Primary Graft Dysfunction (PGD) Following Lung Transplantation

2018 ◽  
Vol 39 (02) ◽  
pp. 148-154 ◽  
Author(s):  
Rupal Shah ◽  
Joshua Diamond

AbstractPrimary graft dysfunction (PGD) is a form of acute lung injury that results from ischemia reperfusion injury (IRI) and is the major cause of early posttransplant morbidity and mortality. Patients who survive PGD have decreased quality of life, an increased risk of chronic lung allograft dysfunction, specifically bronchiolitis obliterans syndrome, and a significantly increased risk of death. In 2017, the International Society for Heart and Lung Transplantation released updated consensus statements on the PGD definition, most up-to-date PGD risk factors, mechanisms of PGD development, and the state-of-the-art for PGD therapeutics. Risk factor identification has led to the development of PGD predictive algorithms, although their clinical utility remains limited. Ongoing areas of controversy and discussion include further refinements to the PGD grading scheme to account for technologic advances such as extracorporeal membrane oxygenation and the increased utilization of high flow nasal cannula, the use of PGD as an outcome measure in clinical trials of ex vivo lung perfusion, enhancement of predictive algorithms incorporating biochemical risk factors, and the need for development of therapies targeted at improving PGD outcomes.

2021 ◽  
Vol 42 (03) ◽  
pp. 368-379
Author(s):  
Jake G. Natalini ◽  
Joshua M. Diamond

AbstractPrimary graft dysfunction (PGD) is a form of acute lung injury after transplantation characterized by hypoxemia and the development of alveolar infiltrates on chest radiograph that occurs within 72 hours of reperfusion. PGD is among the most common early complications following lung transplantation and significantly contributes to increased short-term morbidity and mortality. In addition, severe PGD has been associated with higher 90-day and 1-year mortality rates compared with absent or less severe PGD and is a significant risk factor for the subsequent development of chronic lung allograft dysfunction. The International Society for Heart and Lung Transplantation released updated consensus guidelines in 2017, defining grade 3 PGD, the most severe form, by the presence of alveolar infiltrates and a ratio of PaO2:FiO2 less than 200. Multiple donor-related, recipient-related, and perioperative risk factors for PGD have been identified, many of which are potentially modifiable. Consistently identified risk factors include donor tobacco and alcohol use; increased recipient body mass index; recipient history of pulmonary hypertension, sarcoidosis, or pulmonary fibrosis; single lung transplantation; and use of cardiopulmonary bypass, among others. Several cellular pathways have been implicated in the pathogenesis of PGD, thus presenting several possible therapeutic targets for preventing and treating PGD. Notably, use of ex vivo lung perfusion (EVLP) has become more widespread and offers a potential platform to safely investigate novel PGD treatments while expanding the lung donor pool. Even in the presence of significantly prolonged ischemic times, EVLP has not been associated with an increased risk for PGD.


2013 ◽  
Vol 187 (5) ◽  
pp. 527-534 ◽  
Author(s):  
Joshua M. Diamond ◽  
James C. Lee ◽  
Steven M. Kawut ◽  
Rupal J. Shah ◽  
A. Russell Localio ◽  
...  

2012 ◽  
Vol 44 (8) ◽  
pp. 2462-2468 ◽  
Author(s):  
M.N. Samano ◽  
L.M. Fernandes ◽  
J.C.B. Baranauskas ◽  
A.T. Correia ◽  
J.E. Afonso ◽  
...  

2016 ◽  
Vol 8 (11) ◽  
pp. 3275-3282 ◽  
Author(s):  
Sungwoo Moon ◽  
Moo Suk Park ◽  
Jin Gu Lee ◽  
Ji Ye Jung ◽  
Young Ae Kang ◽  
...  

2009 ◽  
Vol 23 (6) ◽  
pp. 819-830 ◽  
Author(s):  
Catherine L. Kuntz ◽  
Denis Hadjiliadis ◽  
Vivek N. Ahya ◽  
Robert M. Kotloff ◽  
Alberto Pochettino ◽  
...  

2006 ◽  
Vol 131 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Bryan A. Whitson ◽  
Dilip S. Nath ◽  
Adam C. Johnson ◽  
Adam R. Walker ◽  
Matthew E. Prekker ◽  
...  

2021 ◽  
Author(s):  
Haider Ghaidan ◽  
Martin Stenlo ◽  
Nika Gvazava ◽  
Anna Niroomand ◽  
Dag Edstrom ◽  
...  

Abstract Despite improvements, lung transplantation (LTx) remains hampered by both a scarcity of donor organs and by mortality following primary graft dysfunction (PGD). Since acute respiratory distress syndrome (ARDS) limits donor lungs utilization, we investigated cytokine filtration as a means of restoring ARDS donor lungs. We induced mild to moderate ARDS using lipopolysaccharide in 12 donor pigs. Lungs were then treated with or without cytokine filtration during ex vivo lung perfusion (EVLP) and post-transplantation using extracorporeal hemoperfusion. The treatment significantly decreased cytokine levels during EVLP and decreased levels of immune cells post-transplantation. Histology demonstrated fewer signs of lung injury across both treatment periods and the incidence of PGD was significantly reduced among treated animals. Overall, cytokine filtration was able to restore lung function and reduce PGD in lung transplantation. We suggest this treatment will increase the availability of donor lungs and increase the tolerability of donor lungs in the recipient.


Sign in / Sign up

Export Citation Format

Share Document