193 research outputs found

    Analysis of the joint kinematics of the 5 iron golf swing

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    The purpose of this study was to identify the performance determining factors of the 5-iron golf swing. Joint kinematics were obtained from thirty male golfers using a twelve camera motion analysis system. Participants were divided into two groups, based on their ball launch speed (high vs. low). Those in the high ball speed group were deemed to be the more skillful group. Statistical analysis was used to identify the variables which differed significantly between the two groups, and could therefore be classified as the performance determining factors. The following factors were important to performance success: (i) the ability of the golfer to maintain a large X Factor angle and generate large X Factor angular velocity throughout the downswing, (ii) maintain the left arm as straight as possible throughout the swing, (iii) utilise greater movement of the hips in the direction of the target and a greater extension of the right hip during the downswing and (iv) greater flexion of both shoulders and less left shoulder internal rotation during the backswing

    The Quit Benefits Model: a Markov model for assessing the health benefits and health care cost savings of quitting smoking

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    BACKGROUND: In response to the lack of comprehensive information about the health and economic benefits of quitting smoking for Australians, we developed the Quit Benefits Model (QBM). METHODS: The QBM is a Markov model, programmed in TreeAge, that assesses the consequences of quitting in terms of cases avoided of the four most common smoking-associated diseases, deaths avoided, and quality-adjusted life-years (QALYs) and health care costs saved (in Australian dollars, A).Quittingoutcomescanbeassessedformalesandfemalesin14fiveyearagegroupsfrom1519to8084years.Exponentialmodels,basedondatafromlargecasecontrolandcohortstudies,weredevelopedtoestimatethedeclineovertimeafterquittingintheriskofacutemyocardialinfarction(AMI),stroke,lungcancer,chronicobstructivepulmonarydisease(COPD),anddeath.Australiandatafortheyear2001weresourcedfordiseaseincidenceandmortalityandhealthcarecosts.Utilityoflifeestimatesweresourcedfromaninternationalregistryandametaanalysis.Inthispaper,outcomesarereportedforsimulatedsubjectsfollowedupfortenyearsafterquittingsmoking.Lifeyears,QALYsandcostswereestimatedwith0). Quitting outcomes can be assessed for males and females in 14 five year age-groups from 15–19 to 80–84 years. Exponential models, based on data from large case-control and cohort studies, were developed to estimate the decline over time after quitting in the risk of acute myocardial infarction (AMI), stroke, lung cancer, chronic obstructive pulmonary disease (COPD), and death. Australian data for the year 2001 were sourced for disease incidence and mortality and health care costs. Utility of life estimates were sourced from an international registry and a meta analysis. In this paper, outcomes are reported for simulated subjects followed up for ten years after quitting smoking. Life-years, QALYs and costs were estimated with 0%, 3% and 5% per annum discount rates. Summary results are presented for a group of 1,000 simulated quitters chosen at random from the Australian population of smokers aged between 15 and 74. RESULTS: For every 1,000 males chosen at random from the reference population who quit smoking, there is a an average saving in the first ten years following quitting of A408,000 in health care costs associated with AMI, COPD, lung cancer and stroke, and a corresponding saving of A328,000forevery1,000femalequitters.Theaveragesavingper1,000randomquittersisA328,000 for every 1,000 female quitters. The average saving per 1,000 random quitters is A373,000. Overall 40 of these quitters will be spared a diagnosis of AMI, COPD, lung cancer and stroke in the first ten years following quitting, with an estimated saving of 47 life-years and 75 QALYs. Sensitivity analyses indicated that QBM predictions were robust to variations of ± 10% in parameter estimates. CONCLUSION: The QBM can answer many of the questions posed by Australian policy-makers and health program funders about the benefits of quitting, and is a useful tool to evaluate tobacco control programs. It can easily be re-programmed with updated information or a set of epidemiologic data from another country

    Early Childhood Development (ECD) services in the Southern Adelaide Health Service region.

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    This report documents the findings of a review conducted by the South Australian Community Health Research Unit (SACHRU) at the request of the Southern Adelaide Health Service (SAHS) into the provision of Early Childhood Development services in southern Adelaide. This review was undertaken between June and December 2006 and overseen by a Project Management group consisting of representatives from the SAHS, the primary health services managers, practitioners, an acute service manager and the researchers. The review examined the early childhood services provided by primary health services across the region, the models used, intake procedures and referral pathways. The findings were to be used for future service planning, implementation and resourcing

    Cost-effectiveness of ranibizumab for neovascular age-related macular degeneration

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    <p>Abstract</p> <p>Background</p> <p>Intravitreal ranibizumab prevents vision loss and improves visual acuity in patients with neovascular age-related macular degeneration, but it is expensive, and efficacy beyond 2 years is uncertain.</p> <p>Methods</p> <p>We assessed the cost-effectiveness of ranibizumab compared with no ranibizumab over 10 years, using randomized trial efficacy data for the first 2 years, post-trial efficacy assumptions, and ranibizumab acquisition costs ranging from the wholesale price (1,950perdose)tothepriceofbevazicumab(1,950 per dose) to the price of bevazicumab (50), a similar molecule which may be equally efficacious. We used a computer simulation model to estimate the probability of blindness, the number of quality-adjusted life-years (QALYs), direct costs (in 2004 U.S. dollars), and cost-effectiveness ratios for a 67-year old woman. Costs and QALYs were discounted at 3% per year.</p> <p>Results</p> <p>The probability of blindness over 10 years was reduced from 56% to 34% if ranibizumab was efficacious for only 2 years, 27% if efficacy was maintained for a further 2 years only (base-case scenario), and 17% if visual acuity at 4 years was then sustained. It was cost-saving under all price assumptions, when caregiver costs were included. When caregiver costs were excluded, the cost per QALY for the base-case ranged from 5,600,assumingthebevazicumabprice,to5,600, assuming the bevazicumab price, to 91,900 assuming the wholesale ranibizumab price. The cost per QALY was < 50,000whenthecostofranibizumabwaslessthan50,000 when the cost of ranibizumab was less than 1000.</p> <p>Conclusion</p> <p>From a societal perspective, ranibizumab was cost-saving. From a health care funder's perspective, ranibizumab was an efficient treatment when it cost less than $1000 per dose.</p

    Families empowered: a strengths based approach. An evaluation of FEAT, Families Empowered to Act Together.

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    The South Australian Community Health Research Unit undertook an evaluation of the FEAT program to track the progress of a number of families through the Families Empowered to Act Together (FEAT) program and capture the experiences and perspectives of children, families and stakeholders. Interviews were undertaken with carers and children both currently in the program and those recently exited. The evaluation also documents the development of the FEAT model of service and its aims and objectives; relates the operation of FEAT to understandings in the current literature regarding best practice principles and models for family support programs; and identifies other agencies, programs and services that the FEAT program links with in order to meet the needs of referred families. The evaluation adopted an action research framework employing qualitative and quantitative methods, and has encouraged participation by key stakeholders in the research process

    Cost-effectiveness of smoking cessation to prevent age-related macular degeneration

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    <p>Abstract</p> <p>Background</p> <p>Tobacco smoking is a risk factor for age-related macular degeneration, but studies of ex-smokers suggest quitting can reduce the risk.</p> <p>Methods</p> <p>We fitted a function predicting the decline in risk of macular degeneration after quitting to data from 7 studies involving 1,488 patients. We assessed the cost-effectiveness of smoking cessation in terms of its impact on macular degeneration-related outcomes for 1,000 randomly selected U.S. smokers. We used a computer simulation model to predict the incidence of macular degeneration and blindness, the number of quality-adjusted life-years (QALYs), and direct costs (in 2004 U.S. dollars) until age 85 years. Cost-effectiveness ratios were based on the cost of the Massachusetts Tobacco Control Program. Costs and QALYs were discounted at 3% per year.</p> <p>Results</p> <p>If 1,000 smokers quit, our model predicted 48 fewer cases of macular degeneration, 12 fewer cases of blindness, and a gain of 1,600 QALYs. Macular degeneration-related costs would decrease by 2.5millionifthecostsofcaregiversforpeoplewithvisionlosswereincluded,orby2.5 million if the costs of caregivers for people with vision loss were included, or by 1.1 million if caregiver costs were excluded. At a cost of 1,400perquitter,smokingcessationwascostsavingwhencaregivercostswereincluded,andcostabout1,400 per quitter, smoking cessation was cost-saving when caregiver costs were included, and cost about 200 per QALY gained when caregiver costs were excluded. Sensitivity analyses had a negligible impact. The cost per quitter would have to exceed 77,000forthecostperQALYforsmokingcessationtoreach77,000 for the cost per QALY for smoking cessation to reach 50,000, a threshold above which interventions are sometimes viewed as not cost-effective.</p> <p>Conclusion</p> <p>Smoking cessation is unequivocally cost-effective in terms of its impact on age-related macular degeneration outcomes alone.</p

    Bile acids and neurological disease

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    This review will focus on how bile acids are being used in clinical trials to treat neurological diseases due to their central involvement with the gut-liver-brain axis and their physiological and pathophysiological roles in both normal brain function and multiple neurological diseases. The synthesis of primary and secondary bile acids species and how the regulation of the bile acid pool may differ between the gut and brain is discussed. The expression of several bile acid receptors in brain and their currently known functions along with the tools available to manipulate them pharmacologically are examined, together with discussion of the interaction of bile acids with the gut microbiome and their lesser-known effects upon brain glucose and lipid metabolism. How dysregulation of the gut microbiome, aging and sex differences may lead to disruption of bile acid signalling and possible causal roles in a number of neurological disorders are also considered. Finally, we discuss how pharmacological treatments targeting bile acid receptors are currently being tested in an array of clinical trials for several different neurodegenerative diseases

    Transformational change in health systems: a road strewn with obstacles.

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    This research study assesses the impact on primary health care of the reform changes in the South Australian health system from 2005 to 2007. The research follows a pilot study conducted in one of the newly created health regions in 2005 to 2006 and reported in: Governance change in the southern metropolitan Adelaide health region: implications for Primary Health Care (Baum et al. 2006). Both studies were intended as scoping exercises to contribute towards the development of an evaluation framework for primary health care

    The social support and service needs of Australia’s ageing Greek migrants: a pilot project

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    This article explores the social support and service needs of Greek-speakers in Australia who migrated as young adults mostly in the 1940s and 1950s. The article reports the findings of a pilot research project initiated by the Modern Greek department at Flinders University in conjunction with social, health and ageing researchers. Focus groups and interviews were held in Adelaide and Darwin in 2010 with older Greek-speakers born in Greece and Cyprus; a survey of service organisations was also conducted. All older Greeks chose to be interviewed in Greek. They reported using a range of formal services, although some were confused about how to access services and lacked awareness of services. Interrupted primary education had resulted in low reading proficiency in Greek, while settlement experiences had contributed to low proficiency in reading, writing and speaking English. These were major barriers to accessing services with no Greek-speaking staff. In line with cultural expectations, a key support role was played by adult children, while some Greek-speaking GPs and MPs also mediated information and service access. Many older Greeks appear to be living independently in the community, but this is only possible because of high levels of informal support from close family. Those without children may therefore be more vulnerable to social isolation. The Modern Greek researchers who were integral members of the research team acted as ‘insiders’ who shared the culture and language of interviewees. Since all interviewees chose to be interviewed in Modern Greek, the ability to conduct interviews in Greek clearly enabled their participation, whereas they may have declined to participate had interviews only been available in English. At the same time, the non-Greek researchers provided a critical ‘outsider’ view which strengthened the data analysis and interpretation. We conclude that this project has demonstrated the important role that Modern Greek academics can play in research on social and health issues among the Greek diaspora
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