Regional Study of Care for the Dying: methods and sample characteristics.
about
Factors associated with home death for individuals who receive home support services: a retrospective cohort study.Perceptions of health care need in lung cancer. Can prospective surveys provide nationally representative data?Nationwide monitoring of end-of-life care via the Sentinel Network of General Practitioners in Belgium: the research protocol of the SENTI-MELC study.Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: does location matter?Ethical arguments for providing palliative care to non-cancer patients.Dying of lung cancer or cardiac failure: prospective qualitative interview study of patients and their carers in the community.Nationwide continuous monitoring of end-of-life care via representative networks of general practitioners in Europe.Effective partnerships in action: radical options or more of the same?Challenges and strategies in the administration of a population based mortality follow-back survey designA randomised controlled trial of postal versus interviewer administration of a questionnaire measuring satisfaction with, and use of, services received in the year before death.Respite in palliative care: a review and discussion of the literature.Determinants of care outcomes for patients who die in hospital in Ireland: a retrospective study.Te Pākeketanga: living and dying in advanced age--a study protocol.Factors Associated with Participation, Active Refusals and Reasons for Not Taking Part in a Mortality Followback Survey Evaluating End-of-Life Care.Dying at home or in an institution: perspectives of Dutch physicians and bereaved relatives.Improving palliative care provision for patients with heart failure.Caregivers for people with end-stage lung disease: characteristics and unmet needs in the whole population.How well do current instruments using bereaved relatives' views evaluate care for dying patients?Timing of Survey Administration After Hospice Patient Death: Stability of Bereaved Respondents.A systematic review of instruments related to family caregivers of palliative care patients.Assessing quality of care for the dying: the development and initial validation of a postal self-completion questionnaire for bereaved relatives.Outcome assessment instruments in palliative and hospice care--a review of the literature.Prevalence, distress, management, and relief of pain during the last 3 months of cancer patients' life. Results of an Italian mortality follow-back survey.Dying from cancer: results of a national population-based investigation.Accounts of carers' satisfaction with health care at the end of life: a comparison of first generation black Caribbeans and white patients with advanced disease.Dementia deaths in hospice: a retrospective case note audit.The challenge of patients' unmet palliative care needs in the final stages of chronic illness.Improving end-of-life care for patients with chronic heart failure: "Let's hope it'll get better, when I know in my heart of hearts it won't".What's the diagnosis? Organisational culture and palliative care delivery in residential aged care in New Zealand.The Views of Informal Carers' Evaluation of Services (VOICES): Toward an adaptation for the New Zealand bicultural context.Towards a culturally acceptable end-of-life survey questionnaire: a Bengali translation of VOICES.Palliative care services: what needs assessment?'All the services were excellent. It is when the human element comes in that things go wrong': dissatisfaction with hospital care in the last year of life.Dying from heart failure: lessons from palliative care. Many patients would benefit from palliative care at the end of their lives.Defining distinct caregiver subpopulations by intensity of end-of-life care provided.An investigation into the use of palliative care services by patients with prostate cancer.Human papilloma virus (HPV) status, p16INK4a, and p53 overexpression in epithelial malignant and borderline ovarian neoplasms.End of life care preferences among people of advanced age: LiLACS NZ.Symptoms experienced in the last six months of life in patients with end-stage heart failure.Understanding how a palliative-specific patient-reported outcome intervention works to facilitate patient-centred care in advanced heart failure: A qualitative study.
P2860
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P2860
Regional Study of Care for the Dying: methods and sample characteristics.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh-hant
name
Regional Study of Care for the Dying: methods and sample characteristics.
@en
Regional Study of Care for the Dying: methods and sample characteristics.
@nl
type
label
Regional Study of Care for the Dying: methods and sample characteristics.
@en
Regional Study of Care for the Dying: methods and sample characteristics.
@nl
prefLabel
Regional Study of Care for the Dying: methods and sample characteristics.
@en
Regional Study of Care for the Dying: methods and sample characteristics.
@nl
P2860
P1433
P1476
Regional Study of Care for the Dying: methods and sample characteristics.
@en
P2093
J Addington-Hall
M McCarthy
P2860
P356
10.1177/026921639500900105
P577
1995-01-01T00:00:00Z