Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-25T13:40:09.787Z Has data issue: false hasContentIssue false

Olanzapine in practice

Published online by Cambridge University Press:  02 January 2018

David Taylor*
Affiliation:
Maudsley Hospital Denmark Hill London SE5 8AZ
Siobhan Drummond
Affiliation:
Chelsea and Westminster Hospital London
Joanne Pendlebury
Affiliation:
Charing Cross Hospital London
*
Correspondence
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Prescription charts including a prescription for olanzapine were evaluated for 202 patients from 15 National Health Service trusts. In patients prescribed olanzapine for less than six weeks, the mean dose was found to be 12.4mg/day but 56% of patients were prescribed olanzapine as the sole antipsychotic. For patients prescribed olanzapine for longer than six weeks (when dose titration and drug crossovers were assumed to be complete) the mean dose of olanzapine was 15.8mg/day and 64% received olanzapine as the sole antipsychotic. A substantial proportion of patients were prescribed concurrent anticholinergic drugs (but relatively few when on olanzapine alone). Olanzapine was used in doses higher than the standard dose recommended by the manufacturers, often in combination with typical antipsychotics. Such practices increase costs and, at least in the latter case, very probably adversely affect outcome. Studies are needed to evaluate the relative effectiveness of commonly used antipsychotic regimens in naturalistic settings. In the absence of these, olanzapine should be used as the sole antipsychotic and patients should be property assessed on lower doses before dose increases are undertaken.

Type
Original Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © 1998 The Royal College of Psychiatrists

References

Beasley, C. M., Tollefson, G. D., Tran, P. V., et al (1996a) Olanzapine versus placebo and haloperidol. Acute phase results of the North American double-blind olanzapine trial. Neuropsychopharmacology, 14, 111123.CrossRefGoogle ScholarPubMed
Beasley, C. M., Sanger, T., Satterlee, W., et al (1996b) Olanzapine versus placebo: results of a double-blind, fixed-dose olanzapine trial. Psychopharmacology, 124, 159167.CrossRefGoogle ScholarPubMed
Tollefson, G. D., Beasley, C. M., Tran, P. V., et al (1997a) Olanzapine versus haloperidol in the treatment of schizophrenia and schizoaffective and schizophreniform disorders: results of an international collaborative trial. American Journal of Psychiatry, 154, 457465.Google Scholar
Tollefson, G. D., Beasley, C. M., Tamura, R. N., et al (1997b) Blind, controlled, long-term study of the comparative incidence of treatment-emergent tardive dyskinesia with olanzapine or haloperidol. American Journal of Psychiatry, 154, 12481254.Google ScholarPubMed
Submit a response

eLetters

No eLetters have been published for this article.