4.4 Article

Ethnic inequalities in clozapine use among people with treatment-resistant schizophrenia: a retrospective cohort study using data from electronic clinical records

Journal

SOCIAL PSYCHIATRY AND PSYCHIATRIC EPIDEMIOLOGY
Volume 57, Issue 7, Pages 1341-1355

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00127-022-02257-3

Keywords

Refractory psychosis; Clozapine; Benign ethnic neutropenia; Black British; Asian British; Health inequalities

Categories

Funding

  1. National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London
  2. NIHR Advanced Fellowship [NIHR301690]
  3. Medical Research Council (MRC) Health Data Research UK Fellowship [MR/S003118/1]
  4. Academy of Medical Sciences [SGL015/1020]
  5. Wellcome Trust
  6. MRC
  7. British Heart Foundation
  8. Arthritis Research UK
  9. Royal College of Physicians
  10. NIHR Clinician Science Fellowship award [CS2018-18-ST2-014]
  11. MRC Clinical Research Training Fellowship [MR/L017105/1]
  12. Psychiatry Research Trust Peggy Pollak Research Fellowship in Developmental Psychiatry
  13. Diabetes UK
  14. National Institutes of Health Research (NIHR) [NIHR301690] Funding Source: National Institutes of Health Research (NIHR)

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This study investigates the ethnic equity in access to clozapine treatment for people with treatment-resistant schizophrenia spectrum disorder, and finds that black service-users are less likely to receive clozapine compared to white British service-users.
Purpose Clozapine is the most effective intervention for treatment-resistant schizophrenia (TRS). Several studies report ethnic disparities in clozapine treatment. However, few studies restrict analyses to TRS cohorts alone or address confounding by benign ethnic neutropenia. This study investigates ethnic equity in access to clozapine treatment for people with treatment-resistant schizophrenia spectrum disorder. Methods A retrospective cohort study, using information from 11 years of clinical records (2007-2017) from the South London and Maudsley NHS Trust. We identified a cohort of service-users with TRS using a validated algorithm. We investigated associations between ethnicity and clozapine treatment, adjusting for sociodemographic factors, psychiatric multi-morbidity, substance misuse, neutropenia, and service-use. Results Among 2239 cases of TRS, Black service-users were less likely to be receive clozapine compared with White British service-users after adjusting for confounders (Black African aOR = 0.49, 95% CI [0.33, 0.74], p = 0.001; Black Caribbean aOR = 0.64, 95% CI [0.43, 0.93], p = 0.019; Black British aOR = 0.61, 95% CI [0.41, 0.91], p = 0.016). It was additionally observed that neutropenia was not related to treatment with clozapine. Also, a detention under the Mental Health Act was negatively associated clozapine receipt, suggesting people with TRS who were detained are less likely to be treated with clozapine. Conclusion Black service-users with TRS were less likely to receive clozapine than White British service-users. Considering the protective effect of treatment with clozapine, these inequities may place Black service-users at higher risk for hospital admissions and mortality.

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