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About the HSRAANZ

Founded in 2001, the Health Services Research Association of Australia & New Zealand (HSRAANZ) supports and promotes the conduct and dissemination of applied research to improve the delivery and organisation of health services in Australia and New Zealand. With a wide range of individual and corporate members from universities, research centres, government departments, independent government agencies, and consumer groups the Association bridges the gap between research and policy, as well as reflecting consumer issues. We also have two special interest groups, focussing on Emerging Researchers and Indigenous Health Services Research, both of which have a prominent role at our main conference. [read more]
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Our latest member profile is Mark F Owusu who is a researcher at the  the School of Health Sciences, University of Canterbury.  Mark's research interests are non-communicable disease management, health systems research and policy, evidence in health services research, implementation science

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    • 20 OCT 17

    International Open Access Week 2017 -23-29 October

    Next week in international open access week. This year’s theme is ‘Open in order to…’, which asks us to imagine what achievements can be reached by making research openly available. Take a look at the open access events being held around Australia and New Zealand and send us your views on what open access would mean for health services researchers.

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    • 19 OCT 17

    10th Health Services and Policy Research Conference

    Only 11 days to go! Don’t miss out! Register Now for the 10th Health Services and Policy Research Conference. The full program is now online with exciting keynote and concurrent sessions and pre-conference workshops and breakfast sessions.

    The workshops and breakfasts are open to conference delegates and non-delegates and there is something for everyone. Take a closer look.

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    • 19 OCT 17

    HSRAANZ Webinar Series – “Futile” treatment and why doctors provide it to patients at the end of life: some empirical findings – 25 October

    Don’t forget to register for our latest webinar. Drawing on the results of 96 semi-structured interviews with doctors from a range of specialties in three Queensland public tertiary hospitals Professor Lindy Wilmott and Professor Ben White will explore how doctors understand the term “futility” and use it in the clinical setting at the end of life for adult patients.

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    • 18 OCT 17

    50 years since citizenship: successes and challenges in Indigenous Health

    How far have we come in improving the health outcomes of Aboriginal and Torres Strait Islanders in the past 50 years? The latest issue of Public Health Research & Practice (PHRP) explores some of the changes that have occurred since the 1967 referendum saw Australians vote “yes” to changing the constitution and allowing the Federal Government to create laws for Indigenous people.

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    • 12 OCT 17

    NHMRC – New Grant Program Public Consultation on Peer Review

    The NHMRC is inviting submissions to its consultation paper on peer review in the new grant program. It is also inviting researchers to nominate themselves to be considered for appointment to NHMRC peer review panels that will assess applications submitted to the 2018 round of funding schemes.

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    • 25 SEP 17

    Australia’s health system is enviable, but there’s room for improvement

    In this article from the Conversation’s global series about health systems, examining different health care systems all over the world, Stephen Duckett, Grattan Institute takes a look at the Australian system. He concludes that, although Australian’s are rightly proud of their health system and value Medicare highly, this is not to say they see the health system through rose-coloured glasses. Health care regularly rates as one of the top three issues of concern to voters.

    The general directions of policy in Australia are similar to international trends – more efforts to establish better relationships between hospitals and family doctors; more emphasis on rewarding health care providers for improved outcomes; and implementing new methods to pay doctors for managing the care of people with chronic conditions.

    But core to all reform proposals in Australia is a commitment to maintain universal access and tax-based financing.

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    • 21 SEP 17

    Over 45s report positive experiences with Australia’s health care system

    The Australian Bureau of Statistics (ABS) and the Australian Institute of Health and Welfare (AIHW) jointly present information from the Survey of Health Care, Australia, 2016. This survey explored the experiences of people aged 45 years and over who had seen a GP in the previous 12 months, with a focus on coordination of health care, including information transfer between GPs, specialists and hospitals in Australia. Coordination of care is important for quality health care and has been shown to improve people’s health outcomes. It found that “Overall, the majority of people believe they are well-informed about their medical care or treatment but there are differing levels of satisfaction”.

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    • 21 SEP 17

    As Victorian MPs debate assisted dying, it is vital they examine the evidence, not just the rhetoric

    In this article from The Conversation Ben White, Queensland University of Technology; Andrew McGee, Queensland University of Technology, and Lindy Willmott, Queensland University of Technology consider how Victorian MPs will sift through competing claims as they prepare to debate an assisted dying bill.

    In late October Ben and Lindy will present a joint webinar for the Association on “Futile treatment and why doctors provide it to patients at the end of life: some empirical findings”

    Assisted dying in Australia is no longer a matter of “if” but “when”. Will the “when” be 2017 through the Voluntary Assisted Dying Bill likely to be tabled in the Victorian parliament this week?

    The politics of assisted dying are notoriously unpredictable, and how our politicians ultimately vote may turn on last-minute lobbying. However, a robust process to develop the bill, coupled with government and high-profile political support, means reform is a real possibility.

    As with previous Australian assisted dying bills, Victorian parliamentarians have been offered a conscience vote. As politicians ponder how they will respond, interest groups on both sides of the debate are lobbying fiercely. MPs are being provided with a range of conflicting information about how assisted dying regimes operate overseas and the risks or benefits of these regimes.

    How can politicians sift through and assess these competing claims?

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