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Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment

BACKGROUND: Clozapine is the only licensed medication for treatment-resistant schizophrenia. The metabolism of clozapine is affected by multiple pharmacokinetic interactions, so the co-administration of adjunct medications can have a significant clinical effect. The anti- tuberculosis medication rif...

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Autores principales: Gee, Siobhan, Dixon, Thomas, Docherty, Mary, Shergill, Sukhwinder S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542109/
https://www.ncbi.nlm.nih.gov/pubmed/26265348
http://dx.doi.org/10.1186/s12888-015-0536-4
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author Gee, Siobhan
Dixon, Thomas
Docherty, Mary
Shergill, Sukhwinder S
author_facet Gee, Siobhan
Dixon, Thomas
Docherty, Mary
Shergill, Sukhwinder S
author_sort Gee, Siobhan
collection PubMed
description BACKGROUND: Clozapine is the only licensed medication for treatment-resistant schizophrenia. The metabolism of clozapine is affected by multiple pharmacokinetic interactions, so the co-administration of adjunct medications can have a significant clinical effect. The anti- tuberculosis medication rifampicin is a potent inducer of the cytochrome P450 system and therefore can cause a reduction in the plasma concentration of clozapine. There is limited clinical evidence regarding co-administration of these medications; in particular there is a lack of data regarding the effect on plasma clozapine levels, which is the key factor determining clinical efficacy. This is clinically relevant given evidence of an increased risk of tuberculosis in patients with schizophrenia. CASE PRESENTATION: We present a case of a 28 year old British man with a diagnosis of schizoaffective disorder who presented with persistent psychotic symptoms. He developed a systemic inflammatory condition, diagnosed as tuberculosis, and was commenced on a six month course of treatment that included rifampicin. This case presents comprehensive data to illustrate the effect on clozapine plasma levels of a complete course of tuberculosis therapy. CONCLUSION: This case report provides guidance to clinicians in managing drug interactions between clozapine and rifampicin to enable safe and effective treatment. The co-administration of these medications is likely to increase as the existing underuse of clozapine is recognised whilst the incidence of tuberculosis increases.
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spelling pubmed-45421092015-08-21 Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment Gee, Siobhan Dixon, Thomas Docherty, Mary Shergill, Sukhwinder S BMC Psychiatry Case Report BACKGROUND: Clozapine is the only licensed medication for treatment-resistant schizophrenia. The metabolism of clozapine is affected by multiple pharmacokinetic interactions, so the co-administration of adjunct medications can have a significant clinical effect. The anti- tuberculosis medication rifampicin is a potent inducer of the cytochrome P450 system and therefore can cause a reduction in the plasma concentration of clozapine. There is limited clinical evidence regarding co-administration of these medications; in particular there is a lack of data regarding the effect on plasma clozapine levels, which is the key factor determining clinical efficacy. This is clinically relevant given evidence of an increased risk of tuberculosis in patients with schizophrenia. CASE PRESENTATION: We present a case of a 28 year old British man with a diagnosis of schizoaffective disorder who presented with persistent psychotic symptoms. He developed a systemic inflammatory condition, diagnosed as tuberculosis, and was commenced on a six month course of treatment that included rifampicin. This case presents comprehensive data to illustrate the effect on clozapine plasma levels of a complete course of tuberculosis therapy. CONCLUSION: This case report provides guidance to clinicians in managing drug interactions between clozapine and rifampicin to enable safe and effective treatment. The co-administration of these medications is likely to increase as the existing underuse of clozapine is recognised whilst the incidence of tuberculosis increases. BioMed Central 2015-08-12 /pmc/articles/PMC4542109/ /pubmed/26265348 http://dx.doi.org/10.1186/s12888-015-0536-4 Text en © Gee et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (http://creativecommons.org/licenses/by/4.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Gee, Siobhan
Dixon, Thomas
Docherty, Mary
Shergill, Sukhwinder S
Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
title Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
title_full Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
title_fullStr Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
title_full_unstemmed Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
title_short Optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
title_sort optimising plasma levels of clozapine during metabolic interactions: a review and case report with adjunct rifampicin treatment
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542109/
https://www.ncbi.nlm.nih.gov/pubmed/26265348
http://dx.doi.org/10.1186/s12888-015-0536-4
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