The influence of pulsatile preservation on renal transplantation in the 1990s

被引:121
作者
Polyak, MMR
Arrington, BO
Stubenbord, WT
Boykin, J
Brown, T
Jean-Jacques, MA
Estevez, J
Kapur, S
Kinkhabwala, M
机构
[1] Cornell Univ, Weill Med Coll, New York Presbyterian Hosp, Dept Surg,Div Transplantat,Organ Preservat Unit, New York, NY USA
[2] Cornell Univ, Weill Med Coll, New York Presbyterian Hosp,Div Transplantat, Ctr Organ Preservat & Transplantat Res,Dept Surg, New York, NY USA
关键词
D O I
10.1097/00007890-200001270-00010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Unlike simple cold storage (CS), pulsatile machine preservation (MP) of kidneys for transplantation permits pharmacologic manipulation of the perfusate and aids in the pretransplant assessment of the kidney graft. These characteristics of MP may have importance in the era of increasing use of extended criteria donor kidneys. The overall aim of this article is to critically assess practices at our preservation unit with respect to graft function. Specific aims are to (1) compare the influence of MP versus CS on graft function, (2) determine which pretransplant variables have significance in pretransplant assessment, and (3) determine whether pharmacologic manipulation during MP is advantageous, Methods. There were 650 consecutive kidneys preserved in our laboratory between January 1, 1993 and March 1, 999, by either MP or CS. All MP kidneys were preserved by continuous hypothermic pulsatile perfusion using Belzer-MPS or Belzer II solution. Perfusion parameters and electrolytes were measured serially during pulsatile perfusion. All CS kidneys were stored in University of Wisconsin solution, All kidneys obtained from donors exhibiting extended criteria features underwent pretransplant frozen section biopsies. Transmission electron microscopy (EM) was performed on a subset of kidneys undergoing pharmacologic manipulation. Four agents were assessed prospectively for their ability to influence MP characteristics when added to perfusate: PGE,, trifluoperazine, verapamil, and papaverine. Results. MP was associated with improved immediate, 1-, and 2-year graft function and reduced length of initial hospital stay when compared with CS grafts. Changes in the machine perfusion variables flow and resistance, and the [Ca++] in perfusate, were significantly associated with delayed graft function (DGF) after the transplant. Biopsy information was not predictive of DGF, The addition of PGE, to perfusate improved MP characteristics, reduced the release of [Ca++] into perfusate, and ameliorated mitochondrial ischemic injury in transmission EM images, Early graft function was improved in the presence of PGE(1)+MP, compared with function in the presence of other pharmacologic agents or CS alone. Conclusions. MP is associated with improved early and long term renal function. Moreover, PGE, augments MP in improving graft function. The combination of MP+PGE(1) may be important in optimizing the ability to use extended donor criteria kidneys and, thereby, improve the overall efficiency of cadaveric renal transplantation.
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页码:249 / 258
页数:10
相关论文
共 41 条
  • [1] ADMINISTRATION OF PROSTAGLANDIN E(1) AFTER LUNG TRANSPLANTATION IMPROVES EARLY GRAFT FUNCTION
    AOE, M
    TRACHIOTIS, GD
    OKABAYASHI, K
    MANCHESTER, JK
    LOWRY, OH
    COOPER, JD
    PATTERSON, GA
    [J]. ANNALS OF THORACIC SURGERY, 1994, 58 (03) : 655 - 661
  • [2] BARBER WH, 1990, TRANSPLANT P, V22, P446
  • [3] BELTZER FO, 1988, TRANSPLANTATION, V45, P673
  • [4] CORRECT USE OF UNIVERSITY-OF-WISCONSIN PRESERVATION SOLUTION
    BELZER, FO
    [J]. LANCET, 1990, 335 (8685) : 362 - 362
  • [5] CA-2+ FLUX AS AN INITIAL EVENT IN PHAGOCYTOSIS BY RAT KUPFFER CELLS
    BIRMELIN, M
    DECKER, K
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 131 (03): : 539 - 543
  • [6] BLANKENSTEJIN JD, 1991, HEPATOLOGY, V13, P1236
  • [7] BURDOWNE KW, 1985, J BIOL CHEM, V260, P11619
  • [8] CHEUNG JY, 1986, NEW ENGL J MED, V314, P1670
  • [10] Glutathione S-transferase as predictor of functional outcome in transplantation of machine-preserved non-heart-beating donor kidneys
    Daemen, JWHC
    Oomen, APA
    Janssen, MA
    vandeSchoot, L
    vanKreel, BK
    Heineman, E
    Kootstra, G
    [J]. TRANSPLANTATION, 1997, 63 (01) : 89 - 93