Chapter 15 - Services for children and youth, older people and cald communities
Introduction
15.1
Mental health services are failing some of the most
vulnerable groups in society; medical health care will need to be the overhauled
and revitalised if community expectations are to be met:
There are still too many gaps in current programs and services,
resulting in some people with mental illness falling out of the health care
system. These may include those with co-morbid mental health and alcohol or
drug problems, people with mental illness who are inappropriately in the
criminal justice system, people in the immigration system, Indigenous
Australians, and young people.
The indication of increased demand for mental health care,
together with the increased expectation of high quality care from consumers and
carers, will logically have an impact on how well existing resources and the
current workforce can effectively meet the increased demand. Evidence would
suggest that these are key areas for future attention, particularly if the pace
of reform is to be increased in the future to keep pace with community
expectations.[1720]
15.2
This part of the report will provide a needs assessment
of particular groups—those requiring a more specialised service response—within
the broad-spectrum of needs addressed in the body of the report. Some of the
groups identified above as 'falling out of the health care system' are discussed;
others have been dealt with in detail elsewhere in the report.[1721] The groups covered in this chapter
comprise children, youth, older people and CALD communities. The service
requirements of rural, remote and Indigenous Australians are explored in
Chapter 16.
15.3
Obviously, there is much room for duplication in this assessment; most chapters canvass the diverse
needs of particular groups to some extent. Discussion of children and youth inevitably
highlights the importance of early intervention programs covered in Chapter 7,
while the growing prevalence of youth with dual diagnosis, touched upon here,
is a focus of Chapter 14. In other areas information of service requirements
was comparatively limited. Less was received on older people with mental
illness, perhaps supporting the view that older Australians are a 'voiceless'
and neglected group. The situation of Australia's
Culturally and Linguistically Diverse (CALD) communities is distinctive, and is
addressed in terms of established community groups, and of refugees or new
arrivals. Some consideration is given to the situation of Temporary Protection
Visa (TPV) holders and immigration detainees with mental disorders in the
discussion on refugees, reflecting the importance of the matter to submitters.[1722]
Children and youth
15.4
It well known that social disadvantage, violence and
instability in childhood reduces the chance of an individual enjoying good
mental and physical health in later life.[1723]
Experts have conjectured that improved living standards would reduce the
incidence of health problems. Studies have recently shown, however, that
despite the general increase in amenity in the lives of people in developed
countries compared with 40 years ago, there has been an alarming deterioration in the overall health of children
in recent decades. Pre-eminent in that is a dramatic increase in the incidence
of mental illness among the young.[1724]
15.5
In Australia,
between 14 and 18 per cent of children and young people between the ages of 4
and 18 years now experience mental health problems of clinical significance.
This equates to in excess of 500 000 individuals nationally.[1725] On this basis Professor Fiona
Stanley, Australia of the Year 2003 and child health expert, has argued for a
more a holistic approach to child health, one that recognises the interaction
of social, economic and health policies, to produce a society which can foster
and sustain the physical and emotional health of children and young people.
Essential to her vision is the promotion of an early intervention approach,
away from the 'end of pathway' policy responses currently modelled:
Modernity’s paradox is that in contemporary Australia we just
have not been providing enough good early childhood experiences and for some
children, our Indigenous children, this has had major negative impacts on their
life chances, in spite of us having such a success with our economy...the policy responses
on the whole have been at the end of pathways and, whilst that’s
understandable, they will not deliver the long-term solutions to reduce those
problems and neither have researchers actually adequately investigated these
problems...we need to respond to this by acknowledging these issues and
acknowledging this is happening in today’s Australia and we need to start to
change our emphasis and activities to make it a better place for our children
and young people.[1726]
15.6
This report cannot address the wider issues of social
and economic policy which affect the happiness and well being of Australian
youth. It can nevertheless acknowledge that the capacity to reduce the
incidence and impact of mental health problems in the community[1727] is
affected by broader social and economic frameworks set up by Australian
governments. As discussed in Chapter 7, the lack of support for early
intervention is just one, albeit very important, aspect of this. This section
will not focus on early intervention services for children as discussed in that
chapter, but will look across the spectrum of child and youth need to discuss
major service gaps affecting these groups.
15.7
The first and foremost issue is the extent of unmet
need. Studies[1728] have shown that
alarmingly few young people have access
to the necessary mental health services:
Only one in four young
people with mental health problems receive help and even among those with most
severe mental health problems, only 50 per cent receive professional help.
Family doctors, school-based counsellors and paediatricians provide the
services that are most frequently used by young people with mental health
problems but even then young people are
under-represented in the number of general practice visits as a percentage of
the population. Of greater concern, they are also under-represented in visits for mental health issues, even though
this issue provides the highest morbidity in this age group.[1729]
15.8
Submitters
identified multiple deficiencies in national policy as underpinning this low
rate of access:
-
first,
the absence of a national template to drive development of services that are
both targeted and better integrated;
-
second,
insufficient recognition of the diversity of child and adolescent health needs
in the structure and provision of services; and
-
third,
the need for adequate funding to develop the necessary family and community
support systems.
15.9
These
failures articulated into significant service gaps in high areas of need,
including those for youth and young adults with emergent mental health
problems.
National child and adolescent mental health framework
15.10
The lack of an articulated plan for addressing child
and adolescent mental health has been identified as a major policy flaw in an
otherwise progressive National Mental Health
Plan 2003–2008. AICAFMHA advised:
A recent study reviewing international policy development on
child and adolescent mental health by Shatkin and Belfer (2004) ranked
Australia a B (on a scale from A-D) which reflected that Australia had national
policies that recognised the unique needs of this population but did not enumerate a unifying plan of action.
This finding is consistent with previous commentary by AICAFMHA on former
drafts of the now current National Mental Health
Plan 2003-2008.
The minimal recognition of the difference between
child/adolescent mental health and adult mental health in the language of the
National Mental Health Plans may also be a contributing
factor in the National Mental Health Strategy
policy areas being inadequately implemented in the infant, child and adolescent
mental health fields.[1730]
15.11
The West
Australian Child and Adolescent Mental Health Services Advisory Committee supports the view that, without such
a template for action, child and adolescent services will continue run second
in the struggle to fund adult mental health demands:
CAMHSAC is constantly frustrated with the inability to attend to
these issues due to the absence of capacity to marshal resources given the
relative position of CAMHS providers within the current organizational structure
and the demand for acute clinical services. The current organisational
structure is based on mental health districts in which CAMHS service leaders
report to the local mental health district Clinical Director who are almost always
preoccupied with adult mental health services requirements and imperatives.
This leads to a tendency to overlook the needs of children, adolescents and
their families and carers and to view them as the “next issue” needing
attention. “When the needs of adults are fixed then we will attend to the needs
of children” This has been the refrain of senior mental health management for
decades.[1731]
15.12
Child development studies suggest that models
responding to the diverse needs of children and youth across the spectrum of
growth, rather than focusing on distinct age based service provision, will be
the foundation of improved treatment outcomes for these groups:
Infants, children and young people are not small adults. They
have particular emotional, social and physical needs that should be considered
within a developmental framework. Services should be designed specifically for
infants, children and young people that work within this framework and address
these specific needs.[1732]
15.13
The absence of transition frameworks for children
moving between service tiers and, in particular, for those moving out of
adolescent services into adult streams, creates service gaps for patients with
complex needs. The problems of youth aged 14 to 24 with co-occurring disorders,
as discussed in the chapter on dual diagnosis, are indicative, and are
recognised by government:
Young people with emerging mental health problems or disorders
often have multiple difficulties that make diagnosis difficult and may mean the
young people do not clearly fit into specific programs or criteria. The report,
Barriers to Service Provision for Young
People with Presenting Substance Misuse and Mental Health Problems, published in 2004 by the
National Youth Affairs Research Scheme, found that a lack of holistic
professional expertise covering both mental health and substance misuse issues
was one of the key barriers to services for young people with dual diagnosis.[1733]
15.14
Clearly, greater coordination and cooperation within an
interagency framework between child and family focused services and other
agencies is needed. This is essential to support the early intervention and
prevention services discussed in Chapter 7:
In a well functioning mental health system which truly cares for
children, services should be child centred, family focussed, community based,
and culturally sensitive with adequate access to a variety of services suited
to their needs including clinic, home based, school based services and crisis
services, residential centres, and social services which provide attention
tailored to their individual needs. In order for this to happen the health, community and education sectors need
to be integrated for families requiring assistance.[1734]
15.15
However, as Professor Margot Prior of the School of
Health and Behavioural Sciences, University of Melbourne noted, despite these
ideals being well articulated in the National Mental Health
Strategy 'current systems are light years away from the ideal', especially when
the low access and high rates of need are taken
into account.[1735]
Responding to the diversity of child and adolescent health needs
15.16
What is lacking in child and adolescent services is the
capacity to provide appropriately tailored services and treatment responses
within a care pathway that ensures easy transition between service streams.
15.17
As noted in Chapter 7, there are some concerns about
early identification of mental health problems in young people. The NSW
Commission for Children and Young People advised that the issue is really about
appropriate service access, not the 'labelling' of young people with disorders:
Discussion should continue to clarify and share definitions of
terms like mental health, mental illness, mental disorder and mental health
problem. While it is important that agencies are clear about their
responsibilities within the service system, we need also to avoid excluding
people with manifest problems in behaviour, conduct or mental health from
service provision because no agency role statement includes their particular
problem.[1736]
15.18
The Commission
considered that to achieve 'universal non-stigmatising service delivery'
for children and families, general health services need to have, or have access
to, mental health expertise.[1737] However,
Professor Prior advised that because of the generic service model currently
imposed on service providers, diagnosis and treatment methodologies for child
and youth mental health disorders are poorly developed, even among mainstream
health specialists:
Many clinicians working in this field are significantly under
trained for the work that is required, lacking specialist graduate
qualifications in child and adolescent mental health. The wholesale adoption of
the generic model in these services means that treatment is not matched with
assessed needs of the client, and when referral is taken
up it is likely to be potluck what kind of professional (eg nurse, occupational
therapist, psychologist etc ) is allotted to the case. Further those
professionals who are well trained in the field often do not have adequate
opportunity to practise the assessment and therapy skills in which they have
been trained and which are needed because of pressures for 'case management'.[1738]
15.19
The
very serious consequence of this is that evidence-based treatments, even where
known, are not often applied:
Much of the treatment provided in current Child and Adolescent
mental health Services is not evidence based. Two salient examples illustrate
this point. Numbers of children with anti-social or conduct disorders are seen
in psychotherapy over long periods of time. Not only is this absorbing scarce
funds but it is known that this mode of treatment is ineffective for children
with such difficulties. Children with anxiety disorders often do not receive
the treatment for which evidence is strong, ie. Cognitive Behavioural Therapy.[1739]
15.20
Screening tools are important for early recognition of
the different childhood mental health problems. While sensitivities exist about
early screening of children for mental health problems, the case for
introducing screening to assist early identification for high risk groups is
strong. One such group would be children entering out of home care:
Young people entering care for the first time usually do not
have comprehensive psychiatric or medical assessments despite the fact that
this group are a high risk group for both physical and mental disorders. We
undertook a pilot project (Stargate Project) providing such assessments for all
children entering care over a twelve month period, combined with parent and
carer interventions. We reasoned that early intervention might reduce the
difficulties and produce better outcome for a highly vulnerable group,
preventing further potential trauma from being in care. We found that there was
indeed a high prevalence of psychiatric disorder, learning difficulties, and
physical and dental problems in this group. Prompt intervention and assessment
enabled better planning for the young people and resulted in a more rapid
reunification where this was possible but also enabled carers to manage the
young people and their problems more effectively, providing support for foster
carers, who are unsung heroes looking after some of the most difficult
children. Unfortunately the funding for this pilot project was not recurrent.[1740]
15.21
Beyondblue argued that screening mechanisms should be
more broadly applied by mainstream health services for early identification of
emerging disorders in children, and to address the growing incidence of
co-morbidity among the young:
Areas recommended as most likely to produce best outcomes
include community screening and treatment for disorders in childhood and
well-trained service providers who are adequately versed in the detection,
management and referral of people with co-morbid problems. Particular focus is
being placed on primary care as a key setting for the identification and treatment
of co-morbid alcohol misuse and mental health problems and, while a number of small
projects underway are investigating potential models for co-morbid clients,
there is little focus on co-morbidity with high prevalence disorders. More
focus and investment in this area is required.[1741]
15.22
Mainstream and recurrent funding under the national
health budget could be an incentive to the states to develop routine health
screening mechanisms of identified high risk groups for nascent mental health
problems. The Central Australian Aboriginal Congress reported the success, for
example, of the new 710 Aboriginal Adult Health Check, which it uses to assess
emotional and social disorders in Indigenous people aged 15 to 55. This
project, however, is not funded as part of mainstream health services.[1742]
15.23
Given the lack of agreed methodologies on early
intervention and prevention across the spectrum of child and youth mental
health disorders, funding for research and developmental consultation mechanisms
seems essential. As a case in point, the risks of pharmacological treatment of
children and youth with depression and anxiety are not established nor well
understood by practitioners, indicating that definitive action must be taken
to identify and promulgate key findings on the subject:
There are some specific issues in regard to the prescribing of
antidepressants in regard to young people and children, with little being known
about the optimal duration of treatment and the effectiveness of pharmacotherapy
in this group. There have been calls for the withdrawal of SSRIs for young
children and protocols regarding labelling to highlight potential side effects,
including suicidal ideation and attempts. beyondblue has facilitated a national
focus group including The Australian Medical Association, The Mental
Health Council of Australia, The Royal Australian College of
General Practitioners and The Royal Australian and New Zealand College of
Psychiatrists and the group are developing a joint statement and highlighting
the research in regard to the use of anti-depressant medication in the
treatment of depression in children and young people, with a view to ongoing
review of this issue.[1743]
15.24
The difficulties of achieving appropriate diagnosis for
children can place extreme emotional
and other demands on their families; then comes the challenge of accessing
appropriate services. When the child's disorder involves high support needs,
the consequences of not providing early and adequate assistance can be very grave
for all concerned. A4 Autism Aspersers Advocacy Australia cited the case of Jason
Dawes and his family, heard at Parramatta,
on 2 June 2004:
Jason Dawes was born on 2
Sept 1992. His autism was diagnosed in March 1994 when he was
eighteen months old. His parents were advised that Jason was in need of early
intervention, but [the local service] advised that they did not have a place
for him. He went for years without intervention.
Jason’s mother was required to educate, feed, toilet, bathe,
entertain and love Jason...She constantly lived with the fact that her son had
lost his best chance of acquiring later life skills because of the failure of
authorities to provide appropriate intervention during his early formative
years.
Jason’s father said autism caused constant stress in the family
and pervaded all their relationships, “[His mother] had to fight so hard for
help for Jason – early on I couldn’t cope at all".
Judge Ellis said...it is clear that the present system within New
South Wales leaves a lot to be desired and was a
significant stressor for Jason’s mother over an extended period of time.
On 24 August 2003...Jason’s
mother held his hand, placed her hand over his mouth and nose and held him
until he ceased struggling. In so doing she took her son’s life... [Jason’s
mother] then went into the bathroom, took a razor and severely lacerated her
wrists.[1744]
15.25
The submission concluded: 'Jason Dawes had autism, a
mental disorder that required treatment that the state did not provide and that
he did not get. The fact that authorities failed to provide appropriate
intervention for his autism contributed to his parents’ mental illnesses and to
his death'.[1745]
15.26
To address the urgent and diverse unmet needs of
children and adolescents with mental health problems, submissions requested
comprehensive review of 'service silos' which prevent the development of
expertise, and the marshalling of scarce resources to treat the range of
disorders across the age spectrum. Beyondblue recommended that a research project
of national significance is required to develop best practice approaches for wholesale
youth mental health service reform, and research be undertaken
to establish and promote:
-
an expanded developmental phase to encompass a
youth population;
-
the epidemiology of mental disorders in young
people; and
-
young people’s access to standard health care
systems.[1746]
Youth transition—specialised
services
15.27
A significant body of evidence to this inquiry
concentrated on the particular obstacles to service access for the young people
with mental illness, early teen through to age 24 years. This group, as
acknowledged by government, has the highest incidence of mental illness of all
age cohorts, and the lowest access rate of services:
-
mental disorders are most prevalent during
adolescence and young adulthood, and account for 55 per cent of the disease
burden of those aged 15 to 24 years.
-
only 25 per cent of young people aged 13 to 17
with mental health problems used one or more services.[1747]
15.28
The 1997 ABS National Survey of Mental
Health and Wellbeing found that rates of mental disorder peak
at age 18 to 24 years, with more than one in every four young adults having one
or more mental disorders. The prevalence rate of anxiety disorders for young people
aged 18 to 24 was 11 per cent, 7 per cent for affective disorders, such as
depression, and 16 per cent for substance use disorders. Substance use
disorders were most common in young males and depressive disorders were most
common in young females.[1748]
15.29
Happily, the suicide rate for young people continues to
decline,[1749] although levels among
young males, particularly regional or rural males, remain high.[1750] Young people overall continue to
record substantially higher rates of self harm than those of older adults:
-
suicide accounted for 22.5 per cent of all
deaths for young people, second only to motor vehicle accidents; and
-
42 per cent of adolescents experiencing very
high levels of mental health problems had seriously considered suicide and one
in four had made a serious attempt in the last 12 months.[1751]
15.30
Reflecting
this data, young people’s hospitalisation rates for mental disorders have also
risen over recent years with about 43 000
hospitalisations for mental health and behavioural disorders recorded between
2000 and 2001 alone. The most common causes for these hospitalisations are
depression, schizophrenia, severe stress and eating disorders.[1752]
15.31
As widely discussed in
this report, the acute care focus of mental health services yields
contradictory and very negative service consequences for people with mental
illness. On one hand, under deinstitutionalisation, acute care services have
been wound back creating a shortage of available beds. On the other,
underdevelopment of the necessary community based and crisis management
services ensures people with mental illness in desperate situations have no
recourse but to go to hospital emergency departments, which are not adequately
equipped to deal with them:
In particular, young people between the ages of 16 years and 18
years have no dedicated emergency response for acute mental disorders and
frequently are hospitalised in adult facilities which are not adequately
resourced, staffed and structured to meet the needs of this population.[1753]
15.32
Submitters
maintained that emergency departments are the worst place for young people in
acute states of need. The committee received numerous reports from young
consumers lamenting their treatment in hospitals, such as shackling and forced
injection, sometimes simply because the consumer expressed frustration at being
left in the waiting area, or mentioned suicide ideation.[1754] Insane australia reported:
If you talk about suicidal feelings, it is quite likely that you
are going to be locked up and then you will have quite invasive treatments
imposed on you against your wishes. We find that people are absconding from our
mental health services, whether they be voluntary or involuntary, specifically
to go and kill themselves. There is quite clear data about that but no-one is
asking the question: what is happening in these services that people are
escaping to go and kill themselves? To me it is very understandable: if you
present to someone seeking help—perhaps your last grasp at staying alive—and
you find yourself being assaulted, it is to be expected that you will flee that
situation.[1755]
15.33
As serious as
this is, the main systemic obstacle to better youth service access is the
age-based clinical distinctions establishing child and adolescent services, as
against adult services, from years 16 to 18.[1756] Mr Jurgen Hemmerling, a youth worker
from the Albury Wodonga, reports that this unhelpful division militates against
children and younger teens accessing out-of-hours emergency care in his region:
Working in the youth sector has highlighted some serious short
comings in the child and adolescent mental health fields. In Victoria, child
and adolescent mental health services do not operate an after hours service, so
only persons aged 16yrs and above are eligible for the adult mental health
system after hours intervention, young people are required to wait til 9am-5pm
service delivery. Currently the wait list for service in this region is at
least six weeks, hardly satisfactory.[1757]
15.34
At the
other end of the spectrum, turning 18 can mean losing access to whatever
specialised services are available:
To date the service structure is such that upon turning 18 a
young person must utilize the services of an adult service only if they have a
defined ‘serious mental illness’ (meaning in most cases psychosis, especially
schizophrenia). Therefore the mental health problems of most young people in
the 18-25 age group largely go either undetected or receive no intervention
whatsoever.[1758]
15.35
In addition, youth with complex disorders must
negotiate the gaps between other service 'silos'. As discussed in Chapter 14,
dual diagnosis youth for example may 'slip through the cracks'[1759]between mental health and alcohol
and drugs services:
Up to 50 per cent of our current client
group, who are aged 12-21yrs with serious alcohol and other drug issues, have
significant psychiatric pathology, ranging from self harm to depression,
anxiety and psychosis. These young people...are poorly serviced by the current
mental health system. It is well known, that young people are one of the most
difficult of client groups to engage in service delivery, long wait lists, lack
of after hours services and the stigma often attached to mental health services
are a constant barrier to service access for these young people.[1760]
15.36
In addition to
the development of transition frameworks and restructuring services to
comprehensively address the needs of the young teen to 24 age group, submitters
asked for a more holistic approach to support youth mental health needs:
Basically it is only hard-core psychotic illness that can be
looked after in the public system, with access to adjuvant supports such as
case managers, linkage to employment and rehabilitation services etc. Yet there
are a huge number of needy, but not wealthy people who simply cannot access the
services that would help them. A large number of these have mood or personality
disorders, and many of them are young. There are significant financial barriers
to accessing medical models of mental health care with declining rates of
bulk-billing and the rise of a “user-pays” system, and even greater barriers to
accessing non-medical models of care which are known to have lasting
therapeutic value. General Practitioners (GPs) cannot offer all that is required.
Community mental health services are overwhelmed with mostly young people
referred for assessment by GPs, who need longer-term talking or behavioural therapies,
yet no affordable and available services can be found.[1761]
15.37
The
focus on symptomatic assessment does not provide young consumers with the
emotional or practical support needs to
negotiate life with a mental illness:
When children and young people do present to services, it is
often for other matters, such as homelessness or family problems, and the
mental health issue may not be immediately apparent. Agencies need to work
collaboratively, focus on building trusting and lasting relationships with
children and young people and be linked to specialist mental health services.
The existing mental health service system is complicated and
frequently compartmentalised to focus on single issues or acute problems. As a
result, responses to vulnerable children and young people are sometimes limited
to the treatment of a mental illness, rather than recognising and addressing
the full range of problems which the child or young person may face.[1762]
15.38
To
overcome the stigma and other difficulties faced by young consumers, targeted
youth friendly services were suggested. The Youth Mental Health Coalition advised:
Young people are often
reluctant to seek help and are very discerning about when, where and from whom
they seek assistance. There is a critical need for youth oriented services.
Young people who don’t necessarily have a ‘serious mental illness’, and even
those who do, must also deal with the stigma associated with attending a mental
health clinic.[1763]
15.39
ORYGEN Research Centre advocated the national implementation of a model which combines
the best of clinical and life skills assistance:
Young people with emerging severe mental illnesses should have
access to specialist youth mental health services. Young people aged 12-25
should be treated in publicly funded youth mental health services alongside
their peers where the therapies, physical environments, group activities,
vocational support, staff and work-practices are appropriate to the needs of
young people. Access to such specialist youth mental health services should not
be a quirk of geographic location—currently access to the only such publicly
funded service in Australia
is confined to residents of the Western and North Western regions of Melbourne.[1764]
15.40
Essential to
the model is consumer participation. AICAFMHA recommended that the 'voice of
children and young people' be heard in the development of mental health policy,
services, interventions and programs which affect them.[1765] The report of a young ORYGEN
client, cited by the Youth Mental Health
Coalition, exemplifies the note of
hope that recovery based services of this type can achieve:
I like to think of myself as an ORYGEN graduate, not a mental
health patient, yes I am one of those crazed and deranged people that society
is so cautious about. It's funny that, because when I look at what’s happening
in society today it seems to be on the brink of madness, materialism,
consumerism, terrorism, genetics and morals.
You must have viewed or at least heard of the saying "the worlds
gone mad". Maybe a bunch of people like me in society should get together
sometime, us crazy people know our stuff, we could help out.[1766]
Funding child and youth services
adequately
15.41
Many service providers reported the alarming extent of
unmet need in their practices. Professor Peter Birleson, Director, Eastern
Health CAMHS, Adjunct Professor in Psychology, Deakin
University, felt the urgency of the
situation personally:
As I see more children being turned away from my service, and
see my staff becoming more stressed trying to meet impossible demands, I am
more convinced that we cannot give up. We must communicate about the personal
and financial costs of not having enough services, must ally with consumers to
make more noise about this problem, and must show we deploy our resources as
efficiently and effectively as we can. We can all do this locally, but the
College can help us by strengthening its policies, building political
partnerships with consumer organizations, actively including the Child Faculty
and providing information.[1767]
15.42
Professor Birleson considered a reasonable a response
by government would be to double the funding allocated to specialist CAMHS from
7.5 per cent to 15 per cent of the specialist mental health budget.[1768]
15.43
In similar vein, the AICAFMHA calls on government to 'undertake
specific child and adolescent national mental health policy and planning
development with defined accountabilities'. It suggested an increase of 15 per
cent of mental health funding by 2010 for infant, child and adolescent mental
health care, with a further target of 20 per cent of mental health funding by
2015 to facilitate servicing the 30per cent of the population who are in this
target age range.[1769]
15.44
The announcement
of the successful tender of ORYGEN Research Centre, with the Sydney-based Mind
and Brain Institute, to run a National Youth Mental Health
Foundation is promising for youth mental health reform. The $54 million funding
for national service provision will be a good start,[1770] but the Government should consider
its commitment as a long term one, and act promptly to implement
recommendations.
Older people with mental illness
15.45
Australia
has an ageing population but the provision of mental health services to the
aged is underdeveloped compared with other groups in the community.[1771] The ratio of mental illness among
the aged is lower than in the general population, at around 6 per cent for
those aged 65 and over, compared with 18 per cent for general population.[1772] Studies
have suggested that getting older might reduce anxiety and depression,[1773] implying
perhaps that there is less unmet need among the elderly. Other factors suggest that
older people with mental illness are another particularly vulnerable group
neglected by current mental health services frameworks.
15.46
The concurrence of dementia with other mental
illness presents special challenges. As the population ages, dementia is
increasingly common. As the number of people in dementia rises, so too does the
number of those with another mental illness, such as anxiety, depression, or
personality disorder. These consumers, particularly the last group, can not be
readily managed in mainstream aged care facilities, which lack services to
assist them. At the same time specialised community based or acute services
remain underdeveloped for this cohort.
15.47
One indicator of this is the very high suicide
rate for males over 65: 29 suicides per 100 000. The risk factors for
depression and suicide for this age group are influential: death of a spouse,
loss of independence, income and status through retirement, increased social
isolation and loneliness, reduced capacity or inability to participate in
favourite leisure activities and pastimes concomitant to physical illness, and
chronic pain associated with injury or disease.[1774]
Limited progress under the National Mental Health
Strategy
15.48
The National Mental Health
Strategy has had limited effect in improving mental health services to older
people with mental illness. Dr Roderick McKay of the Royal Australian and New Zealand College of
Psychiatrists reported findings that suggest medical service access for those
over 64 years is actually in decline:
The National Mental Health
Strategy has had limited effect in improving the mental health care of older
Australians in NSW. Although there has been a reduction in patients managed in
long term mental health beds there has been no co-ordinated system developed
across the State to optimally manage older people with mental health disorders
in the community. There is a marked shortage of inpatient resources of all
types. There is an even greater, severe, shortage of resources to manage older
people with mental illness in the community in all areas of NSW. Some areas
have no access to specialist mental health services for older people. As a
consequence of this older people with mental illness do not have access to a
comprehensive range of mental health interventions. Furthermore older people
have less access to private psychiatric services in Australia.
An analysis of 1998 Medicare data revealed that per capita the proportion of Medicare
expenditure allocated to adults aged less than 65 years was 4.1 times that for
adults over 64 years. This was a decline since 1985–1986.[1775]
15.49
The main objective articulated in the 2003 Public
Health Action Plan for an Ageing Australia is to reduce the future incidence of
aged debility, rather than addressing current unmet need of older consumers.[1776] The
Federal government has funded the ANU's Centre for Mental
Health Research to conduct research for this purpose. The
Beyond Ageing Project focuses on prevention of depression or cognitive
impairment, and improvement of mental health literacy for this cohort. The
project will report late in 2006.[1777]
The Federal Government otherwise reports only one targeted seniors initiative,
the Seniors Portal, an internet site providing information about service
access. It noes that other broader
'whole of community' 'may address some risk factors'.
15.50
Lack of clarity regarding responsibility for funding
between different levels of government, and within each level, is a significant
ongoing barrier to improvements in mental health care for older Australians. Similarly, state
governments do not appear to be moving at any pace on unmet need for the
elderly. The NSW Government’s Plan for Mental Health
Services released in March 2005 proposes the development of only one aged care mental
health unit in the state, in the Illawarra.[1778]
Dr McKay
concluded 'there is a pressing need for clear policy responsibility at a
national level for older persons with mental illness'.[1779]
Service comparison with other groups
15.51
Submissions remarked that specialist services for older
people in all settings are markedly under-resourced, and are significantly less
developed than mental health services for the remainder of the population. The
lack of research and well trained staff were listed as major obstacles to
adequate care for the elderly.[1780]
15.52
While some evidence based models for elderly care have
been developed, service systems are not well defined to address the coexistence
of dementia and mental illness in the elderly. The Australian Government
submission advised:
While dementia is included in the definition of a mental health
problem, it is not considered to be a mental illness. The overlap between
dementia and mental health remains problematic, with the impact felt most
acutely when the person affected, or their carer, needs to interact with the
mental health and aged care sectors.[1781]
15.53
At hearings, Professor
Henry Brodaty,
appearing with Dr Roderick
McKay of the Royal Australian and New Zealand College of
Psychiatrists, explained the stark implications of this:
We know that dementia is largely looked after by Commonwealth
policies and services and mental health problems are looked after by states. If
you have both, often you are not looked after by either. We know that rates of mental
health problems in people with dementia are huge. Ninety per cent will have
some behavioural or psychological symptom at some time during their dementia.
Having aggression, depression, delusions or hallucinations is a big risk factor
for institutionalisation. We currently spend about $3 billion a year on nursing
home costs, and direct costs for dementia are set to rise to $6 billion by
about 2011. A large part of that is accounted for by the mental health problems
associated with dementia.[1782]
15.54
The South Australian Division of General Practice
reported the care response in that state:
Dementia, depression and confusion can be seen by families,
carers and the health care system as part of ageing, which leads to acceptance
of these problems and not enough attention paid to potential solutions...The Home
and Community Care (HACC) system has had difficulty accepting mental health as
a source of disability despite figures demonstrating mental health as the
largest cause of non-fatal burden of disease. As with all areas, comorbidities
with physical illnesses and disabilities impose additional strain on consumers
and carers but are not well managed or treated.[1783]
15.55
Elderly people with coexisting mental health disorders
and substance abuse problems are reported to have extremely poor access to drug
and alcohol services. Dr McKay noted
that the national drug and alcohol plan has no policy initiatives with regards
to the elderly, and that a focus on youth co-occurring disorders disregards
incidence of dual diagnosis with dementia.[1784]
The Department of Veteran Affairs has targeted the needs of veterans generally
in this area, particularly for alcohol based co morbid conditions, and has
increased its focus on aged mental health.[1785]
Depression in aged care facilities
15.56
Older Australians in residential aged care facilities
are at particular risk of depression, but have poor access to services. In
2004, the Department of Health's Challenge Depression Project reported the
results of its national survey of 1758 residents in 168 aged care homes. The
project found that 51 per cent of high care and 30 per cent of low care
residents are depressed. Assessments of those with severe cognitive impairment
able to participate indicated that 38 per cent of high care and 26 per cent of
low care residents are depressed. The report concluded that, under normal
circumstances, a significant proportion of depressed residents go unnoticed, as
staff are poorly informed about and have no framework for systematic assessment
of depression in their patients.[1786]
15.57
Improved training for nursing home staff is clearly
required, as the depression carer support organisation blueVoices observed:
In reviewing education around the country, we would recommend
that a program is funded which offers appropriate education and input into
depression and anxiety disorders in older Australians for the many staff who
work in these types of facilities. The majority of direct client care in
Residential Aged Care is carried out by Grade III Certified Nursing Staff
(Assistants in Nursing). These staff often have minimal educational
qualifications, and therefore do not have very high levels of knowledge around
the areas of depression and anxiety and other mental disorders. This in turn
can quite unwittingly contribute to the further deterioration of their clients,
instead of assisting older Australians to optimise their level of
functionality.[1787]
15.58
The New South Wales Branch of the Faculty of Psychiatry
of Old Age, Royal Australian and New Zealand College of Psychiatrists, observed
that the lack of long term acute inpatient care and community care options for
people with low prevalence disorders such as bipolar disorder has potential to
increase the likelihood that residential aged care facilities will have to
accommodate more older people with these disorders, to the disadvantage of all
concerned.[1788]
15.59
Dr Georgina Phillips advised that the current situation
for these patients is untenable, as many have no where to go but to hospital
emergency departments:
There is a growing trend for EDs to be used as a form of crisis
containment for the mentally unwell aged (psychogeriatric) person. By the time
these people end up in an ED, their degree of
mental and behavioural disturbance is severe, and chemical and/or physical
restraint is necessitated. It is a particularly frustrating phenomenon as often
the mental and behavioural issue is not new, but because of inadequate
community assessment, management and support, the nursing
home/hostel/families/neighbours end up in a crisis situation. The aged are
particularly vulnerable to the stresses of ED care and can suffer exacerbations
of their mental illness, dementia or delirium simply from prolonged time in
such a non-therapeutic environment, as well as a higher risk of physical injury
from falls, physical restraints etc.[1789]
15.60
To address pressures on care systems and to reduce the
level of depression and other mental illness among older people, the NSW
Department of Health recommended that more supported accommodation should be
made available in the community.[1790]
Positive results could be also achieved by implementing a national network of
suicide prevention workers.[1791]
The case for more specialised
services
15.61
The capacity building of community support
services for older people with mental illness is clearly essential. Support
packages such as those developed in Tasmania
for assisting people with mental illness in the community, for example, could
be extended to offer specialised support to aged consumers and their carers.[1792]
15.62
However, experts in the field of geriatric psychiatry
also argued that the distinct needs of the aged with mental disorders needs better
systemic recognition:
Mental health problems
in old age are different. It is not that older people are just adults grown
older. In the same way that child and adolescent psychiatry is qualitatively
different from adult mental health, in old age mental health there are
qualitatively different conditions, different reactions to medication and
different treatment strategies. Old people do not do well in mainstream
psychiatric services. The clinicians are not particularly interested in older
people. In psychiatric wards they often get knocked around by younger, violent
psychotic patients. There are strong arguments for having dedicated, discrete
services for older people, as we do for children and adolescents.[1793]
15.63
The development of discrete targeted services of the
aged seems inevitable given the very real limitations of the present
arrangements to provide both timely and continuous care, particularly for the
acute patient:
Problems arising from lack of expert assessment and definitive care [are] particularly delayed in the
aged population, as CAT teams, psychiatric triage and community mental health
services limit themselves according to patient age (usually < 60yrs).
Psychogeriatric services are ess experienced in acute care and crisis
management, and often do not have resources to provide immediate or even
‘same-day’ assessment. Similarly, psychogeriatric inpatient beds do not have a
high patient turnover, and the delay to accessing these in an acute situation
often stretches to days.[1794]
15.64
The demands that aged people with these disorders put
on their carers, often elderly also, needs an urgent and sympathetic service
response. At present, older people with mental illness and their carers have
little input in the increasingly important consumer and carer movements within mental
health, which may explain their relative neglect. Factors such as stigma, very
prevalent in rural areas,[1795] as
well as cognitive impartment, and lack of respite care may reduce the capacity of
this cohort for lobbying and involvement and service planning—and all are indicators
of their relative powerlessness to change their circumstances.[1796] Dr
Roderick McKay concluded:
In summary, despite the
increasing concern in the broader community regarding the impact of an ageing
population upon our health system, the delivery of services to improve the
mental health of older Australians has received very limited resources, and
development is hindered by lack of clear responsibility for planning or funding
of services. This situation is exacerbated by the reality that older
Australians with mental illness and their carers are not as vocal, nor as
likely to be in the media, as their younger counterparts. There are known
effective systems for improving the mental health of older people, but they
require adequate resourcing. We believe that nation has a responsibility to
offer equivalent access to mental health care to older Australians as it does
to younger Australians. We do not believe this is currently the situation.[1797]
15.65
Statistical projections suggest that the need for
improved services for older Australians with mental illness and their carers
will soon become more urgent. With the number of baby boomers in their eighties
likely to quadruple in the next 40 to 50 years, the case for expanded services
must inevitably be put on the agenda.[1798]
CALD communities and refugees
15.66
Australian society is culturally and linguistically
diverse. One in three identify as having a culturally and linguistically
diverse background; two and a half million were born in countries where English
is not the primary language, and 15 per cent of the population speak a language
other than English at home.[1799]
15.67
During 2003-04 the Australian Government commenced
consultation with multicultural organisations to produce the Framework for
Implementation of the National Mental Health
Plan 2003-08, which identifies priorities for action on multicultural mental
health services. Multicultural Mental Health Australia
took part in the process and expressed support for the plan but cautioned that
the Framework must be progressed with commitment by the Federal Government
according to a comprehensive implementation plan, with agreement by all
governments, and must be supported by adequate resources and infrastructure in
all jurisdictions.[1800]
15.68
Submitters questioned whether this commitment would be
forthcoming, given that the pressures on mainstream mental health services
around the country are so great. The Forum of Australian Services for Survivors
of Torture and Trauma (FASST) noted: 'In most states and territories mental
health services are not appropriately resourced to provide continuity of care
and culturally sensitive assessment interviews'.[1801]
15.69
This section will assess the capacity of and identify
the challenges to service providers to people with mental health problems from
CALD backgrounds, including that subset of the most vulnerable: refugees and
other humanitarian entrants.
CALD established communities
15.70
Information on the level of mental illness and service
access in CALD communities is not freely available. This is partly because of
underdevelopment of mechanisms of collect and collate information, and partly
because available data is not published.[1802] The Victorian Transcultural Psychiatry Unit
provides advice from known studies in a comprehensive coverage of significant
CALD service issues, some of which are:
-
there is great variation in prevalence of mental
disorders across CALD communities, and higher rates of mental disorder in some,
including several of the more established resident communities;
-
CALD communities have greater difficulties in
gaining access to specialist mental health services (both inpatient and
community services) compared with the Australian-born;
-
they have higher rates of involuntary admissions
to inpatient facilities and evidence suggests that they may access services at
a late stage when the clinical state is more severe;
-
representation in community mental health
services is lower than in inpatient facilities and representation in any form
of mental health services is particularly low for those with lower English
language facility;
-
stigma associated with mental illness— both
among CALD communities (consumers, carers and families) and health
professionals— remains a major problem;
-
competence in conducting clinical work across
language and cultural barriers remains low among many mental health clinicians
and workforce turnover;
-
community development and partnerships
strategies have been difficult to establish given the structure and funding
priorities of mental health services; and
-
consumer and carer participation in the
development and delivery of mental health programmes continues to lag behind
for CALD communities relative to the mainstream.[1803]
15.71
These issues are discussed in relation to stigma and
access to information, and provision of culturally appropriate services.
Stigma and access to information
15.72
For many non-English speaking communities, mental
illness is a taboo subject.[1804] Submissions
reported that traditional prejudices and fears about mental illness endure
among many Australian CALD communities, acting as a powerful disincentive to
self referral.[1805] This is despite
the significant psychological stresses experienced in those communities, which
can be transgenerational.[1806]
15.73
Jesuit Social Services, which runs the Vietnamese
Welfare Resource Centre in Melbourne,
for example, reported a high prevalence of significant anxiety and depression
among people presenting for housing and other assistance.[1807] Despite the level of need, program
participants generally deny the existence of mental health problems. They may
seek advice from family or GPs, but avoid professional help until the need
becomes acute:
...the stigma attached to mental illness within the Vietnamese
community is so profound that the mere association with a mental health
professional is believed to bring shame and disgrace on the self and the
family—for example at one of the information sessions, the mental health worker
asked to be introduced as a general health worker for fear being rejected by
the group.[1808]
15.74
A lack of knowledge about mental illnesses and about
the potential to recover or manage disorders through early invention and other
services supports the stigma associated with mental illness and supports the reluctance
to access care:
In many CALD communities the concept of recovery is rare or
unknown. Mental illness is seen as a lifetime disease from which consumers do
not recover. Their families and carers are also permanently affected by the
stigma associated with mental illness. These community perceptions, beliefs and
judgments about mental illness, based often on lack of information on mental
health and wellbeing and the absence of effective promotion can reinforce
social isolation and potentially override an individual’s positive outlook
about their recovery.[1809]
15.75
An assessment of Victoria's
CALD communities indicated that Hong Kong and Malaysian
communities access mental health care at less than one quarter the rate than
the Australian born.[1810] One
submission reported that that residents from the People's Republic of China
access mental health services 75 per cent less than do the general population:
They don’t have basic knowledge of mental
disorders and are not aware of existing mainstream mental health service and
approaches (such as counselling and psychotherapy) to be able to combat with
mental health problems. In P. R China, such services and related ideas on
mental health do not exist. Thus, without well-planned and long term mental
health awareness promotion, they will not use the services and they will
continue suffering silently.[1811]
15.76
Submitters urged the need for appropriate culturally
based information campaigns to address this problem:
Whilst there may be some similar attitudes towards mental
illness that cross cultural and linguistic groups, education programs are not
effective unless there is an understanding of the attitudes and experiences of
each community towards mental illness, the availability of treatments and services
in other countries that may influence how a particular community views the
issues. Education to de-stigmatise mental illness can only be effective when it
is developed in collaboration with the community, the “correct” language is
used to reach each community and genuine attempts are made to provide
culturally and linguistically relevant information and support.[1812]
15.77
The
Victorian Transcultural Mental Health Centre model was criticised for inefficiencies in this respect:
Developing one single
standardised model or promotion material and then translating them into
different languages in a hope of one-meeting-all often miss out the crucial
characteristics of the specific community. If considering there are many such
mini projects going on at the same time and sum of money being spent, it is
even no more cost-effective than a single, holistic, systematic and long term
project rooted deeply in the specific culture community.[1813]
15.78
Multicultural Mental Health
Australia also
urged support for CALD carers, who need training to better understand their
role. An important aspect of this is the provision of accurately translated
information on the rights and responsibilities of mental health consumers and
carers. This and other information should be circulated to community leaders
and through the ethnic media.[1814]
15.79
There has been some recognition of the needs of carers
in the area of mental health first aid course development. Professor Anthony
Jorm and Ms Betty Kitchener, forerunners in course development advised:
The Mental Health First Aid
program has core elements that translate across various cultural groups.
However, there is always a need for some cultural modification. In Australia,
we have developed the course to suit the mainstream of society, but we recognise
this is not suitable for cultural minority groups. Versions of the course are currently
being developed for Aboriginal Australians and have recently been developed for
a number of groups with non-English speaking backgrounds, including Vietnamese,
Croatian and Italian. Instructors have been trained from each of these
communities.[1815]
Provision of culturally appropriate
services
15.80
To overcome the significant cultural resistance to
admission of mental health problems by CALD consumers and they families,
services to CALD groups must be culturally and linguistically accessible.
Overall, mental health service provision to CALD communities was considered to
be patchy at best. Multicultural Mental Health
Australia
contended that, nationwide:
-
service availability 'lacks consistency in both
range and quality';
-
project based funding is undermining development
of sustainable programs which can build partnerships with mainstream services,
and
-
the lack of adequate data collection on the
quality of services prevents establishment of performance and accountability
benchmarks.[1816]
15.81
Short-term project grants to both government and
non-government organisations are a much criticised feature of the mental health
funding model. CALD support groups maintained that mainstream services, even when
funded to progress nationally identified mental health programs, can try to
offload their responsibilities onto resource poor CALD communities.[1817] The experiences of the Australian
Polish Community Services tend to support this view:
When we approached one agency specifically funded to respond to
depression in the community, particularly prevention and early intervention, to
determine the availability of information in community languages, we were
informed that they don’t provide materials in community languages but if we
wanted to translate it for them, that’s okay. Unfortunately, that’s not okay.
As an agency we are not funded to undertake translations for other services and
agencies, and more importantly, our staff are not accredited translators. The implications
of taking this approach displays a lack of professionalism on the part of the
other agencies and a lack of understanding about the importance of accurately
and appropriately translated information to ensure the correct message is being
passed along.[1818]
15.82
Scarce funding can also be hijacked by issues with
political significance, to the detriment of real community needs. Mr David Han Yan, a case worker to the
Chinese community advised:
...sudden availability of
funding from Casino Benefit Fund in NSW has created a field of Chinese Gambling
Counselling. My
observation is that underlining the gambling problem, it is the great mental
health problems in CALD community. Immigration stress, relationship problems,
loneliness and isolation and other mental disorders all find their “legitimate”
expressive form in gambling problems. Restricted by funding requirement while I
was working in the gambling counselling field, I found difficult to go to
tackle real, deep issues.[1819]
15.83
The submission
from the Victorian Transcultural Psychiatry Unit confirmed that while
VicHealth made a large investment CALD mental health in 2001, the funding was
for 'demonstration' projects and will not be incorporated in the mental health
system.[1820] This supports the view
that funded CALD mental health projects tend to be 'innovative' and 'one off',
rather than integral steps in the capacity buildings of mainstream mental
health services to address CALD community needs.[1821]
15.84
A lack of language trained
practitioners and mental health professionals is a problem for culturally
diverse communities, and for the aged in particular. Submitters suggested
developing specific training programs
in tertiary institutions to support transcultural mental health research, and
to develop the capacity of the bilingual workforce. [1822]
Fostering the knowledge of GPs under the Better Outcomes initiative was another
important way that early identification and continuous care could be initiated
and maintained:
Primary care needs to be culturally appropriate and to provide interventions
of an enduring nature, where service providers are engaged as part of their
everyday practice in cross cultural awareness, understanding stigma and dealing
in an informed way with the needs of people from culturally and linguistically
diverse backgrounds, their families and communities. All primary health care
providers, including general practitioners need cross-cultural competency
education, to develop increased capacity in early recognition and intervention,
accurate diagnosis, referral and follow-up.[1823]
Refugees
15.85
Australia,
like many other countries, has become a recipient in recent years of refugees who
have experienced extremes of social and cultural dislocation.[1824] As a subset of the CALD community,
these 'humanitarian entrants' as termed by the Department of Immigration and Multicultural Affairs (DIMA) have
significantly more complex needs. Discussion of these groups in the evidence
included reference to 'temporary' entrants—Temporary Protection Visa Holders
and Immigration detainees.
15.86
The Report on the
Review of Settlement Services for Migrants and Humanitarian Entrants (released
in May 2003) records that between 1
July and 31 December 2002, the largest groups of entrants were from Sudan (28.5 per cent), Iraq (27.0 per cent), Afghanistan (8.7 per cent) and Ethiopia (4.8 per cent). The report advised:
Feedback from public
consultations and submissions to the review has suggested that this shift
towards Middle Eastern and Horn of Africa countries is resulting in a greater proportion
of new arrivals with high level of poverty, larger families and lower levels of
education and English proficiency. They are facing more complex barriers to
settlement.[1825]
15.87
The review reports that these people, in most cases, have
significant mental and physical health issues related directly to torture or
trauma associated with their refugee experience.[1826] Studies have found that between 39
per cent and 100 per cent of these people suffer from post traumatic stress
disorder (compared to 1 per cent of the general population) while 47 to 72 per
cent suffer from depression.[1827] FASST provides the following breakdown the
mental health effects of refugee experience:
Table 15.1 Mental health effects of the refugee experience[1828]
Mental
health effects |
Key
issues |
- depression
- anxiety
- grief
- guilt
- somatic disorders
- attachment and relationship difficulties
- a loss of a sense of hope, meaning and purpose to life
- loss of identity and a diminished sense of belonging
- internalised mistrust and post traumatic stress disorder symptoms
- cultural adjustment suspicion and intergenerational issues
|
- mental health effects associated with exposure to traumatic experiences
and other antecedents in the course of the refugee experience
- may persist long after arrival in a safe country
- can be exacerbated by stresses and lack of resources in the period of
resettlement.
|
15.88
Over the last decade Australia
has settled over 110 000 people under its Humanitarian program. The Government
has recently increased this program to 13 000 places per year.[1829] Of
these, 6 000 places are allocated to refugees (a 50 per cent increase on
previous years), and 7000 places are allocated to the Special Humanitarian
Program and onshore protection. About 75 per cent of the offshore places are
planned to come from Africa and about 20 per cent from
the Middle East and South West Asia.[1830] Yet despite the predictable and
growing need, submissions reported significant under-resourcing is preventing
development of sustainable programs to support these complex cases.
Capacity building of refugee services
15.89
Humanitarian
entrants to Australia are processed under DIMA's Integrated
Humanitarian Settlement Strategy (IHSS).
The IHSS is designed to provide intensive initial settlement support to
newly-arrived humanitarian entrants. The aim of the IHSS is to ensure that all
of these entrants have access to the information, personal tools, services and
basic material requirements they need to rebuild their lives in Australia. The
IHSS works with the Early Health Assessment and Intervention (EHAI), Community Support
for Refugees and other support services to provide this initial assistance.[1831]
Services are provided to refugees, defined as 'people who have
experienced persecution in their countries', and Temporary Protection Visa
Holders, who are entitled to limited services, including EHAI and torture and
trauma entitlements, during the life of the visa. [1832]
15.90
The Forum of Australian Services for Survivors of
Torture and Trauma (FASSTT) agencies are the principal contractors to the DIMA to provide EHAI services. These
services are in part funded through the Department of Health and Ageing’s
Program of Assistance to Survivors of Torture and Trauma (PASTT). FASSTT
reports significant pressure on services as PASST funding levels have been
frozen for ten years, with only CPI increases. This is not commensurate with
the increased level of need:[1833]
The level of funding forces FASSTT agencies into a reactive
rather than proactive position. For example, we recognise the need to develop,
in addition to conventional one-to-one interventions, a range of community
based interventions in response to the needs of certain client groups (for
example African clients). However some FASSTT agencies are struggling to
maintain existing services levels, making it difficult to work in a developmental
way. Instead, resources that ideally would be spent on training and sector development
particularly in regional and rural areas get diverted into acute response— particularly,
in some states, with respect to the needs of clients holding Temporary Protection
and Bridging visas.[1834]
15.91
Other service providers working with recent African
arrivals, the projected source of most future refugees, confirmed that the
capacity of mainstream and community mental health services to assist this high
needs group is extremely limited. Eastern and Central Africa Communities of
Victoria (EACACOV) advised:
It is our experience as African, social and community support
workers in the field that when we have clients who display psychotic disorders
symptoms/behaviour or suffering from psychological disorders; mental
disorder/illness, on a number of times we have contacted many mental health
services providers and we have found that there are no strategies for
prevention or early intervention....Mainstream service providers lack awareness
about pre and post migration experiences, such as: torture and trauma, vast
differences in cultural, religious and gender issues between countries of
origin and Australia and their impact on family relationships and mental
well-being.[1835]
15.92
FASSTT
argued that mainstream services ugently need resources to build the responsiveness necessary to treat this category
of patient, whose diagnosis is complicated by post traumatic stress disorders
and cultural and communication barriers:
In all States and
Territories there is now a significant proportion of the population who have
particular needs as a result of trauma impacts from their refugee or
refugee-like experience. All mental health service providers whether in the
acute or community sector need to be more aware of the needs of refugee survivors
of torture and trauma. For example, practices such as the use of restraints,
placing distressed individuals in isolation and forcibly administering
medication replicate torture and other experiences that have led to trauma. This
greatly increases the level of an individual’s distress and potential
retraumatisation. Working with such survivors requires specialist skills to
recognise their specific needs. Failure to recognise these needs compounds the
failures of the mainstream mental health system to deliver coordinated
continuity of care.[1836]
15.93
Particular concerns were expressed about the
lack of early prevention services to refugee children, now the largest entrant
group.[1837] FASST notes that
preventative measures have been found effective in dealing with the trauma and
dislocation experienced by these children have experienced,[1838] however the emphasis on parental
and family assistance means these measures are not systematically employed.[1839] A case study shows how, with the
service gap in place, identification of even the most plangent needs can be
serendipitous:
A teacher noticed a 15 year old girl in the classroom who was
withdrawn and had scarring on her hand which she was trying to hide. The
teacher contacted the FASSTT service in her state who arranged through the
school to seek permission to speak with her parents. Her parents had in fact
been killed and she was living with her relatives who had recently arrived. The
young girl was assessed as depressed and suffering severe post traumatic stress
disorder symptoms. She had witnessed her mother’s face blown off in a sniper
attack and suffered burn injuries. She formed a close relationship with the
Early Intervention counsellor-advocate, with whom she was able to share her grief.
He was able to find a suitable school work-experience placement for her,
something she had been dreading and he facilitated a referral to a plastic
surgeon. These interventions led to an immediate improvement in active
participation at school. Her guardians were offered support which they felt
they did not need but they supported the assistance being provided to their
niece.[1840]
15.94
Concerns
were expressed that DIMA's policy of dispersing humanitarian entrants into regional areas will make
delivery of approriate servces to children and young people more difficult to
achieve.[1841] The children of TPV
holders are at particular risk, given the limited access this group have to
health and other services and the degree of anxiety, and perception of
prejudice, they experience as a result of their temporary status.[1842] To address this, FASSTT
recommmended that the IHSS should build the capacity of the education system in regional and rural areas to
provide a supportive environment to refugee students, working closely with new
arrivals programs.[1843]
15.95
The
Department's policy of regional placement, for both humanitarian entrants and
TPV holders, is directed by client choice and access to appropriate services. Service capacity exists in number of
regional centres.[1844] However submissions warned that the present level
of need is not being met. Hume
City Council reported that a large proportion of new entrants to Hume
City require counselling and
support services, and should be receiving long-term assistance:
There is a need to develop specialist mental health services for
culturally diverse communities, and for these services to be located in
communities, such as Hume City,
where new arrivals are settled by DIMIA. The culturally specific mental health
services should be developed in partnership between all levels of government,
Migrant Resource Centres and other organisations, including the Foundation for Survivors
of Torture. Any government assistance for new arrivals to access mental health
services needs to recognise the lifetime impacts of trauma and torture, and not
be time limited to the initial period of settlement.[1845]
15.96
Like
other CALD groups, lack of knowledge and understanding about mental illness and
of available services, in combination with fear and stigma, supports the
tendency of refugees to avoid assistance until crisis point.[1846] EACACOV reported that African refugees in acute states
commonly present at emergency departments in the care of police. On release
many end up extremely disoriented, homeless, and may be taken to immigration detention centres:
In January 2005, one of our clients with a mental disorder was
locked up in Villa Wood Detention centre Sydney,
because he had no identification or travel documents with him, he had not been
taking his medication, he was confused and he had lost all his documents, plus
his mobile phone. He was released from the detention centre and admitted to
Banksia Mental Health Hospital/Psychiatrist Unit
when an inmate from Sudan
contacted EACACOV’s workers on the client’s behalf. The staff faxed a copy of
his travel document which was on his client file to the case worker/officer.[1847]
15.97
A number of proposals were made to address the threat
to CALD people with mental illness under the government’s detention policy. EACACOV
took a holistic view, stressing the importance of the capacity building of
community based services to reduce the possibility of such circumstances. These
services should provide culturally appropriate assistance and advice,
reflecting traditional customs, to address the extreme social dislocation
experienced by these people, and to reduce the incidence and severity of mental
health problems. It was also suggested that DIMA should advertise any
detainment of individuals taken from
community, and in particular, utilise the knowledge of CALD community groups
and ethno-specific organisations to identify individuals.
15.98
The Mental Health Foundation
ACT thought a nationwide missing persons
system an imperative as there are many
situation in which individuals wander from state to state and cannot be found
by loved ones and fall through the cracks in the system or end up in
inappropriate situation such as happened to Cornelia Rau.[1848]
Mental health of detainees
15.99
In the wake of the Palmer
report and the sequential revelation of harms and inefficiency in its detention
centres, a number of submissions questioned the wisdom of continuing with the
Government's detention policy. Suicide Prevention Australia (SPA) was among the
many who saw that the custodial nature of a detention centre is counterintuitive
to delivery of appropriate mental health care:
Mental illness is neglected in immigration detention for a
number of reasons. The framework for managing detainees treats them as
law-breakers whose behaviour must be deterred. Such a deterrent approach treats
suffering and psychological harm to detainees as acceptable ‘collateral
damage’. Former Minister Philip Ruddock asserted that depression among
detainees is not a mental illness, and that self-harm is manipulation (rather
than a reflection of despair). He frequently referred to asylum seeker
self-harm ‘inappropriate behaviours’ and ‘moral blackmail’, and suggested
actions such as lip-sewing stemmed from their cultures and were repugnant to
Australians. IDCs [Immigration Detention Centres] are therefore custodial and
punitive, rather than being treatment- based. They resemble prisons in that
they hold people under maximum security, use solitary confinement, employ
prison staff etc, but differ from them in that the inmates are indefinitely
detained.[1849]
15.100
Submitters called on government to recognise that the
policy of detention is conducive to mental illness, referring to conclusive
findings:
In ten asylum-seeker families held for protracted periods in a
remote IDC, all adults and children met diagnostic criteria for at least one
current psychiatric disorder with disorders identified among 14 adults, and 52
disorders among 20 children. Persistent suicidal ideation was reported by all
but one adult, and over half the children; five adults and five children had engaged
in self-harm or attempted suicide. Retrospective comparisons indicated that
adults displayed a threefold and children a tenfold increase in psychiatric
disorder subsequent to detention. Exposure to trauma within detention was
commonplace. All adults and the majority of children were regularly distressed
by sudden and upsetting memories about detention, intrusive images of events
that had occurred, and feelings of sadness and hopelessness. The majority of
parents felt they were no longer able to care for, support, or control their
children.[1850]
15.101
Various suggestions were made about how the situation
should be addressed. The Mental
Health Foundation ACT recommended the government should
‘change its 'hardline' attitude to refugees held in detention’ which it considered
informs ‘an uncaring culture' in the IDCs. It suggested that the centres should
be located in less isolated locations so that detainees can readily access
specialist services when required and that Detention centre staff be given
training or refreshment courses on duty of care.[1851]
15.102
The Victorian Transcultural Psychiatry maintained that
detainees, being at high risk of mental illness, should become an identified
group for preventative assistance under the National Mental
Health Plan. It recommended in particular that DIMA develop
an approach for treatment of detainees with dual diagnosis, and that tensions
between detention and other service providers be resolved by developing
interagency agreements.[1852] The SPA argued that a judicial inquiry into
the detention process should be held, referring to sustained international
criticism of the human rights affront
represented by the policy:
Australia remains the only industrialised country in
western civilisation that continues to routinely impose mandatory detention on
those who seek refugee protection. Those who arrive on our shores without a
valid visa, including unaccompanied children, are detained in facilities in
remote areas for several months, even years. Such practices have been condemned
by the international community as breaching human rights standards with the ill
treatment of refugees in Australia being clearly documented by the United
Nations Human Rights Commission and the Human Rights and Equal Opportunity
Commission (HREOC). Such international instruments demand that each person is
afforded the highest attainable standard of physical and mental health
available. To date, every independent inquiry into the immigration detention
centres of Australia have highlighted the poor mental health of
detainees with particular emphasis on the risks to children’s wellbeing.[1853]
15.103
The Senate Legal and Constitutional References
Committee, recently reiterated that view, concluding:
...the prolonged and indeterminate immigration detention is
inherently harmful to psychological well being and its abolition should be a
priority.[1854]
15.104 The
recent court decision awarding compensatory payment to the family of 11 year
old Iranian child Shayan Badraie sets a precedent which may prompt the
Government to further review its detention policy. During the proceedings,
former DIMA (then DIMIA) officials, reversed the official view, and acknowledged
the connection between detention and mental illness[1855] also confirming the system is not
functioning as intended.[1856]
15.105
DIMIA facilitated a visit of the Senate Select
Committee to Baxter Immigration Detention Facility on Wednesday, 28 September 2005. The Baxter
facility is in remote South Australia,
and while controlled by DIMIA it is run by a private service provider. The
facility is built to house up to 660 detainees,[1857] but at the time of the visit there
were around 125, all adults. The visit included briefings from the DIMIA
manager of the facility, and from a representative of service provider Global
Solutions Limited (GSL). The Committee toured the facility, and held a round table
discussion with some of the detainees.
15.106
In the wake of the problems revealed by the erroneous
detention of Cornelia Rau, the Federal Government began implementing changes in
immigration detention. The Committee saw some of the first changes already
underway during its visit to Baxter, such as modifications to
the living environment and the way the movement of detainees within the
facility is regulated. GSL stated that their new environmental change program
was intended to reflect a community rather than an institutional approach to
detention. Procedural changes at Baxter
since the Palmer Inquiry into the Circumstances of the Immigration Detention of
Cornelia Rau delivered its findings included:
-
a ‘revamp’ of operational procedures;
-
mental health screening;
-
changes to seclusion times;
-
a different approach to mental health services;
and
-
all GSL officers attended a one day training
course run by the mental health team within Baxter.
15.107
A discussion (facilitated by an interpreter) was held
with three immigration detainees who volunteered to talk to the committee
following a letter from DIMA. The length of stay of the three detainees varied
between 4 months and 3 years. There was a sense of isolation and depression
amongst the detainees with whom the committee met:
It is quite obvious we are like a bird in a cage. We would be
better happier outside. Of course we
would be happier waiting for a visa outside.
Here we can only see the sky and the ground - we would be free outside.
15.108
Discussions with medical staff at Baxter
indicated that there were difficulties in providing services. Baxter
was deliberately established to be remote, and that very remoteness has made it
hard to recruit health professionals, challenging to retain them, and adds to
the logistic challenges involved in securing effective treatment in cases of
serious mental illness. Despite these difficulties, medical staff did say that
they were able to communicate successfully with most detainees and overcome
barriers to building effective relationships with them.
15.109 Responding
to a contemporaneous review of its detention services, DIMA moved quickly to
implement a package of reforms. One aspect will be the national implementation
of an improved mental health care program being trialled at Baxter Detention
Centre, under the auspices of an MOU signed with the South Australian
Department of Health. DIMA will also re-tender all detention services, and will
award separate health and psychological services contracts, to be managed by
the department.[1858]
15.110 These
developments answer requests for official acknowledgment of the mental health
implications of the Government's detention policy, and show the department's
responsiveness in that direction[1859].
They do not however address the strongly expressed concerns to this inquiry
about the long-term mental health consequences of the detention process, or the
damage done to Australia's
reputation as friendly nation proud of its cultural diversity.
15.111 The
shift to community based accommodation progressed by DIMA for those with
identified special needs,[1860] and
for women and children is a positive development; the Government may wish to
review its position on detention in the interests of ensuring unauthorised
entrants with mental illness are treated 'humanly, decently and fairly', as
intended.[1861]
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