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Antipsychotic medication for childhood-onset schizophrenia

Published online by Cambridge University Press:  16 April 2020

A. Kumar
Affiliation:
Leeds Partnerships Foundation Trust, Leeds, UK
E. Kennedy
Affiliation:
Child and Family Department, Tavistock Clinic, London, UK
S. Datta
Affiliation:
South London and Maudsley NHS Foundation Trust, London, UK

Abstract

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Background

Childhood-onset schizophrenia is onset prior to the age of 13 years. Although rare, people who suffer from schizophrenia at an early age appear to have a severe form of the illness with poor long-term prognosis. Antipsychotic medication is one way of managing this serious mental illness.

Aims/objectives

To examine the effects of antipsychotics for childhood-onset schizophrenia.

Methods

We searched the Cochrane Schizophrenia Group Trials Register, inspected references and contacted pharmaceutical companies and authors of trials. We included all randomised clinical trials.

Results

From a total of 2062 citations, we identified six relevant trials. Three comparisons: atypical versus typical, atypical versus atypical and typical versus typical antipsychotic drugs. The only comparison to find any differences was atypical versus typical antipsychotic drugs. A few results from one study favoured the atypical antipsychotic clozapine over haloperidol in treating treatment resistant childhood-onset schizophrenia (n = 21, WMD CGAS 17.00 CI 7.74 to 26.26). Participants on clozapine, however, were three times more likely to have drowsiness (1 RCT, n = 21, RR 3.30 CI 1.23 to 8.85, NNH 2 CI 2 to 17) and half of the children receiving clozapine had neutropenia (1 RCT, n = 21, RR 12, CI 0.75 to192.86).

Conclusions

There are few relevant trials and, presently, there is little conclusive evidence regarding the effects of antipsychotic medication for those with early onset schizophrenia. Some benefits were identified in using the atypical antipsychotic clozapine compared with haloperidol but the benefits were offset by an increased risk of serious adverse effects. Larger, more robust, trials are required.

Type
P01-315
Copyright
Copyright © European Psychiatric Association2011
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