Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study

Introduction and aim: The interleukin-2 receptor antagonist; basiliximab is used to allow delayed introduction of Calcineurin inhibitors (CNI) after liver transplantation and thus delay their renal insult. However, there is only little evidence for the safety and the efficacy of this regimen. This s...

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Main Authors: Mohamed Hashim, Ayman Alsebaey, Amr Ragab, Hossam Eldeen Soliman, Imam Waked
Format: Article
Language:English
Published: Elsevier 2020-09-01
Series:Annals of Hepatology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1665268120300818
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author Mohamed Hashim
Ayman Alsebaey
Amr Ragab
Hossam Eldeen Soliman
Imam Waked
author_facet Mohamed Hashim
Ayman Alsebaey
Amr Ragab
Hossam Eldeen Soliman
Imam Waked
author_sort Mohamed Hashim
collection DOAJ
description Introduction and aim: The interleukin-2 receptor antagonist; basiliximab is used to allow delayed introduction of Calcineurin inhibitors (CNI) after liver transplantation and thus delay their renal insult. However, there is only little evidence for the safety and the efficacy of this regimen. This study aimed to evaluate the effectiveness and safety of basiliximab induction in liver transplantation. Materials and methods: This study included 89 patients who were classified into two groups: standard triple immunosuppression (IS) regimen of steroid, tacrolimus (TAC) and mycophenolate mofetil (MMF) (n = 47) and induction IS regimen of basiliximab, low dose steroids and MMF with delayed introduction of CNI (n = 42). All patients were followed after liver transplantation for at least six months or until death. Results: There were no significant differences in patient survival, graft dysfunction, infection rate or type, or wound healing between both groups. The acute rejection rate was equivalent in both groups. Renal dysfunction in the first six months post-transplant was less in the basiliximab group in comparison to the other group (7.1% and 19.1% respectively). Conclusion: Basiliximab-induced IS protocol is a safe regimen that reduces medium-term renal dysfunction and achieves similar survival without increasing the acute rejection or infection rate in liver transplantation recipients.
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spelling doaj.art-d8aeb29f864f48ae99c4ce2720af0d052022-12-21T22:30:38ZengElsevierAnnals of Hepatology1665-26812020-09-01195541545Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center studyMohamed Hashim0Ayman Alsebaey1Amr Ragab2Hossam Eldeen Soliman3Imam Waked4Department of Hepatology, National Liver Institute, Menoufiya University, Shebin Elkom, Egypt; Corresponding author at: National Liver Institute, Menoufiya University, Meleg Road, Shebin ElKom, Egypt.Department of Hepatology, National Liver Institute, Menoufiya University, Shebin Elkom, EgyptDepartment of Hepatology, National Liver Institute, Menoufiya University, Shebin Elkom, EgyptDepartment of Hepatobiliary and Pancreatic Surgery, National Liver Institute, Menoufiya University, Shebin Elkom, EgyptDepartment of Hepatology, National Liver Institute, Menoufiya University, Shebin Elkom, EgyptIntroduction and aim: The interleukin-2 receptor antagonist; basiliximab is used to allow delayed introduction of Calcineurin inhibitors (CNI) after liver transplantation and thus delay their renal insult. However, there is only little evidence for the safety and the efficacy of this regimen. This study aimed to evaluate the effectiveness and safety of basiliximab induction in liver transplantation. Materials and methods: This study included 89 patients who were classified into two groups: standard triple immunosuppression (IS) regimen of steroid, tacrolimus (TAC) and mycophenolate mofetil (MMF) (n = 47) and induction IS regimen of basiliximab, low dose steroids and MMF with delayed introduction of CNI (n = 42). All patients were followed after liver transplantation for at least six months or until death. Results: There were no significant differences in patient survival, graft dysfunction, infection rate or type, or wound healing between both groups. The acute rejection rate was equivalent in both groups. Renal dysfunction in the first six months post-transplant was less in the basiliximab group in comparison to the other group (7.1% and 19.1% respectively). Conclusion: Basiliximab-induced IS protocol is a safe regimen that reduces medium-term renal dysfunction and achieves similar survival without increasing the acute rejection or infection rate in liver transplantation recipients.http://www.sciencedirect.com/science/article/pii/S1665268120300818TransplantationImmunosuppressionBasiliximabCalcineurin inhibitorsinterleukin-2Rejection
spellingShingle Mohamed Hashim
Ayman Alsebaey
Amr Ragab
Hossam Eldeen Soliman
Imam Waked
Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study
Annals of Hepatology
Transplantation
Immunosuppression
Basiliximab
Calcineurin inhibitors
interleukin-2
Rejection
title Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study
title_full Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study
title_fullStr Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study
title_full_unstemmed Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study
title_short Efficacy and safety of basiliximab as initial immunosuppression in liver transplantation: A single center study
title_sort efficacy and safety of basiliximab as initial immunosuppression in liver transplantation a single center study
topic Transplantation
Immunosuppression
Basiliximab
Calcineurin inhibitors
interleukin-2
Rejection
url http://www.sciencedirect.com/science/article/pii/S1665268120300818
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