Unlocking the potential of uncontrolled DCD in lung transplantation: A review of 2 decades of experience

Otros/as autores/as

Institut Català de la Salut

[Bello I] Servei de Cirurgia Toràcica i Trasplantament Pulmonar, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Donació i Trasplantament d’Òrgans, Teixits i Cèl·lules, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Palleschi A] Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy. Thoracic Surgery and Lung Transplantation Unit, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan, Italy. [Cypel M] Toronto Lung Transplant Program, University of Toronto, Toronto, Canada. [Argudo E] Servei de Medicina Intensiva, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Shock, Disfunció Orgànica i Ressuscitació, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Sandiumenge A] Grup de Recerca de Donació i Trasplantament d’Òrgans, Teixits i Cèl·lules, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Coordinació de Programes de Donació i Trasplantament, Vall d’Hebron Hospital Universitari, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Fecha de publicación

2025-10-29T09:04:42Z

2025-10-29T09:04:42Z

2025-11



Resumen

Exvivo lung perfusion; Lung donor; Lung transplantation


Perfusión pulmonar ex vivo; Donante de pulmón; Trasplante de pulmón


Perfusió pulmonar ex vivo; Donant de pulmó; Trasplantament de pulmó


Uncontrolled donation after circulatory death (uDCD) represents a promising yet underutilized approach to expanding the lung donor pool amid persistent organ shortages. Since the first successful lung transplantation from a uDCD donor in 2001, increasing clinical experience and advancements in organ preservation have demonstrated its feasibility. This review critically explores historical evolution, physiological basis, preservation techniques, ethical and legal considerations, and clinical outcomes of uDCD lung transplantation. The lung's unique ability to maintain viability through passive oxygen diffusion in the absence of perfusion supports its potential in the uDCD context. Compared to donors after brain death (DBD), uDCD donors may avoid systemic inflammatory response, potentially preserving graft quality. However, concerns persist regarding ischemia-reperfusion injury and mitochondrial dysfunction, highlighting the need for mitigation strategies such as ex vivo lung perfusion and normothermic ventilation. Ethical and legal challenges-particularly those related to the determination of death and consent-remain key obstacles. Organizational demands, including rapid coordination between prehospital, hospital teams and transplant teams, further limit broader implementation. Despite these barriers, reported outcomes are encouraging: to date, over 70 transplants from uDCD donors have been documented, with 1-year survival rates ranging from 71% to 87.5% and long-term outcomes comparable to DBD transplants. Integration of uDCD into routine clinical practice will require standardized protocols, robust public engagement, and institutional commitment. When appropriately implemented, uDCD lung transplantation offers a viable opportunity to increase donor availability and improve access to life-saving treatment.

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Elsevier

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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