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A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome
Primary graft dysfunction (PGD) is the clinical syndrome of acute lung injury after lung transplantation (LTx). However, PGD is an umbrella term that encompasses the ongoing pathophysiological and -biological mechanisms occurring in the lung grafts. Therefore, we aim to provide a focused review on t...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870290/ https://www.ncbi.nlm.nih.gov/pubmed/35203392 http://dx.doi.org/10.3390/cells11040745 |
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author | Van Slambrouck, Jan Van Raemdonck, Dirk Vos, Robin Vanluyten, Cedric Vanstapel, Arno Prisciandaro, Elena Willems, Lynn Orlitová, Michaela Kaes, Janne Jin, Xin Jansen, Yanina Verleden, Geert M. Neyrinck, Arne P. Vanaudenaerde, Bart M. Ceulemans, Laurens J. |
author_facet | Van Slambrouck, Jan Van Raemdonck, Dirk Vos, Robin Vanluyten, Cedric Vanstapel, Arno Prisciandaro, Elena Willems, Lynn Orlitová, Michaela Kaes, Janne Jin, Xin Jansen, Yanina Verleden, Geert M. Neyrinck, Arne P. Vanaudenaerde, Bart M. Ceulemans, Laurens J. |
author_sort | Van Slambrouck, Jan |
collection | PubMed |
description | Primary graft dysfunction (PGD) is the clinical syndrome of acute lung injury after lung transplantation (LTx). However, PGD is an umbrella term that encompasses the ongoing pathophysiological and -biological mechanisms occurring in the lung grafts. Therefore, we aim to provide a focused review on the clinical, physiological, radiological, histological and cellular level of PGD. PGD is graded based on hypoxemia and chest X-ray (CXR) infiltrates. High-grade PGD is associated with inferior outcome after LTx. Lung edema is the main characteristic of PGD and alters pulmonary compliance, gas exchange and circulation. A conventional CXR provides a rough estimate of lung edema, while a chest computed tomography (CT) results in a more in-depth analysis. Macroscopically, interstitial and alveolar edema can be distinguished below the visceral lung surface. On the histological level, PGD correlates to a pattern of diffuse alveolar damage (DAD). At the cellular level, ischemia-reperfusion injury (IRI) is the main trigger for the disruption of the endothelial-epithelial alveolar barrier and inflammatory cascade. The multilevel approach integrating all PGD-related aspects results in a better understanding of acute lung failure after LTx, providing novel insights for future therapies. |
format | Online Article Text |
id | pubmed-8870290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88702902022-02-25 A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome Van Slambrouck, Jan Van Raemdonck, Dirk Vos, Robin Vanluyten, Cedric Vanstapel, Arno Prisciandaro, Elena Willems, Lynn Orlitová, Michaela Kaes, Janne Jin, Xin Jansen, Yanina Verleden, Geert M. Neyrinck, Arne P. Vanaudenaerde, Bart M. Ceulemans, Laurens J. Cells Review Primary graft dysfunction (PGD) is the clinical syndrome of acute lung injury after lung transplantation (LTx). However, PGD is an umbrella term that encompasses the ongoing pathophysiological and -biological mechanisms occurring in the lung grafts. Therefore, we aim to provide a focused review on the clinical, physiological, radiological, histological and cellular level of PGD. PGD is graded based on hypoxemia and chest X-ray (CXR) infiltrates. High-grade PGD is associated with inferior outcome after LTx. Lung edema is the main characteristic of PGD and alters pulmonary compliance, gas exchange and circulation. A conventional CXR provides a rough estimate of lung edema, while a chest computed tomography (CT) results in a more in-depth analysis. Macroscopically, interstitial and alveolar edema can be distinguished below the visceral lung surface. On the histological level, PGD correlates to a pattern of diffuse alveolar damage (DAD). At the cellular level, ischemia-reperfusion injury (IRI) is the main trigger for the disruption of the endothelial-epithelial alveolar barrier and inflammatory cascade. The multilevel approach integrating all PGD-related aspects results in a better understanding of acute lung failure after LTx, providing novel insights for future therapies. MDPI 2022-02-21 /pmc/articles/PMC8870290/ /pubmed/35203392 http://dx.doi.org/10.3390/cells11040745 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Van Slambrouck, Jan Van Raemdonck, Dirk Vos, Robin Vanluyten, Cedric Vanstapel, Arno Prisciandaro, Elena Willems, Lynn Orlitová, Michaela Kaes, Janne Jin, Xin Jansen, Yanina Verleden, Geert M. Neyrinck, Arne P. Vanaudenaerde, Bart M. Ceulemans, Laurens J. A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome |
title | A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome |
title_full | A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome |
title_fullStr | A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome |
title_full_unstemmed | A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome |
title_short | A Focused Review on Primary Graft Dysfunction after Clinical Lung Transplantation: A Multilevel Syndrome |
title_sort | focused review on primary graft dysfunction after clinical lung transplantation: a multilevel syndrome |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870290/ https://www.ncbi.nlm.nih.gov/pubmed/35203392 http://dx.doi.org/10.3390/cells11040745 |
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