Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-18T15:40:57.525Z Has data issue: false hasContentIssue false

YPSP01-12 - Lipid Metabolism Changes After Switching To Ziprasidone

Published online by Cambridge University Press:  17 April 2020

J. Dragasek
Affiliation:
1st Dept. of Psychiatry, Faculty of Medicine, University of P. J. Safarik, Slovak Republic University Hospital of L. Pasteur, Kosice, Slovak Republic
E. Palova
Affiliation:
1st Dept. of Psychiatry, Faculty of Medicine, University of P. J. Safarik, Slovak Republic
I. Lukacsova
Affiliation:
University Hospital of L. Pasteur, Kosice, Slovak Republic
M. Drimalova
Affiliation:
Dept. of Psychiatry, Jessenius Faculty of Medicine, Comenius University, Martin, Slovak Republic
D. Breznoscakova
Affiliation:
1st Dept. of Psychiatry, Faculty of Medicine, University of P. J. Safarik, Slovak Republic
P. Mirossay
Affiliation:
University Hospital of L. Pasteur, Kosice, Slovak Republic

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.
Introduction

Increasing numbers of reports concerning lipid dysregulation, diabetes and hyperglycaemia in patients treated with atypical antipsychotics have raised concerns about a possible association between these metabolic effects and treatment with these medications.

Objectives

The available literature notes that ziprasidone is a weight-neutral antipsychotic and that lipids anomalies improve when patient are switched from other atypical antipsychotics to ziprasidone.

Aims

The purpose of this study was to examine the association of treatment with ziprasidone and changes in serum levels of cholesterol, triglycerides, serum levels of glucose and BMI changes.

Methods

Prospective, cohort, multicenter, open design in 373 in- and outpatients treated with ziprasidone for broad spectrum of psychotic disorders in flexible dose manner. The analysis was done in group of patients with no previous antipsychotic treatment or discontinuation of antipsychotic treatment longer than 3 months compared to group of patients directly switched from another antipsychotic treatment to ziprasidone.

Results

Changes in fasting serum levels of total cholesterol were significant from baseline at week 24 in subgroup of patients directly switched from another antipsychotic treatment to ziprasidone (5,12 vs 4,94 mmol/l, p< 0,05, ANOVA).

Conclusions

We have observed statistical significant difference in fasting serum levels of total cholesterol in patients directly switched from another antipsychotic treatment to ziprasidone.

Type
YP Scholar poster
Copyright
Copyright © European Psychiatric Association 2010
Submit a response

Comments

No Comments have been published for this article.