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Clozapine and COVID-19

Published online by Cambridge University Press:  28 July 2020

Edward Silva
Affiliation:
Consultant Psychiatrist, Ashworth Hospital, Mersey Care NHS Foundation Trust, UK; email: ed.silva@merseycare.nhs.uk
Siobhan Gee
Affiliation:
Principal Pharmacist, South London and Maudsley NHS Foundation Trust, Maudsley Hospital, UK
Shubulade Smith
Affiliation:
Consultant Psychiatrist, South London and the Maudsley NHS Foundation Trust and Visiting Senior Lecturer, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK
Fiona Gaughran
Affiliation:
Consultant Psychiatrist, National Psychosis Unit, South London and the Maudsley NHS Foundation Trust and Reader, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK
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Abstract

Type
Correspondence
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s) 2020

The COVID-19 pandemic presents psychiatrists prescribing clozapine with complexities over and above the general difficulties already described among Chinese psychiatric in-patients.Reference Xiang, Zhao, Liu, Li, Zhao and Cheung1 Some common initiation effects of clozapine: isolated fever, tachycardia or a mildly raised C-reactive proteinReference Roge, Moller, Andersen, Correll and Nielsen2 may be difficult to differentiate from intercurrent infection, including COVID-19.Reference Maharaj3 Other laboratory anomalies may add to confusion. Given COVID-19 infection deaths that are not the result of acute respiratory distress syndrome are often from fulminant myocarditis, for which a raised troponin is a poor prognostic feature, troponin levels taken routinely during clozapine initiation will need to be interpreted carefully. However, while leucopenia is a reported blood dyscrasia with COVID-19, to date neither neutropenia nor agranulocytosis is.

In the absence of an antibody test for COVID-19Reference Bedford, Enria, Giesecke, Heymann, Ihekweazu and Kobinger4 we rely on reverse-transcriptase polymerase chain reaction COVID-19 testing, which does not have 100% sensitivity in the initial phase of infection, so a single negative test does not exclude infection. Once an antibody test becomes available it will be a useful addition to pre-clozapine investigations.

Comorbidities such as diabetes, hypertension, respiratory illness and cardiovascular disease are very common in patients taking clozapine but are associated with adverse outcomes in the event of COVID-19 infection, including increased mortality rates. It is not known whether the antibody deficiency described in patients taking clozapine will further compromise this vulnerable group.Reference Ponsford, Castle, Tahir, Robinson, Wade and Steven5 These are not, however, indications to stop clozapine, which itself has serious adverse consequences. Rather patients need clear advice and, if possible, assistance regarding self-isolation and other precautions advised. Obesity and sleep apnoea may also contribute to poor outcomes and continuous positive airway pressure treatment, which can be an aerosol-generating procedure,Reference Genta and Lorenzi-Filho6 may be a risk to staff.

Individuals already established on clozapine and managed in the community may require changes to their management. In view of recommendations for social distancing, the use of clozapine clinics for routine blood testing should be reconsidered. Instead, blood tests may be better performed in patient's homes, with staff using personal protective equipment and at, or near, the maximum intervals permitted. While the standard blood monitoring frequencies are at weekly (weeks 1–18), fortnightly (weeks 19–52) and four-weekly (over 52 weeks) intervals, clozapine can still be dispensed and administered with satisfactory monitoring at 14-, 21- and 42-day intervals, respectively.

Inevitably many patients taking clozapine will present with flu-like symptoms. An urgent full blood count will be required to exclude neutropenia with appropriate action. Many, however, will have another cause and so the evolving National Health Service recommendations regarding isolation and hopefully testing for COVID-19 infection should be followed. The combination of flu-like symptoms, chest pain and shortness of breath will, as community prevalence of COVID-19 increases, be much more likely to be because of COVID-19 than clozapine-induced myocarditis, except perhaps within the first 60 days of treatment.Reference Ronaldson, Fitzgerald, Taylor, Topliss and McNeil7 However, such a presentation will still need investigation and cessation of clozapine may on occasion be required as well as urgent general medical assistance. Careful documentation of symptom profiles and investigations will aid subsequent decisions regarding clozapine re-challenge. In the event of COVID-19 infection the acute-phase reaction may result in reduced activity of cytochrome P450 1A2, raising clozapine levels and so an urgent trough clozapine level will be needed with a reduction in clozapine dose if required. This effect may be amplified if hospital admission is indicated necessitating abrupt change in smoking habits.

In summary; COVID-19 presents us with extreme difficulties regards clozapine initiation, the risks of COVID-19 are insufficient to justify stopping clozapine, an action which presents its own serious problems, precautions must be taken now to help protect our high-risk patients as COVID-19 infection may jeopardise both their physical and mental health.

Declaration of interest

F.G. has received honoraria for advisory work and lectures or continuing medical education activity support from Roche, BMS, Lundbeck, Otsuka, Janssen and Sunovion, is a collaborator on an NHS Innovations project co-funded by Janssen and has a family member with professional links to Lilly and GSK, including shares. E.S. has received speaker fees from Janssen and Novartis.

References

Xiang, Y-T, Zhao, Y-J, Liu, Z-H, Li, X-H, Zhao, N, Cheung, T, et al. . The COVID-19 outbreak and psychiatric hospitals in China: managing challenges through mental health service reform. Intern J Biol Sci 2020; 16: 1741–4.10.7150/ijbs.45072CrossRefGoogle ScholarPubMed
Roge, R, Moller, BK, Andersen, CR, Correll, CU, Nielsen, J. Immunomodulatory effects of clozapine and their clinical implications: what have we learned so far? Schizophr Res 2012; 140: 204–13.10.1016/j.schres.2012.06.020CrossRefGoogle ScholarPubMed
Maharaj, R. King's Critical Care - Evidence Summary Clinical Management of COVID-19. King's College Hospital NHS Foundation Trust, 2020.Google Scholar
Bedford, J, Enria, D, Giesecke, J, Heymann, DL, Ihekweazu, C, Kobinger, G, et al. COVID-19: towards controlling of a pandemic. Lancet 2020; 395: 1015–8.10.1016/S0140-6736(20)30673-5CrossRefGoogle ScholarPubMed
Ponsford, M, Castle, D, Tahir, T, Robinson, R, Wade, W, Steven, R, et al. Clozapine is associated with secondary antibody deficiency. Br J Psychiatry 2019; 214: 83–9.10.1192/bjp.2018.152CrossRefGoogle Scholar
Genta, PR, Lorenzi-Filho, G. Sealing the leak: a step forward in improving CPAP adherence. Chest 2018; 153: 774–5.10.1016/j.chest.2017.10.023CrossRefGoogle ScholarPubMed
Ronaldson, KJ, Fitzgerald, PB, Taylor, AJ, Topliss, DJ, McNeil, JJ. Clinical course and analysis of ten fatal cases of clozapine-induced myocarditis and comparison with 66 surviving cases. Schizophr Res 2011; 128: 161–5.10.1016/j.schres.2011.01.017CrossRefGoogle ScholarPubMed
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