Basiliximab With Delayed Tacrolimus Improves Short-Term Renal Outcomes Post-Liver Transplantation-a Real-World Experience.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 11 12 2020
revised: 16 03 2021
accepted: 05 04 2021
pubmed: 3 6 2021
medline: 13 7 2021
entrez: 2 6 2021
Statut: ppublish

Résumé

Acute kidney injury (AKI) is common after liver transplantation (LT). Induction with interleukin-2 receptor antagonists is often used as a "renal-sparing" strategy. The aim of this study was to assess this approach in a real-world setting in an LT center. A retrospective cohort analysis of LTs between 2011 and 2018 was performed to assess the impact of a renal-sparing strategy using basiliximab in conjunction with mycophenolate mofetil and corticosteroids from day 0 post-LT along with delayed introduction of tacrolimus. This was compared with a group receiving tacrolimus, mycophenolate mofetil, and corticosteroids from the outset. The renal-sparing regimen was associated with significantly lower incidence of all-stage AKI at day 7 post-LT (36% vs 55%, P = .006) and less decline in renal function at 3 months (39% vs 57%, P = .01). No further significant differences in renal outcomes were observed at other time points on follow-up to 1 year post-LT. There was no significant difference in the incidence of acute cellular rejection, inpatient length of stay or graft survival. The decision to adopt a renal-sparing regimen was predominantly made on a clinically reactive basis within the first 24 hours post-LT in 77%, and was preordained in 23%. Cost-effectiveness analysis did not find evidence of a significant cost saving when using a renal-sparing strategy. This study provides real-world analysis of the use of a renal-sparing immunosuppression regimen in LT. Although improvements in incidence of AKI in the short term were demonstrated, this did not translate to cost savings or improved renal outcomes after 3 months.

Sections du résumé

BACKGROUND BACKGROUND
Acute kidney injury (AKI) is common after liver transplantation (LT). Induction with interleukin-2 receptor antagonists is often used as a "renal-sparing" strategy. The aim of this study was to assess this approach in a real-world setting in an LT center.
METHODS METHODS
A retrospective cohort analysis of LTs between 2011 and 2018 was performed to assess the impact of a renal-sparing strategy using basiliximab in conjunction with mycophenolate mofetil and corticosteroids from day 0 post-LT along with delayed introduction of tacrolimus. This was compared with a group receiving tacrolimus, mycophenolate mofetil, and corticosteroids from the outset.
RESULTS RESULTS
The renal-sparing regimen was associated with significantly lower incidence of all-stage AKI at day 7 post-LT (36% vs 55%, P = .006) and less decline in renal function at 3 months (39% vs 57%, P = .01). No further significant differences in renal outcomes were observed at other time points on follow-up to 1 year post-LT. There was no significant difference in the incidence of acute cellular rejection, inpatient length of stay or graft survival. The decision to adopt a renal-sparing regimen was predominantly made on a clinically reactive basis within the first 24 hours post-LT in 77%, and was preordained in 23%. Cost-effectiveness analysis did not find evidence of a significant cost saving when using a renal-sparing strategy.
CONCLUSION CONCLUSIONS
This study provides real-world analysis of the use of a renal-sparing immunosuppression regimen in LT. Although improvements in incidence of AKI in the short term were demonstrated, this did not translate to cost savings or improved renal outcomes after 3 months.

Identifiants

pubmed: 34074467
pii: S0041-1345(21)00249-9
doi: 10.1016/j.transproceed.2021.04.001
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Immunosuppressive Agents 0
Basiliximab 9927MT646M
Mycophenolic Acid HU9DX48N0T
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1541-1547

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Alexander Boyd (A)

The Liver Unit, NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust and University of Birmingham, Birmingham, United Kingdom; The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom; The Liver Unit, University of Birmingham, Birmingham, United Kingdom. Electronic address: alexander.boyd3@nhs.net.

Andrew Brown (A)

The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Jaimin Patel (J)

Department of Critical Care, The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom; Department of Critical Care, University of Birmingham, Birmingham, United Kingdom.

Peter Nightingale (P)

Department of Statistics, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

M Thamara P R Perera (MTPR)

The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

James Ferguson (J)

The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom; The Liver Unit, University of Birmingham, Birmingham, United Kingdom.

James Neuberger (J)

The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Neil Rajoriya (N)

The Liver Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom; The Liver Unit, University of Birmingham, Birmingham, United Kingdom.

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Classifications MeSH