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Immunosuppression minimization vs. complete drug withdrawal in liver transplantation
被引:78
|作者:
Londono, Maria-Carlota
[1
]
Rimola, Antoni
[1
]
O'Grady, John
[2
]
Sanchez-Fueyo, Alberto
[2
]
机构:
[1] Univ Barcelona, Hosp Clin Barcelona, IDIBAPS,CIBEREHD, Liver Unit, Barcelona, Spain
[2] Kings Coll London, Kings Coll Hosp London, Inst Liver Studies, London, England
基金:
英国医学研究理事会;
关键词:
Immunosuppression minimization;
Immunosuppression withdrawal;
Liver transplantation;
HEPATITIS-C VIRUS;
RANDOMIZED CONTROLLED-TRIAL;
CHRONIC RENAL DYSFUNCTION;
HOT-TOPIC DEBATE;
CALCINEURIN INHIBITOR;
TACROLIMUS MONOTHERAPY;
OPERATIONAL TOLERANCE;
SIROLIMUS CONVERSION;
MYCOPHENOLATE-MOFETIL;
ORGAN-TRANSPLANTATION;
D O I:
10.1016/j.jhep.2013.04.003
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Despite the increase in long-term survival, liver transplant recipients still exhibit higher morbidity and mortality than the general population. This is in part attributed to the lifelong administration of immunosuppression and its associated side effects. Several studies reported in the last decades have evaluated the impact of immunosuppression minimization in liver transplant recipients, but results have been inconsistent due to the heterogeneity of study designs and insufficient sample sizes. On the other hand, complete immunosuppression withdrawal has proven to be feasible in approximately 20% of carefully selected liver transplant recipients, especially in older patients and those with longer duration after transplantation. The long-term risks and clinical benefits of this strategy, however, also need to be clarified. As a consequence, and despite the general perception that a large proportion of liver recipients are over-immunosuppressed, it is currently not possible to derive evidence-based guidelines on how to manage long-term immunosuppression to improve clinical outcomes. Large clinical trials of drug minimization and/or withdrawal focused on clinically-relevant long-term outcomes are required. Development of personalized medicine tools and a deeper understanding of the pathogenesis of idiopathic inflammatory graft lesions will be pre-requisites to achieve these goals. (C) 2013 Published by Elsevier B. V. on behalf of the European Association for the Study of the Liver.
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页码:872 / 879
页数:8
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