600 research outputs found

    sj-pdf-1-pmj-10.1177_02692163231172243 – Supplemental material for Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study

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    Supplemental material, sj-pdf-1-pmj-10.1177_02692163231172243 for Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study by Wendy English, Jackie Robinson and Merryn Gott in Palliative Medicine</p

    sj-pdf-2-pmj-10.1177_02692163231172243 – Supplemental material for Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study

    No full text
    Supplemental material, sj-pdf-2-pmj-10.1177_02692163231172243 for Health professionals’ experiences of rapport during telehealth encounters in community palliative care: An interpretive description study by Wendy English, Jackie Robinson and Merryn Gott in Palliative Medicine</p

    sj-docx-1-pcr-10.1177_26323524231164162 – Supplemental material for Dying at home for people experiencing financial hardship and deprivation: How health and social care professionals recognise and reflect on patients’ circumstances

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    Supplemental material, sj-docx-1-pcr-10.1177_26323524231164162 for Dying at home for people experiencing financial hardship and deprivation: How health and social care professionals recognise and reflect on patients’ circumstances by Sam Quinn, Naomi Richards and Merryn Gott in Palliative Care and Social Practice</p

    861925_Supplementary_file_1 – Supplemental material for Comparison of financial support for family caregivers of people at the end of life across six countries: A descriptive study

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    Supplemental material, 861925_Supplementary_file_1 for Comparison of financial support for family caregivers of people at the end of life across six countries: A descriptive study by Clare Gardiner, Beth Taylor, Jackie Robinson and Merryn Gott in Palliative Medicine</p

    Inscription in Nova Solyma, the ideal city; or, Jerusalem regained; an anonymous romance written in the time of Charles I

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    Probable editor's gift inscription, "Jacobo Hiltonio Amico Suo Amicissimo D. D. D Libri hujus Editor et Interpres. W. B. A.D. CMMII".Nova Solyma, the ideal city; or, Jerusalem regained; an anonymous romance written in the time of Charles I. Now first drawn from obscurity, and attributed to the illustrious John Milton. With introduction, translation, literary essays and a bibliography by the Rev. Walter Begley. Begley, Walter, 1845-1905, ed. and tr. Gott, Samuel, 1613-1671, supposed author. Milton, John, 1608-1674, supposed author

    The development and implementation of evidence-based palliative care guidelines for residential care: Lessons for other countries

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    Guidelines are 'systematically developed statements to assist practitioner and patient decisions about appropriate health care for specific clinical circumstances' (1). In the last decade there has been worldwide interest in development and use of evidence-based guidelines. This has been driven by the imperative to limit variations in clinial practice for people with the same condition, uncertainty about the effectiveness of interventions in making a change in people's health, and making the best of limited health resources within fiscal constraints. Whiles initially the focus was on how guidelines should be developed, this is now well defined and in Australia the National Health and Medical Research Council (NMHRC) (1) provides details of this process as does the National Institute for Health and Clinical Excellence(NICE) (2) in the UK. Several countries such as Australia, the UK, the USA, and Canada have national bodies that collate, synthesize, and publish evidence. [Extract

    “You get pushed to the limit… but it was worth it”: Experiences of working carers supporting older adults in advanced age at end of life

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    Full Text is available to authenticated members of The University of Auckland only.Background: To better respond to the palliative and end-of-life (EOL) care needs of our growing ageing population, policies have advocated shifting palliative care from hospital settings to the community. This has strained informal or family or ‘lay’ carers who are the main providers of palliative and EOL care within the community. Many informal carers are also juggling their employment with caring. However, there is a lack of research that elucidates the experiences of those who are caring for someone in advanced age at EOL while also working. Aim: This study aimed to gain insight into the experiences of working carers by exploring the interaction between caregiving and employment for those who are caring for a person in advanced age at EOL. Methods: Guided by social constructionism, I conducted qualitative secondary research using data from the Te Pākeketanga: Living and Dying in Advanced Age study. After reading all 58 Te Pākeketanga interview transcripts, I selected 41 transcripts that discussed balancing work and care responsibilities. Data was analysed using reflexive thematic analysis and narrative analysis. Findings: I identified three key themes in the data. First, participants discussed the process that helped them to transition to their dual role as carer and worker. Second, being a supporter who worked and cared meant constantly negotiating their dual role to meet the increasing EOL care needs of the older adult in advanced age. This was not easy; involving balancing work and care responsibilities, finding all available resources that allowed them to continue working and caring, and making difficult decisions. Third, participants reflected on their experiences of juggling work and care after the death of their older adult. They emphasised that negotiating work and care was demanding and future working carers require more support. Despite the challenges, participants knew that the care and dedication they provided to the older person made a difference to their EOL experience. Conclusion: This is the first study in New Zealand to explore the experiences of working carers for those in advanced age at EOL. Findings from this study provide valuable insight into an under-researched group, but further research is needed to build on existing knowledge. Future policy and service delivery should explore opportunities to better support community-based palliative care that responds to the needs of older adults in advanced age and their supporters
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