OBJECTIVE: Clozapine is an atypical neuroleptic with superior efficacy
in severely ill, treatment-resistant inpatients with schizophrenia. To
determine if clozapine's differential efficacy generalizes to less ill,
outpatients populations, the authors examined the effects of clozapine on
positive and negative symptoms in outpatients with schizophrenia. METHOD:
Outpatients with schizophrenia who had histories of partial response to
conventional neuroleptics and who had not responded to a prospective 6-week
trial of fluphenazine participated in a 10-week, double-blind,
parallel-groups comparison of clozapine and haloperidol. Thirteen men and
six women were given clozapine, and 15 men and five women were given
haloperidol. Clinical response rates were determined and effects on primary
versus secondary negative symptoms were addressed. Doses of clozapine and
haloperidol at the end of the 10-week trial were 410.5 mg/day (SD = 45.8)
and 24.8 mg/day (SD = 5.5), respectively. RESULTS: Clozapine was superior
to haloperidol for treating positive symptoms. In addition, eight of the
patients given clozapine and only one of the patients given haloperidol
fulfilled clinical responder criteria. Clozapine was also superior to
haloperidol for treating negative symptoms, although these effects were
relatively minor. Negative symptoms were significantly affected in the
subgroup of patients with nondeficit schizophrenia but not in the subgroup
with deficit schizophrenia. Overall, clozapine was well tolerated.
CONCLUSIONS: Clozapine has superior efficacy for treating positive symptoms
in partially responsive outpatients with chronic schizophrenia, suggesting
that it has utility for a broad spectrum of patients with schizophrenia
beyond the most severely ill.
Abstract Teaser