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Living donor transplant options in end-stage renal disease patients with ABO incompatibility

INTRODUCTION: The options available to CKD 5 patients with donor shortage due to incompatibilities is to either get enlisted in cadaver transplant program or opt for three other alternatives viz; ABO-incompatible transplant (ABO-I), ABO-incompatible transplant with Rituximab (ABO-R) or paired-kidney...

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Autores principales: Waigankar, Santosh S., Kamat, Madhav H., Joshi, Shriram, Gandhi, Bhupendra V., Bahadur, Madan, Deshpande, Rushi V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737666/
https://www.ncbi.nlm.nih.gov/pubmed/23956512
http://dx.doi.org/10.4103/0970-1591.114031
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author Waigankar, Santosh S.
Kamat, Madhav H.
Joshi, Shriram
Gandhi, Bhupendra V.
Bahadur, Madan
Deshpande, Rushi V.
author_facet Waigankar, Santosh S.
Kamat, Madhav H.
Joshi, Shriram
Gandhi, Bhupendra V.
Bahadur, Madan
Deshpande, Rushi V.
author_sort Waigankar, Santosh S.
collection PubMed
description INTRODUCTION: The options available to CKD 5 patients with donor shortage due to incompatibilities is to either get enlisted in cadaver transplant program or opt for three other alternatives viz; ABO-incompatible transplant (ABO-I), ABO-incompatible transplant with Rituximab (ABO-R) or paired-kidney exchange transplant (PKE). At our institute we have performed ABO-I, ABO-R and PKE transplants and we are presenting the results of these transplants performed at our institution. Here, we report our experiences of living donor kidney transplantation in highly sensitized patients. OBJECTIVE: To review the options available to CKD 5 patients with incompatible donor. MATERIALS AND METHODS: Between January 2008 and June 2011, 7 PKE, 26 ABO-I and 7 ABO-R transplants were carried out at our institute. Evaluation of both the recipients and donors involved biochemical, serological and radiological investigations. In case of PKE, recipients were operated simultaneously in different operation theaters. In ABO-I splenectomy was done while in ABO-R was given. Post-transplant the recipient management protocol remained the same. Expenditure following each transplant was calculated. RESULTS: The graft and patient survival of ABO-I, ABO-R and PKE transplants 12-18 months after transplant were 78.9%:80%, 85.7%:85.7% and 100%:100%, respectively. CONCLUSIONS: The inclusion of Rituximab in the transplant protocol appears promising. The existing donor shortage could be addressed by encouraging other options like PKE. The limiting factor for ABO-R and PKE transplants is time and cost, respectively. The decision depends on the informed consent between the patient and the nephrologists.
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spelling pubmed-37376662013-08-16 Living donor transplant options in end-stage renal disease patients with ABO incompatibility Waigankar, Santosh S. Kamat, Madhav H. Joshi, Shriram Gandhi, Bhupendra V. Bahadur, Madan Deshpande, Rushi V. Indian J Urol Original Article INTRODUCTION: The options available to CKD 5 patients with donor shortage due to incompatibilities is to either get enlisted in cadaver transplant program or opt for three other alternatives viz; ABO-incompatible transplant (ABO-I), ABO-incompatible transplant with Rituximab (ABO-R) or paired-kidney exchange transplant (PKE). At our institute we have performed ABO-I, ABO-R and PKE transplants and we are presenting the results of these transplants performed at our institution. Here, we report our experiences of living donor kidney transplantation in highly sensitized patients. OBJECTIVE: To review the options available to CKD 5 patients with incompatible donor. MATERIALS AND METHODS: Between January 2008 and June 2011, 7 PKE, 26 ABO-I and 7 ABO-R transplants were carried out at our institute. Evaluation of both the recipients and donors involved biochemical, serological and radiological investigations. In case of PKE, recipients were operated simultaneously in different operation theaters. In ABO-I splenectomy was done while in ABO-R was given. Post-transplant the recipient management protocol remained the same. Expenditure following each transplant was calculated. RESULTS: The graft and patient survival of ABO-I, ABO-R and PKE transplants 12-18 months after transplant were 78.9%:80%, 85.7%:85.7% and 100%:100%, respectively. CONCLUSIONS: The inclusion of Rituximab in the transplant protocol appears promising. The existing donor shortage could be addressed by encouraging other options like PKE. The limiting factor for ABO-R and PKE transplants is time and cost, respectively. The decision depends on the informed consent between the patient and the nephrologists. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3737666/ /pubmed/23956512 http://dx.doi.org/10.4103/0970-1591.114031 Text en Copyright: © Indian Journal of Urology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Waigankar, Santosh S.
Kamat, Madhav H.
Joshi, Shriram
Gandhi, Bhupendra V.
Bahadur, Madan
Deshpande, Rushi V.
Living donor transplant options in end-stage renal disease patients with ABO incompatibility
title Living donor transplant options in end-stage renal disease patients with ABO incompatibility
title_full Living donor transplant options in end-stage renal disease patients with ABO incompatibility
title_fullStr Living donor transplant options in end-stage renal disease patients with ABO incompatibility
title_full_unstemmed Living donor transplant options in end-stage renal disease patients with ABO incompatibility
title_short Living donor transplant options in end-stage renal disease patients with ABO incompatibility
title_sort living donor transplant options in end-stage renal disease patients with abo incompatibility
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737666/
https://www.ncbi.nlm.nih.gov/pubmed/23956512
http://dx.doi.org/10.4103/0970-1591.114031
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