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Published on: June 6, 2025
Donation after circulatory death: current practices, ongoing challenges, and potential improvements
Paul E Morrissey1, Anthony P Monaco
11 Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI. 2 Beth Israel-Deaconess Medical Center, Harvard Medical School, Boston, MA. 3 Address correspondence to: Paul E. Morrissey, M.D., Division of Organ Transplantation, Rhode Island Hospital, 593 Eddy St, APC 921, Providence, RI 02903.
Insights
Organ donation after circulatory death (DCD) offers a vital source of organs, though challenges like ischemia impact utilization. Strategies to mitigate injury and improve organ recovery are crucial for expanding DCD transplantation.
Area of Science:
- Transplantation Medicine
- Organ Donation
- Nephrology
Background:
- Organ donation after circulatory death (DCD) is a globally recognized practice, yet faces challenges impacting organ utilization.
- While donor candidacy criteria are generally agreed upon, DCD practices vary, leading to limitations in organ perfusion and increased ischemic injury.
- Existing DCD protocols often result in higher rates of graft nonfunction, delayed function, and discard compared to donation after brain death.
Purpose of the Study:
- To review current DCD practices, identify associated problems and challenges.
- To explore clinical strategies for improving DCD organ utilization and outcomes.
- To assess the potential of emerging technologies and approaches in DCD transplantation.
Main Methods:
- Comprehensive review of current DCD practices and literature.
- Analysis of factors limiting DCD organ utilization, including ischemia and reperfusion injury.
- Evaluation of existing and novel clinical strategies for DCD organ procurement and preservation.
Main Results:
- DCD kidneys show comparable long-term function to brain death kidneys but higher rates of initial complications.
- Extra-renal DCD organs are less utilized due to concerns over ischemic injury and lack of supportive therapies.
- Emerging techniques like machine perfusion and normothermic regional perfusion show promise in mitigating ischemic injury and increasing organ viability.
Conclusions:
- Despite challenges, DCD offers a significant organ pool, with ongoing research focused on improving organ quality and utilization.
- Advancements in preservation techniques and strategies to minimize ischemic injury are key to enhancing DCD transplantation outcomes.
- Expanding DCD donor criteria and exploring innovative approaches like extended criteria donor utilization can further increase transplantable organs.
Abstract:
Organ donation after circulatory death (DCD) has been endorsed by the World Health Organization and is practiced worldwide. This overview examines current DCD practices, identifies problems and challenges, and suggests clinical strategies for possible improvement. Although there is uniform agreement on DCD donor candidacy (ventilator-dependent individuals with nonrecoverable or irreversible neurologic injury not meeting brain death criteria), there are variations in all aspects of DCD practice. Utilization of DCD organs is limited by hypoxia, hypotension, reduced--then absent--organ perfusion, and ischemia/reperfusion syndrome. Nevertheless, DCD kidneys exhibit comparable function and survival to donors with brain death kidneys, although they have higher rates of primary graft nonfunction, delayed graft function, discard, and retrieval associated injury. Concern over ischemic organ injury underscores the reluctance to recover extrarenal DCD organs since lack of medical therapy to support inadequate allograft function limits their acceptability. Nevertheless, limited results with DCD pancreas, liver, and lung allografts (but not heart) are now approaching that of donors with brain death organs. Pretransplant machine perfusion of DCD kidneys (vs. static storage) may reduce delayed graft function but has no effect on long-term organ function and survival. Normothermic regional perfusion used during DCD abdominal organ retrieval may reduce ischemic organ injury and increase the number of usable organs, although critical confirmative studies have yet to be done. Minor increases in usable DCD kidneys could accrue from increased use of pediatric DCD kidneys and from selective use of DCD/ECD kidneys, whereas a modest increase could result through utilization of donors declared dead beyond 1 hr from withdrawal of life support therapy. A significant increase in transplantable kidneys could be achieved by extension of the concept of living kidney donation in relation to imminent death of potential DCD donors. Progress in research to identify, prevent, and repair DCD-associated organ retrieval injury should improve utilization of DCD organs. Recent results using ex situ pretransplant organ perfusion of DCD organs has been encouraging in this regard.
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