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<title>Australian Health Services Research Institute</title>
<copyright>Copyright (c) 2013 University of Wollongong All rights reserved.</copyright>
<link>http://ro.uow.edu.au/ahsri</link>
<description>Recent documents in Australian Health Services Research Institute</description>
<language>en-us</language>
<lastBuildDate>Wed, 27 Mar 2013 01:39:47 PDT</lastBuildDate>
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<title>Primary care vs specialist sleep center management of obstructive sleep apnea and daytime sleepiness and quality of life: a randomized trial</title>
<link>http://ro.uow.edu.au/ahsri/205</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/205</guid>
<pubDate>Mon, 25 Mar 2013 14:10:14 PDT</pubDate>
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	<p>Importance: Due to increasing demand for sleep services, there has been growing interest in ambulatory models of care for patients with obstructive sleep apnea. With appropriate training and simplified management tools, primary care physicians are ideally positioned to take on a greater role in diagnosis and treatment. Objective: To compare the clinical efficacy and within-trial costs of a simplified model of diagnosis and care in primary care relative to that in specialist sleep centers. Design, Setting, and Patients: A randomized, controlled, noninferiority study involving 155 patients with obstructive sleep apnea that was treated at primary care practices (n=81) in metropolitan Adelaide, 3 rural regions of South Australia or at a university hospital sleep medicine center in Adelaide, Australia (n=74), between September 2008 and June 2010. Interventions: Primary care management of obstructive sleep apnea vs usual care in a specialist sleep center; both plans included continuous positive airway pressure, mandibular advancement splints, or conservative measures only. Main Outcome and Measures: The primary outcome was 6-month change in Epworth Sleepiness Scale (ESS) score, which ranges from 0 (no daytime sleepiness) to 24 points (high level of daytime sleepiness). The noninferiority margin was -2.0. Secondary outcomes included disease-specific and general quality of life measures, obstructive sleep apnea symptoms, adherence to using continuous positive airway pressure, patient satisfaction, and health care costs. Results: There were significant improvements in ESS scores from baseline to 6 months in both groups. In the primary care group, the mean baseline score of 12.8 decreased to 7.0 at 6 months (P < .001), and in the specialist group, the score decreased from a mean of 12.5 to 7.0 (P < .001). Primary care management was noninferior to specialist management with a mean change in ESS score of 5.8 vs 5.4 (adjusted difference, -0.13; lower bound of 1-sided 95% CI, -1.5; P = .43). There were no differences in secondary outcome measures between groups. Seventeen patients (21%) withdrew from the study in the primary care group vs 6 patients (8%) in the specialist group. Conclusions and Relevance: Among patients with obstructive sleep apnea, treatment under a primary care model compared with a specialist model did not result in worse sleepiness scores, suggesting that the 2 treatment modes may be comparable. Trial Registration: anzctr.org.au Identifier: ACTRN12608000514303.</p>

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<author>Ching L. Chai-Coetzer</author>


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<title>The International Society for Occupational Science: a critique of its role in facilitating the development of occupational science through international networks and intercultural dialogue</title>
<link>http://ro.uow.edu.au/ahsri/188</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/188</guid>
<pubDate>Thu, 28 Feb 2013 17:10:09 PST</pubDate>
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<author>Alison Wicks</author>


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<title>Value of information and pricing new healthcare interventions</title>
<link>http://ro.uow.edu.au/ahsri/189</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/189</guid>
<pubDate>Thu, 28 Feb 2013 17:10:09 PST</pubDate>
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	<p>Previous application of value-of-information methods to optimal clinical trial design have predominantly taken a societal decision-making perspective, implicitly assuming that healthcare costs are covered through public expenditure and trial research is funded by government or donation-based philanthropic agencies. In this paper, we consider the interaction between interrelated perspectives of a societal decision maker (e.g. the National Institute for Health and Clinical Excellence [NICE] in the UK) charged with the responsibility for approving new health interventions for reimbursement and the company that holds the patent for a new intervention. We establish optimal decision making from societal and company perspectives, allowing for trade-offs between the value and cost of research and the price of the new intervention. Given the current level of evidence, there exists a maximum (threshold) price acceptable to the decision maker. Submission for approval with prices above this threshold will be refused.</p>
<p>Given the current level of evidence and the decision maker's threshold price, there exists a minimum (threshold) price acceptable to the company. If the decision maker's threshold price exceeds the company's, then current evidence is sufficient since any price between the thresholds is acceptable to both. On the other hand, if the decision maker's threshold price is lower than the company's, then no price is acceptable to both and the company's optimal strategy is to commission additional research. The methods are illustrated using a recent example from the literature.</p>

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<author>Andrew R. Willan</author>


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<title>Lower-limb amputee rehabilitation in Australia: analysis of a national data set 2004-10</title>
<link>http://ro.uow.edu.au/ahsri/190</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/190</guid>
<pubDate>Thu, 28 Feb 2013 17:05:09 PST</pubDate>
<description>
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	<p>Objective. Examine demographics, clinical characteristics and rehabilitation outcomes of lower-limb amputees, using the Australasian Rehabilitation Outcomes Centre (AROC) database.</p>
<p>Methods. Lower-limb amputee rehabilitation separations between 2004 and 2010 were identified using AROC impairment codes 5.3-5.7.1 Analysis was conducted by year, impairment code, Australian National Sub-acute and Non-Acute Patient (AN-SNAP) classification (S2-224, Functional Independence Measure (FIM) motor(Mot) score 72-91; S2-225, FIM (Mot) score 14-71) and states of Australia.</p>
<p>Results. Mean length of stay (LOS) for all lower-limb amputee episodes was 36.1 days (95% confidence interval (CI): 35.4-36.9). Majority of episodes were unilateral below knee (63.6%), males (71.8%) with a mean age of 67.9 years (95% CI: 67.6-68.3). Year-on-year analysis revealed a trend for increasing LOS and decreasing age. Analysis by impairment code demonstrated no significant difference in rehabilitation outcomes. Analysis by AN-SNAP found that LOS was 16.2 days longer for S2-225 than for S2-224 (95% CI: 14.7-17.8,P < 0.001), andFIM(Mot) change was 12.0 points higher for S2-225 than for S2-224 (95% CI: 11.5-12.6, P < 0.001). Analysis by states revealed significant variation in LOS, FIM (Mot) change and FIM (Mot) efficiency which may be associated with variations in organisation of rehabilitation services across states.</p>
<p>Conclusion. Although amputees represented a comparatively small proportion of all rehabilitation episodes in Australia, their LOS was significant. Unlike many other rehabilitation conditions, there was no evidence of decreasing LOS over time. AN-SNAP classes were effective in distinguishing rehabilitation outcomes, and could potentially be used more effectively in planning rehabilitation programs.</p>

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<author>Brenton G. Hordacre</author>


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<title>Use of PCOC assessment tools in driving and supporting design of specialist palliative care community team meetings/case conferences.</title>
<link>http://ro.uow.edu.au/ahsri/193</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/193</guid>
<pubDate>Thu, 28 Feb 2013 17:00:18 PST</pubDate>
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	<p>This presentation will describe the introduction of the PCOC assessment tools into a specialist palliative care community team on the Northern beaches of Sydney. One of the misconceptions found within the sector regarding PCOC, is that is it "just data". Many services, who for differing reasons cannot submit data, still find the use of PCOC assessment tools to have a profound impact on service delivery and design. This is such a service. For the past six months, whilst awaiting the introduction of a new database, and thus the ability to submit data and gain a report, the Hammond care Northern beaches team have used the tools to influence their practice.</p>

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<author>Jane Connolly</author>


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<title>The use of common assessment tools: supporting connections</title>
<link>http://ro.uow.edu.au/ahsri/194</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/194</guid>
<pubDate>Thu, 28 Feb 2013 17:00:18 PST</pubDate>
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	<p>Implementation of common assessment tools across care settings facilitates a shared language that supports better communication between team members and between services. The use of common assessment tools supports the development of referral triggers and clinical decision tools that improve clinical outcomes and patient and family experience - ensuring for all people the right care, at the right time, in the right place.</p>
<p>The importance of '<em>impeccable</em>' clinical assessment has been understood from the very beginning of the modern hospice movement, along with the need for 'exquisite' attention to detail. While these definitions may be disputed in the palliative care movement of the 21st century the underlying principle that quality, patient -centred, holistic care begins with good assessment cannot be disputed. The NSAP Quality Report (NSAP 2011) revealed that clinical assessment was identified by two-thirds of palliative care services as a priority for improvement. Clinical assessment data is routinely collected by the Palliative Care Outcomes Collaboration (PCOC) to report service performance against national benchmarks in clinical care, and is used to drive improvement effort.</p>
<p>This presentation will explore the links between clinical assessment and improved quality of care for people approaching and reaching the end of life - a shared commitment and collaboration between PCOC and Calvary Health, Aged and Community Care services. The use of the validated assessment tools utilised by PCOC to support quality improvement initiatives for the care of people approaching and reaching the end of life within Calvary services will be described.</p>

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<author>Sue Hanson</author>


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<title>PCOC assessment workshops: a common language- improved communication</title>
<link>http://ro.uow.edu.au/ahsri/195</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/195</guid>
<pubDate>Thu, 28 Feb 2013 16:55:08 PST</pubDate>
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	<p>In the last 18 months PCOC has developed and delivered workshop style education on the use of PCOC assessment tools. 25 workshops have been delivered to 450 participants in metropolitan, regional and rural NSW.</p>
<p>The workshops were introduced in an attempt to improve the ability of the sector to meet the national benchmarks. We are seeing an improved trend towards meeting the benchmarks since the introduction of the workshops. However the focus of this presentation will be the increased understanding of the assessment tools post workshop as evidenced by evaluation feedback.</p>

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<author>Sabina Clapham</author>


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<title>Proof is in the outcomes: change in practice through PCOC (Palliative Care Outcomes Collaboration)</title>
<link>http://ro.uow.edu.au/ahsri/196</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/196</guid>
<pubDate>Thu, 28 Feb 2013 16:55:08 PST</pubDate>
<description>
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	<p>Palliative Care Outcomes Collaboration (PCOC) is a national voluntary quality program to introduce standardised clinical assessment tools in palliative care in order to benchmark patient outcomes. It is funded under the National Palliative Care Program and supported by the Australian Government Department of Health and Ageing. Since its inception in 2005, PCOC has increased awareness of outcome measurement to support care planning, service development and quality activities. Currently there are 102 palliative care services across Australia participating in this program.</p>

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<author>Sabina Clapham</author>


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<title>Critical appraisal, systematic literature reviews and evidence based practice</title>
<link>http://ro.uow.edu.au/ahsri/200</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/200</guid>
<pubDate>Thu, 28 Feb 2013 16:45:12 PST</pubDate>
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<author>Jan Sansoni</author>


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<title>The revised urinary incontinence scale: a comparison with other short urinary incontinence measures</title>
<link>http://ro.uow.edu.au/ahsri/201</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/201</guid>
<pubDate>Thu, 28 Feb 2013 16:45:11 PST</pubDate>
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	<p>The Revised Urinary Incontinence Scale (RUIS) contains 5 items drawn from the Urogenital Distress Inventory-6 (UDI-6) and the Incontinence Severity Index (ISI). Selection of the RUIS items was based on the examination of the psychometric properties of the items within these scales in a large community survey (N = 2915). The RUIS was developed to provide a short, psychometrically sound measure of urinary incontinence (UI) for both epidemiological and outcomes research.</p>
<p>As part of the clinical validation of the RUIS this study aims to provide comparisons with other short scales used to assess urinary incontinence: the International Consultation of Incontinence - Short Form (ICIQ-SF) scale, the UDI-6 and the ISI.</p>

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<author>Jan Sansoni</author>


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<title>PCOC Assessment as a quality improvement tool</title>
<link>http://ro.uow.edu.au/ahsri/202</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/202</guid>
<pubDate>Thu, 28 Feb 2013 16:40:12 PST</pubDate>
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<author>Claire Johnson</author>


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<title>PCOC Report 13: An overview of the Western Australian and National PCOC</title>
<link>http://ro.uow.edu.au/ahsri/203</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/203</guid>
<pubDate>Thu, 28 Feb 2013 16:40:12 PST</pubDate>
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<author>Tanya Pidgeon</author>


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<title>The Sydney Multisite Intervention of LaughterBosses and ElderClowns (SMILE) study: cluster randomised trial of humour therapy in nursing homes</title>
<link>http://ro.uow.edu.au/ahsri/204</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/204</guid>
<pubDate>Thu, 28 Feb 2013 16:35:09 PST</pubDate>
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	<p>Objectives: To determine whether humour therapy reduces depression (primary outcome), agitation and behavioural disturbances and improves social engagement and quality-of-life in nursing home residents. Design: The Sydney Multisite Intervention of LaughterBosses and ElderClowns study was a singleblind cluster randomised controlled trial of humour therapy. Setting: 35 Sydney nursing homes. Participants: All eligible residents within geographically defined areas within each nursing home were invited to participate. Intervention: Professional 'ElderClowns' provided 9-12 weekly humour therapy sessions, augmented by resident engagement by trained staff 'LaughterBosses'. Controls received usual care. Measurements: Depression scores on the Cornell Scale for Depression in Dementia, agitation scores on the Cohen-Mansfield Agitation Inventory, behavioural disturbance scores on the Neuropsychiatric Inventory, social engagement scores on the withdrawal subscale of Multidimensional Observation Scale for Elderly Subjects, and self-rated and proxy-rated quality-of-life scores on a health-related quality-of-life tool for dementia, the DEMQOL. All outcomes were measured at the participant level by researchers blind to group assignment. Randomisation: Sites were stratified by size and level of care then assigned to group using a random number generator. Results: Seventeen nursing homes (189 residents) received the intervention and 18 homes (209 residents) received usual care. Groups did not differ significantly over time on the primary outcome of depression, or on behavioural disturbances other than agitation, social engagement and quality of life. The secondary outcome of agitation was significantly reduced in the intervention group compared with controls over 26 weeks (time by group interaction adjusted for covariates: p=0.011). The mean difference in change from baseline to 26 weeks in Blom-transformed agitation scores after adjustment for covariates was 0.17 (95% CI 0.004 to 0.34, p=0.045). Conclusions: Humour therapy did not significantly reduce depression but significantly reduced agitation.</p>

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<author>Lee-Fay Low</author>


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<title>Building better systems of care for Aboriginal and Torres Strait Islander people: findings from the Kanyini health systems assessment</title>
<link>http://ro.uow.edu.au/ahsri/187</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/187</guid>
<pubDate>Tue, 05 Feb 2013 16:37:37 PST</pubDate>
<description>
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	<p>Background Australian federal and jurisdictional governments are implementing ambitious policy initiatives intended to improve health care access and outcomes for Aboriginal and Torres Strait Islander people. In this qualitative study we explored Aboriginal Medical Service (AMS) staff views on factors needed to improve chronic care systems and assessed their relevance to the new policy environment.</p>
<p>Methods Two theories informed the study: (1) 'candidacy', which explores "the ways in which people's eligibility for care is jointly negotiated between individuals and health services"; and (2) kanyini or 'holding', a Central Australian philosophy which describes the principle and obligations of nurturing and protecting others. A structured health systems assessment, locally adapted from Chronic Care Model domains, was administered via group interviews with 37 health staff in six AMSs and one government Indigenous-led health service. Data were thematically analysed.</p>
<p>Results Staff emphasised AMS health care was different to private general practices. Consistent with kanyini, community governance and leadership, community representation among staff, and commitment to community development were important organisational features to retain and nurture both staff and patients. This was undermined, however, by constant fear of government funding for AMSs being withheld. Staff resourcing, information systems and high-level leadership were perceived to be key drivers of health care quality. On-site specialist services, managed by AMS staff, were considered an enabling strategy to increase specialist access. Candidacy theory suggests the above factors influence whether a service is 'tractable' and 'navigable' to its users. Staff also described entrenched patient discrimination in hospitals and the need to expend considerable effort to reinstate care. This suggests that Aboriginal and Torres Strait Islander people are still constructed as 'non-ideal users' and are denied from being 'held' by hospital staff.</p>
<p>Conclusions Some new policy initiatives (workforce capacity strengthening, improving chronic care delivery systems and increasing specialist access) have potential to address barriers highlighted in this study. Few of these initiatives, however, capitalise on the unique mechanisms by which AMSs 'hold' their users and enhance their candidacy to health care. Kanyini and candidacy are promising and complementary theories for conceptualising health care access and provide a potential framework for improving systems of care.</p>

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<author>David Peiris</author>


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<title>Community care assessment and the web: what do we know already and where are we heading?</title>
<link>http://ro.uow.edu.au/ahsri/176</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/176</guid>
<pubDate>Sun, 20 Jan 2013 21:30:18 PST</pubDate>
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	<p>The use of Information and Communication Technologies (ICT) by the Non Government sector and the broader community care sector, including the interface with health services, has developed rapidly in the last decade and more recently has begun to generate some useful tools that may actually improve the consumers experience of receiving services. The development of ICT tools utilising different modalities (electronic data collection and storage, web pages, sms, podcasts) may improve the community care systems capacity to describe consumer needs and risks, to organise a service response, and to more easily report on their programs activities. This improved capacity may in turn help to redefine how service systems are planned and managed and improve the quality of how services are delivered. The first part of this paper describes some of the lessons for community care in the age of electronic data manipulation that are already well understood: the intractability of integration problems (your integration is my fragmentation); the requirement for a common language of client/consumer and carer assessment; requirement for common data elements and common data transmission standards that enable information sharing; and the requirement for trust and shared protocols for exchanging information at a local level. The second part of the paper is much more speculative in looking forward, given the current rapidly evolving nature of the technology, and the various governments policy and service development agendas, to map a path towards a more interesting electronic future and arguably a more useful service system. The road map includes ways to improve the capacity of community care systems to build skills and competencies, exchange useful information and build a knowledge base over time. The map also includes some directions through dangerous territory, with some signposts to avoid the inherent tendency towards service system fragmentation, and ways we may be able to use the new technologies to enhance civil society and offset the tendencies towards greater centralised control. Finally, the paper asserts the need to develop an ongoing program of research and development of ICT and promote its responsible use by community care workers and communities.</p>

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<author>Andrew Clark</author>


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<title>Consistently estimating risk difference in a jurisdiction of interest: odds solution to relative risk fallacies</title>
<link>http://ro.uow.edu.au/ahsri/177</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/177</guid>
<pubDate>Sun, 20 Jan 2013 21:25:11 PST</pubDate>
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	<p>Economic analyses in health technology assessment often require estimation of absolute risk difference (ARD) for outcomes such as survival or progression, given base risk in the jurisdiction of interest and trial evidence of treatment effects. We demonstrate that odds ratios (OR) provide distinct advantages over relative risk (RR) in consistently estimating such ARD independent of the framing of effects (e.g. mortality or survival) for direct and indirect comparisons. METHODS: Use of RR is shown to lead to inferential anomalies in estimating ARD, while consistently estimated using OR. These inferential anomalies and odds solution are illustrated for indirect comparison of Natiluzimab versus Interferon beta-1b for multiple sclerosis, as well as direct comparisons. RESULTS: Standard use of relative risk to calculate ARD in indirect comparison suggests Natiluzimab is more effective than Interferon for progression (RR = 0.70, ARD = 21% for a base risk of 70% progression) but less effective than Interferon for no progression (RR = 0.84, ARD = 4.8%). This inferential anomaly is avoided using OR, with odds of progression (0.83) the reciprocal of that for no progression (1.21), and ARD of 4.1% in favor of Nataluzimab with progression or no progression. For direct comparisons ARD is shown to be consistently estimated with OR but change with framing of effects using RR wherever epidemiological risk differs from trial risk in the comparator arm. CONCLUSIONS: Odds ratios allow consistent estimation of absolute risk differences regardless of framing of effects in direct and indirect comparisons. This overcomes inferential anomalies that arise with use of relative risk in such comparisons whenever base risk differs in the jurisdiction of interest from that in trials, or base risk in the common arms differs in indirect comparisons. Consequently, odds ratios avoid selection biases in framing of effects inherent with risk ratios and are suggested as the preferred metric in estimating such risk differences.</p>

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<author>Simon Eckermann</author>


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<title>Child injury in an urban Australian indigenous community: the safe koori kids intervention</title>
<link>http://ro.uow.edu.au/ahsri/178</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/178</guid>
<pubDate>Sun, 20 Jan 2013 21:05:08 PST</pubDate>
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	<p>Objective To design and evaluate an intervention targeting urban indigenous Australian children in order to increase their self-effi cacy, knowledge and attitudes towards safety. Methods The Safe Koori Kids intervention was developed and delivered to 790 children primary school aged children (13% indigenous) in 24 middle and upper primary classes across fi ve schools in Sydney, Australia. The intervention, consisting of fi ve safety modules, was evaluated using a mixed-methods approach. A pre-test post-test research design was applied to evaluate changes in key outcomes namely child self-effi cacy, knowledge and attitudes towards safety. Qualitative and quantitative data were collected from teachers. Findings There was a signifi cant increase (p<0.05) in self-effi cacy among children from pre- to post-intervention for both Indigenous (6%) and non-Indigenous children (2%). Safety knowledge among Indigenous children increased from pre- to post intervention by 17% (p<0.01) and non-Indigenous children by 15%, (p<0.01). However, there were no signifi cant improvements in attitudes towards safety (indigenous children 2%, p=0.288, non-Indigenous children 1%, p=0.0721). Overall, Indigenous children scored lower than non-Indigenous children post intervention on self-effi cacy (75%:77%), knowledge (56%:63%) and attitudes towards safety (79%:84%). Teacher focus groups provided further evidence of the programs impact on children's safety knowledge and attitudes. Conclusions The study contributes to our limited knowledge about effective child injury prevention for disadvantaged Indigenous minorities in high income countries. This is the fi rst intervention of its type in an urban indigenous setting in Australia which has positively contributed to the resilience of indigenous children and families with respect to safety and their environment.</p>

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<author>Kathleen F. Clapham</author>


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<title>Researching the safety of Indigenous children and youth: an urban perspective</title>
<link>http://ro.uow.edu.au/ahsri/179</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/179</guid>
<pubDate>Sun, 20 Jan 2013 21:01:18 PST</pubDate>
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	<p>Injury is one of the leading causes of Indigenous mortality in Australia and safety in Indigenous communities has become increasingly prominent in commentary on Indigenous communities. However, our knowledge of urban Indigenous people and their experiences has been largely ignored in these debates; most of the discussions to date have focused on remote areas, despite the fact that around one-third of Indigenous Australians live in urban settings. This paper reports on the Safe Koori Kids study, which addressed the safety of Indigenous children, carried out in Sydney's outer metropolitan area of Campbelltown between 2006 and 2009 (Clapham et al. 2006a, 2006b). The study aimed to increase our understanding of the broad range of factors involved in injury in Indigenous communities and to create a culturally acceptable and effective intervention program by addressing child and youth resilience. The program, delivered to Indigenous and non-Indigenous primary-aged children across 11 primary schools and evaluated in five of these schools, drew on local knowledge and resources to address safety issues. The program was underpinned by recognising that a multitude of factors affect the safety of children and families. Additionally, the program embedded positive messages to reinforce the cultural identity of Indigenous people living in urban areas. The theme of connections and reconnections embedded in our study emerged as children responded positively to the way urban Indigenous identity was represented in the program. Researchers recorded an increase in self-efficacy in questionnaire responses among the primary-aged children after the program was delivered over one school term in five schools. Qualitative data collected from teachers also revealed that Indigenous children responded to the program with an increased sense of achievement and pride in Aboriginal heritage. Improving the safety of Indigenous children in urban areas is complex and currently not well understood. Intervention programs need to incorporate a much better comprehension of the factors that increase the vulnerability of urban Indigenous children. Safety programs must recognise the social and cultural context in which children live, draw on local resources and reinforce a sense of pride in Indigenous identity to build resilience among vulnerable children.</p>

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<author>Kathleen F. Clapham</author>


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<title>Stephanie Alexander Kitchen Garden National Program Evaluation: Final Report</title>
<link>http://ro.uow.edu.au/ahsri/183</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/183</guid>
<pubDate>Sun, 20 Jan 2013 20:55:10 PST</pubDate>
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<author>Heather Yeatman</author>


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<title>Stephanie Alexander Kitchen Garden National Program Evaluation: Supporting Information</title>
<link>http://ro.uow.edu.au/ahsri/184</link>
<guid isPermaLink="true">http://ro.uow.edu.au/ahsri/184</guid>
<pubDate>Sun, 20 Jan 2013 20:55:10 PST</pubDate>
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<author>Heather Yeatman</author>


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