Weight-based tacrolimus trough concentrations post liver transplant.


Journal

Internal medicine journal
ISSN: 1445-5994
Titre abrégé: Intern Med J
Pays: Australia
ID NLM: 101092952

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 23 03 2018
revised: 30 06 2018
accepted: 17 07 2018
pubmed: 26 7 2018
medline: 21 9 2019
entrez: 26 7 2018
Statut: ppublish

Résumé

Tacrolimus is one of the most widely used liver transplant medications. With the increasing number of obese patients requiring liver transplants, knowledge of the effect of body size affecting post-transplant outcomes, for example drug exposure is increasingly required. (i) To investigate whether patient body size (i.e. total bodyweight) affects trough plasma concentrations of tacrolimus when a standard mg/kg dosing regimen is used; and (ii) to investigate whether obese patients have different numbers of plasma concentrations outside the therapeutic range compared to non-obese patients in the first months after liver transplant. Using a transplant database, data tacrolimus concentrations were available for 69 patients. Tacrolimus was initially dosed at a standard 0.1 mg/kg/day after liver transplant, and adjusted to maintain a target trough concentration. Trough blood samples, phenotypic and outcome variables were analysed. Trough concentrations were similar between obese and non-obese patients (P > 0.05) at each sampling day. At day 7 post-transplant, 85.7% and 79.5% of the observed plasma concentrations were outside the recommended therapeutic range for obese and non-obese patients respectively, at day 30, 52.9% and 57.4%, and at 6 months, 18.7% and 27.5%. In the first week post-transplant, tacrolimus trough concentrations after standard mg/kg dosing post liver transplant appear to be corrected by total bodyweight. Obese patients have a similar number of trough plasma concentrations outside the therapeutic range compared to non-obese patients.

Sections du résumé

BACKGROUND BACKGROUND
Tacrolimus is one of the most widely used liver transplant medications. With the increasing number of obese patients requiring liver transplants, knowledge of the effect of body size affecting post-transplant outcomes, for example drug exposure is increasingly required.
AIMS OBJECTIVE
(i) To investigate whether patient body size (i.e. total bodyweight) affects trough plasma concentrations of tacrolimus when a standard mg/kg dosing regimen is used; and (ii) to investigate whether obese patients have different numbers of plasma concentrations outside the therapeutic range compared to non-obese patients in the first months after liver transplant.
METHODS METHODS
Using a transplant database, data tacrolimus concentrations were available for 69 patients. Tacrolimus was initially dosed at a standard 0.1 mg/kg/day after liver transplant, and adjusted to maintain a target trough concentration. Trough blood samples, phenotypic and outcome variables were analysed.
RESULTS RESULTS
Trough concentrations were similar between obese and non-obese patients (P > 0.05) at each sampling day. At day 7 post-transplant, 85.7% and 79.5% of the observed plasma concentrations were outside the recommended therapeutic range for obese and non-obese patients respectively, at day 30, 52.9% and 57.4%, and at 6 months, 18.7% and 27.5%.
CONCLUSION CONCLUSIONS
In the first week post-transplant, tacrolimus trough concentrations after standard mg/kg dosing post liver transplant appear to be corrected by total bodyweight. Obese patients have a similar number of trough plasma concentrations outside the therapeutic range compared to non-obese patients.

Identifiants

pubmed: 30043532
doi: 10.1111/imj.14043
doi:

Substances chimiques

Immunosuppressive Agents 0
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-83

Informations de copyright

© 2018 Royal Australasian College of Physicians.

Auteurs

Zheng Liu (Z)

School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia.
Clinical Pharmacology, Department of Medicine, The Royal Children's Hospital, Melbourne, Victoria, Australia.

Jeffrey Cheng (J)

School of Medicine, University of Queensland, Brisbane, Queensland, Australia.
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Elizabeth Powell (E)

School of Medicine, University of Queensland, Brisbane, Queensland, Australia.
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Graeme Macdonald (G)

Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
PA-Southside Clinical School, University of Queensland, Brisbane, Queensland, Australia.
Translational Research Institute, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Jonathan Fawcett (J)

School of Medicine, University of Queensland, Brisbane, Queensland, Australia.

Stephen Lynch (S)

School of Medicine, University of Queensland, Brisbane, Queensland, Australia.
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Jennifer Martin (J)

School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia.

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