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 :...

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Main Authors: Eun Sung Jeong, Kyo Won Lee, Sang Jin Kim, Hee Jin Yoo, Kyung A Kim, Jae Berm Park
Format: Article
Language:English
Published: Korean Society for Transplantation 2019-12-01
Series:Korean Journal of Transplantation
Subjects:
Online Access:http://journaleditor.inforang.com/journal/view.html?doi=10.4285/jkstn.2019.33.4.118
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author Eun Sung Jeong
Kyo Won Lee
Sang Jin Kim
Hee Jin Yoo
Kyung A Kim
Jae Berm Park
author_facet Eun Sung Jeong
Kyo Won Lee
Sang Jin Kim
Hee Jin Yoo
Kyung A Kim
Jae Berm Park
author_sort Eun Sung Jeong
collection DOAJ
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).Conclusion : s: 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.
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spelling doaj.art-ce9e2c04980c456f9d84ce03a47384d32024-02-02T04:20:13ZengKorean Society for TransplantationKorean Journal of Transplantation2671-87902019-12-0133411812710.4285/jkstn.2019.33.4.118jkstn.2019.33.4.118Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapiesEun Sung Jeong0Kyo Won Lee1Sang Jin Kim2Hee Jin Yoo3Kyung A Kim4Jae Berm Park5Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, KoreaDepartment of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, KoreaDepartment of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, KoreaBiostatistics and Clinical Epidemiology Center, Samsung Medical Center, Seoul, KoreaBiostatistics and Clinical Epidemiology Center, Samsung Medical Center, Seoul, KoreaDepartment of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, KoreaBackground : 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).Conclusion : s: 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.http://journaleditor.inforang.com/journal/view.html?doi=10.4285/jkstn.2019.33.4.118kidney transplantation; immunosuppressive agent; graft rejection
spellingShingle Eun Sung Jeong
Kyo Won Lee
Sang Jin Kim
Hee Jin Yoo
Kyung A Kim
Jae Berm Park
Comparison of clinical outcomes of deceased donor kidney transplantations, with a focus on three induction therapies
Korean Journal of Transplantation
kidney transplantation; immunosuppressive agent; graft rejection
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 kidney transplantation; immunosuppressive agent; graft rejection
url http://journaleditor.inforang.com/journal/view.html?doi=10.4285/jkstn.2019.33.4.118
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