Background; Clozapine is an atypical antipsychotic indicated for the manage
ment of severely ill patients with schizophrenia who have failed to respond
adequately to standard drug treatment. The significant risk of agranulocyt
osis and seizure associated with clozapine has led to the restrictions in i
ts use. Additionally, drug-induced sedation, sialorrhea, enuresis, and weig
ht gain are often cited as problematic consequences of clozapine treatment.
Our primary objective was to determine the effectiveness and safety of a m
ethod of slow cross-titration from clozapine to olanzapine among patients r
esponsive to clozapine treatment but experiencing medication-induced advers
e events.
Method: Changes in symptomatology, mood, subjective response, and safety we
re examined in 20 outpatients meeting DSM-IV criteria for schizophrenia or
schizoaffective disorder who converted from clozapine to olanzapine. Patien
ts were considered clozapine-responsive as evidenced by improved social fun
ction and decreased symptoms with clozapine therapy; however, they were int
erested in alternative pharmacologic treatment because of clozapine-related
side effects.
Results: Equivalent efficacy of olanzapine to clozapine was found in 90% of
the patients (18/20) in the study group, without rehospitalization or suic
idal behavior in any of the patients. Also notable was a reduction in drug-
induced side effects and improved subjective response to pharmacotherapy.
Conclusion; The successful conversion from clozapine to olanzapine has the
potential to provide great benefits for the patient, including reducing dru
g-induced side effects while maintaining symptom control. These preliminary
results suggest that further research on converting clozapine responders t
o olanzapine is warranted.