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ABSTRACTS - World Psychiatric Association

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Health Organization has recently released global recommendations<br />

and guidelines on task shifting for scaling up HIV care and proposes<br />

the “adoption or expansion of a task shifting approach as one method<br />

of strengthening and expanding the health workforce to rapidly<br />

increase access to HIV and other health services”. The scarcity of specialist<br />

mental health human resources in developing countries, compounded<br />

by their inequitable distribution and inefficient utilization,<br />

has been well documented. This human resource gap will remain<br />

large for the foreseeable future, and is likely to be worsened as populations<br />

grow in many countries and as specialists emigrate. We present<br />

a perspective on the role of task shifting to scale up mental health<br />

care, by empowering community and primary health workers to<br />

deliver specific tasks, the evidence base which supports the effectiveness<br />

of task shifting interventions in mental health care, the role of<br />

mental health specialists in such intervention programs, and future<br />

research and program opportunities.<br />

US15.3.<br />

THE INTERFACE BETWEEN PRIMARY CARE<br />

AND SPECIALIZED MENTAL HEALTH SERVICES:<br />

IS IT LOSING IMPETUS<br />

R. Araya<br />

University of Bristol, UK<br />

There was great interest in the 1980s and 1990s to propose and test a<br />

variety of working models for the interface between primary care and<br />

mental health services. There is some evidence to suggest that gradually<br />

this interest may have diminished. Some reasons that may explain<br />

this situation include the preferential attention given to research and<br />

development on models to improve the resolution of selected priority<br />

health problems in primary care or the difficulties to break the existing<br />

formal and informal boundaries between primary care and psychiatry.<br />

The situation is rather different in countries with different levels<br />

of development. In some low-income countries there are few psychiatrists<br />

but there are other forms of specialized mental health services.<br />

Unsurprisingly in those countries psychiatrists may not be at the<br />

centre of this interface. In other more resourceful middle-income<br />

countries with a reasonable number of psychiatrists, other members<br />

of the team – often psychologists – play a much more active role in<br />

this interface. In some high-income countries, some people have<br />

argued that perhaps the central role of the psychiatrist in this interface<br />

should be scrutinized more carefully. Several successful experiences<br />

with nurse specialists and psychologists are worth a more careful<br />

evaluation. There is some evidence to suggest that some treatment<br />

practices deeply established in developed countries may have little<br />

empirical support for their existence. Some have argued that disinvesting<br />

in some of these costly practices may be an option.<br />

US16.<br />

EFFECTIVENESS AND COST-EFFECTIVENESS<br />

OF PHARMACOLOGICAL TREATMENTS<br />

IN PSYCHIATRY: EVIDENCE FROM PRAGMATIC<br />

TRIALS<br />

US16.1.<br />

UTILIZING THE RESULTS OF PRACTICAL CLINICAL<br />

TRIALS TO OPTIMIZE TREATMENT FOR INDIVIDUAL<br />

PATIENTS<br />

J.A. Lieberman<br />

Columbia University College of Physicians and Surgeons,<br />

New York State <strong>Psychiatric</strong> Institute, New York, NY, USA<br />

There is a saying that doctors should “use a new treatment fast while<br />

it still works”. This is because clinicians have grown accustomed to<br />

the fact that new drugs are approved based on their testing in rigorous<br />

clinical trials with great fanfare and high expectations, which they<br />

rarely live up to when used in routine clinical settings. This disconnect<br />

reflects the so-called “efficacy-effectiveness gap”. This gap refers to the<br />

reasons why the results of randomized clinical trials designed largely<br />

to gain regulatory approval for new drugs or additional indications for<br />

the marketed drugs do not accurately reflect how drugs work when<br />

they are applied to broad patient populations in real world settings<br />

and can best be filled by the conduct of practical clinical trials which<br />

aim to determine treatment effectiveness in representative patient<br />

populations in ecologically valid clinical settings. Consequently, there<br />

is an increasing recognition of the urgent need for more practical clinical<br />

trials that will evaluate the comparative effectiveness of currently<br />

marketed treatments, so that we know how best to utilize them and<br />

whether they justify their cost. This paper describes the role of the various<br />

types of studies in the course of drug development and then<br />

emphasizes the unique features and information that practical trials<br />

can provide. In this context the recently published CATIE, CUTLASS,<br />

EUFEST and TEOSS trials are reviewed and analyzed.<br />

US16.2.<br />

EFFECTIVENESS OF SECOND-GENERATION<br />

ANTIPSYCHOTICS IN FIRST EPISODE<br />

SCHIZOPHRENIA: THE EUFEST STUDY<br />

R.S. Kahn<br />

Department of Psychiatry, Rudolf Magnus Institute<br />

of Neuroscience, University Medical Centre Utrecht,<br />

The Netherlands<br />

Second-generation antipsychotic drugs were introduced over a decade<br />

ago for the treatment of schizophrenia; however, their purported clinical<br />

effectiveness compared with first-generation antipsychotic drugs is<br />

still debated. We aimed to compare the effectiveness of second-generation<br />

antipsychotic drugs with that of a low dose of haloperidol, in firstepisode<br />

schizophrenia. We did an open randomised controlled trial of<br />

haloperidol vs. second-generation antipsychotic drugs in 50 sites, in 14<br />

countries. Eligible patients were aged 18-40 years, and met diagnostic<br />

criteria for schizophrenia, schizophreniform disorder, or schizoaffective<br />

disorder. 498 patients were randomly assigned by a web-based<br />

online system to haloperidol (1-4 mg/day; n=103), amisulpride (200-<br />

800 mg/day; n=104), olanzapine (5-20 mg/day; n=105), quetiapine<br />

(200-750 mg/day; n=104), or ziprasidone (40-160 mg/day; n=82). Follow-up<br />

was at one year. The primary outcome measure was all-cause<br />

treatment discontinuation. Patients and their treating physicians were<br />

not blinded to the assigned treatment. Analysis was by intention to<br />

treat. The number of patients who discontinued treatment for any<br />

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