4.4 Article

Real-world effectiveness of clozapine in patients with bipolar disorder: results from a 2-year mirror-image study

Journal

BIPOLAR DISORDERS
Volume 14, Issue 8, Pages 863-869

Publisher

WILEY
DOI: 10.1111/bdi.12018

Keywords

antipsychotic agents; bipolar disorder; clozapine; effectiveness; mood stabilizer; treatment resistance

Funding

  1. Aalborg Psychiatric Hospital
  2. Lundbeck
  3. Pfizer
  4. Chempaq
  5. Bristol-Myers Squibb
  6. AstraZeneca
  7. Janssen-Cilag
  8. Hemocue
  9. Eli Lilly Co.
  10. National Institute of Mental Health (NIMH)
  11. Feinstein Institute for Medical Research
  12. NIMH
  13. National Alliance for Research in Schizophrenia and Depression (NARSAD)
  14. Ortho-McNeill/Janssen/Johnson Johnson

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Nielsen J, Kane JM, Correll CU. Real-world effectiveness of clozapine in patients with bipolar disorder: results from a 2-year mirror-image study. ?Bipolar Disord 2012: 14: 863869. (C) 2012 John Wiley & Sons A/S.Published by Blackwell Publishing Ltd. Objectives: Clozapine remains the drug of choice for treatment-resistant schizophrenia but the evidence for its use in severe bipolar disorder (BD) remains sparse. Methods: A pharmaco-epidemiologic database study was carried out in Denmark, investigating the effectiveness of clozapine in BD patients (without a schizophrenia-spectrum disorder), between 1996 and 2007, using a two-year mirror-image design. Results: A total of 21473 patients with a lifetime diagnosis of International Classification of Diseases-10 (ICD-10) BD were identified, of which only 326 (1.5%) were treated with clozapine and were included in the mirror-image analysis. The mean follow-up time was 544 +/- 280 days, the mean clozapine dose was 307.4 mg [95% confidence interval (CI): 287.9328.2], and 39.3% were male. During clozapine treatment, the mean number of bed-days decreased from 177.8 (95% CI: 149.4211.6) to 34.6 (95% CI: 24.848.2) (p < 0.001). The mean number of admissions was reduced from 3.2 (95% CI: 2.93.7) to 2.0 (95% CI: 1.62.4) (p < 0.001). Overall, 240 patients (73.6%) had reduced bed-days and 130 (39.9%) were not admitted while treated with clozapine. Moreover, the number of psychotropic co-medications was reduced from 4.5 defined daily doses (DDD) (2575 percentiles: 2.48.2) to 3.9 DDD (2575 percentiles: 2.46.1) (p = 0.045). Somatic hospital visits for intentional self-harm/overdose reduced significantly from 8.3% to 3.1% (p = 0.004). However, non-psychotropic co-medication use for medical conditions did not increase; 0.7 DDD (2575 percentiles: 0.02.9) to 0.8 DDD (2575 percentiles: 0.12.89) (p = 0.3). Conclusions: Clozapine use for BD was associated with a significant and clinically relevant reduction in the number of bed-days, psychiatric admissions, psychotropic co-medications, and hospital contact for self-harm/overdose, without increased medical treatments. Clozapine seems to be an appropriate choice for treatment-resistant BD and should be investigated in randomized controlled trials.

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