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S834

25th European Congress of Psychiatry / European Psychiatry 41S (2017) S772–S846

Results

The sample consisted of 72 inpatients (schizophrenia

55.6%, SZA 20% and cluster A PD 19.4%). The negative and the

general psychopathology scales directly correlated at different

degrees in the three groups (schizophrenia:

r

= 0.750;

P

< 0.001;

SZA:

r

= 0.625,

P

= 0.006; cluster A PD:

r

= 0.541,

P

= 0.046). The

symptom “depression” directly correlated with 5 out of 7 neg-

ative symptoms: blunted affect (

r

= 0.616,

P

< 0.001), emotional

withdrawal (

r

= 0.643,

P

< 0.001), poor rapport (

r

= 0.389,

P

= 0.001),

passive/apathetic social withdrawal (

r

= 0.538,

P

< 0.001), lack of

spontaneity & flow of conversation (

r

= 0.399,

P

= 0.001).

Conclusions

Our study confirmed the existence of the

“schizophrenia spectrum” with combined different disorders lying

on a continuum in which negative symptoms mainly correlated

with the psychopathological functioning. Noteworthy, the symp-

toms of the negative scale strongly correlatedwith the “depression”

symptom, underlying the impact of the affective symptoms on the

severity of the “schizophrenia spectrum” disorders.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.1638

EV1309

Ultra-resistant schizophrenia and

potentiation strategies

S. Khouadja

, R. Ben Soussia , S. Younes , A. Bouallagui , I. Marrag ,

M. Nasr

University Hospital, Psychiatry, Mahdia, Tunisia

Corresponding author.

Introduction

Treatment resistance to clozapine is estimated at

40–70% of the treated population. Several clozapine potentiation

strategies have come into clinical practice although often without

evidence-based support.

Objective

The aim of our work was to identify the potentiation

strategies in ultra-resistant schizophrenia depending on the sub-

type of schizophrenia.

Methodology

This is a prospective study conducted on patients

with the diagnosis of schizophrenia, based on DSM-IV-TR criteria,

and hospitalized in the psychiatric department of the univer-

sity hospital in Mahdia, Tunisia. The study sample consisted of

patients meeting the resistant schizophrenia criteria as defined by

national institute for clinical excellence (NICE), and the prescrip-

tion of clozapine for 6 to 8 weeks was shown without significant

improvement.

Results

we have collected 10 patients. The mean serum level

of clozapine was 462.25mg/L. The potentiation strategies were

different depending on the subtype of schizophrenia. For the undif-

ferentiated schizophrenia, we have chosen ECT sessions. For the

disorganized schizophrenia, we opted for amisulpiride and arip-

iprazole. For the paranoid forms, we have chosen the association

of risperidone and ECT. A psychometric improvement was noted in

BPRS ranging from 34 to 40%.

Conclusion

Every potentiation strategy entails a cost, whether it

is an additional monetary cost, adverse effects or greater stress to

caregivers. The cost/benefit equation should be thoroughly evalu-

ated and discussed before commencing a strategy.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.1639

EV1310

Increased prevalence of toxoplasma

gondii seropositivity in patients with

treatment-resistant schizophrenia

M. Sagud

1 ,

, S. Vlatkovic

2

, D. Svob Strac

3

, M. Sviben

4

,

M. Zivkovic

5

, M. Vilibic

2

, B. Vuksan-Cusa

6

, A. Mihaljevic-Peles

7

,

N. Pivac

3

1

Psychiatrist, Assistant Professor, School of Medicine, University of

Zagreb, Zagreb, Croatia

2

University Psyciatric Clinic Vrapce, Psychiatry, Zagreb, Croatia

3

Rudjer Boskovic Institute, Laboratory for Molecular

Neuropsychiatry Division of Molecular Medicine, Zagreb, Croatia

4

Croatian National Institute of Public Health, Department of

Parasitology and Mycology, Zagreb, Croatia

5

University Psychiatric Clinic Vrapce, Psychiatry, Zagreb, Croatia

6

School of Medicine, University of Osijek, University Hospital Centre

Zagreb, Psychiatry, Zagreb, Croatia

7

School of Medicine, University of Zagreb, Psychiatry, Zagreb, Croatia

Corresponding author.

Introduction

Previous studies suggested that patients with

schizophrenia had an increased prevalence of antibodies against

toxoplasma gondii (TG) and that those seropositive patients had

higher symptom severity. However, there is no data on the rela-

tionship between treatment-resistant schizophrenia (TRS) and TG

seroprevalence.

Objectives

To determine the association between TRS and TG

seropositivity, and to further investigate the relationship between

TG seropositivity and different clinical features of schizophrenia.

Methods

In this cross-sectional study, we included 210 male

inpatients with schizophrenia. TG seropositivity was determined

by ELFA assay. Treatment-resistance was defined as a failure of at

least 2 adequate anti-psychotic trials. Data were analyzed using

2

test or Mann–Whitney test.

Results

The rate of TG seropositivity in the entire sample

was 52.3%, whereas 47.6% of patients met the definition for

treatment-resistance. Seropositive patients had twice the rate of

treatment–resistance compared to seronegative patients (63.6%

vs. 30.0%,

P

< 0.0001). Moreover, in the seropositive group, the

patients were older (47.6

±

12.2 vs. 39.81

±

12.01 years,

P

< 0.0001),

had higher number of previous hospitalizations (13.9

±

11.7 vs.

9.6

±

8.5,

P

= 0.0073), and increased Calgary depression scale for

schizophrenia (CDSS) total score (7.8

±

4.5 vs. 6.3

±

3.8,

P

= 0.012).

There were no differences between the groups in the age of dis-

ease onset, smoking, positive and negative syndrome scale (PANSS)

total, positive and negative scores, and the life-time history of sui-

cide attempts.

Conclusions

Our results support the hypothesis that TG seropos-

itivity might contribute to treatment-resistance in schizophrenia,

at least in male patients.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.1640

EV1311

From polipharmacy to monotheraphy

a case about schizoaffective disorder

S.F. Salonia

1 ,

, P.E. Asensio Pascual

1

, B. Pérez Molina

1

,

A.M. García Herrero

1

, M.D.C. Martinez Tomás

1

,

J. Martinez Martinez

2

, Á.A. Maroto Hernández

2

,

A.M. Gea Jimenez

2

, F.J. Sanchís Lledó

3

,

M. Infante Sánchez de Lugarnuevo

3

1

CSM Yecla, Psychiatry, Yecla, Spain

2

CSM Yecla, Nursing, Yecla, Spain

3

CSM Yecla, Psychology, Yecla, Spain

Corresponding author.

The aim of the present poster is to describe an initial complex case

of schizoaffective disorder with other clinical adverse conditions

(metabolic disorders) in a young adult male, which gradually went

into a positive treatment way from polipharmacy to monotera-

phy. His psychiatric history started when he was 25-year-old, he

was diagnosed of heroine dependence, hypercholesterolemia and

hypertrigliceridemia. In 2000 he had a suicide attempt in a context

of depressive mood and delusions. He needed a psychiatric hospi-

talization for the first time in his life and he received anti-psychotics