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P-1013 - Psychopathological Assessment of the Ultra-high Risk State of Psychosis: a Five Factor Solution

Published online by Cambridge University Press:  15 April 2020

S. Ruhrmann
Affiliation:
Department of Psychiatry and Psychotherapy, University of Cologne, Cologne, Germany
F. Schultze-Lutter
Affiliation:
Department of Psychiatry and Psychotherapy, University of Cologne, Cologne, Germany University Hospital of Child and Adolescent Psychiatry, University of Bern, Bern, Switzerland
M. Bodatsch
Affiliation:
Department of Psychiatry and Psychotherapy, University of Cologne, Cologne, Germany
D. Linszen
Affiliation:
Department of Psychiatry, Academic Medical Centre, Amsterdam Maastricht University Medical Centre, University of Maastricht, Maastricht, The Netherlands
R.K.R. Salokangas
Affiliation:
Turku University Central Hospital, Turku University, Turku, Finland
M. Birchwood
Affiliation:
School of Psychology, University of Birmingham, Birmingham, UK
G. Juckel
Affiliation:
Dept. of Psychiatry and Psychotherapy, Ruhr University Bochum, Bochum, Germany
S. Lewis
Affiliation:
School of Medicine, The University of Manchester, Manchester, UK
J. Klosterkotter
Affiliation:
Department of Psychiatry and Psychotherapy, University of Cologne, Cologne, Germany

Abstract

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The ultra-high risk state of developing a psychosis is mainly characterized by attenuated or transient full-blown psychotic symptoms. It can be assessed with the structured interview for prodromal symptoms (SIPS), comprising four domains: positive, negative, disorganization and general symptoms. As the scores of the SOPS sub-domains are regularly used to perform domain-related analyses the stability of the suggested domain structure and item composition is of major interest.

Method

SIPS (version 3.0) data from n = 243 participants of the European Prediction of Psychosis Study (EPOS) were used for the current analysis. Inclusion criteria comprised ultra-high risk criteria and the basic symptom criterion COGDIS. The EPOS investigators received extensive training by one of the scale's authors (Tandy J. Miller, PhD). Pairwise interrater concordance for SIPS was 77%, which was determined acceptable by the training team. A principal component analysis was performed (Eigenvalues > 1, varimax rotation).

Results

A five factor solution emerged. Factor 1 was primarily defined by a loss of intentionality, functioning and stress tolerance, factor 2 by anhedonia and affective blunting, factor 3 by cognitive and behavioural disorganization, factor 4 by delusions. Sleep disturbances and perceptual abnormalities/hallucinations have both been associated with dopaminergic disturbances, this may explain their common appearance on factor 5.

Discussion

The originally suggested structure of the SIPS proofed not to be stable and was replaced by a five-factor solution. Our results suggest considering a different item and factor structure in future SIPS based data analyses.

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Copyright
Copyright © European Psychiatric Association 2012
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