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Ex Situ Normothermic Machine Perfusion of Donor Livers
Published on: May 26, 2015
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Maximizing organs for donation: the potential for ex situ normothermic machine perfusion
C Griffiths1,2, W E Scott1,2, S Ali1,2
1From the NIHR Blood and Transplant Research Unit in Organ Donation and Transplantation, Institute of Transplantation, Freeman Hospital, Newcastle Upon Tyne, NE7 7DN, UK.
QJM : Monthly Journal of the Association of Physicians
|January 17, 2020
Summary
Organ transplantation faces donor shortages, leading to expanded criteria and increased risks. Normothermic machine perfusion (NMP) assesses and potentially improves organ function and outcomes using novel therapeutics.
Area of Science:
- Organ transplantation and regenerative medicine.
- Machine perfusion technologies in transplantology.
- Pharmacological interventions for organ preservation.
Background:
- Global organ transplant waiting lists are long due to a shortage of suitable donor organs.
- Expanded donor criteria, including donation after circulatory death, increase the risk of primary graft dysfunction.
- Prolonged ischemia times associated with extended criteria donors can impair organ viability.
Approach:
- Normothermic machine perfusion (NMP) allows ex vivo assessment and potential reconditioning of donor organs.
- NMP provides a platform for targeted delivery of therapeutics directly to the organ.
- This approach minimizes systemic side effects often seen with in vivo drug administration.
Key Points:
- NMP enables objective evaluation of donor organ function before transplantation.
- Therapeutic agents can be tested and administered directly to the organ during NMP.
- Potential to improve graft function and long-term transplant outcomes.
Conclusions:
- NMP is a promising technology for addressing organ shortages and improving transplant success rates.
- Investigating novel therapeutics within NMP platforms may enhance organ viability and reduce post-transplant complications.
- This strategy supports the use of extended criteria donors and reduces primary graft dysfunction.

