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Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies
BACKGROUND: Graft survival rate of kidney transplantation recipients improves after induction therapy. However, there is no conclusive evidence on which regimen is superior for deceased donor kidney transplantation (DDKT). This study aims at discussing effective induction therapy in DDKT. METHODS: B...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Transplantation
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188948/ https://www.ncbi.nlm.nih.gov/pubmed/35769973 http://dx.doi.org/10.4285/jkstn.2019.33.4.118 |
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author | Jeong, Eun Sung Lee, Kyo Won Kim, Sang Jin Yoo, Hee Jin Kim, Kyung A Park, Jae Berm |
author_facet | Jeong, Eun Sung Lee, Kyo Won Kim, Sang Jin Yoo, Hee Jin Kim, Kyung A Park, Jae Berm |
author_sort | Jeong, Eun Sung |
collection | PubMed |
description | BACKGROUND: Graft survival rate of kidney transplantation recipients improves after induction therapy. However, there is no conclusive evidence on which regimen is superior for deceased donor kidney transplantation (DDKT). This study aims at discussing effective induction therapy in DDKT. METHODS: Between 2003 and 2016, 395 DDKT recipients were divided into three groups following induction therapy. Recipients of the basiliximab group (n=184) received basiliximab (20 mg/kg) on days 0 and 4. Recipients of the low-dose rabbit anti-thymocyte globulin (rATG) group (n=113) received rATG (1.5 mg/kg) on days 0, 1, and 2, while those of the high-dose rATG group (n=98) received it for more than 4 days. We retrospectively reviewed and analyzed the clinical outcomes and adverse effects of induction therapy. RESULTS: Compared to other groups, the low-dose rATG group donors were older (P<0.001); rATG group donors had higher serum creatinine levels (P<0.001), and the basiliximab group showed a lower delayed graft function rate (P=0.004). In graft failure, the low-dose rATG group did not differ significantly from the basiliximab group (P=0.080), but was significantly different from the high-dose rATG group (P=0.004). CONCLUSIONS: The low-dose rATG group had the best graft survival rate, although it had older donors and higher serum creatinine levels. Therefore, low-dose rATG may be considered an effective induction therapy in DDKT. |
format | Online Article Text |
id | pubmed-9188948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Society for Transplantation |
record_format | MEDLINE/PubMed |
spelling | pubmed-91889482022-06-28 Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies Jeong, Eun Sung Lee, Kyo Won Kim, Sang Jin Yoo, Hee Jin Kim, Kyung A Park, Jae Berm Korean J Transplant Original Article BACKGROUND: Graft survival rate of kidney transplantation recipients improves after induction therapy. However, there is no conclusive evidence on which regimen is superior for deceased donor kidney transplantation (DDKT). This study aims at discussing effective induction therapy in DDKT. METHODS: Between 2003 and 2016, 395 DDKT recipients were divided into three groups following induction therapy. Recipients of the basiliximab group (n=184) received basiliximab (20 mg/kg) on days 0 and 4. Recipients of the low-dose rabbit anti-thymocyte globulin (rATG) group (n=113) received rATG (1.5 mg/kg) on days 0, 1, and 2, while those of the high-dose rATG group (n=98) received it for more than 4 days. We retrospectively reviewed and analyzed the clinical outcomes and adverse effects of induction therapy. RESULTS: Compared to other groups, the low-dose rATG group donors were older (P<0.001); rATG group donors had higher serum creatinine levels (P<0.001), and the basiliximab group showed a lower delayed graft function rate (P=0.004). In graft failure, the low-dose rATG group did not differ significantly from the basiliximab group (P=0.080), but was significantly different from the high-dose rATG group (P=0.004). CONCLUSIONS: The low-dose rATG group had the best graft survival rate, although it had older donors and higher serum creatinine levels. Therefore, low-dose rATG may be considered an effective induction therapy in DDKT. The Korean Society for Transplantation 2019-12-31 2019-12-31 /pmc/articles/PMC9188948/ /pubmed/35769973 http://dx.doi.org/10.4285/jkstn.2019.33.4.118 Text en Copyright: © 2019 The Korean Society for Transplantation https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jeong, Eun Sung Lee, Kyo Won Kim, Sang Jin Yoo, Hee Jin Kim, Kyung A Park, Jae Berm Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
title | Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
title_full | Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
title_fullStr | Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
title_full_unstemmed | Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
title_short | Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
title_sort | comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9188948/ https://www.ncbi.nlm.nih.gov/pubmed/35769973 http://dx.doi.org/10.4285/jkstn.2019.33.4.118 |
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