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REVIEW ARTICLE |
Cochrane Schizophrenia Group, Summertown Pavilion, Oxford
Institute of Psychiatry & Guy's, King's and St Thomas' School of Medicine, London
Correspondence: Professor Anthony S. David, Institute of Psychiatry & GKT School of Medicine, Denmark Hill, London SE5 8AF, UK. Tel: 020 7848 0138; Fax: 020 7848 0572; e-mail: a.david{at}iop.kcl.ac.uk
Declaration of interest Funded by the NHS Health Technology Assessment programme. A.S.D. is participating in a trial funded by janssen-Cilag and has been an advisor for them. The Cochrane Schizophrenia Group has received funding from pharmaceutical companies, the NHS and Department of Health.
See pp. 300 307, this
issue.
Background Long-acting depot antipsychotic medication is a widely used treatment for schizophrenia.
Aims To synthesise relevant systematic Cochrane reviews.
Method The Cochrane Database was searched and summary data were extracted from randomised controlled clinical trials of depots.
Results Standard dose depot v. placebo resulted in significantly less relapse but more movement disorders. Those on depots (v. oral drugs) showed more global change on one outcome measure; relapse and adverse effects showed no difference. Comparisons showed no convincing advantages for one depot over another.
Conclusions Depot antipsychotics are safe and effective. They may confer a small benefit over oral drugs on global outcome. Those for whom depots are most indicated may not be represented. Large studies are required to discern differences in relapse rates and long-term adverse effects, and data on satisfaction, quality of life and economics.
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