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ABSTRACTS - World Psychiatric Association

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useful in clinical practice as an adjuvant treatment for hospitalized<br />

patients with severe, drug-resistant major depression.<br />

PO1.166.<br />

VAGUS NERVE STIMULATION AND RESISTANT<br />

DEPRESSION: A SYSTEMATIC REVIEW<br />

C. Daban, A. Martinez-Aran, N. Cruz, M. Bonin, E. Vieta<br />

Clinical Institute of Neurosciences, Hospital Clinic, University<br />

of Barcelona, Spain<br />

Since 2005, vagus nerve stimulation (VNS) is considered as an<br />

adjunctive for treatment-resistant depression (TRD) (unipolar or<br />

bipolar). Our objective is to give a clear overview of the safety and<br />

efficacy of the VNS by means of a systematic review. The review was<br />

made using the major databases beginning in January 2000 until April<br />

2008. A total of 108 references were found, but only 20 add-on studies<br />

meeting the required criteria were selected for this review. Since<br />

only one double-blind randomized study was published, a metaanalysis<br />

was not feasible. Regarding the efficacy, VNS is associated to<br />

a reduction of depressive symptoms in a majority of the open studies.<br />

Unfortunately, in the only double-blind study the results are rather<br />

disappointing and inconclusive. Regarding safety, despite its invasive<br />

nature, VNS can be considered as safe and feasible. VNS therapy is<br />

an interesting new approach for the treatment of TRD. Although the<br />

results are rather promising, we must be cautious in our conclusions<br />

since the evidence is only based on open studies. Further clinical trials<br />

are needed in bipolar patients, regarding the predictors of<br />

response, the cost-efficacy and the mechanism of action to better<br />

understand and develop VNS therapy for affective disorder.<br />

PO1.167.<br />

FUNCTIONAL OUTCOME AFTER 12 MONTHS<br />

OF DEEP BRAIN STIMULATION FOR TREATMENT<br />

RESISTANT MAJOR DEPRESSIVE DISORDER<br />

S.H. Kennedy, S. Rizvi, H. McNeely, P. Giacobbe, H.S. Mayberg,<br />

A.M. Lozano<br />

University of Toronto, Ontario, Canada; St. Joseph’s Hamilton<br />

Healthcare, Hamilton, Canada; McMaster University, Hamilton,<br />

Canada; Emory University, Atlanta, GA, USA<br />

Although improvements in function are fundamental to recovery<br />

from a depressive episode, reductions of individual symptoms often<br />

precede objective increases in a patient’s functional capacity. In order<br />

to assess the full utility of an antidepressant therapy, it is not only necessary<br />

to explore the rate of symptom decline, but also the trajectory<br />

for improvement across various domains of function. In 20 patients<br />

with treatment resistant major depressive disorder, measures of mental,<br />

physical, and sexual function, and neuropsychology tests that<br />

assess executive function, memory and emotional responsivity, were<br />

administered before and at various times up to 12 months after deep<br />

brain stimulation to the subcallosal ingulated gyrus. The rate and<br />

degree of functional improvement across measures was analyzed for<br />

all patients. The influence of executive function, memory and emotional<br />

responsivity and personality dimensions was also examined in<br />

relation to functional outcome. The results extend the emerging evidence<br />

base on deep brain stimulation as an alternative to existing<br />

options for treatment resistant depression.<br />

PO1.168.<br />

APPLYING TWO TRANSCRANIAL MAGNETIC<br />

STIMULATION SESSIONS PER DAY COULD HELP<br />

IN THE FASTER REDUCTION OF DEPRESSIVE<br />

SYMPTOMS<br />

P. Sakkas, C. Theleritis, C. Psarros, V. Masdrakis,<br />

T. Paparrigopoulos, G.N. Papadimitriou<br />

First Psychiatry Department, Athens University Medical School,<br />

Eginition Hospital, Athens, Greece<br />

During the last seven years, we completed various pilot studies using<br />

repetitive transcranial magnetic stimulation (rTMS), trying to evaluate<br />

its efficiency. In this context we selected some patients suffering<br />

from drug resistant major depression, who wanted to be treated with<br />

rTMS, and gave them an intensive treatment. We raised the magnetic<br />

intensity to 110-120% of the motor threshold. We gave them about 40<br />

trains of 20-25 Hz per session, using two electromagnetic coils. Also,<br />

we extended the overall duration of treatment to three weeks.<br />

Patients were evaluated with the Hamilton Depression Rating Scale<br />

(HDRS) at baseline as well as at the end of every week thereafter. In<br />

addition, we extended our period of clinical assessment to two more<br />

weeks, because we had an indication from some of our patients that<br />

rTMS sometimes produces a late effect. Ten patients were treated with<br />

two daily sessions (one in the morning, and another in the afternoon)<br />

for five days every week and for three consecutive weeks. Preliminary<br />

results indicate that patients who were treated with two daily sessions<br />

of rTMS had a faster reduction of depressive symptoms on the HDRS,<br />

and some of them also a faster remission of depressive symptoms, in<br />

comparison to patients treated with one rTMS session per day. Further<br />

investigations in larger patient populations should verify this preliminary<br />

result.<br />

PO1.169.<br />

NON-ECT TREATMENT OF CATATONIA<br />

M. El-Shazly, M. Chandran<br />

Department of Neurosciences, University of Birmingham; Hallam<br />

Street Hospital, Birmingham, UK<br />

Catatonia is considered a rare and potentially lethal condition. It is a<br />

syndrome that encompasses multiple motor signs. It can be the only<br />

presenting feature in a patient with underlying multiple neuropsychiatric<br />

syndrome. It is, however, more usually associated with schizophrenia<br />

and to a lesser extent with mixed manic episodes in bipolars.<br />

Electroconvulsive therapy (ECT) is generally considered the treatment<br />

of choice for various forms of catatonia, e.g., organic, lethal and<br />

schizophrenic. The use of benzodiazepines in catatonia remains unlicensed.<br />

There are reports of the use of intravenous (i.v.) low-dose<br />

lorazepam in treating excited catatonia, while higher doses are reported<br />

to have worsened the condition. We present the treatment of four<br />

different types of catatonia (one of organic/antipsychotic induced,<br />

one of iatrogenic, one of schizophrenic and one of depressive catatonia)<br />

without the resort to ECT or i.v. medication. In all cases benzodiazepines<br />

were used, mostly during the stuporous phase. The use was<br />

judicious and time limited. Other treatment strategies were used such<br />

as withdrawing certain drugs or the introduction of others. All cases<br />

responded satisfactorily. In no case ECT was needed. We discuss these<br />

cases in detail and present a review of the literature on the use of benzodiazepines<br />

in catatonia. We present an argument for including catatonia<br />

as one of the indications for benzodiazepine use.<br />

197

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