Med Short Report BACKGROUND: The drug pirfenidone has been shown to slow the progression and decrease mortality of idiopathic pulmonary fibrosis (IPF). Its exact mechanism is unknown, but it likely inhibits pro-fibrotic cytokine transforming growth factor beta, a known contributor to wound healing. We evaluated whether patients taking pirfenidone until lung transplantation had increased risk of impaired wound healing post-transplant. This information could determine whether pirfenidone should be discontinued prior to listing to allow for a wash-out period. METHODS: We retrospectively reviewed patients who underwent lung transplantation for pulmonary fibrosis at Norton Thoracic Institute in Phoenix, Arizona, from January 2014 to December 2015. RESULTS: We describe 18 patients who took pirfenidone up to a month before transplant. Aside from one patient who experienced sternal dehiscence due to a surgical issue, all remaining patients did well with no evidence of airway dehiscence. Each of these 17 patients had been on pirfenidone for at least 30 days; nine patients had been on pirfenidone for over 90 days. Baseline characteristics including age, sex, body mass index, renal function, liver function, glucose level, pre-transplant corticosteroid use, and post-transplant immunosuppressant therapy were similar. CONCLUSIONS: In our experience, pirfenidone may be safely continued until lung transplantation. Only one patient in our series experienced impaired wound healing related to a surgical issue, even when pirfenidone was continued until lung transplantation. We found no evidence of impaired wound healing or airway complications after lung transplantation in patients who were treated with pirfenidone before lung transplantation. BioMed Central 2018-06-14 /pmc/articles/PMC6001132/ /pubmed/29946463 http://dx.doi.org/10.1186/s40248-018-0129-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Mortensen, Amber Cherrier, Lauren Walia, Rajat Effect of pirfenidone on wound healing in lung transplant patients |
title | Effect of pirfenidone on wound healing in lung transplant patients |
title_full | Effect of pirfenidone on wound healing in lung transplant patients |
title_fullStr | Effect of pirfenidone on wound healing in lung transplant patients |
title_full_unstemmed | Effect of pirfenidone on wound healing in lung transplant patients |
title_short | Effect of pirfenidone on wound healing in lung transplant patients |
title_sort | effect of pirfenidone on wound healing in lung transplant patients |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001132/ https://www.ncbi.nlm.nih.gov/pubmed/29946463 http://dx.doi.org/10.1186/s40248-018-0129-4 |
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