Abstract

102
ANTIDEPRESSANTS AS IMMUNOMODULATORS
Brian Leonard
Pharmacology Department National University of Ireland and Institute for Brain and Behaviour Research, University of Maastricht, The Netherlands
Epidemiological studies have implicated chronic depression as an important predisposing factor for dementia. Furthermore, chronic inflammatory diseases such as rheumatoid arthritis are frequently associated with depression. The therapeutic use of inflammatory cytokines such as interferon, used to treat chronic hepatitis, frequently cause depressive episodes in psychiatrically normal patients.
More direct evidence shows that in patients with major depression, the pro-inflammatory cytokines are raised in the plasma and cerebrospinal fluid (CRF). Other inflammatory mediators such as prostaglandin E2 are also raised in the plasma and CSF. In addition to the increase in inflammatory mediators that correlate with the major symptoms of depression (and which forms the basis for the macrophage theory of depression) the brain microglia and astrocytes, as well as the blood macrophages and monocytes, are overactive in depression. Hypercortisolaemia is also a common feature of major depression and while cortisol would be expected to attenuate the inflammatory changes, this mechanism would not appear to be functional in such patients. As a consequence of these immune and endocrine changes, there is an impairment of neuronal repair and neurogenesis.
Recently it has become apparent that in depression the activity of the tryptophan-kynurenine pathway increases, the activity of key enzyme, indoleamine dioxygenase being increased by the pro-inflammatory cytokines. As a consequence, the synthesis of serotonin is impaired while the end products of this pathway, 3-hydroxykynurenine and quinolinic acid, activate the NMDA glutamate receptors in the brain to cause neuronal damage. Such neurotoxic damage initiates neurodegeneration, an event that could predispose to dementia.
As most effective antidepressants attenuate the inflammatory changes, it seems possible that antidepressants could have a neuroprotective role. There is also evidence that, in patients in the early phase of the disorder, antidepressants reverse the accumulation of the neurodegenerative mediators of the kynurenine pathway. However, in those with chronic depression, antidepressants no longer appear to be neuroprotective. This hypothesis helps to explain not only the psychopathology of depression but also the possible reasons for the link between depression and chronic inflammatory disorders.
103
ALCOHOL, WINE AND MENTAL HEALTH
Roger M Pinder
Pharma Consultant, The Netherlands
Alcohol is both a poison and a tonic. It all depends upon the dose. The beneficial effects of regular consumption of modest levels of alcohol (<24g/day) have been amply demonstrated in the prevention of coronary heart disease (CHD). The evidence points to wine being better than beer or distilled spirits because it contains grape-derived polyphenols with antioxidant properties, more so in red than in white wine. There is much emerging data, mainly from population-based epidemiological studies, that the risks of stroke, dementia and cognitive decline in the elderly are also reduced by regular consumption of alcohol particularly (red) wine. The risks for CHD, stroke, cognitive decline and dementia follow a J-shaped curve-modest drinkers fare better than both abstainers and heavy drinkers. Plausible biological mechanisms for the beneficial influence of alcohol and wine upon diverse disease states include effects upon glucose metabolism as well as anti-thrombotic, anti-inflammatory and anti-atherosclerotic effects. Wine also uniquely increases heart rate variability and has important antioxidant properties. For Alzheimer's disease, where 5 studies from geographically diverse populations (Denmark, France, Italy, the Netherlands and the USA) have suggested reduced risk in modest and regular drinkers, it is highly likely that the antioxidant and anti-inflammatory properties of red wine in particular play major roles.
104
MATERNAL DEPRIVATION AND CORTICOSTERONE ADMINISTRATION IN RATS AS A NEURODEVELOPMENTAL MODEL OF SCHIZOPHRENIA: EFFECT ON PREPULSE INHIBITION
Maarten van den Buuse
Mental Health Research Institute, Australia
It has been hypothesized that schizophrenia is caused by at least two disruptions during the lifespan. The first disruption is genetic or occurs during an early developmental stage and increases vulnerability to the disease. The second stressful disruption occurs later in life and triggers the onset of overt symptoms. We have investigated this model in rats by combining maternal deprivation and ‘adolescent’ treatment with the stress hormone, corticosterone. Initial studies compared different ages of maternal deprivation and of corticosterone treatment. From these studies, we chose a protocol consisting of 24 hour maternal deprivation on postnatal day 9, followed by implantation of a 100 mg corticosterone pellet from 8 to 10 weeks of age. Controls were briefly handled (nondeprived) or implanted with cholesterol control pellets, respectively. Rats were tested at 10 or 12 weeks of age for psychotropic druginduced locomotor hyperactivity, a model of psychosis, and for prepulse inhibition (PPI), a model of sensorimotor gating.
We did not observe changes in the locomotor hyperactivity response of the animals to amphetamine or phencyclidine treatment at either 10 or 12 weeks of age. In contrast, while apomorphine treatment disrupted PPI in rats that either underwent maternal deprivation or were treated with corticosterone, there was no effect of apomorphine on PPI in rats with the combined neonatal and ‘adolescent’ stress hormone treatment. This effect was seen both at 10 weeks and 12 weeks of age. The disruption of PPI by treatment with the serotonin-1A receptor agonist, 8-OH-DPAT, was similar in all groups. This suggests prolonged and selective changes in dopaminergic regulation of PPI in rats by two disruptions along the neurodevelopmental axis. Current studies are addressing the neurochemical and molecular mechanisms by which maternal deprivation and corticosterone treatment alter behavioural responses.
105
FETAL AND NEONATAL ORIGINS OF ALTERED BRAIN DEVELOPMENT: IMPLICATIONS FOR NEUROLOGICAL DISORDERS
Sandra M Rees
Department of Anatomy and Cell Biology, University of Melbourne, Australia
106
GENE–ENVIRONMENT INTERACTIONS AND EXPERIENCE-DEPENDENT CORTICAL PLASTICITY IN MOUSE MODELS OF PSYCHIATRIC DISORDERS
Anthony J Hannan
Howard Florey Institute, University of Melbourne, Australia
Huntington's disease (HD) is caused by an expanded trinucleotide (CAG) repeat encoding an extended polyglutamine tract in the huntingtin protein. Affected individuals display progressive motor, cognitive and psychiatric symptoms (including depression and psychosis), leading to terminal decline. Given that transgenic HD mice have decreased hippocampal cell proliferation, and that a deficit in neurogenesis has been postulated as an underlying cause of depression, we hypothesised that decreased hippocampal neurogenesis contributes to depressive symptoms and cognitive decline in HD. Fluoxetine, a serotonin reuptake inhibitor commonly prescribed for the treatment of depression, is known to increase neurogenesis in the dentate gyrus of wild-type mouse hippocampus. We have shown that hippocampal-dependent cognitive and depressive-like behavioural symptoms occur in HD mice, and that the administration of fluoxetine produces a marked improvement in these deficits. Furthermore, fluoxetine was found to rescue deficits of neurogenesis and volume loss in the dentate gyrus of HD mice. We have also recently demonstrated that specific environmental manipulations can have similar effects.
We are also focusing on specific glutamate, serotonin and muscarinic acetylcholine receptors, and associated G protein-coupled signalling pathways, which mediate experience-dependent changes in the structure and function of neurons in the postnatal neocortex and hippocampus. We know that some of the genes we are examining have been recently linked to schizophrenia, and we are attempting to understand how disruption of these molecular signalling pathways can lead to the abnormal cortical maturation seen in this disease. These molecular changes have now been compared with behavioural changes in knockout mice, suggesting that these signalling pathways are crucial for development of various cognitive functions, including working memory and sensorimotor gating, which are known to be disrupted in schizophrenia. We have identified specific behavioural deficits that can be rescued by increased levels of environmental stimulation, providing evidence for gene-environment interactions of relevance to the pathogenesis of schizophrenia.
107
DEVELOPMENTAL VITAMIN D DEFICIENCY AND BRAIN DEVELOPMENT: AN INFORMATIVE ANIMAL MODEL OF SCHIZOPHRENIA
Tom H Burne
Queensland Centre for Mental Health Research (QCMHR), Australia
John J McGrath
Queensland Centre for Mental Health Research (QCMHR), Australia
Alan Mackay-Sim
Griffith University, Australia
Darryl W Eyles
Queensland Centre for Mental Health Research (QCMHR), Australia
There is growing evidence that vitamin D is active in the brain but until recently there was a lack of evidence about its role during brain development. Guided by certain features of the epidemiology of schizophrenia, we have explored the role of vitamin D in the developing brain and behaviour using whole animal models. Prenatal vitamin D deficiency results in subtle alterations in maternal behaviour as well as long lasting effects on the adult offspring, despite a return to normal vitamin D levels during postnatal life. These affects are specific to transient prenatal vitamin D depletion as adult vitamin D depletion, combined prenatal and chronic postnatal vitamin D depletion, or ablation of the vitamin D receptor in mice lead to markedly different outcomes. The developmental vitamin D (DVD) model now draws strength from epidemiological evidence of schizophrenia and animal experiments. Although the DVD model does not replicate every aspect of schizophrenia, it has several attractive features: (1) the exposure is based on clues from epidemiology; (2) it reproduces the increase in lateral ventricles; (3) it reproduces well-regarded behavioural phenotypes associated with schizophrenia (e.g. MK-801 induced hyperlocomotion and impaired LI); and (4) it implicates a disturbance in dopamine signaling. In summary, low prenatal levels of vitamin D can influence critical components of orderly brain development and that this has a long lasting effect on the adult brain.
108
ANIMALS MODELS OF DEPRESSION: DO THEY EXIST?
Trevor Norman
Department of Psychiatry, University of Melbourne, Austin Hospital, Australia
Studies in animals are widely used for the screening of new molecules as potential antidepressants in man. Additionally, examination of biochemical and physiological changes occurring in animals after acute and chronic administration of existing clinically proven antidepressant molecules have been used to advance an understanding of their mechanism of action. The ability of such studies to predict, with few false positives, drugs which have already been shown to be antidepressant in the clinic has been used to advance the case for a particular model to be one of depression. From such studies a number of models of depression have been developed with predictive validity. Rarely have such models been used to understand the pathophysiology of certain aspects of the depression. For this latter application models need to demonstrate face and construct validity as well as predictive validity. This presentation focuses on two models of depression developed from different perspectives: the bilateral olfactory bulbectomised rat and the chronic mild stress model. Face, construct and predictive validity will be compared and contrasted for the two models and their relative contributions to understanding the neuro-chemical basis of depression presented. The bulbectomised rat, a neuronal damage model, relies heavily on predictive validity, where it has been successful in demonstrating antidepressant properties of novel agents. A series of studies in recent years has suggested that the model also demonstrates both construct and face validity. The chronic mild stress model, an aetiological model, also has high predictive validity for antidepressant drugs. Both face and construct validity are also demonstrated by this model. However the usefulness of this model is limited by the difficulties in establishing it in different laboratories.
109
THE 2ND AUSTRALIAN NATIONAL SURVEY OF MENTAL HEALTH AND WELL-BEING: OVERVIEW AND FUTURE DIRECTIONS
Tim Slade
University of New South Wales, Australia
Jane Pirkis
University of Melbourne, Australia
In 2007 a second survey of the mental health of the Australian adult general population will be conducted. The planning for this second mental health survey is just underway. The current presentation will provide background information about the aims and purposes of the second survey along with a more detailed discussion of the issues associated with developing the instrument to be used in the survey. The strengths and weaknesses of the first survey will be discussed with the aim of identifying gaps in knowledge regarding the epidemiology of mental disorders. The presentation will conclude by describing some potential research questions that will be answered with the new survey.
110
DEVELOPMENT AND EVALUATION OF A YOUTH MENTAL HEALTH COMMUNITY AWARENESS CAMPAIGN – THE COMPASS STRATEGY
Annemarie Wright
ORYGEN Research Centre, University of Melbourne, Australia
Anthony F Jorm
ORYGEN Research Centre, University of Melbourne, Australia
Meredith G Harris
ORYGEN Research Centre, University of Melbourne and School of Population Health, University of Queensland, Australia
Patrick D McGorry
ORYGEN Research Centre, University of Melbourne, Australia
Kerryn Pennell
ORYGEN Research Centre, University of Melbourne, Australia
111
CHALLENGES IN THE EPIDEMIOLOGICAL STUDY OF INTELLECTUAL DISABILITY COMORBID WITH PSYCHIATRIC MORBIDITY. DATA FROM A WESTERN AUSTRALIAN RECORD LINKAGE STUDY
Vera A Morgan
School of Psychiatry and Clinical Neurosciences, The University of Western Australia, Australia
Helen Leonard
Institute for Child Health Research, The University of Western Australia, Australia
Assen Jablensky
School of Psychiatry and Clinical Neurosciences, The University of Western Australia, Australia
In 1919, Kraepelin used the term “pfropfschizophrenie” to describe schizophrenia comorbid with intellectual disability. In recent years, there has been a renewed interest in studying the relationship between psychiatric morbidity and intellectual disability in general, and between schizophrenia and intellectual disability specifically. Research findings have not been consistent, with the variation in prevalence estimates reflecting methodological, diagnostic and administrative issues. However, it is estimated that some 3% of persons with intellectual disability will have schizophrenia compared to a population figure of around 1%. In Western Australia, we had an opportunity to study intellectual disability comorbid with psychiatric morbidity using whole-of-population data. We linked 11,576 individuals on the Western Australian intellectual disability register to the statewide mental health register in order (i) to get estimates of comorbidity and (ii) to describe the profile of persons with comorbid illness.
Our results highlight the importance of using both psychiatric and disability registers to study comorbidity. We found that psychiatric morbidity is poorly recorded in disability services records and intellectual disability is poorly recorded in mental health services records. Using the linked dataset, psychiatric morbidity affected up to 1 in 5 persons with an intellectual disability. The prevalence of psychotic episodes was high (4% of all disability services clients) but may be underestimated unless we also use psychiatric registers to identify cases.
The challenges of researching comorbid disorders will be discussed. However, despite the difficulties, our estimates are in line with some of the more reliable estimates in the literature and, for the first time in Western Australia, we are able to describe the clinical profile of this group of people and characterise their use of services. The linked database also provides a rare opportunity to test specific hypotheses on the association between intellectual disability and psychiatric disorders and our ongoing work is focusing specifically on intellectual disability comorbid with psychotic disorders.
112
PERFORMANCE OF THE SF-12 AND RAND-12 PHYSICAL AND MENTAL HEALTH SUMMARY SCALES IN A POPULATION-BASED SAMPLE OF 20–24, 40–44 AND 60–64 YEAR-OLDS: THE PATH THROUGH LIFE PROJECT
Timothy D Windsor
Australian National University, Australia
Bryan Rodgers
Australian National University, Australia
Peter Butterworth
Australian National University, Australia
Kaarin J Anstey
Australian National University, Australia
Anthony F Jorm
University of Melbourne, Australia
113
THE IMPORTANCE OF THE HOUSEHOLD IN PSYCHIATRIC EPIDEMIOLOGY
Peter Butterworth
Centre for Mental Health Research, The Australian National University, Australia
114
PARTNERSHIPS FOR WELLBEING: THE RURAL RAP PROGRAM
Tracy E Robinson
Charles Sturt University, Australia
Paul Burnett
Charles Sturt University, Australia
Brian Kelly
Centre for Rural and Remote Mental Health, University of Newcastle, Australia
Michael Kiernan
Charles Sturt University, Australia
115
THE RELATIONSHIP BETWEEN THERAPEUTIC ALLIANCE AND RECOVERY ORIENTED BEHAVIOUR IN CLIENTS WITH SEVERE MENTAL ILLNESS AND HIGH SUPPORT NEEDS
Robert J King
The University of Queensland, Australia
Frank Deane
Australia
Lindsay Oades
Australia
Trevor Crowe
Australia
Pete Kelly
Australia
The Aim Hi project (High Support Stream) is an NHMRC funded multisite trial of collaborative mental health service provision using evidencebased procedures within a recovery oriented framework. Mental health practitioners from state operated clinical services in Victoria, NSW and Queensland and non clinical support workers from non-government services in NSW and Queensland were trained in a model of service delivery that emphasised alliance building, collaborative goal setting and client homework. Services were allocated to either an immediate training or a delayed training condition so as to enable evaluation of training impact, having reference to therapy process and client outcome. Standardised process and client outcome measures were used and participating practitioners were required to maintain detailed records of client goal setting and recovery oriented tasks. It was hypothesised that training would promote stronger collaboration and alliance resulting in greater commitment to recovery goals and increased participation in agreed tasks, including homework activities. This paper reports on early data from a sample of approximately 120 clients and examines the relationship between therapy process and active engagement in goal setting and recovery oriented behaviour.
116
HELP-SEEKING BY RURAL RESIDENTS FOR MENTAL HEALTH PROBLEMS: THE IMPORTANCE OF AGRAGARIAN VALUES
Fiona Judd
Centre for Rural Mental Health, Bendigo Health Care Group and Monash University, Australia
Angela Komiti
Centre for Rural Mental Health, Bendigo Health Care Group and Monash University, Australia
Henry Jackson
The University of Melbourne, Australia
Greg Murray
Swinburne University, Australia
Caitlin Fraser
Centre for Rural Mental Health, Bendigo Health Care Group and Monash University, Australia
117
INCIDENCE AND OUTCOME OF PSYCHIATRIC DISORDER IN A LONGITUDINAL RURAL COMMUNITY STUDY (NoRMHS)
John Beard
Public and Environment Health University of Sydney, Australia
Brian Kelly
Centre for Rural and Remote Mental Health, University of Newcastle, Australia
Kathy Heathcote
Centre for Rural and Remote Mental Health, University of Newcastle, Southern Cross University and Department of Rural Health, Australia
Robert Brooks
Centre for Population Mental Health, Liverpool Hospital, Australia
Arul Earnest
Department of Rural Health (Northern Rivers), University of Sydney, Australia
118
AUSTRALIAN NEWSPAPER JOURNALISTS BELIEFS ABOUT DISCRIMINATION: DO THEY HAVE THE WRITE IDEA?
Lara M Bishop
Centre for Mental Health Research, Australian National University, Australia
Kathleen M Griffiths
Centre for Mental Health Research, Australian National University, Australia
Helen M Christensen
Centre for Mental Health Research, Australian National University, Australia
Louise Farrer
Centre for Mental Health Research, Australian National University, Australia
119
A FLEXIBLE MODEL OF PERSONALITY TRAITS ASSOCIATED WITH DEPRESSION: THE BLACK DOG INSTITUTE'S MODEL
Gordon Parker
School of Psychiatry, University of New South Wales and Black Dog Institute, Australia
Lucy A Tully
School of Psychiatry, University of New South Wales and Black Dog Institute, Australia
Joanna Crawford
School of Psychiatry, University of New South Wales and Black Dog Institute, Australia
Vijaya Manicavasagar
School of Psychiatry, University of New South Wales and Black Dog Institute, Australia
120
ARE CHANGES IN ROLE STRAIN AND RUMINATION ASSOCIATED WITH CHANGES IN DEPRESSION AS A FUNCTION OF GENDER?
Holly A Mack
The Centre for Mental Health Research, The Australian National University, Australia
Helen Christensen
The Centre for Mental Health Research, The Australian National University, Australia
Ruth A Parslow
ORYGEN Research Centre, Department of Psychiatry, The University of Melbourne, Australia
It is well established that women experience depression more than men, but it is not completely understood why women are more vulnerable to depressive symptoms. Explanations for this vulnerability have been that women experience greater role strain and rumination than men, which leads to an increase in anxiety and depression. The present study investigates the relationship between changes in role strain and rumination and changes in depression as a function of gender.
The analyzed sample comprised subjects from an ongoing Australian epidemiology study entitled “The PATH Through Life” project (PATH), randomly selected from electoral rolls in the ACT. Initial data collection began in 1999, with follow-up data collected four years later, resulting in a total sample size of 7,485 adults in three age groups (20–24, 40–44, 60–64). Data on the youngest age group (20–24) concerns the current analyses, with 1,162 males and 1,242 females. Goldberg's scales were utilized to measure symptoms of depression and anxiety experienced in the last month. Factors evaluated for possible gender differences in depression and anxiety included education, martial status, employment status, number of children, personality, role strain, mastery, and ruminative style. Latent change models were utilized to evaluate these relationships.
Preliminary results show a significant difference between the number of depression and anxiety symptoms experienced by males and females, with females having higher scores at both time points. For females, there was a significant difference in anxiety between the two time points.
121
EXECUTIVE DYSFUNCTION PREDICTS POOR PSYCHOSOCIAL OUTCOME THREE MONTHS AFTER RECOVERY FROM MAJOR DEPRESSIVE DISORDER
Adrienne Withall
School of Behavioural and Community Health Sciences, University of Sydney, Australia
Lynne Harris
School of Behavioural and Community Health Sciences, University of Sydney, Australia
Steve Cumming
School of Behavioural and Community Health Sciences, University of Sydney, Australia
122
UNDERSTANDING FLIGHT OF IDEAS IN MANIA
Susan L Rossell
Mental Health Research Institute of Victoria, Australia
Characteristically, patients with mania show pressure of speech, rapidly and involuntarily flitting from one topic to the next, which although logical and possible to follow, is often inappropriate. This is called flight of ideas. There have been no previous empirical investigations to uncover the underlying cognitive basis for this symptom. This study predicted that flight of ideas is the result of an associative processing abnormality. 28 patients with mania, 32 patients with schizophrenia and 32 matched normal controls performed eight associative/semantic processing tasks. It was predicted that mania participants would have difficulty performing tasks that required accurate processing of associations (for example deciding whether synonyms are associated or not) but other semantic processing skills would be intact, i.e. fluency and meaning generation. The data supported our hypothesis. We consequently further examined whether the deficits reported in mania were the result of an access or storage difficulty by using task manipulations of consistency, frequency and hyperpriming. It is generally assumed that a storage deficit is signalled by item-specific consistent performance, an exaggerated effect of word frequency, and the occurrence of hyperpriming; an access deficit is signalled by the absence of these effects. The data, in general, supported an access difficulty. In conclusion, individuals with mania have specific controlled associative processing difficulties that are the result of impaired search and retrieval of information.
123
DETERMINANTS OF PSYCHOSOCIAL IMPAIRMENT IN BIPOLAR DISORDER
Philip B Mitchell
University of New South Wales, The Black Dog Institute, Australia
Justine C Corry
Black Dog Institute, Prince of Wales Hospital, Australia
Gin S Malhi
The University of New South Wales, Australia
Dusan Hadzi-Pavlovic
Department of Human Behaviour, School of Psychiatry, The University of New South Wales, Australia
Amy K Johnston
School of Psychiatry, The University of New South Wales, and The Black Dog Institute, Australia
124
BIPOLAR DISORDER IN AUSTRALIA: ASSESSMENT OF CLINICAL OUTCOMES AND DISEASE BURDEN
Jayashri Kulkarni
Alfred Psychiatry Research Centre, The Alfred and Monash University, Australia
Michael Berk
Department of Clinical and Biomedical Sciences, The University of Melbourne, Australia
Fitzgerald B Paul
Alfred Psychiatry Research Centre, The Alfred and Monash University, Department of Psychological Medicine, Australia
Anthony R de Castella
Alfred Psychiatry Research Centre, The Alfred and Monash University, Australia
Dodd Seetal
Department of Clinical and Biomedical Sciences, The University of Melbourne, Australia
Katarina Kelin
Eli Lilly Australia Pty Ltd, Australia
Alan Brnabic
Clinical Outcomes and Research Institute, Eli Lilly Australia Pty Ltd, Australia
William Montgomery
Eli Lilly Australia Pty Ltd, Australia
125
FACTORS DISTINGUISHING SUICIDE IDEATORS FROM SUICIDE ATTEMPTERS IN A COMMUNITY SAMPLE: SOCIAL ISSUES AND PHYSICAL HEALTH PROBLEMS
Alicia K Fairweather
Centre for Mental Health Research, Australian National University, Australia
Kaarin J Anstey
Centre for Mental Health Research, Australian National University, Australia
Bryan Rodgers
National Centre for Epidemiology and Population Health, Australian National University, Australia
Peter Butterworth
Centre for Mental Health Research, Australian National University, Australia
126
UNDERSTANDING SUICIDE IN AUSTRALIAN FARMERS
Henry Jackson
University of Melbourne, Australia
Fiona K Judd
Centre for Rural Mental Health, Monash University, Australia
Caitlin E Fraser
Centre for Rural Mental Health, Bendigo Health Care Group and Monash University, Australia
Greg Murray
Swinburne University, Australia
Garry Robbins
University of Melbourne, Australia
Angela Komiti
University of Melbourne, Australia
Male farmers in Australia have an elevated risk of suicide. In this paper we report the findings of a study examining this serious public health issue. The aims of the study were to investigate the rate of mental health problems, in particular depression, an important factor contributing to suicide, amongst farmers compared to non-farmer rural residents. The study also investigated additional factors that might contribute to an increased risk of suicide amongst farmers. The study used a combination of quantitative and qualitative approaches.
In the study quantitative we found no support for the proposition that farmers experience higher rates of mental health problems than nonfarmer rural residents, but identified potentially important personality differences between farmers and non-farmers. Participants in the study also indicated that farming is an environment in which individuals experienced a range of stressors, but have limited capacity to acknowledge or express these. In addition, there appeared to be significant attitudinal barriers to help seeking for those who may have mental health problems, particularly male farmers.
The study concluded that the elevated rate of suicide amongst farmers does not seem to be simply explained by an elevated rate of mental health problems. Individual personality, gender and community attitudes which limit a person's ability to acknowledge or express mental health problems and seek help for these may be significant risk factors for suicide in farmers.
127
EVALUATION OF THE TOWARDS-WELL-BEING SUICIDE MONITORING PROGRAMME
Pete M Ellis
Wellington School of Medicine and Health Sciences, University of Otago, New Zealand
Don AR Smith
Wellington School of Medicine and Health Sciences, University of Otago, New Zealand
Suicide rates among young people in New Zealand have been among the highest in the OECD. These rates were particularly high among young people under statutory supervision by the Child Youth and Family (Welfare) Service. Guidelines to reduce the rate of suicidal behaviour had been commissioned specifically for this service, but had not led to early change. The Towards Well-Being suicide monitoring programme sought to formally implement these guidelines using a network of clinical advisers supported by an electronic clinical decision support system. Welfare social workers used brief rating scales and their own judgement to refer at risk youth to the programme. The programme provided a low threshold, rapid response and proactive detection of youth at risk from daily reports of social worker screening. Clinical advisers provided consultation-liaison support to assist the social worker plan and carry though appropriate management and provided support in accessing mental health services, but had no direct contact with the young people involved. The implementation of the management plan was monitored electronically and weekly review of the young person's social work casenotes.
The aims of the programme were to reduce deaths by suicide, reduce suicide attempts and to increase appropriate referrals to mental health services.
As this was a national cohort study with no control group, evaluation is against historical control data and the non-welfare group. Over a three-year period the number of young people in CYF care increased by 80%, there was an increase in hospitalisation for suicide attempts and the national rate of death by suicide increased significantly. The rate of suicide attempts and deaths among youth in the welfare group remained stable.
128
METABOLIC ABNORMALITIES IN BIPOLAR PATIENTS ON SODIUM VALPROATE
Richard J Porter
Christchurch School of Medicine & Health Sciences, University of Otago, New Zealand
Jane Elmslie
Christchurch School of Medicine & Health Sciences, University of Otago, New Zealand
Peter R Joyce
Christchurch School of Medicine and Health Sciences, University of Otago, New Zealand
Andrea Bartram
Christchurch School of Medicine & Health Sciences, University of Otago, New Zealand
Penny Hunt
Christchurch School of Medicine & Health Sciences, University of Otago, New Zealand
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