Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-18T17:59:16.194Z Has data issue: false hasContentIssue false

P0113 - Duloxetine for major depressive episodes in the course of psychotic disorders: A prospective clinical trial

Published online by Cambridge University Press:  16 April 2020

S. Englisch
Affiliation:
Zentralinstitut Für Seelische Gesundheit, Mannheim, Germany
U. Knopf
Affiliation:
Psychiatrisches Zentrum Nordbaden, Wiesloch, Germany
B. Scharnholz
Affiliation:
Zentralinstitut Für Seelische Gesundheit, Mannheim, Germany
A. Kuwilsky
Affiliation:
Zentralinstitut Für Seelische Gesundheit, Mannheim, Germany
M. Deuschle
Affiliation:
Zentralinstitut Für Seelische Gesundheit, Mannheim, Germany
M. Zink
Affiliation:
Zentralinstitut Für Seelische Gesundheit, Mannheim, Germany

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.
Background and Aims:

Patients with psychotic disorders often suffer from intercurrent major depressive episodes (MDEs). Case reports suggested successful antidepressive treatment with duloxetine, a selective dual reuptake inhibitor of serotonin and norepinephrine (SSNRI). We initiated this open prospective clinical trial in order to evaluate efficacy, safety and tolerability of this approach.

Methods:

Patients with a psychotic lifetime diagnosis suffering from mildly severe MDEs were treated with duloxetine over a period of 6 weeks. We evaluated effects on mood, monitored the psychotic psychopathology and assessed side effects, basal clinical and pharmacological parameters.

Results:

Twenty patients were included and experienced a significant improvement of their MDE during the observation period (CDSS: Calgary Depression Scale for Schizophrenia, HAMD: Hamilton Depression scale). Psychotic positive symptoms remained stably absent while negative syndrome and global psychopathology considerably improved (PANSS: Positive and Negative Syndrome Scale). In general, the treatment was well tolerated, serum prolactin levels stayed unchanged, but pharmacokinetic interactions with a number of antipsychotic agents were observed.

Conclusions:

This open prospective evaluation revealed antidepressive efficacy of duloxetine in patients with co-morbid psychotic disorders. With regard to the psychotic disorder, the treatment appears to be safe and well tolerable. Further investigations should involve a randomized control group.

Type
Poster Session I: Schizophrenia and Psychosis
Copyright
Copyright © European Psychiatric Association 2008
Submit a response

Comments

No Comments have been published for this article.