Publication

Performance-enhancing strategies for deceased donor kidneys

van Rijt, G., 2014, [S.l.]: [S.n.]. 205 p.

Research output: ThesisThesis fully internal (DIV)Academic

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  • Title and contents

    Final publisher's version, 198 KB, PDF-document

  • Chapter 1

    Final publisher's version, 419 KB, PDF-document

  • Chapter 2

    Final publisher's version, 960 KB, PDF-document

  • Chapter 3

    Final publisher's version, 4 MB, PDF-document

  • Chapter 4

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  • Chapter 5

    Final publisher's version, 642 KB, PDF-document

  • Chapter 6

    Final publisher's version, 3 MB, PDF-document

  • Chapter 7

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  • Chapter 8

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  • Chapter 9

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  • Chapter 10

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  • Chapter 11

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  • Complete dissertation

    Submitted manuscript, 14 MB, PDF-document

  • Propositions

    Final publisher's version, 41 KB, PDF-document

  • Geert van Rijt
Renal transplantation is the most effective treatment of end-stage renal disease. The major part of renal transplants is derived from deceased brain dead- or cardiac dead donors. Unfortunately, outcome of deceased donor kidneys is inferior compared to living donor kidneys. In this thesis three strategies are tested in experimental models to improve outcome after deceased donor kidney transplantation.
Earlier experiments showed that α-melanocyte stimulating hormone (α-MSH) is able to protects kidneys against ischemic injury. Recipients of a deceased brain dead donor kidney were therefore treated with α-MSH. Surprisingly, α-MSH impaired recovery of renal function. Thus, α-MSH seems no potential treatment for recipients of a deceased brain dead donor kidney.
The second strategy is normothermic recirculation of deceased cardiac death donor kidneys. The effectiveness of this treatment has already been shown in clinical trials, but the experimental evidence is limited. In this study, we were not able to reproduce the protective effect of normothermic recirculation in an experimental model in the rat.
Erythropoietin (EPO) has a tissue-protective function, besides its regulation of the production of red blood cells. The major disadvantage of protective EPO treatment is an increased risk for cardiovascular adverse events due to stimulation of the production of red blood cells. ARA290 is a protective EPO derivative and does not affect the production of red blood cells. In experimental ischemia/reperfusion models, administration of ARA290 after reperfusion reduced inflammation and improved renal function. ARA290 treatment of recipients of a deceased donor kidney is therefore a promising strategy to improve outcome of renal transplantation.
Translated title of the contributionPrestatie bevorderende strategieën voor donornieren afkomstig van postmortale donoren
Original languageEnglish
QualificationDoctor of Philosophy
Awarding Institution
Supervisors/Advisors
Award date29-Sep-2015
Place of Publication[S.l.]
Publisher
Print ISBNs978-90-367-7214-3
Electronic ISBNs978-90-367-7213-6
Publication statusPublished - 2014

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