TY - JOUR
T1 - Case Report
T2 - Optimal utilization of marginal lung allografts by considering donor–recipient PGD risk compatibility and by mitigating allograft and recipient inflammatory risk
AU - Braithwaite, Sue A.
AU - Jennekens, Jitte
AU - Berg, Elize M.
AU - de Heer, Linda M.
AU - Ramjankhan, Faiz
AU - de Jong, Michel
AU - Luc Charlier, Jean
AU - Dessing, Thomas C.
AU - Veltkamp, Marcel
AU - Scheren, Amy S.
AU - Ruigrok, Dieuwertje
AU - Schönwetter, Rob H.J.
AU - Buhre, Wolfgang F.F.A.
AU - van der Kaaij, Niels P.
N1 - Publisher Copyright:
2024 Braithwaite, Jennekens, Berg, de Heer, Ramjankhan, de Jong, Luc Charlier, Dessing, Veltkamp, Scheren, Ruigrok, Schönwetter, Buhre and van der Kaaij.
PY - 2024/10/3
Y1 - 2024/10/3
N2 - Reducing the risk of high-grade primary graft dysfunction (PGD) is vital to achieve acceptable short- and long-term outcomes for recipients following lung transplantation. However, the utilization of injured lung allografts, which may confer a higher risk of PGD, must be considered due to the disparity between the increasing number of patients requiring lung transplantation and the limited donor pool. We describe a case in which highly marginal lung allografts were utilized with a good post-transplant outcome. Donor–recipient PGD risk compatibility was taken into consideration. Normothermic ex vivo lung perfusion (EVLP) was utilized to functionally assess the allografts. A second cold ischemia time following EVLP was avoided by converting the EVLP mode to a hypothermic oxygenated perfusion setup from which the lungs were transplanted directly. We attempted to mitigate lung ischemia-reperfusion injury in the recipient by employing cytokine adsorption both during the EVLP and intraoperatively during the implant procedure. In this case report, we describe our hypothermic oxygenated perfusion setup on EVLP for the first time. Furthermore, we describe the utilization of cytokine adsorption in two phases of the same transplant process.
AB - Reducing the risk of high-grade primary graft dysfunction (PGD) is vital to achieve acceptable short- and long-term outcomes for recipients following lung transplantation. However, the utilization of injured lung allografts, which may confer a higher risk of PGD, must be considered due to the disparity between the increasing number of patients requiring lung transplantation and the limited donor pool. We describe a case in which highly marginal lung allografts were utilized with a good post-transplant outcome. Donor–recipient PGD risk compatibility was taken into consideration. Normothermic ex vivo lung perfusion (EVLP) was utilized to functionally assess the allografts. A second cold ischemia time following EVLP was avoided by converting the EVLP mode to a hypothermic oxygenated perfusion setup from which the lungs were transplanted directly. We attempted to mitigate lung ischemia-reperfusion injury in the recipient by employing cytokine adsorption both during the EVLP and intraoperatively during the implant procedure. In this case report, we describe our hypothermic oxygenated perfusion setup on EVLP for the first time. Furthermore, we describe the utilization of cytokine adsorption in two phases of the same transplant process.
KW - cytokine adsorption
KW - EVLP
KW - hypothermic oxygenated lung perfusion
KW - lung ischemia-reperfusion injury
KW - lung transplant continuum
KW - lung transplantation outcome
KW - primary graft dysfunction
UR - https://www.scopus.com/pages/publications/85207259234
U2 - 10.3389/frtra.2024.1450376
DO - 10.3389/frtra.2024.1450376
M3 - Article
C2 - 39421646
AN - SCOPUS:85207259234
SN - 2813-2440
VL - 3
JO - Frontiers in Transplantation
JF - Frontiers in Transplantation
M1 - 1450376
ER -