TY - JOUR
T1 - Centralized Static Ex Vivo Lung Perfusion in the United States
AU - Chen, Qiudong
AU - Malas, Jad
AU - Bowdish, Michael E.
AU - Chikwe, Joanna
AU - Krishna, Vikram
AU - Zaffiri, Lorenzo
AU - Rampolla, Reinaldo E.
AU - Catarino, Pedro
AU - Megna, Dominick
N1 - Publisher Copyright:
© 2025
PY - 2025/3
Y1 - 2025/3
N2 - Background: Ex vivo lung perfusion (EVLP) may improve donor lung utilization but requires significant infrastructure and expertise. Centralized EVLP facilities may mitigate these requirements. Methods: From the United Network for Organ Sharing database, we identified 345 adults undergoing isolated, first-time lung transplantation using donor lungs perfused by static EVLP (March 1, 2018-December 31, 2022). Recipients of lungs perfused at centralized EVLP facilities (n = 165) were compared with recipients of lungs perfused at individual transplant centers (n = 180). Propensity score matching was used to create balanced groups for comparison. Results: Centralized EVLP facilities were increasingly used from 2018 to 2022 (35.3% vs 55.8%, P =.04) and were more likely used when the annual center volume of EVLP lung transplants was low. Compared with allografts placed on EVLP at individual transplant centers, those placed on EVLP at centralized facilities had longer median ischemic time (11.3 vs 9.6 hours, P <.001) and were less likely to come from donation after circulatory death donors (25.4% vs 39.5%, P =.003) or be used for double-lung transplant (73.3% vs 83.9%, P =.02). In 102 well-matched recipient pairs, 2-year survival was equivalent between those receiving allografts perfused at centralized facilities (77.9%; 95% CI, 68.0%-85.1%) vs individual transplant centers (77.7%; 95% CI, 67.8%-84.9%; P =.90). Multivariable Cox regression analysis also showed equivalent 2-year survival (adjusted hazard ratio, 1.02; 95% CI, 0.57-1.84; P =.95). Conclusions: Transplanting lung allografts that underwent static EVLP at centralized facilities had similar outcomes compared with transplanting lungs perfused at individual transplant centers. The centralized model of clinical EVLP can potentially improve access to EVLP.
AB - Background: Ex vivo lung perfusion (EVLP) may improve donor lung utilization but requires significant infrastructure and expertise. Centralized EVLP facilities may mitigate these requirements. Methods: From the United Network for Organ Sharing database, we identified 345 adults undergoing isolated, first-time lung transplantation using donor lungs perfused by static EVLP (March 1, 2018-December 31, 2022). Recipients of lungs perfused at centralized EVLP facilities (n = 165) were compared with recipients of lungs perfused at individual transplant centers (n = 180). Propensity score matching was used to create balanced groups for comparison. Results: Centralized EVLP facilities were increasingly used from 2018 to 2022 (35.3% vs 55.8%, P =.04) and were more likely used when the annual center volume of EVLP lung transplants was low. Compared with allografts placed on EVLP at individual transplant centers, those placed on EVLP at centralized facilities had longer median ischemic time (11.3 vs 9.6 hours, P <.001) and were less likely to come from donation after circulatory death donors (25.4% vs 39.5%, P =.003) or be used for double-lung transplant (73.3% vs 83.9%, P =.02). In 102 well-matched recipient pairs, 2-year survival was equivalent between those receiving allografts perfused at centralized facilities (77.9%; 95% CI, 68.0%-85.1%) vs individual transplant centers (77.7%; 95% CI, 67.8%-84.9%; P =.90). Multivariable Cox regression analysis also showed equivalent 2-year survival (adjusted hazard ratio, 1.02; 95% CI, 0.57-1.84; P =.95). Conclusions: Transplanting lung allografts that underwent static EVLP at centralized facilities had similar outcomes compared with transplanting lungs perfused at individual transplant centers. The centralized model of clinical EVLP can potentially improve access to EVLP.
UR - http://www.scopus.com/inward/record.url?scp=85208531294&partnerID=8YFLogxK
U2 - 10.1016/j.athoracsur.2024.08.008
DO - 10.1016/j.athoracsur.2024.08.008
M3 - Article
C2 - 39197634
AN - SCOPUS:85208531294
SN - 0003-4975
VL - 119
SP - 661
EP - 669
JO - Annals of Thoracic Surgery
JF - Annals of Thoracic Surgery
IS - 3
ER -