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Department of Psychiatry,University of Toronto Faculty of Medicine, Toronto, Ontario, Canada
Department of Psychiatry,University of North Carolina School of Medicine, Chapel Hill, North Carolina
Department of Psychiatry, Dartmouth Medical School, Hanover, New Hampshire
Department of Psychiatry,University of North Carolina School of Medicine, Chapel Hill, North Carolina
Lilly Research Laboratories, Indianapolis, Indiana
Department of Psychiatry, Duke University School of Medicine, Durham, North Carolina
Department of Psychiatry, University of Cincinnati, Cincinnati, Ohio, USA
Clinical Neuroscience Research Centre, Kent, UK
Department of Psychiatry, University of Utrecht Medical School,Utrecht,The Netherlands
University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
Lilly Research Laboratories, Indianapolis, Indiana
Department of Psychiatry, College of Physicians and Surgeons, Columbia University, New York,USA
on behalf of the HGDH Study Group
Correspondence: Dr Robert B. Zipursky, Schizophrenia Programme,Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario, Canada M5T 1R8. Tel: +1 416 979 6913; fax: +1 416 979 4676; e-mail: robert_zipursky{at}camh.net
Declaration of interest This work was financially supported by Lilly Research Laboratories. M.F.T. and G.D.T. are employees of Lilly Research Laboratories.
Background Substantial weight gain is common with many atypical antipsychotics.
Aims To evaluate the extent, time course and predictors of weight gain and its effect on study retention among people with first-episode psychosis treated with olanzapine or haloperidol.
Method Survival analysis assessed time to potentially clinically
significant weight gain (
7%) and the effect of weight gain on study
retention. Weight gain during the 2-year study was summarised using
last-observation-carried-forward (LOCF), observed cases and study completion
approaches.
Results After 2 years of treatment, LOCF mean weight gain was 10.2 kg (s.d.=10.1) for olanzapine (n=131) and 4.0 kg (s.d.=7.3) for haloperidol (n=132); observed cases mean weight gain was 15.4 kg (s.d.=10.0) for olanzapine and 7.5 kg (s.d.=9.2) for haloperidol. Change in body massindex was significantly predicted only by treatment group (P < 0.0001).
Conclusions Olanzapine was associated with significantly greater weight gain than haloperidol, with both leading to greater weight gain than previously described.
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