The impact of clozapine initiation and cessation on psychiatric hospital admissions and bed days: a mirror image cohort study.


Journal

Psychopharmacology
ISSN: 1432-2072
Titre abrégé: Psychopharmacology (Berl)
Pays: Germany
ID NLM: 7608025

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 24 10 2018
accepted: 23 01 2019
pubmed: 5 2 2019
medline: 29 10 2019
entrez: 5 2 2019
Statut: ppublish

Résumé

Clozapine is the most effective medication for the positive symptoms of treatment-refractory schizophrenia. Although clozapine use is associated with fewer admissions, less is known about the impact of clozapine cessation on hospitalisation. The aims of this study were to investigate whether clozapine-reduced psychiatric inpatient admissions and bed days, and investigate patient factors associated with these changes from a sample of 1906 people commenced on clozapine. All people commencing clozapine during an acute hospitalisation over a 10-year period in Queensland, Australia, were included in this retrospective cohort study. A mirror image design was used to compare psychiatric bed days and hospitalisations 2 years before and after clozapine treatment, and the impact of clozapine continuation or early cessation. Changes in psychiatric bed days and hospitalisations were analysed using linear regression, adjusting for the duration on clozapine, sex, age, indigenous status, country of origin and time to clozapine commencement. There was a significant reduction in bed days (29.55 days vs 24.46 days, p < 0.001) and admissions (2.27 vs 1.87 < 0.001) associated with clozapine commencement. This remained significant among clozapine continuers, but not among those with early cessation. Longer duration on clozapine was associated with greater reductions in psychiatric bed days and admissions. Age, sex and time to clozapine commencement, indigeneity and country of origin did not impact outcomes. Longer clozapine therapy led to a greater reduction in psychiatric bed days and hospitalisations. Early cessation was associated with a return to pre-clozapine levels of bed days and admissions.

Sections du résumé

BACKGROUND BACKGROUND
Clozapine is the most effective medication for the positive symptoms of treatment-refractory schizophrenia. Although clozapine use is associated with fewer admissions, less is known about the impact of clozapine cessation on hospitalisation.
AIMS OBJECTIVE
The aims of this study were to investigate whether clozapine-reduced psychiatric inpatient admissions and bed days, and investigate patient factors associated with these changes from a sample of 1906 people commenced on clozapine.
METHODS METHODS
All people commencing clozapine during an acute hospitalisation over a 10-year period in Queensland, Australia, were included in this retrospective cohort study. A mirror image design was used to compare psychiatric bed days and hospitalisations 2 years before and after clozapine treatment, and the impact of clozapine continuation or early cessation. Changes in psychiatric bed days and hospitalisations were analysed using linear regression, adjusting for the duration on clozapine, sex, age, indigenous status, country of origin and time to clozapine commencement.
RESULTS/OUTCOMES RESULTS
There was a significant reduction in bed days (29.55 days vs 24.46 days, p < 0.001) and admissions (2.27 vs 1.87 < 0.001) associated with clozapine commencement. This remained significant among clozapine continuers, but not among those with early cessation. Longer duration on clozapine was associated with greater reductions in psychiatric bed days and admissions. Age, sex and time to clozapine commencement, indigeneity and country of origin did not impact outcomes.
CONCLUSION/INTERPRETATION CONCLUSIONS
Longer clozapine therapy led to a greater reduction in psychiatric bed days and hospitalisations. Early cessation was associated with a return to pre-clozapine levels of bed days and admissions.

Identifiants

pubmed: 30715572
doi: 10.1007/s00213-019-5179-6
pii: 10.1007/s00213-019-5179-6
doi:

Substances chimiques

Antipsychotic Agents 0
Clozapine J60AR2IKIC

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1931-1935

Subventions

Organisme : Medical Research Council
ID : MR/L011794/1
Pays : United Kingdom
Organisme : National Health and Medical Research Council
ID : APP1111136

Références

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Auteurs

D Siskind (D)

Metro South Addiction and Mental Health Service, Brisbane, Australia. d.siskind@uq.edu.au.
School of Medicine, University of Queensland, Brisbane, Australia. d.siskind@uq.edu.au.

T Reddel (T)

School of Medicine, University of Queensland, Brisbane, Australia.
The Park Centre for Mental Health, Brisbane, Australia.

J H MacCabe (JH)

Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

S Kisely (S)

Metro South Addiction and Mental Health Service, Brisbane, Australia.
School of Medicine, University of Queensland, Brisbane, Australia.

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Classifications MeSH