Olanzapine response in psychotic depression
by
Rothschild AJ, Bates KS,
Boehringer KL, Syed A
Department of Psychiatry,
University of Massachusetts Medical School,
Worcester 01655, USA.
J Clin Psychiatry 1999 Feb; 60(2):116-8
ABSTRACT
BACKGROUND: Psychotic depression is more common than is generally realized,
occurring in an estimated 16% to 54% of depressed patients. In controlled
studies of patients with schizophrenia, the atypical antipsychotic olanzapine
has been shown to be superior in efficacy to haloperidol at doses of 10 mg/day.
Since olanzapine may have antidepressant effects in addition to its
antipsychotic properties, the purpose of this study was to assess the safety and
efficacy of olanzapine in the treatment of psychotic depression. METHOD:
Hospitalized patients with the discharge diagnosis of DSM-IV psychotic
depression (major depression with psychotic features or bipolar I disorder,
depressed phase...with psychotic features) who had been treated with olanzapine
during the first 9 months of its availability in the United States were
identified. An age- and sex-matched sample of hospitalized patients with
psychotic depression treated with other antipsychotics during the same time
period was also identified. The medical records were expunged of all references
to medication treatment and then reviewed and scored in a blind fashion for
indications, doses, response, and side effects. RESULTS: Fifteen psychotic
depression patients (10 women, 5 men), aged 36.9 +/- 10.1 years, who were
treated with olanzapine were retrospectively compared with 15 psychotic
depression patients (10 women, 5 men), aged 35.0 +/- 8.2 years, treated with
other antipsychotics. Ten (67%) of 15 patients taking olanzapine were much or
very much improved upon discharge compared with only 4 (27%) of 15 patients
taking other antipsychotics (Fisher exact test, p = .037). Olanzapine was well
tolerated: no patient discontinued the medication because of side effects.
Twelve (80%) of 15 patients in each group were taking antidepressants in
addition to the antipsychotic. Of the 3 patients taking olanzapine but not
taking an antidepressant, 2 were much or very much improved (1 patient taking
olanzapine alone, 1 taking olanzapine plus valproate sodium). CONCLUSION:
Olanzapine appears to be effective and safe for patients with psychotic
depression. Further prospective studies are warranted to ascertain whether
olanzapine's unique pharmacologic profile may make it particularly useful for
the treatment of psychotic depression either alone or in combination with
antidepressants.
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