582 results on '"Addington-Hall, Julia"'
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2. Assessing the Quality of Care for Dying Patients From the Bereaved Relatives' Perspective: Further Validation of “Evaluating Care and Health Outcomes–for the Dying”
3. A Survey of Joint and Muscle Aches, Pain, and Stiffness Comparing Women With and Without Breast Cancer
4. From ‘conductor’ to ‘second fiddle’: Older adult care recipients’ perspectives on transitions in family caring at hospital admission
5. Living into old age with the consequences of breast cancer
6. Challenges in transition from intervention to end of life care in intensive care: A qualitative study
7. Negotiated dying: A grounded theory of how nurses shape withdrawal of treatment in hospital critical care units
8. What methods do stakeholders prefer for feeding back performance data: a qualitative study in palliative care
9. Spiritual Needs In Health Care: May Be Distinct From Religious Ones And Are Integral To Palliative Care
10. Place of death in metropolitan regions: Metropolitan versus non-metropolitan variation in place of death in Belgium, The Netherlands and England
11. Measuring Quality Of Life: Who Should Measure Quality Of Life?
12. Randomised Controlled Trial Of Non-Directive Counselling, Cognitive-Behaviour Therapy, And Usual General Practitioner Care For Patients With Depression. I: Clinical Effectiveness
13. ‘You canʼt say, “what about me?” Iʼm not the one with cancer’: information and support needs of relatives
14. Palliative Care Needs to Be Provided on Basis of Need Rather than Diagnosis
15. A Randomised Controlled Trial of Postal versus Interviewer Administration of a Questionnaire Measuring Satisfaction with, and Use of, Services Received in the Year before Death
16. Dying from Heart Failure: Lessons from Palliative Care: Many Patients Would Benefit from Palliative Care at the End of Their Lives
17. ABC of Palliative Care: The Carers
18. Carers' health status: is it associated with their evaluation of the quality of palliative care?
19. What to eat when off treatment and living with involuntary weight loss and cancer: a systematic search and narrative review
20. Conflict rationalisation: How family members cope with a diagnosis of brain stem death
21. Nursing the dying within a generalist caseload: A focus group study of district nurses
22. What Facilitates or Impedes Family Communication Following Genetic Testing for Cancer Risk? A Systematic Review and Meta-Synthesis of Primary Qualitative Research
23. The palliative care needs of acute stroke patients: a prospective study of hospital admissions
24. Development and initial validation of a new outcome measure for hospice and palliative care: the St Christopherʼs Index of Patient Priorities (SKIPP)
25. Physiciansʼ experiences and perspectives regarding the use of continuous sedation until death for cancer patients in the context of psychological and existential suffering at the end of life
26. End-of-life care and achieving preferences for place of death in England: Results of a populationbased survey using the VOICES-SF questionnaire
27. Discontinuity of care at end of life: a qualitative exploration of OOH end of life care
28. Non-cancer patients as an under-served group
29. How do proxies' perceptions of patients' pain, anxiety, and depression change during the bereavement?
30. Place of death and use of health services in the last year of life
31. Outcomes After Unplanned Admission to Hospital in Older People: Ill-Defined Conditions as Potential Indicators of the Frailty Trajectory
32. What is important to measure in the last months and weeks of life?: A modified nominal group study
33. Palliative Care Research in the Face of Uncertainty
34. Secondary analysis of qualitative data: a valuable method for exploring sensitive issues with an elusive population?
35. End-Stage Renal Disease: A New Trajectory of Functional Decline in the Last Year of Life
36. Survey research: methods of data collection, questionnaire design and piloting
37. How to write a paper
38. Survey Design
39. Introduction
40. Place of Death of Older Persons with Dementia. A Study in Five European Countries
41. End-of-life issues in acute stroke care: a qualitative study of the experiences and preferences of patients and families
42. The experiences of older adults in the community dying from cancer and non-cancer causes: a national survey of bereaved relatives
43. Memory in depression
44. Experiences of hospital care reported by bereaved relatives of patients after a stroke: a retrospective survey using the VOICES questionnaire
45. Feeding back survey research findings within palliative care. Findings from qualitative research
46. Patient descriptions of breathlessness in heart failure
47. Improving district nursesʼ confidence and knowledge in the principles and practice of palliative care
48. The quality and adequacy of care received at home in the last 3 months of life by people who died following a stroke: a retrospective survey of surviving family and friends using the Views of Informal Carers Evaluation of Services questionnaire
49. How people with motor neurone disease talk about living with their illness: a narrative study
50. Supportive and palliative care research collaboratives in the United Kingdom: an unnatural experiment?
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