This edition combines analytical feature articles on a variety of contemporary welfare issues with short statistical snapshots following a life-course approach. It covers: Understanding welfare; Australia's welfare spending and workforce; Child wellbeing; Young people; Working age; Growing older; Diversity and disadvantage in Australia; Indicators of Australia's welfare.
The main report is accompanied by Australia's welfare 2015-in brief: a summary report presenting highlights from Australia's welfare 2015 .
In 2014, 91.7% of all registered nurses and midwives were in the nursing and midwifery workforce (323,711). Of these, 9,110 were looking for work in nursing and midwifery, up from 8,151 in 2013. In 2014 the overall supply of employed nurses and midwives was 1,134 full-time equivalents or FTEs for every 100,000 people. This compares with the figure of 1,107 FTEs per 100,000 in 2011. In 2011 and 2014, there were more employed nurses and midwives in the 50-54 year age group than any other age group. The proportion aged 50 and over grew from 38.3% to 39.4%.
The mental health of children and adolescents: report on the second Australian child and adolescent survey of mental health and wellbeing
It documents the prevalence and type of mental health problems, the impact of those problems on families and young people themselves and the role of health and education services in providing assistance. While the primary sources of information were parents and carers, the survey also engaged directly with young people 11 years and older who completed their own survey. This information provides unique insights about aspects of their emotional lives and behaviour that are generally not visible to parents and carers.
"There is abundant evidence about what works to prevent suicide, but it is often patchily implemented," Mr Feneley said. "By combining these proven strategies within an overarching systems approach, we believe we may have a chance to amplify their effect and make a dramatic difference to the number of lives lost."
Mr Feneley was commenting on the launch of the Proposed Suicide Prevention Framework for NSW, developed by the National Health and Medical Research Council's Centre of Research Excellence in Suicide Prevention with the Black Dog Institute.
The researchers, led by Professor Helen Christensen, identified 9 strategies that could be applied in parallel at a local or regional level to reduce the number of completed suicides. They are:
- Reducing access to lethal means
- Responsible reporting of suicide by the media
- Promotion of national suicide awareness programs
- School-based peer support and mental health literacy
- Gatekeeper training for those like to be in contact with high risk individuals, including teachers, clergy, and community social workers
- Regular suicide prevention training for emergency services
- Training GPs to assess risk and start conversations
- Adequate access to tailored evidence-based therapies such as cognitive behavior therapy (CBT) to high risk groups
- Targeted support for people who have made a previous attempt or are in current crisis through phone and online counselling, training for emergency department staff and out-patient support.
The Proposed Framework,responds to a key Action (3.4.2) within Living Well: A Strategic Plan for Mental Health in NSW 2014-2024, adopted as the Government's mental health reform policy in December 2014.
We have an array of prevention agencies, lifeline programs and public mantras about “being in life”. So why don’t they seem to work in rural and remote communities?The obvious – but always avoided – response is that we don’t know why people, particularly young people, take their lives.
We can’t get to the soul of the suicide. And prevention is a somewhat pretentious term: suicide isn’t measles or smallpox and there are neither overt symptoms nor vaccinations to hand.
Nearly half of all patients hospitalised after suicide attempt receive no follow-up mental health treatment, research shows
Every year, more than 60,000 Australians attempt to take their life and the majority of these people will be taken to a hospital setting.
Research by the Black Dog Institute shows, of the patients who do receive follow-up mental health care following a suicide attempt, more than half receive one 30-minute session.
Aboriginal and Torres Strait Islander people experience dementia at an earlier age then the general population and this, combined with the steadily growing number of older Aboriginal and Torres Strait Islander people, will result in the number of people effected by dementia growing significantly in the coming years.
Although higher rates of dementia have been reported in Aboriginal and Torres Strait Islander people, the disease is often overlooked by Aboriginal and Torres Strait Islander communities, health workers and service providers. Geographical constraints in the provision of services, a lack of education and awareness in communities and by health workers and the prevalence of other chronic diseases have all posed considerable barriers to the recognition of dementia as an emerging health issue.
This paper includes recommendations to ensure that Aboriginal and Torres Strait Islander people, family members and communities have access to awareness, information, and appropriate support services for people with dementia.
Workshop report : Addressing Dementia in Aboriginal and Torres Strait Islander Communities
The website includes Condition Summaries, Gene Summaries, Gene Family Summaries, Chromosome Summaries and a resources section providing links to other online resources based on users ie families, researchers or health professionals.
Genetics Home Reference also provides a free printable version of the entire Handbook, complete with illustrations. One of the latest additions to the site is Stevens-Johnson syndrome/toxic epidermal necrolysis.
Reposted from: HealthInfo Blog.
It defines cultural competency; reports on available evidence; identifies approaches and strategies that are effective in improving cultural competency among health services staff, examines the relationship between cultural competency and health outcomes, and documents an evidence-informed conceptual framework.
Better Cardiac Care measures for Aboriginal and Torres Strait Islander people: first national report 2015 (AIHW)
It shows that: the age-standardised death rate due to cardiac conditions for Indigenous people was 1.6 times that for non-Indigenous people; mortality from cardiac conditions for Indigenous Australians decreased by 41% between 1998 and 2012, while access to cardiac care has improved over time.