Rates of treatment-resistant schizophrenia from first-episode cohorts: systematic review and meta-analysis.


Journal

The British journal of psychiatry : the journal of mental science
ISSN: 1472-1465
Titre abrégé: Br J Psychiatry
Pays: England
ID NLM: 0342367

Informations de publication

Date de publication:
03 2022
Historique:
pubmed: 21 1 2022
medline: 28 4 2022
entrez: 20 1 2022
Statut: ppublish

Résumé

Treatment-resistant schizophrenia (TRS) is associated with high levels of functional impairment, healthcare usage and societal costs. Cross-sectional studies may overestimate TRS rates because of selection bias. We aimed to quantify TRS rates by using first-episode cohorts to improve resource allocation and clozapine access. We undertook a systematic review of TRS rates among people with first-episode psychosis and schizophrenia, with a minimum follow-up of 8 weeks. We searched PubMed, PsycINFO, EMBASE, CINAHL and the Cochrane Database of Systematic Reviews, and meta-analysed TRS rates from included studies. Twelve studies were included, totalling 11 958 participants; six studies were of high quality. The rate of TRS was 22.8% (95% CI 19.1-27.0%, P < 0.001) among all first-episode cohorts and 24.4% (95% CI 19.5-30.0%, P < 0.001) among first-episode schizophrenia cohorts. Subgroup sensitivity analyses by location of recruitment, TRS definition, study quality, time of data collection and retrospective versus prospective data collection did not lead to statistically significant differences in heterogeneity. In a meta-regression, duration of follow-up and percentage drop-out did not significantly affect the overall TRS rate. Men were 1.57 times more likely to develop TRS than women (95% CI 1.11-2.21, P = 0.010). Almost a quarter of people with first-episode psychosis or schizophrenia will develop TRS in the early stages of treatment. When including people with schizophrenia who relapse despite initial response and continuous treatment, rates of TRS may be as high as a third. These high rates of TRS highlight the need for improved access to clozapine and psychosocial supports.

Sections du résumé

BACKGROUND
Treatment-resistant schizophrenia (TRS) is associated with high levels of functional impairment, healthcare usage and societal costs. Cross-sectional studies may overestimate TRS rates because of selection bias.
AIMS
We aimed to quantify TRS rates by using first-episode cohorts to improve resource allocation and clozapine access.
METHOD
We undertook a systematic review of TRS rates among people with first-episode psychosis and schizophrenia, with a minimum follow-up of 8 weeks. We searched PubMed, PsycINFO, EMBASE, CINAHL and the Cochrane Database of Systematic Reviews, and meta-analysed TRS rates from included studies.
RESULTS
Twelve studies were included, totalling 11 958 participants; six studies were of high quality. The rate of TRS was 22.8% (95% CI 19.1-27.0%, P < 0.001) among all first-episode cohorts and 24.4% (95% CI 19.5-30.0%, P < 0.001) among first-episode schizophrenia cohorts. Subgroup sensitivity analyses by location of recruitment, TRS definition, study quality, time of data collection and retrospective versus prospective data collection did not lead to statistically significant differences in heterogeneity. In a meta-regression, duration of follow-up and percentage drop-out did not significantly affect the overall TRS rate. Men were 1.57 times more likely to develop TRS than women (95% CI 1.11-2.21, P = 0.010).
CONCLUSIONS
Almost a quarter of people with first-episode psychosis or schizophrenia will develop TRS in the early stages of treatment. When including people with schizophrenia who relapse despite initial response and continuous treatment, rates of TRS may be as high as a third. These high rates of TRS highlight the need for improved access to clozapine and psychosocial supports.

Identifiants

pubmed: 35049446
doi: 10.1192/bjp.2021.61
pii: S0007125021000611
doi:

Substances chimiques

Antipsychotic Agents 0
Clozapine J60AR2IKIC

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

115-120

Subventions

Organisme : Medical Research Council
ID : MR/L011794/1
Pays : United Kingdom

Auteurs

Dan Siskind (D)

School of Clinical Medicine, University of Queensland, Australia; Metro South Addiction and Mental Health Service, Metro South Health, Brisbane, Australia; and Queensland Centre for Mental Health Research, Faculty of Medicine, University of Queensland, Australia.

Stacy Orr (S)

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

Surabhi Sinha (S)

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

Ou Yu (O)

School of Clinical Medicine, University of Queensland, Australia.

Bhavna Brijball (B)

School of Clinical Medicine, University of Queensland, Australia.

Nicola Warren (N)

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

James H MacCabe (JH)

Institute for Psychiatry, Psychology and Neuroscience, King's College London, UK; and National Psychosis Unit, South London and Maudsley NHS Foundation Trust, UK.

Sophie E Smart (SE)

MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, UK.

Steve Kisely (S)

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

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Classifications MeSH