family and carer participation in the recovery...
TRANSCRIPT
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Family and carer participation in the recovery process
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Aim of this session
To explore the importance of family/ carers
and the role they can play in the recovery
process
To highlight the carer perspective on being
involved in the recovery process
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Session Overview
Brief historical overview of family/ carer
participation
Current situation re. participation
Reasons to involve family/ carers
Barriers to involvement
Best practice
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‘Carer’ population
One in five experience mental
health problems in their lifetime
15% adults in a caregiver role (Jane Pirkis et.al. (2009), Melbourne University)
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Who are Carers?
Someone actively caring for a person with a
mental illness
They need not be living with the person with
mental illness
May be a family member, friend or someone
who has a significant role in the person’s life
The caring role may vary over time according
to the needs of the person and the carer
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Historical Overview
Deinstitutionalisation
Western model of care
Blaming families
Issues of privacy & confidentiality
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3. Step Guide to the Law David Leggatt , lawyer
1. Respect confidential information
2. Treat the patient
3. Avoid harm
A reasoned use of information will
always be supported
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Current situation
Carers often perceived by service
providers as being of little importance
MH policy suggests collaboration with
carers
BUT … carers often receive little
education or support in their role
Vital to keep carers in the loop
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Impact of mental illness on family members
The trauma model
The caring journey – experiences & emotions
facing carers
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Impact of Excluding Carers
Reducing carer well-being
– Studies show negative impacts on carers
– Added burden for the carer
Compromising the carer-consumer
relationship
– Contributes to culture of blame between
consumer & carer
– Lack of information can lead to families potentially
hindering consumer recovery
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Challenges for families
Mental illness – difficult to process
cognitively, emotionally
Family histories, traditions, values, beliefs
influence attempts to cope and adapt
Families not helped to manage impacts of
guilt, blame, loss, grief
Families of mentally ill have own needs – but
not considered per se
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Challenges for families
Patient-centred focus by clinicians - no outcome
measures for family members
Many families unsure how to ask for help – often
ignored & feel powerless
Social stigma related mental illness – reluctant to
reveal caring status
Rural communities stigma more firmly entrenched
CALD communities stigmas of mental illness even
more deeply entrenched
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CALD Communities & Mental Illness
Consistently lower rates of access to public
community & inpatient mental health services
– e.g. Non English speaking countries – comprise
20% of Vic population, but only 13% mental
health services, 15% hospital inpatients
Represent higher proportion of involuntary
admissions
www.vtpu.org.au
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Evidence Research Base for Working With Families
Evidence from over 40 randomised
controlled trials over 30 years support
inclusion family & other carers in
treatment of mentally ill persons
– better outcomes for all
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Research evidence Benefits from family involvement
Decrease in relapse rates (up to 20%)
through early detection of symptoms and
early intervention
Decrease in hospital admissions
Better adherence to medication
Reduction in psychiatric symptoms
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Other Significant Outcomes
Improved functioning of consumer
> employment rates
> involvement in community
< burden experienced by family carers
Improved relationship between family
members
Cost effectiveness - < treatment costs,
significant savings for health system
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Barriers to Implementation
Issues of consumers not wanting to involve
family/ carers
Engagement of families can be difficult
Professionals not trained to work with
families
Services feel under pressure without adding
in involvement of families
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Barriers (cont.)
Systemic culture of excluding families
Failure to identify carers
Carer confidentiality often disregarded
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Overcoming Barriers
Promoting clinical attitudes re. value of
involving families
Prioritising resources to support involvement
of family/ carer
Identifying practical ways in which family/
carer can be involved at various points in
diagnosis, treatment and rehabilitation
Examples from co-design action plans
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Overcoming Barriers (example)
Support for carers
– Accessible information for carers
– Carer involvement in treatment and planning (eg
early contact, review points, discharge)
– Support for carers (eg peer support, access to
services)
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Dr Alex Cochrane
Film Clip
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Good information sharing outcomes
Support needs of consumers & carers often
interdependent
Carer involvement & understanding of
consumer situation assists better recovery
This also associated with greater satisfaction
for clinicians
Carers can convey important information to
clinicians
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Key Principles for working with carers/families
They must be recognised, valued &
supported in care giving role
Clearly defined roles and responsibilities for
clinicians & carers – understood by all
They should be consulted & engaged ASAP
in an episode of care
Clinicians, consumers & carers need to
communicate effectively with each other
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Key Principles for working with carers/families cont
Clinicians must have sound knowledge what
information may be given to carers under
different circumstances
Services need to ensure language & cultural
needs of family are considered
Consumer rights not to involve family to be
respected – but explore reasons.
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Benefits working with families/carers - summary
Assessment – better diagnosis
Service delivery – 2nd source of information
Treatment outcomes – better care, support
Relapse admissions – reduced
Cost effectiveness – in improving treatment
outcomes
Carer support – < adverse impacts of caring
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Reference
“Families as Partners in Mental Health Care: a Guidebook for implementing Family Work“ (2007)
by
Diane Froggatt
GrÃinne Fadden
Dale L. Johnson
Margaret Leggatt
Radha Shankar
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Vic Mental Health Carers Network
Peak body
Awareness raising
Info, education, training
Ensure fed & state govt
recognise carers
Facilitation
communication carers
& key stakeholders
Systemic advocacy for
carers
Encourage best practice
research in carer support
Support carer
involvement
Support carer
participation