A comparison of the quality of care provided to cancer patients in the UK in the last three months of life in in-patient hospices compared with hospitals, from the perspective of bereaved relatives: results from a survey using the VOICES questionnai
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End-of-life care pathways as tools to promote and support a good death: a critical commentary.Quality of life, psychological burden, needs, and satisfaction during specialized inpatient palliative care in family caregivers of advanced cancer patients.Nationwide continuous monitoring of end-of-life care via representative networks of general practitioners in Europe.Determinants of care outcomes for patients who die in hospital in Ireland: a retrospective study.The prevalence of severe pain, its etiopathological characteristics and treatment profile of patients referred to a tertiary cancer care pain clinic.No Negative Impact of Palliative Sedation on Relatives' Experience of the Dying Phase and Their Wellbeing after the Patient's Death: An Observational Study.Inpatient transfer to a care home for end-of-life care: What are the views and experiences of patients and their relatives? A systematic review and narrative synthesis of the UK literature.Patients' perceptions of palliative care quality in hospice inpatient care, hospice day care, palliative units in nursing homes, and home care: a cross-sectional study.Does the 'Liverpool Care Pathway' facilitate an improvement in quality of care for dying cancer patients?Hospice caregivers' experiences with pain management: "I'm not a doctor, and I don't know if I helped her go faster or slower".Measuring Experience With End-of-Life Care: A Systematic Literature ReviewHow well is cancer pain treated?Perceived risks around choice and decision making at end-of-life: a literature review.Assessing quality of care for the dying: the development and initial validation of a postal self-completion questionnaire for bereaved relatives.Initiating end-of-life care pathways: a discussion paper.Patient and family experiences of palliative care in hospital: what do we know? An integrative review.How do researchers conceive of spousal grief after cancer? A systematic review of models used by researchers to study spousal grief in the cancer context.Dignity and patient-centred care for people with palliative care needs in the acute hospital setting: A systematic review.The care experiences of patients who die in residential hospice: A qualitative analysis of the last three months of life from the views of bereaved caregivers.Understanding the bereavement care roles of nurses within acute care: a systematic review.The Experience of Hospital Death.Palliative Care Experience in the Last 3 Months of Life: A Quantitative Comparison of Care Provided in Residential Hospices, Hospitals, and the Home From the Perspectives of Bereaved Caregivers.End-of-life care in residential care homes: a retrospective study of the perspectives of family members using the VOICES questionnaire.Hospital care following emergency admission: a critical incident case study of the experiences of patients with advanced lung cancer and Chronic Obstructive Pulmonary Disease.The Views of Informal Carers' Evaluation of Services (VOICES): Toward an adaptation for the New Zealand bicultural context.Influence of caregiver personality on the burden of family caregivers of terminally ill cancer patients.Validation of a modified VOICES survey to measure end-of-life care quality: the CaregiverVoice survey.Using maps and funnel plots to explore variation in place of death from cancer within London, 2002-2007.Pain: a quality of care issue during patients' admission to hospital.Measuring Patient-Centeredness of Care for Seriously Ill Individuals: Challenges and Opportunities for Accountability Initiatives.The relationships between the combination of person- and organization-related conditions and patients' perceptions of palliative care quality.Adaptation and validation of the VOICES (SF) questionnaire - for evaluation of end-of-life care in Sweden.Measuring the quality of end-of-life care: Development, testing, and cultural validation of the Danish version of Views of Informal Carers' Evaluation of Services-Short Form.Assessing needs of family members of inpatients with advanced cancer.Achieving Goal-Concordant Care: A Conceptual Model and Approach to Measuring Serious Illness Communication and Its Impact.A quality registers impact on community nurses' in end-of-life care - a grounded theory study.Bereaved relatives' views about participating in cancer research.Privacy and dignity in a hospice environment-the development of a clinical audit.Palliative care team consultation and quality of death and dying in a university hospital: A secondary analysis of a prospective studyResearch in public health and end-of-life care – Building on the past and developing the new
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P2860
A comparison of the quality of care provided to cancer patients in the UK in the last three months of life in in-patient hospices compared with hospitals, from the perspective of bereaved relatives: results from a survey using the VOICES questionnai
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2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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name
A comparison of the quality of ...... y using the VOICES questionnai
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A comparison of the quality of ...... y using the VOICES questionnai
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type
label
A comparison of the quality of ...... y using the VOICES questionnai
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A comparison of the quality of ...... y using the VOICES questionnai
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prefLabel
A comparison of the quality of ...... y using the VOICES questionnai
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A comparison of the quality of ...... y using the VOICES questionnai
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P2860
P356
P1433
P1476
A comparison of the quality of ...... y using the VOICES questionnai
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P2093
A C O'Callaghan
J M Addington-Hall
P2860
P304
P356
10.1177/0269216309102525
P577
2009-02-27T00:00:00Z