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P-1210 - Comparative Study of the Effectiveness of Long Acting Injectable Risperidone in Front of Oral Antipsychotics in Early Onset Schizophrenia

Published online by Cambridge University Press:  15 April 2020

P. Barrio
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain
D. Hidalgo
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain
M. García
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain
A. Batalla
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain
P. Castellví
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain
A. Pons
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain
E. Parellada
Affiliation:
Schizophrenia Program, Clinic Hospital, Barcelona, Spain

Abstract

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Introduction

Long-acting injectable antipsychotics in early-onset schizophrenia improve treatment adherence, and this may lead to decreased rates of hospital admission, better rates of clinical remission and better psychosocial adjustment.

Objectives

To compare clinical remission rates, number of hospital readmissions and personal and social functioning after two years between patients with early-onset schizophrenia (EOS;≤ 2 years), either in treatment with long-acting injectable risperidone (LAIR) or oral antipsychotics (OA).

Methods

This is a case-control study comparing patients with EOS who initiated LAIR between 2004–2008 (n = 26 cases) with a control group with EOS matched for age and sex (n = 26 controls) treated with OA. The PANSS was administered at baseline; after two years the PANSS, the Personal and Social Functioning Scale (PSP) and the Andreasen remission criteria were administered.

Results

The PANSS score comparison at baseline showed no significant differences between LAIR and OA groups (79.9 vs. 88.5, respectively; CI 95%: −21.6, 4.3; p = 0.185). There were statistical significant differences after two years of treatment in the PANSS scores (47.7 vs. 66.2, respectively; CI 95%: −27.2, −9.8; p < 0.001), the PSP scores (72.4 vs. 59.7, respectively; CI 95%: 4.9, 20.7; p = 0.002) and the clinical remission rates (65.4% vs. 38.5, respectively; p = 0.05). Although no statistically significant, there were differences between hospital readmission rates (19,5% vs. 42.3%, respectively).

Conclusions

Despite case-control studies limitations, data suggest that treatment with LAIR instead of OA in EOS might improve clinical, remission and social functioning rates. This improved effectiveness might be due to a greater treatment adherence achieved with LAIR.

Type
Abstract
Copyright
Copyright © European Psychiatric Association 2012
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