Long-Term Outcome After Tacrolimus-Related Neurotoxicity in Pediatric Living Donor Liver Transplantation.


Journal

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

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 09 12 2021
accepted: 29 12 2021
pubmed: 26 1 2022
medline: 1 4 2022
entrez: 25 1 2022
Statut: ppublish

Résumé

Tacrolimus-related neurotoxicity is a serious complication. Posterior reversible encephalopathy syndrome, which is severe neurotoxicity after pediatric living donor liver transplantation (LDLT), is a medication-induced complication related to calcineurin inhibitors. The purpose of this study was to evaluate the long-term outcome of tacrolimus-related neurotoxicity after pediatric LDLT. Pediatric patients who underwent LDLT between 2007 and 2020 at our institution and developed neurologic symptoms with tacrolimus were included in the study. Tacrolimus-related encephalopathy was defined as encephalopathy that resolved after tacrolimus was discontinued. All patients received tacrolimus and a steroid for immunosuppression starting just after LDLT. During the study period, 128 patients underwent LDLT. All patients received tacrolimus and a steroid. Six patients (5%) developed tacrolimus-related encephalopathy. The median age at transplant was 1.6 years. The original diseases were biliary atresia (n = 5) and progressive familial intrahepatic cholangiopathy type 2 (n = 1). Patients developed encephalopathy at a median of 9 days after LDLT. All patients recovered with conversion to cyclosporine. Posterior reversible encephalopathy syndrome was confirmed by magnetic resonance imaging in 3 patients. The mean tacrolimus level at encephalopathy was 11 ng/dL (range, 5.6-14.6 ng/dL). White blood cell count elevation was observed in all patients. One patient died of pancreatitis. Surviving patients (n = 5) were followed for a median of 9 years. All patients resumed tacrolimus a median of 8 months from onset. No neurologic complications were observed after resuming tacrolimus. We observed tacrolimus-induced encephalopathy in 5% of patients after pediatric LDLT. Patients can resume tacrolimus safely without further neurologic symptoms.

Sections du résumé

BACKGROUND BACKGROUND
Tacrolimus-related neurotoxicity is a serious complication. Posterior reversible encephalopathy syndrome, which is severe neurotoxicity after pediatric living donor liver transplantation (LDLT), is a medication-induced complication related to calcineurin inhibitors. The purpose of this study was to evaluate the long-term outcome of tacrolimus-related neurotoxicity after pediatric LDLT.
METHODS METHODS
Pediatric patients who underwent LDLT between 2007 and 2020 at our institution and developed neurologic symptoms with tacrolimus were included in the study. Tacrolimus-related encephalopathy was defined as encephalopathy that resolved after tacrolimus was discontinued. All patients received tacrolimus and a steroid for immunosuppression starting just after LDLT.
RESULTS RESULTS
During the study period, 128 patients underwent LDLT. All patients received tacrolimus and a steroid. Six patients (5%) developed tacrolimus-related encephalopathy. The median age at transplant was 1.6 years. The original diseases were biliary atresia (n = 5) and progressive familial intrahepatic cholangiopathy type 2 (n = 1). Patients developed encephalopathy at a median of 9 days after LDLT. All patients recovered with conversion to cyclosporine. Posterior reversible encephalopathy syndrome was confirmed by magnetic resonance imaging in 3 patients. The mean tacrolimus level at encephalopathy was 11 ng/dL (range, 5.6-14.6 ng/dL). White blood cell count elevation was observed in all patients. One patient died of pancreatitis. Surviving patients (n = 5) were followed for a median of 9 years. All patients resumed tacrolimus a median of 8 months from onset. No neurologic complications were observed after resuming tacrolimus.
CONCLUSION CONCLUSIONS
We observed tacrolimus-induced encephalopathy in 5% of patients after pediatric LDLT. Patients can resume tacrolimus safely without further neurologic symptoms.

Identifiants

pubmed: 35074159
pii: S0041-1345(21)00956-8
doi: 10.1016/j.transproceed.2021.12.036
pii:
doi:

Substances chimiques

Immunosuppressive Agents 0
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

468-471

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Takehisa Ueno (T)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan. Electronic address: ueno@pedsurg.med.osaka-u.ac.jpl.

Chiyoshi Toyama (C)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Koichi Deguchi (K)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Kazunori Masahata (K)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Motonari Nomura (M)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Miho Watanabe (M)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Masafumi Kamiyama (M)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Yuko Tazuke (Y)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

Kazuhiko Bessho (K)

Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.

Hiroomi Okuyama (H)

Pediatric Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

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Classifications MeSH