Literature DB >> 12352884

Survival of mandatorily shared cadaveric kidneys and their paybacks in the zero mismatch era.

Mark D Stegall1, Patrick G Dean, Maureen A McBride, James J Wynn.   

Abstract

BACKGROUND: The United Network for Organ Sharing has mandated the national sharing of well-matched cadaveric kidneys with payback to the national pool. On March 6, 1995, the policy was extended to include sharing of cadaveric kidneys for which there is a recipient with a 0-HLA mismatch (0-MM). However, the beneficial effects of this policy have been questioned. To address these concerns, we analyzed the effects of this system on graft survival, cold ischemia time, and the transplantation of highly sensitized patients during the 0-MM era.
METHODS: We analyzed cadaveric solitary kidney transplant data in the OPTN/The United Network for Organ Sharing database. Cox proportional hazards analyses were conducted on 29,401 transplants performed between March 6, 1995 and December 31, 1998 to assess the effects of mandatory sharing and paybacks on graft outcome. We also compared the outcome of pairs of kidneys in which one was shared as either an 0-MM kidney (n=833) or as a payback (n=440) and the mate was transplanted locally.
RESULTS: Overall, 36% of kidneys were shared, 15.6% as 0-MM and 20.4% as paybacks or other shares. Although the sharing of 0-MM kidneys significantly increased cold ischemia time, the risk of graft loss was significantly decreased. The survival of payback kidneys was not significantly different from other shared kidneys. Sharing 0-MM kidneys appeared to increase the chances of transplantation of sensitized patients and 47% of the kidneys transplanted in patients with a panel reactive antibody of more than 80% were from 0-MM donors.
CONCLUSIONS: National sharing of 0-MM kidneys appears to lead to a small but significant improvement in intermediate-term graft survival despite increasing cold ischemia time. The current policy also increases access of highly sensitized patients to transplantation.

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Year:  2002        PMID: 12352884     DOI: 10.1097/00007890-200209150-00014

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


  5 in total

1.  Elderly recipients of hepatitis C positive renal allografts can quickly develop liver disease.

Authors:  Tanya R Flohr; Hugo Bonatti; Tjasa Hranjec; Doug S Keith; Peter I Lobo; Sean C Kumer; Timothy M Schmitt; Robert G Sawyer; Timothy L Pruett; John P Roberts; Kenneth L Brayman
Journal:  J Surg Res       Date:  2011-11-19       Impact factor: 2.192

2.  HLA-A, -B, and -DR zero-mismatched kidneys shipped to the University of Wisconsin, Madison, 1993-2006: superior graft survival despite longer preservation time.

Authors:  William J Burlingham; Alejandro Muñoz del Rio; David Lorentzen; Hans W Sollinger; John D Pirsch; Ewa Jankowska-Gan; Anthony D'Alessandro
Journal:  Transplantation       Date:  2010-08-15       Impact factor: 4.939

3.  Resection or transplant-listing for solitary hepatitis C-associated hepatocellular carcinoma: an intention-to-treat analysis.

Authors:  Hiroshi Sogawa; Brian Shrager; Ghalib Jibara; Parissa Tabrizian; Sasan Roayaie; Myron Schwartz
Journal:  HPB (Oxford)       Date:  2012-08-30       Impact factor: 3.647

4.  Influence of Cold Ischemia Time in Kidney Transplants From Small Pediatric Donors.

Authors:  Liise K Kayler; Michelle Lubetzky; Xia Yu; Patricia Friedmann
Journal:  Transplant Direct       Date:  2017-06-27

5.  Impact of Cold Ischemia Time in Kidney Transplants From Donation After Circulatory Death Donors.

Authors:  Liise Kayler; Xia Yu; Carlos Cortes; Michelle Lubetzky; Patricia Friedmann
Journal:  Transplant Direct       Date:  2017-06-23
  5 in total

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