Literature DB >> 2463700

Combined cold storage-perfusion preservation with a new synthetic perfusate.

R M Hoffmann1, R J Stratta, A M D'Alessandro, H W Sollinger, M Kalayoglu, J D Pirsch, J H Southard, F O Belzer.   

Abstract

Based upon encouraging experimental results, we began employing a synthetic perfusate for cadaver kidney preservation. The new perfusate contains hydroxyethyl starch (HES) as the sole colloid for oncotic support; 107 cadaver kidneys were preserved and transplanted (93 primary, 14 nonprimary) using the HES solution and were compared with our previous experience of 180 cadaver kidneys (161 primary, 19 nonprimary) preserved and transplanted utilizing an albumin-based perfusate. All cadaver kidneys were locally harvested and preserved by machine perfusion. Donor and preservation characteristics in the HES (n = 61) and the albumin (n = 101) groups were comparable, with a mean preservation time of 30.9 hr. Cold storage in combination with hypothermic pulsatile perfusion (HPP) preservation was performed more often in the HES group (68.2% vs. 31.1%, P less than 0.001). Recipient characteristics were also comparable, and all received quadruple immunosuppressive therapy with sequential/Minnesota antilymphoblast globulin/(MALG)/cyclosporine. After primary transplantation, the incidence of immediate function (82.6% vs. 89.2%), preservation-related dialysis (14.9% vs. 8.6%), and primary nonfunction (2.5% vs. 0) were similar between the 2 groups, with trends favoring the latter HES data. One-month serum creatinine (1.8 vs. 1.7 mg/dl) and graft survival (95% vs. 97.8%) also were comparable. Similar trends were present in the retransplant group, including a significantly lower 1-month serum creatinine in the HES group (2.2 vs. 1.5 mg/dl; P less than 0.05). The preservation-related dialysis rate did not differ between primary and nonprimary transplants. Primary nonfunction has not occurred with our new perfusate. Combined cold-storage-HPP preservation with HES perfusate offers advantages over standard retrieval technology and provides excellent immediate allograft function.

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Year:  1989        PMID: 2463700     DOI: 10.1097/00007890-198901000-00008

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  7 in total

1.  A new liver perfusion and preservation system for transplantation research in large animals.

Authors:  K Yanaga; L Makowka; G Lebeau; R R Hwang; M Shimada; S Kakizoe; A J Demetris; T E Starzl
Journal:  J Invest Surg       Date:  1990       Impact factor: 2.533

2.  Ethical decisions in the history of organ transplantation.

Authors:  A G Diethelm
Journal:  Ann Surg       Date:  1990-05       Impact factor: 12.969

Review 3.  Current status of renal transplantation.

Authors:  M G Suranyi; B M Hall
Journal:  West J Med       Date:  1990-06

4.  Development of pancreas storage solutions: Initial screening of cytoprotective supplements for β-cell survival and metabolic status after hypothermic storage.

Authors:  Lia H Campbell; Michael J Taylor; Kelvin G M Brockbank
Journal:  Biopreserv Biobank       Date:  2013-02-06       Impact factor: 2.300

5.  Survey of Apoptosis After Hypothermic Storage of a Pancreatic β-Cell Line.

Authors:  Lia H Campbell; Michael J Taylor; Kelvin G M Brockbank
Journal:  Biopreserv Biobank       Date:  2016-03-03       Impact factor: 2.300

6.  The use of UW solution in clinical transplantation. A 4-year experience.

Authors:  F O Belzer; A M D'Alessandro; R M Hoffmann; S J Knechtle; A Reed; J D Pirsch; M Kalayoglu; H W Sollinger
Journal:  Ann Surg       Date:  1992-06       Impact factor: 12.969

7.  Mouse IPK: A Powerful Tool to Partially Characterize Renal Reperfusion and Preservation Injury.

Authors:  Susanne L Lindell; Natascha Williams; Ilia Brusilovsky; Martin J Mangino
Journal:  Open Transplant J       Date:  2011-01-01
  7 in total

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