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25th European Congress of Psychiatry / European Psychiatry 41S (2017) S170–S237

S197

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.2137

EW0268

Diagnostic stability in first psychotic

episode after 5 years follow-up

M. Mota-Oliveira

1 , M.

J. Peixoto

1 , I. F

erraz

1 , E. P

ereira

1 ,

R. Guedes

1 ,

, A . N

orton

2 , C. S

ilveira

1

1

Centro Hospitalar de São João, Clínica de Psiquiatria e Saúde

Mental, Porto, Portugal

2

Hospital Magalhães Lemos, Hospital Magalhães Lemos, Porto,

Portugal

Corresponding author.

Introduction

The diagnosis of psychosis is based on the presence

or absence of characteristic symptoms. The presence of such symp-

toms varies during the course and treatment, raising the question

of diagnostic stability after a first psychotic episode.

Aims and objectives

The aim of this study is to evaluate the diag-

nostic stability after a first psychotic episode in the long term (five

years after the first inpatient admission).

Methodology

A retrospective study that included patients with

first psychotic episode between 2007 and 2011 admitted to the

inpatient unit of the psychiatry and mental health clinic of São João

hospital center, Oporto, Portugal and re-evaluation of the diagnosis

after five years.

Results

We included 60 patients with a first psychosis episode,

22 of which were drop-outs after five years. Of the 38 patients

evaluated, it was possible to see that after 5 years 68.4% (

n

= 26)

maintained the same diagnosis during follow-up. In particular, the

diagnosis of schizophrenia was kept in 83.3% of patients after 5

years (

n

= 15, 18 patients with the diagnosis of schizophrenia after

first admission). Diagnosis of acute and transient psychotic disor-

der and psychosis not otherwise specified were the least stable

diagnosis after 5 years.

Conclusions

The diagnosis after a first psychotic episode has

important therapeutic and prognostic implications. The presence

of characteristic symptomatology, with periods of partial or total

remission between subsequent episodes emphasizes the need for

regular monitoring, since this group of patients appears to be more

vulnerable to changes in diagnosis over time.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.2138

EW0269

Side effects of clozapine and their

relationship with clinical variables in

patients with schizophrenia

G. Gürcan

, S¸ . Hun S¸ enol , A.E. Anıl Ya˘gcıo˘glu , A. Ertu˘grul

Hacettepe University Faculty of Medicine, Psychiatry, Ankara, Turkey

Corresponding author.

Introduction

The side effects of clozapine may affect the treat-

ment process negatively, and increase the disability.

Aims

We aimed to assess the side effects of clozapine, and their

relationship with the clinical variables in schizophrenia patients,

and study the predictors of disability.

Methods

Consecutive 122 outpatients who met DSM-IV criteria

for schizophrenia, and were on clozapine treatment were included

in the study. Information about sociodemographic characteristics,

past and current clinical status were gathered through a clinical

interview and review of the medical records, and physical meas-

ures and laboratory tests, including clozapine plasma levels, were

recorded. The patients were assessed with SCID-I, Positive and

Negative Syndrome Scale, UKU-Side Effect Rating Scale, WHO-

Disability Assessment Schedule-II.

Results

Hypersalivation, weight gain, sedation and constipation

were the most common side effects of clozapine. Although the

mean plasma clozapine levels were high (828.11

±

445.5 ng/mL),

no significant effect of clozapine dose and plasma levels were

detected on the severity of side effects, except for constipation.

Metabolic syndrome prevalence was found to be 50% according to

ATP IIIA criteria. Duration of clozapine treatment, clozapine dose

and plasma levels were not significantly different between patients

with andwithoutmetabolic syndrome. Regression analysis showed

that the severity of schizophrenia psychopathology and the number

of side effects predicted the severity of disability.

Conclusions

Side effects of clozapine increase the disability of

patients with schizophrenia and should be monitored regularly. On

the other hand, clozapine dose and plasma levels do not determine

the severity of most of the common side effects.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.2139

EW0270

Effect of clozapine on psychiatric

comorbidities in patients with

schizophrenia

G. Gürcan

, S¸ . Hun S¸ enol , A.E. Anıl Ya˘gcıo˘glu , A. Ertu˘grul

Hacettepe University Faculty of Medicine, Psychiatry, Ankara, Turkey

Corresponding author.

Introduction

Clozapine has superior efficacy in treatment-

resistant schizophrenia, and has various effects on psychiatric

comorbidities, which may affect the illness course.

Aims

We aimed to assess the past and current psychiatric comor-

bidities in schizophrenia patients treated with clozapine, and study

their relationship with clinical variables.

Methods

Consecutive 122 outpatients who met DSM-IV criteria

for schizophrenia receiving clozapine were included. Information

about past and current clinical status were gathered through a

clinical interview and review of the medical records, along with

laboratory test results. Patients were assessed with structured

clinical interview for Axis-I Disorders for DSM-IV, Clinical Global

Impression Scale, Positive and Negative Syndrome Scale (PANSS),

Calgary Depression Scale, Yale-Brown Obsessive Compulsive Scale

(Y-BOCS), Panic and Agoraphobia Scale (PAS), WHO-Disability

Assessment Schedule-II.

Results

There was a significant decrease in the diagnosis of

depression, alcohol and substance use disorder, number of suicide

attempts, and an increase in the diagnosis of obsessive compul-

sive disorder (OCD) after clozapine initiation. Clozapine related de

novo OCD appeared in 48.4% of the patients, and there was a pos-

itive correlation between Y-BOCS total scores and clozapine dose

and plasma levels. In the de novo OCD group, compulsion scores

were higher than obsession scores with checking most prevalent

among compulsions. Total PANSS, Y-BOCS, PASscores were posi-

tively correlated withtotal disability score.

Conclusions

Clozapine seems to decrease comorbid depression,

alcohol and substance use and number of suicide attempts and

increase OCD. Assessment and treatment of psychiatric comorbidi-

ties in clozapine using schizophrenia patients is vital to decrease

disability.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.2140