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

S823

EV1276

Brain-based psychotherapy for

psychosis

L. Mehl-Madrona

1 ,

, B. Mainguy

2

1

Eastern Maine Medical Center, Family Medicine, Orono, USA

2

Coyote Institute, Education, Orono, USA

Corresponding author.

Introduction

Psychotherapy methods are evolving for patients

with psychosis.

Methods

We present a psychotherapy of psychosis that is brain-

based, along with results of working with patients using these

methods. Patients with psychosis are known to have decreased

connectivity of the elements of the default mode network, also

known as the story-making brain. These patients are known

to tell narratives that lack coherence, of both excessive ele-

ments and inadequate elements. These stories are rigid and

either cacophonous or rigidly monologic. The key brain area

of the precuneus shows diminished connectivity to other brain

areas. We present a narrative approach in which patients are

assisted through rehearsal and modeling to tell more coherent

stories about their life experiences. We work toward achiev-

ing a future orientation in which a sequence of actions leads

toward an achievement of a future goal. The protagonist encounters

obstacles and learns how to overcome them. Through itera-

tive rehearsals, the story achieves more vivid mental imagery

and emotional connectivity. Delusions and voices are accepted

and incorporated into those stories in ways that provide the

patient with improved capacity to cope with their delusions and

voices.

Results

We present the results of 59 patients who worked with

these techniques and compare themto amatched cohort of patients

treated conventionally. The treated patients show statistically sig-

nificant improvement in positive and negative symptoms and in

quality of life.

Discussion

Brain-based narrative psychotherapy approaches can

improve the quality of life and reduce symptoms.

Conclusion

These techniques are worthy of further exploration.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.1606

EV1277

First-episode psychosis

intervention – description of our early

intervention model

B. Melo

, C. Alves Pereira , R. Cajão , J. Ribeiro Silva , S. Pereira ,

E. Monteiro

Centro Hospitalar Tondela Viseu, Department of Psychiatry, Viseu,

Portugal

Corresponding author.

Introduction

The research about the benefits of early diagnosis

and treatment of first-episode psychosis had significantly increased

in last decades. There have been several early intervention pro-

grams in psychotic disease, implemented worldwide, in order to

improve the prognosis of these psychotic patients.

Objectives

To present a brief description of the first-

episode psychosis intervention team of Tondela-Viseu Hospital

Centre–Portugal and its model. We aim to further characterize our

population and describe its evolution since 2008.

Aims

We aim to clarify the benefits of an early intervention in

psychosis.

Methods

We conducted a retrospective cohort study of patients

being followed by our team from November 2008 to September

2016. Demographic and medical data were collected (such as diag-

nosis, duration of untreated psychosis, treatments and its clinical

effectiveness, relapse rate and hospital admissions) in patient’s

clinical records. The intervention model protocol of this team was

also described and analyzed.

Results

This multidisciplinary team consists of three psychia-

trists, one child Psychiatrist, one psychologist and five reference

therapists (areas of nursing, social service and occupational ther-

apy). It includes patients diagnosed with first-episode psychosis,

aged 16 to 42 years old, followed for five years. The team followed,

since its foundation, 123 patients, mostly male. The most prevalent

diagnosis are schizophrenia and schizophreniform psychosis. The

team is currently following 51 patients.

Conclusions

This team’s intervention have progressively

assumed a more relevant importance in the prognosis of patients

with first-episode psychosis, by reducing the duration of untreated

psychosis, the relapse rate and by promoting social reintegration.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.1607

EV1278

Rechallenge of clozapine in a low

secure setting following pericardial

effusion

A. Mohandas

1 ,

, J. McCarthy

1

, A. Hartley

2

, E. Fatima

3

,

L. Shearman

1

1

Devon Partnership NHS Trust, Langdon Hospital, Dawlish, United

Kingdom

2

Devon Partnership NHS Trust, Core Trainee CT3, Exeter, United

Kingdom

3

Devon Partnership NHS Trust, Specialty trainee ST5, Exeter, United

Kingdom

Corresponding author.

Introduction

Clozapine is licensed for treatment-resistant

schizophrenia and when clozapine is not able to be used, less

evidence based practices may be required. Full remission may

require combinations or high doses of psychotropic medications

having greater potential for interactions and side effects. If this

is not successful, symptoms may persist and long-term disability

may occur.

Aims

To explore safety and efficacy of a rechallenge of clozap-

ine in a patient with treatment resistant schizoaffective disorder,

who previously developed pericardial effusion. Collateral history

reported best improvement with clozapine compared to other

medications.

Objectives

To improve level of functioning and reduce need for

less evidence based choices of medication.

Methods

Initial consultation with clozapine monitoring service

over prospects of rechallenge. Full medication history and review.

Consultationwith a cardiologist regarding validity of local monitor-

ing strategy. Obtain consent from the patient and his family. Titrate

clozapine slowly. Once clozapine initiated, measure temperature,

blood pressure, pulse rate and monitoring of symptoms of peri-

carditis including chest pain, cough and dyspnoea daily. ECG and

echocardiography at baseline and 2 and 4 weeks after initiation of

the rechallenge. ECGs monthly thereafter, with a further echocar-

diogram at 3 months. Weekly troponin and CRP for three months

to monitor developing myocarditis and pericarditis.

Results

Successful rechallenge of clozapine with significant

reduction in psychopathology, improvement in functioning and no

adverse events reported. Reduction of risk enabled transfer to open

ward conditions.

Conclusions

There is increasing evidence of successful rechal-

lenges of clozapine however, further research is necessary to aid

such clinical decisions.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.01.1608