Pushing the envelope in renal preservation; improved results with novel perfusate modifications for pulsatile machine perfusion of cadaver kidneys

Transplant Proc. 2004 Jun;36(5):1257-60. doi: 10.1016/j.transproceed.2004.04.083.

Abstract

Introduction: Novel preservation techniques may diminish ischemia/reperfusion (I/R) injury. Our preservation laboratory has modified Belzer MPS for machine perfusion (MP) with prostaglandin E1 (PGE 1), nitroglycerin (NTG), and polyethylene glycol-superoxide dismutase (PEG-SOD) to attenuate I/R injury. We reviewed our recent experience using this novel formulation (NF) compared with standard perfusates.

Results: Between January 1998 and March 2000, 1060 consecutive kidneys were preserved in our laboratory. One hundred forty-eight kidneys (14%) were discarded. Fifty-eight percent of kidneys during this time period underwent MP (n = 532). En bloc kidney pairs were randomly assigned to pulsatile MP using Waters RM3 or MOX-100 perfusion systems using 1 of 3 perfusates; NF (NF; n = 119), Belzer MPS (MPS; n = 201), or Belzer II albumin gluconate (ALB; n = 212) Significant improvements in delayed graft function (DGF) rate were seen with NF versus other perfusates (8% vs 14% vs 19%, respectively; P =.03). At 6 months, graft survival was significantly improved with NF compared with MPS and ALB (96% vs 90% vs 87%, respectively; P =.03). NF also produced a significantly higher percentage of recipients with a serum creatinine level < or = 1.5 mg/dL.

Conclusions: Novel modifications of standard MP perfusate improved outcomes after renal transplantation. Preservation-based interventions targeted to ameliorate I/R injury can improve outcomes and may allow expansion of the donor pool.

MeSH terms

  • Adult
  • Alprostadil
  • Cadaver
  • Cause of Death
  • Female
  • Free Radical Scavengers
  • Graft Survival / physiology
  • Humans
  • Kidney Transplantation / physiology
  • Kidney*
  • Male
  • Middle Aged
  • Nitroglycerin
  • Organ Preservation / methods*
  • Perfusion / methods
  • Polyethylene Glycols
  • Superoxide Dismutase
  • Tissue Donors*

Substances

  • Free Radical Scavengers
  • Polyethylene Glycols
  • Superoxide Dismutase
  • polyethylene glycol-superoxide dismutase
  • Alprostadil
  • Nitroglycerin