2 - Schools incorporating the Life Sciences and Medicine
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Item Health, self-care and the offshore workforce – opportunities for behaviour change interventions : an epidemiological survey(2018-05-26) Gibson Smith, Kathrine; Paudyal, Vibhu; Klein, Susan; Stewart, Derek; University of Aberdeen.Medical Education; University of Aberdeen.Centre for Healthcare Education and Research Innovation (CHERI)Item Personal identity and the role of 'carer' among relatives and friends of people with multiple sclerosis(2013-11-01) Hughes, Nic; Locock, Louise; Ziebland, Sue; University of Aberdeen.Aberdeen Centre for EvaluationItem “Doctor my eyes” : A natural experiment on the demand for eye care services(2016-02) Dickey, H; Ikenwilo, D; Norwood, P; Watson, Verity; Zangelidis, A; University of Aberdeen.Centre for Labour Market Research (CeLMR); University of Aberdeen.Economics; University of Aberdeen.Health Economics Research UnitItem Multicentre, non-interventional study to assess the profile of patients with uncontrolled rhinitis prescribed a novel formulation of azelastine hydrochloride and fluticasone propionate in a single spray in routine clinical practice in the UK(2017-04-01) Scadding, Glenis; Price, David; El-Shanawany, Tariq; Ahmed, Shahzada; Ray, Jaydip; Sargur, Ravishankar; Kumar, Nirwal; University of Aberdeen.Other Applied Health Sciences; University of Aberdeen.Institute of Applied Health SciencesItem Exploring the cost-utility of stratified primary care management for low back pain compared with current best practice within risk-defined subgroups(2012-11) Whitehurst, David G T; Bryan, Stirling; Lewis, Martyn; Hill, Jonathan; Hay, Elaine M; University of Aberdeen.Health Economics Research UnitItem The hidden burden of adult allergic rhinitis : UK healthcare resource utilisation survey(2015-11-20) Price, David; Scadding, Glenis; Ryan, Dermot; Bachert, Claus; Canonica, G Walter; Mullol, Joaquim; Klimek, Ludger; Pitman, Richard; Acaster, Sarah; Murray, Ruth; Bousquet, Jean; University of Aberdeen.Other Applied Health Sciences; University of Aberdeen.Institute of Applied Health SciencesItem Model inter-comparison between statistical and dynamic model assessments of the long-term stability of blanket peat in Great Britain (1940-2099)(2010-12-12) Clark, J. M.; Billett, M. F.; Coyle, M.; Croft, S.; Daniels, S.; Evans, C. D.; Evans, M.; Freeman, C.; Gallego-Sala, A. V.; Heinemeyer, A.; House, J. I.; Monteith, D. T.; Nayak, D.; Orr, H. G.; Prentice, I. C.; Rose, R.; Rowson, J.; Smith, J. U.; Smith, P.; Tun, Y. M.; Vanguelova, E.; Wetterhall, F.; Worrall, F.; University of Aberdeen.Biological Sciences; University of Aberdeen.Environment and Food Security; University of Aberdeen.EnergyItem How young people find out about their family history of Huntington's disease(Elsevier, 2009-03-26) Forrest Keenan, Karen; van Teijlingen, Edwin; McKee, Lorna; Miedzybrodzka, Zosia; Simpson, Sheila A.Family communication about adult-onset hereditary illness can be problematic, leaving some relatives inadequately informed or ignorant of their risk. Although studies have explored the barriers and facilitators in family communication about genetic risk, questions remain about when, what, how and indeed whether to tell relatives. The process of disclosure is also dependent upon the way in which genetic information is realized and understood by recipients, but research here is limited. Our paper explores young people’s experiences of finding out about a family history of the hereditary disorder Huntington’s disease (HD). In-depth interviews explored how and when young people found out, their reactions to different communication styles and any impact on family relations. We recruited young people through the North of Scotland regional genetics clinic and the Scottish Huntington’s Association (SHA). Thirtythree young people (aged 9–28) were interviewed. A qualitative analysis was undertaken which revealed four types of disclosure experiences: (1) having always been told, (2) gradually told, (3) HD was kept a secret, or (4) HD as a new diagnosis. In particular, the timing and style of disclosure from relatives, and one’s stage of awareness, were fundamental in structuring participants’ accounts. This article focuses on questions of when, how and indeed whether to tell children, and sits within a broader set of research and practice issues about what professionals and families (should) tell children about parental illness and genetic risk.Item Health inequalities in England, Scotland and Wales : stakeholders' accounts and policy compared(Elsevier, 2009-01) Harrington, B.E.; Smith, K.E.; Hunter, D.J.; Marks, L; Blackman, T.J.; McKee, Lorna; Greene, A; Elliott, E; Williams, G.H.; University of Aberdeen, Business School, Management Studies; University of Aberdeen, School of Medicine & Dentistry, Division of Applied Health SciencesObjectives The election of a Labour government in 1997 brought the issue of health inequalities firmly back on to the policy agenda across the UK. Since then, in the wake of devolution, the need to tackle health inequalities has been highlighted as a policy priority in all three mainland UK countries, albeit with varying degrees of emphasis. This paper reports on a major cross-national study, funded by the Economic and Social Research Council, investigating how National Health Service bodies, local councils and partnerships make sense of their work on health inequalities, and examining the difference made by the contrasting approaches that have been taken to performance assessment in England, Wales and Scotland. Study design Case studies, semi-structured interviews and analysis of key policy statements. Methods In order to explore how health inequalities have been approached by the three governments (noting that there was a change in governments in Wales and Scotland during this time), key policy statements published between May 1997 and May 2007 were analysed. Concurrently, data from stakeholder interviews carried out in 2006 in case study areas in each country were analysed to determine the extent of alignment between policy and practice at local level. Results This paper suggests that claims about the extent of health policy divergence in post-devolution Britain may have been exaggerated. It finds that, whilst the three countries have taken differing approaches to performance assessment and the setting of targets, policy approaches to health inequalities up until 2007 appear to have been remarkably similar. Furthermore, the first round of interview data suggest that variations in local understandings of, and responses to, health inequalities cannot always be clearly distinguished along national lines. Conclusions Based on the policy analysis, devolution in the UK does not appear to have resulted in substantively different national policy approaches to health inequalities. Indeed, the overall analysis suggests that (prior to the 2007 elections in Scotland and Wales) the differences between local areas within countries may be of as much interest as those between countries.