TY - JOUR
T1 - Ex vivo lung perfusion in donation after circulatory death
T2 - A post hoc analysis of the Normothermic Ex Vivo Lung Perfusion as an Assessment of Extended/Marginal Donors Lungs trial
AU - Gouchoe, Doug A.
AU - Sanchez, Pablo G.
AU - D'Cunha, Jonathan
AU - Bermudez, Christian A.
AU - Daneshmand, Mani A.
AU - Davis, Robert D.
AU - Hartwig, Matthew G.
AU - Wozniak, Thomas C.
AU - Kon, Zachary N.
AU - Griffith, Bartley P.
AU - Lynch, William R.
AU - Machuca, Tiago N.
AU - Weyant, Michael J.
AU - Jessen, Michael E.
AU - Mulligan, Michael S.
AU - D'Ovidio, Frank
AU - Camp, Phillip C.
AU - Cantu, Edward
AU - Whitson, Bryan A.
AU - Ryan, John P.
AU - Wozniak, Thomas
AU - Lynch, William
AU - Nemeh, Hassan
AU - Caldeira, Christiano
AU - Song, Tae
AU - Kreisel, Daniel
AU - Ramzy, Danny
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/9
Y1 - 2024/9
N2 - Objective: Donation after circulatory death (DCD) donors offer the ability to expand the lung donor pool and ex vivo lung perfusion (EVLP) further contributes to this ability by allowing for additional evaluation and resuscitation of these extended criteria donors. We sought to determine the outcomes of recipients receiving organs from DCD EVLP donors in a multicenter setting. Methods: This was an unplanned post hoc analysis of a multicenter, prospective, nonrandomized trial that took place during 2011 to 2017 with 3 years of follow-up. Patients were placed into 3 groups based off procurement strategy: brain-dead donor (control), brain-dead donor evaluated by EVLP, and DCD donors evaluated by EVLP. The primary outcomes were severe primary graft dysfunction at 72 hours and survival. Secondary outcomes included select perioperative outcomes, and 1-year and 3-years allograft function and quality of life measures. Results: The DCD EVLP group had significantly higher incidence of severe primary graft dysfunction at 72 hours (P = .03), longer days on mechanical ventilation (P < .001) and in-hospital length of stay (P = .045). Survival at 3 years was 76.5% (95% CI, 69.2%-84.7%) for the control group, 68.3% (95% CI, 58.9%-79.1%) for the brain-dead donor group, and 60.7% (95% CI, 45.1%-81.8%) for the DCD group (P = .36). At 3-year follow-up, presence observed bronchiolitis obliterans syndrome or quality of life metrics did not differ among the groups. Conclusions: Although DCD EVLP allografts might not be appropriate to transplant in every candidate recipient, the expansion of their use might afford recipients stagnant on the waitlist a viable therapy.
AB - Objective: Donation after circulatory death (DCD) donors offer the ability to expand the lung donor pool and ex vivo lung perfusion (EVLP) further contributes to this ability by allowing for additional evaluation and resuscitation of these extended criteria donors. We sought to determine the outcomes of recipients receiving organs from DCD EVLP donors in a multicenter setting. Methods: This was an unplanned post hoc analysis of a multicenter, prospective, nonrandomized trial that took place during 2011 to 2017 with 3 years of follow-up. Patients were placed into 3 groups based off procurement strategy: brain-dead donor (control), brain-dead donor evaluated by EVLP, and DCD donors evaluated by EVLP. The primary outcomes were severe primary graft dysfunction at 72 hours and survival. Secondary outcomes included select perioperative outcomes, and 1-year and 3-years allograft function and quality of life measures. Results: The DCD EVLP group had significantly higher incidence of severe primary graft dysfunction at 72 hours (P = .03), longer days on mechanical ventilation (P < .001) and in-hospital length of stay (P = .045). Survival at 3 years was 76.5% (95% CI, 69.2%-84.7%) for the control group, 68.3% (95% CI, 58.9%-79.1%) for the brain-dead donor group, and 60.7% (95% CI, 45.1%-81.8%) for the DCD group (P = .36). At 3-year follow-up, presence observed bronchiolitis obliterans syndrome or quality of life metrics did not differ among the groups. Conclusions: Although DCD EVLP allografts might not be appropriate to transplant in every candidate recipient, the expansion of their use might afford recipients stagnant on the waitlist a viable therapy.
KW - DCD
KW - EVLP
KW - donation after circulatory death
KW - ex vivo lung perfusion
KW - lung transplantation
UR - https://www.scopus.com/pages/publications/85190087517
U2 - 10.1016/j.jtcvs.2024.03.011
DO - 10.1016/j.jtcvs.2024.03.011
M3 - Article
C2 - 38508486
AN - SCOPUS:85190087517
SN - 0022-5223
VL - 168
SP - 724-734.e7
JO - Journal of Thoracic and Cardiovascular Surgery
JF - Journal of Thoracic and Cardiovascular Surgery
IS - 3
ER -