Impact of a hospice rapid response service on preferred place of death, and costs
Authors (first, second and last of 5)
Volume 14, issue 1, December 2015
75 articles in this issue
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Te Pākeketanga: living and dying in advanced age - a study protocol
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Benefits and resource implications of family meetings for hospitalized palliative care patients: research protocol
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The characteristics of patients who discontinue their dying process – an observational study at a single university hospital centre
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The prevalence in the general population of advance directives on euthanasia and discussion of end-of-life wishes: a nationwide survey
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Counseling for personal care options at neonatal end of life: a quantitative and qualitative parent survey
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The relationship between pain management and psychospiritual distress in patients with advanced cancer following admission to a palliative care unit
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Palliative care consultation services in hospitals in the Netherlands: the design of the COMPASS study
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Living with AIDS in Uganda: a qualitative study of patients’ and families’ experiences following referral to hospice
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Exploring end of life priorities in Saudi males: usefulness of Q-methodology
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INSPIRE (INvestigating Social and PractIcal suppoRts at the End of life): Pilot randomised trial of a community social and practical support intervention for adults with life-limiting illness
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The development of a complex intervention in China: the ‘Caring for Couples Coping with Cancer “4Cs” Programme’ to support couples coping with cancer
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Pragmatic cluster randomised controlled trial of facilitated family case conferencing compared with usual care for improving end of life care and outcomes in nursing home residents with advanced dementia and their families: the IDEAL study protocol
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Is shared decision-making vanishing at the end-of-life? A descriptive and qualitative study of advanced cancer patients’ involvement in specific therapies decision-making
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Palliative care professionals’ willingness to perform euthanasia or physician assisted suicide
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Determinants of favourable opinions about euthanasia in a sample of French physicians
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Palliative enteral feeding for patients with malignant esophageal obstruction: a retrospective study
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Paediatric palliative care: recommendations for treatment of symptoms in the Netherlands
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Identification of the palliative phase in people with dementia: a variety of opinions between healthcare professionals
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Evaluating the systematic implementation of the ‘Let Me Decide’ advance care planning programme in long term care through focus groups: staff perspectives
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Patients’ perceptions of palliative care: adaptation of the Quality from the Patient’s Perspective instrument for use in palliative care, and description of patients’ perceptions of care received
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Variation in physician recommendations, knowledge and perceived roles regarding provision of end-of-life care
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UK quality statements on end of life care in dementia: a systematic review of research evidence
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Promoting an ethic of engagement in pediatric palliative care research
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Exploring barriers to assessment of bereavement risk in palliative care: perspectives of key stakeholders
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Incidence of pain flare following palliative radiotherapy for symptomatic bone metastases: multicenter prospective observational study
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Strategies to implement evidence into practice to improve palliative care: recommendations of a nominal group approach with expert opinion leaders
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Implementation of a Care Pathway for Primary Palliative Care in 5 research clusters in Belgium: quasi-experimental study protocol and innovations in data collection (pro-SPINOZA)
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Enhancing legacy in palliative care: study protocol for a randomized controlled trial of Dignity Therapy focused on positive outcomes
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A mobile hospice nurse teaching team’s experience: training care workers in spiritual and existential care for the dying - a qualitative study
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End of life care interventions for people with dementia in care homes: addressing uncertainty within a framework for service delivery and evaluation
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Design of, and enrollment in, the palliative care communication research initiative: a direct-observation cohort study
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Strategies for effective goals of care discussions and decision-making: perspectives from a multi-centre survey of Canadian hospital-based healthcare providers
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Efficacy of palliative radiotherapy for gastric bleeding in patients with unresectable advanced gastric cancer: a retrospective cohort study
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Priorities for global research into children’s palliative care: results of an International Delphi Study
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Communication between family carers and health professionals about end-of-life care for older people in the acute hospital setting: a qualitative study
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Comparison of terminally ill cancer- vs. non-cancer patients in specialized palliative home care in Germany – a single service analysis
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Expert views on the factors enabling good end of life care for people with dementia: a qualitative study
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Shared decision-making in end-stage renal disease: a protocol for a multi-center study of a communication intervention to improve end-of-life care for dialysis patients
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Workings of the human spirit in palliative care situations: a consensus model from the Chaplaincy Research Consortium
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Place of death of people living with Parkinson’s disease: a population-level study in 11 countries
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A mixed method feasibility study of a patient- and family-centred advance care planning intervention for cancer patients
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‘I want to feel at home’: establishing what aspects of environmental design are important to people with dementia nearing the end of life
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