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Inferior survival outcomes of pancreas transplant alone in uremic patients

Theoretically, pancreas transplant alone in uremic (PTAU) patients could also be one of the options for those waiting for both pancreas and kidney grafts, but it has never been reported. There were 160 cases of pancreas transplant in this study, including 16% PTAU. The 5-year patient survival was 66...

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Autores principales: Shyr, Bor-Uei, Shyr, Bor-Shiuan, Chen, Shih-Chin, Shyr, Yi-Ming, Wang, Shin-E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548435/
https://www.ncbi.nlm.nih.gov/pubmed/34702876
http://dx.doi.org/10.1038/s41598-021-00621-y
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author Shyr, Bor-Uei
Shyr, Bor-Shiuan
Chen, Shih-Chin
Shyr, Yi-Ming
Wang, Shin-E.
author_facet Shyr, Bor-Uei
Shyr, Bor-Shiuan
Chen, Shih-Chin
Shyr, Yi-Ming
Wang, Shin-E.
author_sort Shyr, Bor-Uei
collection PubMed
description Theoretically, pancreas transplant alone in uremic (PTAU) patients could also be one of the options for those waiting for both pancreas and kidney grafts, but it has never been reported. There were 160 cases of pancreas transplant in this study, including 16% PTAU. The 5-year patient survival was 66.2% after PTAU, 94.5% after SPK, 95.8% after PAK, and 95.4% after PTA. Rejection of pancreas graft was significantly lower in PTAU group (3.8%), followed by 16.7% in pancreas after kidney transplant (PAK), 29.8% in simultaneous pancreas and kidney transplant (SPK) and 37.0% in pancreas transplant alone (PTA). Fasting blood sugar and serum HbA1c levels after PTAU were not significantly different from those by other subgroups. The 5-year death-censored pancreas graft survival was 100% after PTAU and PAK, and 97.0% after SPK and 77.9% after PTA. However, the 5-year death-uncensored pancreas graft survival was 67.0% after PTAU, 100% after PAK, 91.3% after SPK, and 74.0% after PTA. The superior graft survival in the PTAU group was achieved only if deaths with a functioning graft were censored. In conclusion, given the inferior patient survival outcome, PTAU is still not recommended unless SPK and PAK is not available. Although PTAU could be a treatment option for patients with diabetes complicated by end-stage renal disease (ESRD) in terms of surgical risks, endocrine function, and immunological and graft survival outcomes, modification of the organ allocation policies to prioritize SPK transplant in eligible patients should be the prime goal.
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spelling pubmed-85484352021-10-28 Inferior survival outcomes of pancreas transplant alone in uremic patients Shyr, Bor-Uei Shyr, Bor-Shiuan Chen, Shih-Chin Shyr, Yi-Ming Wang, Shin-E. Sci Rep Article Theoretically, pancreas transplant alone in uremic (PTAU) patients could also be one of the options for those waiting for both pancreas and kidney grafts, but it has never been reported. There were 160 cases of pancreas transplant in this study, including 16% PTAU. The 5-year patient survival was 66.2% after PTAU, 94.5% after SPK, 95.8% after PAK, and 95.4% after PTA. Rejection of pancreas graft was significantly lower in PTAU group (3.8%), followed by 16.7% in pancreas after kidney transplant (PAK), 29.8% in simultaneous pancreas and kidney transplant (SPK) and 37.0% in pancreas transplant alone (PTA). Fasting blood sugar and serum HbA1c levels after PTAU were not significantly different from those by other subgroups. The 5-year death-censored pancreas graft survival was 100% after PTAU and PAK, and 97.0% after SPK and 77.9% after PTA. However, the 5-year death-uncensored pancreas graft survival was 67.0% after PTAU, 100% after PAK, 91.3% after SPK, and 74.0% after PTA. The superior graft survival in the PTAU group was achieved only if deaths with a functioning graft were censored. In conclusion, given the inferior patient survival outcome, PTAU is still not recommended unless SPK and PAK is not available. Although PTAU could be a treatment option for patients with diabetes complicated by end-stage renal disease (ESRD) in terms of surgical risks, endocrine function, and immunological and graft survival outcomes, modification of the organ allocation policies to prioritize SPK transplant in eligible patients should be the prime goal. Nature Publishing Group UK 2021-10-26 /pmc/articles/PMC8548435/ /pubmed/34702876 http://dx.doi.org/10.1038/s41598-021-00621-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shyr, Bor-Uei
Shyr, Bor-Shiuan
Chen, Shih-Chin
Shyr, Yi-Ming
Wang, Shin-E.
Inferior survival outcomes of pancreas transplant alone in uremic patients
title Inferior survival outcomes of pancreas transplant alone in uremic patients
title_full Inferior survival outcomes of pancreas transplant alone in uremic patients
title_fullStr Inferior survival outcomes of pancreas transplant alone in uremic patients
title_full_unstemmed Inferior survival outcomes of pancreas transplant alone in uremic patients
title_short Inferior survival outcomes of pancreas transplant alone in uremic patients
title_sort inferior survival outcomes of pancreas transplant alone in uremic patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548435/
https://www.ncbi.nlm.nih.gov/pubmed/34702876
http://dx.doi.org/10.1038/s41598-021-00621-y
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