Outcomes in treatment-resistant schizophrenia: symptoms, function and clozapine plasma concentrations

Author:

Krivoy Amir123ORCID,Whiskey Eromona45ORCID,Webb-Wilson Henrietta4,Joyce Dan6,Tracy Derek K.57ORCID,Gaughran Fiona45,MacCabe James H.45,Shergill Sukhwinder S.45

Affiliation:

1. Geha Mental Health Center, Petach-Tikva, Israel

2. Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King’s College London, 16 De Crespigny Park, London, SE5 8AF, UK

3. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

4. National Psychosis Service, South London and Maudsley NHS Foundation Trust, London, UK

5. Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King’s College London, London, UK

6. National Institute of Health Research Oxford Health Biomedical Research Center and Department of Psychiatry, Warneford Hospital, University of Oxford, Oxford, UK

7. West London NHS Foundation Trust, London, UK

Abstract

Background: Clozapine is the only medication licenced for treating patients with treatment-refractory schizophrenia. However, there are no evidence-based guidelines as to the optimal plasma level of clozapine to aim for, and their association with clinical and functional outcome. Objective: We assessed the relationship between clinical and functional outcome measures and blood concentrations of clozapine among patients with treatment-refractory psychosis. Methods: Data were reviewed in 82 patients with treatment-refractory psychosis admitted to a specialised tertiary-level service and treated with clozapine. Analysis focussed on the relationship between clozapine and norclozapine plasma concentrations and the patient’s clinical symptoms and functional status. Results: Clinical symptom improvement was positively correlated with norclozapine plasma concentrations and inversely correlated with clozapine to norclozapine plasma concentrations ratio. Clozapine concentrations showed a bimodal association with clinical improvement (peaks around 350 and 660 ng/ml). Clinical symptom improvement correlated with functional outcomes, although there was no significant correlation between the latter and clozapine or norclozapine plasma concentrations. Conclusion: Clozapine treatment was associated with optimal clinical improvement at two different peak plasma concentrations around 350 and 650 ng/ml. Clinical improvement was associated with functional outcome; however, functionality was not directly associated with clozapine concentrations. A subset of patients may require higher clozapine plasma concentrations to achieve clinical improvement.

Funder

European Research Council Consolidator Award

NIHR Mental Health Biomedical Research Centre at SLAM NHS Foundation Trust and King’s College London

Boehringer Ingelheim, Otsuka,Takeda and Lundbeck

Publisher

SAGE Publications

Subject

Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Psychology (miscellaneous)

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