There Is Life After the UK Clozapine Central Non-Rechallenge Database

Author:

Oloyede Ebenezer12ORCID,Casetta Cecilia23,Dzahini Olubanke14,Segev Aviv25,Gaughran Fiona23,Shergill Sukhi23,Mijovic Alek6,Helthuis Marinka7,Whiskey Eromona1238,MacCabe James Hunter238,Taylor David14

Affiliation:

1. Pharmacy Department, South London and Maudsley NHS Foundation Trust, London, UK

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

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

4. Institute of Pharmaceutical Science, King’s College, London, UK

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

6. Kings College Hospital NHS Foundation Trust, London, UK

7. Leyden Delta B.V., Nijmegen, The Netherlands

8. NIHR Biomedical Research Centre for Mental Health South London and Maudsley NHS, London, UK

Abstract

Abstract Background and Aims In the United Kingdom, patients on clozapine whose hematological parameters fall below certain thresholds are placed on the Central Non-Rechallenge Database (CNRD), meaning that they cannot be prescribed clozapine again except under exceptional circumstances. This practice was discontinued in the United States in 2015 by expanding the hematological monitoring guidelines, allowing more patients to receive clozapine. Our objective was to investigate the implications this policy change would have on clozapine utilization in the United Kingdom. Methods This was an observational, retrospective analysis of patients registered on the CNRD in a large mental health trust. The first objective was to compare the number of patients placed on the CNRD under the United Kingdom and the US Food and Drug Administration (FDA) criteria. The second objective was to explore the hematological and clinical outcomes of CNRD patients. The third objective was to investigate the hematological outcomes of patients rechallenged on clozapine after nonrechallengeable status. Results One hundred and fifteen patients were placed on CNRD from 2002 to 2019, of whom 7 (6%) met the equivalent criteria for clozapine discontinuation under the FDA guidelines. Clinical outcomes, as measured by the Clinical Global Impression-Severity scale, were worse 3 months after clozapine cessation than on clozapine (t = −7.4862; P < .001). Sixty-two (54%) patients placed on CNRD were rechallenged. Fifty-nine of those (95%) were successfully rechallenged; 3 patients were placed back on CNRD, only one of which would have had to stop clozapine again under FDA criteria. Conclusion Implementation of the updated FDA’s monitoring criteria in the United Kingdom would significantly reduce clozapine discontinuation due to hematological reasons. The evidence suggests an urgent need for revising the UK clozapine monitoring guidelines to improve outcomes in treatment-resistant schizophrenia.

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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