421 results on '"Ingleton, Christine"'
Search Results
2. Predictors of patient-related benefit, burden and feeling safe in relation to hospital admissions in palliative care: A cross-sectional survey
3. What do we know about different models of providing palliative care? Findings from a systematic review of reviews
4. Lay and professional stakeholder involvement in scoping palliative care issues: Methods used in seven European countries
5. Transitions to palliative care in acute hospitals in England: qualitative study
6. Recounting Mathematical Experiences: Emotions in Mathematics Learning.
7. Research passports don't help
8. Care pathways for older people in need of palliative care
9. Gender and Learning: Does Emotion Make a Difference?
10. A qualitative study exploring the benefits of hospital admissions from the perspectives of patients with palliative care needs
11. ‘You have to be mindful of whose story it isʼ: The challenges of undertaking life story work with people with dementia and their family carers
12. Gender and Learning: Does Emotion Make a Difference?
13. Economic impact of hospitalisations among patients in the last year of life: An observational study
14. Autonomy and choice in palliative care: time for a new model?
15. Patient and family experiences of palliative care in hospital: What do we know? An integrative review
16. The role of the nurse in palliative Care settings in a global context: Sheila Payne and colleagues examine the differences and similarities in end-of-life care provided in different countries which, while broadly based on the same models, varies according to resources, cultural attitudes and public health policies
17. Supporting people who have dementia to die with dignity: people with dementia being cared for in acute settings benefit from a relationship-centred approach to their end-of-life care, argue Tony Ryan and colleagues
18. Awareness contexts revisited: indeterminacy in initiating discussions at the end-of-life
19. Evaluation of a scheme to enhance palliative cancer care in rural Wales
20. A narrative literature review of older peopleʼs cancer pain experience
21. Extent of palliative care need in the acute hospital setting: A survey of two acute hospitals in the UK
22. Silent issues for international postgraduate research students: Emotion and agency in academic success
23. Barriers and facilitators to the receipt of palliative care for people with dementia: The views of medical and nursing staff
24. The hospital environment for end of life care of older adults and their families: an integrative review
25. ‘Thatʼs part of everybodyʼs job’: the perspectives of health care staff in England and New Zealand on the meaning and remit of palliative care
26. The role of health care assistants in supporting district nurses and family carers to deliver palliative care at home: findings from an evaluation project
27. An exploration of spiritual needs of Taiwanese patients with advanced cancer during the therapeutic processes
28. Most hospices and palliative care programmes in the USA serve people with dementia; lack of awareness, need for respite care and reimbursement policies are the main barriers to providing this care
29. Barriers to providing palliative care for older people in acute hospitals
30. Mixed methods for evaluation research
31. Unresolved Power for Feminist Researchers Employing Memory-Work
32. Commentary on Green AJ & De-Vries K (2010) Cannabis use in palliative care – an examination of the evidence and the implications for nurses. Journal of Clinical Nursing 19, 2454–2462
33. Research passports havenʼt streamlined processes
34. Actively involving people with dementia in qualitative research
35. The use of life story work with people with dementia to enhance person-centred care
36. Commentary on Huang Y, Yates P & Prior D (2009) Factors influencing oncology nurses’ approach to accommodating cultural needs in palliative care. Journal of Clinical Nursing 18, 3421–3429
37. Commentary on Cronfalk BS, Ternstedt BM & Strang P (2009) ‘Soft tissue massage: early intervention for relatives whose family members died in palliative cancer care’. Journal of Clinical Nursing 19, 1040–1048
38. Commentary on Metcalfe A, Pumphrey R & Clifford C (2009) Hospice nurses’ and genetics: implications for end-of-life care’. Journal of Clinical Nursing 19, 192–207
39. Commentary on Tang W-R (2009) Hospice family caregiversʼ quality of life. Journal of Clinical Nursing 18, 2563–2572
40. Commentary on Hewison A, Badger F, Clifford C & Thomas K (2009) Delivering ‘Gold Standards’ in end-of-life care in care homes: a question of teamwork? Journal of Clinical Nursing 18, 1757-1766
41. Editorial: The beginning of the End (of Life Care Strategy)
42. Commentary on Birch D and Draper J (2008) A critical literature review exploring the challenges of delivering effective palliative care to older people with dementia. Journal of Clinical Nursing 17, 1144–1163
43. Carer satisfaction with end-of-life care in Powys, Wales: a cross-sectional survey
44. Response to: Watsonʼs Guest Editorial ‘Scientific methods are the only credible way forward for nursing research’, Journal of Advanced Nursing 43, 219–220
45. Specialist palliative care: patientsʼ experiences
46. Needs assessment for palliative care: three projects compared
47. Support and supervision in palliative care research
48. Circumstances of hospital admissions in palliative care: A cross-sectional survey of patients admitted to hospital with palliative care needs
49. STAKEHOLDER INVOLVEMENT THROUGHOUT HEALTH TECHNOLOGY ASSESSMENT: AN EXAMPLE FROM PALLIATIVE CARE
50. Predictors of patient-related benefit, burden and feeling safe in relation to hospital admissions in palliative care: A cross-sectional survey
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