Hostname: page-component-84b7d79bbc-2l2gl Total loading time: 0 Render date: 2024-07-26T09:34:29.330Z Has data issue: false hasContentIssue false

1125 – Characteristics Of The Antipsychotic Switch To Amisulpride In Schizophrenia In Romanian Practice- a Multicentric, Retrospective Data Collection (switch Study)

Published online by Cambridge University Press:  15 April 2020

D. Vasile
Affiliation:
University of Medicine and Pharmacy ‘Dr. Carol Davila’ Bucharest, Romania University Emergency Central Military Hospital ‘Dr. Carol Davila’ Bucharest, Bucharest, Romania
O. Vasiliu
Affiliation:
University Emergency Central Military Hospital ‘Dr. Carol Davila’ Bucharest, Bucharest, Romania
A.G. Mangalagiu
Affiliation:
University Emergency Central Military Hospital ‘Dr. Carol Davila’ Bucharest, Bucharest, Romania
B.M. Petrescu
Affiliation:
University Emergency Central Military Hospital ‘Dr. Carol Davila’ Bucharest, Bucharest, Romania

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Objective

To evaluate characteristics of the antipsychotic switch from any antipsychotic to amisulpride (Solian®) through the integration of the significantly variables.

Method

This is an open, non-randomized, multicentric, retrospective, non-interventional study that included 1165 subjects who were already stabilized on amisulpride for at least 6±1 months. These patients were previously switched from other antipsychotic to Solian®. Data were collected retrospectively on the patients’ status 6±1 months ago and their present status.

Results

The population consisted of 38.5% hospitalized patients at the moment of antipsychotic switch and 61.5% outpatients; 56.3% of the patients were in acute exacerbation at that moment. Previous treatment of the patients: 100% antipsychotic, 17.9% antidepressant, 38.8% mood stabilizer, 39.4% benzodiazepine and 22.2% other treatments. Switch type: sudden in 63.7% of the patients, gradual in 35.4% and unknown in 0.9%. The mean dosage of Solian at initiation was 581.04 mg/day. For 38.1% of the patients the initial daily dose of Solian® was of 600 mg, for 29.6% of them 400 mg and for 22.7% 800 mg. The mean dosage of Solian during the 6±1 months was 571.39 mg/day. For 39.8% of the patients the daily dose of Solian® was of 600 mg, for 30.5% of them 400 mg and for 20.7% 800 mg.

Conclusions

The switch to Solian® was made suddenly in a majority of patients, preferred start dose being 600 mg, while the mean dose was similar to baseline values (in almost 40% of cases) or smaller during the 6±1 months of the study.

Type
Abstract
Copyright
Copyright © European Psychiatric Association 2013
Submit a response

Comments

No Comments have been published for this article.