Abstract
Introduction: Using an atypical long-acting antipsychotic may improve patient outcome by offering
the good efficacy and tolerability of an atypical antipsychotic with improved compliance
through depot administration.
Methods: This subanalysis of an international, 6-month, open-label trial of risperidone long-acting
injectable (RLAI) focused on non-acute schizophrenic adult patients switching from
oral or depot conventional antipsychotic. Efficacy assessments included Positive and
Negative Syndrome Scale (PANSS), Global Assessment of Functioning (GAF), quality of
life, treatment satisfaction, hospitalization rates, and treatment-emergent adverse
events (TEAEs).
Results: Over 70% of patients switching from oral (n=100) or depot (n=565) conventional medication
completed treatment. Improvements were observed for PANSS total and subscale scores,
GAF, quality of life, treatment satisfaction and hospitalization. Overall RLAI was
well tolerated. TEAEs occurring in >5% were: anxiety (11.0%), insomnia (9.0%), weight
increase (6.0%) for patients switching from oral, and weight increase (6.0%) and disease
exacerbation (5.3%) for patients switching from depot medication.
Conclusion: Patients with schizophrenia, unsatisfactorily treated with oral or depot conventional
antipsychotics, showed improvement in symptom control, tolerability, and patient satisfaction
after switching to RLAI.
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Correspondence
A. Lex
Janssen-Cilag
Medical Affairs EMEA
Turnhoutseweg 30
2340 Beerse
Belgium
Phone: +49/213/795 54 55
Email: alex@jacde.jnj.com