1,605 research outputs found

    The Ethics of Embodiment

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    A review of Rosalyn Diprose's Corporeal Generosity: On Giving with Nietzsche, Merleau-Ponty, and Levinas (SUNY Press, Albany, New York. 2002)

    Distribution, habitat preferences and population sizes of two threatened tree ferns, Cyathea cunninghamii and Cyathea x marcescens, in south-eastern Australia

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    The distribution, population sizes and habitat preferences of the rare tree ferns Cyathea cunninghamii Hook.f. (Slender Tree Fern) and F1 hybrid Cyathea x marcescens N.A.Wakef. (Skirted Tree Fern) in south-eastern Australia are described, together with the extension of the known distribution range of Cyathea cunninghamii from eastern Victoria into south-eastern New South Wales. Floristic and ecological data, encompassing most of the known habitat types, vegetation associations and population sizes, were collected across 120 locations. Additional information was sought from literature reviews, herbarium collections and field surveys of extant populations. Cyathea cunninghamii is widespread, with the majority of populations occurring in Tasmania and Victoria, one population in south-eastern NSW and a disjunct population in south-eastern Queensland; Cyathea x marcescens is confined to south and eastern Victoria and south and north eastern Tasmania. Both taxa occur on King Island in Bass Strait. Both taxa have a near coastal distribution with most populations occurring in sub-coastal hinterland and escarpment forests with a median altitude of 288 m. Hierarchical cluster analysis of floristic data across the species’ geographic range identified six vegetation communities ranging from rainforest to damp sclerophyll forest. Their micro-habitat preferences were consistently identified as steeply incised gullies of minor headwater streams of coastal and sub-coastal ranges with a plentiful moisture regime and geomorphic protection from extreme stream flow events, flooding and bank scouring. Sporophyte recruitment was associated with exposed soil of stream banks and edges of constructed walking tracks. Population sizes of both taxa are small with the majority of populations consisting of less than five adult individuals, with total populations of Cyathea cunninghamii and Cyathea x marcescens estimated at 919 and 221 mature individuals respectively. Population extinctions in Victoria and Tasmania have primarily been associated with outlier populations in regions subject to agricultural land clearance, habitat modification and changes to fire regimes in crown forests. Nonanthropogenic mortality was associated with land slips, tree falls and stream bank scouring by flood water. Conservation of the hybrid Cyathea x marcescens necessitates the preservation of habitats where both Cyathea cunninghamii and Cyathea australis occur in close proximity to substrates suitable for spore germination. In future, molecular techniques may prove useful for field identification of juvenile stages, facilitating selection of progeny of Cyathea cunninghamii and Cyathea x marcescens for cultivation and re-introduction to sites of previous or possible future extinctions

    Applying the Biopsychosocial Model: Factors Associated with Depression in Mexican-American Adults

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    Although professionals in psychiatry, psychology and medicine claim to endorse the biopsychosocial model as proposed by George L. Engel (1977), clinicians in all three fields still tend to underutilize it. Some academics have also criticized the model for its inadequate emphasis on cultural contextualization. To improve upon the model, I sought to empirically establish the relationship between culturally-specific social factors and psychological disorder, in this case depressive symptoms in Mexican-American adults. Eighty-six Mexican-American participants living on the US-Mexico border completed scales measuring depressive symptoms, bidirectional acculturation, living situation, diabetes, and health beliefs regarding the origins of diabetes. The results revealed that diabetes, acculturation, and gender were not associated with depressive symptoms in this population, even when controlling for mental health biases. This finding is in contrast to findings from other literature that associated diabetes, low acculturation and gender with depression in Hispanic adults. Extended family cohabitation was also not associated with lower numbers of depressive symptoms, despite the importance of familism and the extended family unit in Mexican-American culture. Unemployment was significantly related to number of depressive symptoms in both genders. There was no significant relationship between acculturation and health beliefs. These results indicate the importance of studying psychological disorders within the context of specific population groups that transcend vague censual terms. The discussion addresses methodological concerns and further directions for research concerning gender roles, chronic illness, depression and out-of-home employment in Mexican-American adults

    Primary health care for Aboriginal and Torres Strait Islander children

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    This final report presents the findings from each of the phases of the Engaging Stakeholders in Identifying Priority Evidence-Practice Gaps and Strategies for Improvement in Primary Health Care (ESP) Project. This report is designed for people working in a range of roles including national and jurisdictional policy makers, managers, community-controlled organisations and government health authorities, peak bodies, clinical leaders, researchers, primary health care staff and continuous quality improvement (CQI) practitioners who may have an interest in the interpretation and use of aggregated CQI data to drive decision making. Stakeholders across services and systems that deliver Aboriginal and Torres Strait Islander primary health care (PHC) engaged in a process to analyse and interpret national continuous quality improvement (CQI) data from 132 health centres. We used a consensus process to identify priority evidence-practice gaps in child health care, based on these data. Stakeholders drew on their knowledge and experience working in Aboriginal and Torres Strait Islander PHC to identify barriers and enablers to addressing the priority evidence- practice gaps, and to suggest strategies to overcome barriers and strengthen enablers to addressing the priority evidence-practice gaps. Important messages emerge from these findings

    Chronic illness care for Aboriginal and Torres Strait Islander people: final report

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    This project engage a range of stakeholders across different levels of the primary health care system, including service providers, management, policy-makers and researchers and capture their knowledge on the barriers and enablers to addressing the identified priority-evidence practice gaps and their suggestions on strategies for improvement. Overview The purpose of this project is to engage key stakeholders in the use of aggregate continuous quality improvement (CQI) data to identify and address system-wide evidence-practice gaps in Aboriginal and Torres Strait Islander chronic illness care. We aimed to engage a range of stakeholders across different levels of the primary health care (PHC) system, including service providers, management, policy-makers and researchers and capture their knowledge on the barriers and enablers to addressing the identified priority-evidence practice gaps and their suggestions on strategies for improvement. Our research has highlighted the wide variation in performance between different aspects of care and between health centres. While many aspects of care are being done well in many health centres, there are important gaps between evidence and practice in some aspects of PHC. System-wide gaps are likely to be due to deficiencies in the broader (PHC) system, indicating that system-level action is required to improve performance. Such system-level action should be developed with a deep understanding of the holistic nature of Aboriginal and Torres Strait islander wellbeing beyond just physical health (including healthy connections to culture, community and country), of the impact of Australian colonist history on Aboriginal and Torres Strait Islander people, and of how social systems – including the health system - should be shaped to meet the needs of Aboriginal and Torres Strait Islander people. This project aims to build on the collective strengths within PHC services in order to continue improving the quality of care for Aboriginal and Torres Strait Islander communities

    Status epilepticus on the paediatric intensive care unit—the role of EEG monitoring

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    AbstractA pilot study was undertaken of the feasibility of continuous EEG monitoring of patients admitted to a Paediatric Intensive Care Unit (PICU) for management of status epilepticus or its immediate sequelae. Eight children were studied and seizure activity was recorded in four patients. Additional information influencing management was obtained: the bedside nurse considered decerebrate posturing in one patient to be a seizure: there were no epileptiform EEG changes. Another patient was considered to have seizures (clonic movements of both upper limbs) following cardiac arrest; the EEG showed electrocerebral silence, and thiopentone treatment was discontinued. In another patient, continuing epileptiform activity on EEG gave intensivists the confidence to use higher than usual doses of thiopentone. The problems encountered were delays in monitoring, once for a CT scan and once because of two admissions within hours of each other. We conclude that EEG monitoring on a PICU is feasible and provides clinically useful information
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