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1 ioning, 34 on preservation fluids, and 21 on pulsatile perfusion.
2 d electrolytes were measured serially during pulsatile perfusion.
3 ic kidneys have led to the infrequent use of pulsatile perfusion.
4 These data support routine use of pulsatile perfusion.
7 ere identified in which one kidney underwent pulsatile perfusion and transplantation at our center, w
10 r donor kidney before transplant, could make pulsatile perfusion for the expanded donor financially a
11 nt outcome when organs are preserved through pulsatile perfusion; however, the underlying mechanisms
12 hat these channels are activated by enhanced pulsatile perfusion in vivo and contribute substantially
15 tive pressure mechanical ventilation or from pulsatile perfusion of lungs held motionless by continuo
16 d retrospectively to determine the impact of pulsatile perfusion on initial function and 1-year graft
22 Conflicting literature on the benefit of pulsatile perfusion (PP) over cold storage (CS) warrants
24 a novel servopump system to control mean and pulsatile perfusion pressure within the isolated vascula
25 e baseline flow 66 % markedly amplified this pulsatile perfusion response (+82.6 +/- 14.3 % increase
26 n preservation solutions in conjunction with pulsatile perfusion shows promise in improving early out
29 eys were preserved by continuous hypothermic pulsatile perfusion using Belzer-MPS or Belzer II soluti
30 phasic coronary flow responses to increasing pulsatile perfusion were assessed in anaesthetized dogs,
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