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Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis

BACKGROUND: It is unclear whether continuing anti-fibrotic therapy until the time of lung transplant increases the risk of complications in patients with idiopathic pulmonary fibrosis. OBJECTIVES: To investigate whether the time between discontinuation of anti-fibrotic therapy and lung transplant in...

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Autores principales: Astor, Todd L., Goldberg, Hilary J., Snyder, Laurie D., Courtwright, Andrew, Hachem, Ramsey, Pena, Tahuanty, Zaffiri, Lorenzo, Criner, Gerard J., Budev, Marie M., Thaniyavarn, Tany, Leonard, Thomas B., Bender, Shaun, Barakat, Aliaa, Breeze, Janis L., LaCamera, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126649/
https://www.ncbi.nlm.nih.gov/pubmed/37073794
http://dx.doi.org/10.1177/17534666231165912
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author Astor, Todd L.
Goldberg, Hilary J.
Snyder, Laurie D.
Courtwright, Andrew
Hachem, Ramsey
Pena, Tahuanty
Zaffiri, Lorenzo
Criner, Gerard J.
Budev, Marie M.
Thaniyavarn, Tany
Leonard, Thomas B.
Bender, Shaun
Barakat, Aliaa
Breeze, Janis L.
LaCamera, Peter
author_facet Astor, Todd L.
Goldberg, Hilary J.
Snyder, Laurie D.
Courtwright, Andrew
Hachem, Ramsey
Pena, Tahuanty
Zaffiri, Lorenzo
Criner, Gerard J.
Budev, Marie M.
Thaniyavarn, Tany
Leonard, Thomas B.
Bender, Shaun
Barakat, Aliaa
Breeze, Janis L.
LaCamera, Peter
author_sort Astor, Todd L.
collection PubMed
description BACKGROUND: It is unclear whether continuing anti-fibrotic therapy until the time of lung transplant increases the risk of complications in patients with idiopathic pulmonary fibrosis. OBJECTIVES: To investigate whether the time between discontinuation of anti-fibrotic therapy and lung transplant in patients with idiopathic pulmonary fibrosis affects the risk of complications. METHODS: We assessed intra-operative and post-transplant complications among patients with idiopathic pulmonary fibrosis who underwent lung transplant and had been treated with nintedanib or pirfenidone continuously for ⩾ 90 days at listing. Patients were grouped according to whether they had a shorter (⩽ 5 medication half-lives) or longer (> 5 medication half-lives) time between discontinuation of anti-fibrotic medication and transplant. Five half-lives corresponded to 2 days for nintedanib and 1 day for pirfenidone. RESULTS: Among patients taking nintedanib (n = 107) or pirfenidone (n = 190), 211 (71.0%) had discontinued anti-fibrotic therapy ⩽ 5 medication half-lives before transplant. Anastomotic and sternal dehiscence occurred only in this group (anastomotic: 11 patients [5.2%], p = 0.031 vs patients with longer time between discontinuation of anti-fibrotic medication and transplant; sternal: 12 patients [5.7%], p = 0.024). No differences were observed in surgical wound dehiscence, length of hospital stay, or survival to discharge between groups with a shorter versus longer time between discontinuation of anti-fibrotic therapy and transplant. CONCLUSION: Anastomotic and sternal dehiscence only occurred in patients with idiopathic pulmonary fibrosis who discontinued anti-fibrotic therapy < 5 medication half-lives before transplant. The frequency of other intra-operative and post-transplant complications did not appear to differ depending on when anti-fibrotic therapy was discontinued. REGISTRATION: clinicaltrials.gov NCT04316780: https://clinicaltrials.gov/ct2/show/NCT04316780
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spelling pubmed-101266492023-04-26 Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis Astor, Todd L. Goldberg, Hilary J. Snyder, Laurie D. Courtwright, Andrew Hachem, Ramsey Pena, Tahuanty Zaffiri, Lorenzo Criner, Gerard J. Budev, Marie M. Thaniyavarn, Tany Leonard, Thomas B. Bender, Shaun Barakat, Aliaa Breeze, Janis L. LaCamera, Peter Ther Adv Respir Dis Original Research BACKGROUND: It is unclear whether continuing anti-fibrotic therapy until the time of lung transplant increases the risk of complications in patients with idiopathic pulmonary fibrosis. OBJECTIVES: To investigate whether the time between discontinuation of anti-fibrotic therapy and lung transplant in patients with idiopathic pulmonary fibrosis affects the risk of complications. METHODS: We assessed intra-operative and post-transplant complications among patients with idiopathic pulmonary fibrosis who underwent lung transplant and had been treated with nintedanib or pirfenidone continuously for ⩾ 90 days at listing. Patients were grouped according to whether they had a shorter (⩽ 5 medication half-lives) or longer (> 5 medication half-lives) time between discontinuation of anti-fibrotic medication and transplant. Five half-lives corresponded to 2 days for nintedanib and 1 day for pirfenidone. RESULTS: Among patients taking nintedanib (n = 107) or pirfenidone (n = 190), 211 (71.0%) had discontinued anti-fibrotic therapy ⩽ 5 medication half-lives before transplant. Anastomotic and sternal dehiscence occurred only in this group (anastomotic: 11 patients [5.2%], p = 0.031 vs patients with longer time between discontinuation of anti-fibrotic medication and transplant; sternal: 12 patients [5.7%], p = 0.024). No differences were observed in surgical wound dehiscence, length of hospital stay, or survival to discharge between groups with a shorter versus longer time between discontinuation of anti-fibrotic therapy and transplant. CONCLUSION: Anastomotic and sternal dehiscence only occurred in patients with idiopathic pulmonary fibrosis who discontinued anti-fibrotic therapy < 5 medication half-lives before transplant. The frequency of other intra-operative and post-transplant complications did not appear to differ depending on when anti-fibrotic therapy was discontinued. REGISTRATION: clinicaltrials.gov NCT04316780: https://clinicaltrials.gov/ct2/show/NCT04316780 SAGE Publications 2023-04-19 /pmc/articles/PMC10126649/ /pubmed/37073794 http://dx.doi.org/10.1177/17534666231165912 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Astor, Todd L.
Goldberg, Hilary J.
Snyder, Laurie D.
Courtwright, Andrew
Hachem, Ramsey
Pena, Tahuanty
Zaffiri, Lorenzo
Criner, Gerard J.
Budev, Marie M.
Thaniyavarn, Tany
Leonard, Thomas B.
Bender, Shaun
Barakat, Aliaa
Breeze, Janis L.
LaCamera, Peter
Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
title Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
title_full Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
title_fullStr Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
title_full_unstemmed Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
title_short Anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
title_sort anti-fibrotic therapy and lung transplant outcomes in patients with idiopathic pulmonary fibrosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126649/
https://www.ncbi.nlm.nih.gov/pubmed/37073794
http://dx.doi.org/10.1177/17534666231165912
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