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Lung transplantation for acute respiratory distress syndrome: A multicenter experience
Acute respiratory distress syndrome (ARDS) is a rapidly progressive lung disease with a high mortality rate. Although lung transplantation (LTx) is a well‐established treatment for a variety of chronic pulmonary diseases, LTx for acute lung failure (due to ARDS) remains controversial. We reviewed po...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441742/ https://www.ncbi.nlm.nih.gov/pubmed/34254423 http://dx.doi.org/10.1111/ajt.16759 |
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author | Frick, Anna E. Gan, Christiaan T. Vos, Robin Schwarz, Stefan Kraft, Felix Kifjak, Daria Neyrinck, Arne P. Van Raemdonck, Dirk E. Klepetko, Walter Jaksch, Peter Verschuuren, Erik A. M. Hoetzenecker, Konrad |
author_facet | Frick, Anna E. Gan, Christiaan T. Vos, Robin Schwarz, Stefan Kraft, Felix Kifjak, Daria Neyrinck, Arne P. Van Raemdonck, Dirk E. Klepetko, Walter Jaksch, Peter Verschuuren, Erik A. M. Hoetzenecker, Konrad |
author_sort | Frick, Anna E. |
collection | PubMed |
description | Acute respiratory distress syndrome (ARDS) is a rapidly progressive lung disease with a high mortality rate. Although lung transplantation (LTx) is a well‐established treatment for a variety of chronic pulmonary diseases, LTx for acute lung failure (due to ARDS) remains controversial. We reviewed posttransplant outcome of ARDS patients from three high‐volume European transplant centers. Demographics and clinical data were collected and analyzed. Viral infection was the main reason for ARDS (n = 7/13, 53.8%). All patients were admitted to ICU and required mechanical ventilation, 11/13 were supported with ECMO at the time of listing. They were granted a median LAS of 76 (IQR 50–85) and waited for a median of 3 days (IQR 1.5–14). Postoperatively, median length of mechanical ventilation was 33 days (IQR 17–52.5), median length of ICU and hospital stay were 39 days (IQR 19.5–58.5) and 54 days (IQR 43.5–127). Prolongation of peripheral postoperative ECMO was required in 7/13 (53.8%) patients with a median duration of 2 days (IQR 2–7). 30‐day mortality was 7.7%, 1 and 5‐year survival rates were calculated as 71.6% and 54.2%, respectively. Given the lack of alternative treatment options, the herein presented results support the concept of offering live‐saving LTx to carefully selected ARDS patients. |
format | Online Article Text |
id | pubmed-8441742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84417422021-09-15 Lung transplantation for acute respiratory distress syndrome: A multicenter experience Frick, Anna E. Gan, Christiaan T. Vos, Robin Schwarz, Stefan Kraft, Felix Kifjak, Daria Neyrinck, Arne P. Van Raemdonck, Dirk E. Klepetko, Walter Jaksch, Peter Verschuuren, Erik A. M. Hoetzenecker, Konrad Am J Transplant ORIGINAL ARTICLES Acute respiratory distress syndrome (ARDS) is a rapidly progressive lung disease with a high mortality rate. Although lung transplantation (LTx) is a well‐established treatment for a variety of chronic pulmonary diseases, LTx for acute lung failure (due to ARDS) remains controversial. We reviewed posttransplant outcome of ARDS patients from three high‐volume European transplant centers. Demographics and clinical data were collected and analyzed. Viral infection was the main reason for ARDS (n = 7/13, 53.8%). All patients were admitted to ICU and required mechanical ventilation, 11/13 were supported with ECMO at the time of listing. They were granted a median LAS of 76 (IQR 50–85) and waited for a median of 3 days (IQR 1.5–14). Postoperatively, median length of mechanical ventilation was 33 days (IQR 17–52.5), median length of ICU and hospital stay were 39 days (IQR 19.5–58.5) and 54 days (IQR 43.5–127). Prolongation of peripheral postoperative ECMO was required in 7/13 (53.8%) patients with a median duration of 2 days (IQR 2–7). 30‐day mortality was 7.7%, 1 and 5‐year survival rates were calculated as 71.6% and 54.2%, respectively. Given the lack of alternative treatment options, the herein presented results support the concept of offering live‐saving LTx to carefully selected ARDS patients. John Wiley and Sons Inc. 2021-07-24 2022-01 /pmc/articles/PMC8441742/ /pubmed/34254423 http://dx.doi.org/10.1111/ajt.16759 Text en © 2021 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ORIGINAL ARTICLES Frick, Anna E. Gan, Christiaan T. Vos, Robin Schwarz, Stefan Kraft, Felix Kifjak, Daria Neyrinck, Arne P. Van Raemdonck, Dirk E. Klepetko, Walter Jaksch, Peter Verschuuren, Erik A. M. Hoetzenecker, Konrad Lung transplantation for acute respiratory distress syndrome: A multicenter experience |
title | Lung transplantation for acute respiratory distress syndrome: A multicenter experience |
title_full | Lung transplantation for acute respiratory distress syndrome: A multicenter experience |
title_fullStr | Lung transplantation for acute respiratory distress syndrome: A multicenter experience |
title_full_unstemmed | Lung transplantation for acute respiratory distress syndrome: A multicenter experience |
title_short | Lung transplantation for acute respiratory distress syndrome: A multicenter experience |
title_sort | lung transplantation for acute respiratory distress syndrome: a multicenter experience |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441742/ https://www.ncbi.nlm.nih.gov/pubmed/34254423 http://dx.doi.org/10.1111/ajt.16759 |
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