211 results on '"Higginson, Irene J"'
Search Results
2. Deaths at home, area-based deprivation and the effect of the Covid-19 pandemic: An analysis of mortality data across four nations
3. Face and content validity, acceptability, feasibility, and implementability of a novel outcome measure for children with life-limiting or life-threatening illness in three sub-Saharan African countries
4. Experiences of staff providing specialist palliative care during COVID-19: a multiple qualitative case study
5. Understanding the impact of the Covid-19 pandemic on delivery of rehabilitation in specialist palliative care services: An analysis of the CovPall-Rehab survey data
6. Changes in mortality patterns and place of death during the COVID-19 pandemic: A descriptive analysis of mortality data across four nations
7. Identification of palliative care needs among people with dementia and its association with acute hospital care and community service use at the end-of-life: A retrospective cohort study using linked primary, community and secondary care data
8. Preparedness to Face the COVID-19 Pandemic in Hospice and Palliative Care Services in the Asia-Pacific Region: A Rapid Online Survey
9. ‘Necessity is the mother of invention’: Specialist palliative care service innovation and practice change in response to COVID-19. Results from a multinational survey (CovPall)
10. Relationships between prolonged physical and social isolation during the COVID-19 pandemic, reduced physical activity and disability in activities of daily living among people with advanced respiratory disease
11. Changing patterns of mortality during the COVID-19 pandemic: Population-based modelling to understand palliative care implications
12. Response and role of palliative care during the COVID-19 pandemic: A national telephone survey of hospices in Italy
13. Towards person-centred quality care for children with life-limiting and life-threatening illness: Self-reported symptoms, concerns and priority outcomes from a multi-country qualitative study
14. Drivers of care costs and quality in the last 3 months of life among older people receiving palliative care: A multinational mortality follow-back survey across England, Ireland and the United States
15. Short-term integrated rehabilitation for people with newly diagnosed thoracic cancer: a multi-centre randomized controlled feasibility trial
16. End-of-life care and place of death in adults with serious mental illness: A systematic review and narrative synthesis
17. Establishing key criteria to define and compare models of specialist palliative care: A mixed-methods study using qualitative interviews and Delphi survey
18. A brief, patient- and proxy-reported outcome measure in advanced illness: Validity, reliability and responsiveness of the Integrated Palliative care Outcome Scale (IPOS)
19. Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique
20. Symptoms and anxiety predict declining health-related quality of life in multiple myeloma: A prospective, multi-centre longitudinal study
21. Predicting outcomes following holistic breathlessness services: A pooled analysis of individual patient data
22. Recommendations for services for people living with chronic breathlessness in advanced disease: Results of a transparent expert consultation
23. Finding a ‘new normal’ following acute illness: A qualitative study of influences on frail older people’s care preferences
24. Symptom prevalence and quality of life of patients with end-stage liver disease: A systematic review and meta-analysis
25. Use of mirtazapine in patients with chronic breathlessness: A case series
26. Is end-of-life care a priority for policymakers? Qualitative documentary analysis of health care strategies
27. Patient empowerment, what does it mean for adults in the advanced stages of a life-limiting illness: A systematic review using critical interpretive synthesis
28. A framework for complexity in palliative care: A qualitative study with patients, family carers and professionals
29. Understanding how a palliative-specific patient-reported outcome intervention works to facilitate patient-centred care in advanced heart failure: A qualitative study
30. What is the impact of population ageing on the future provision of end-of-life care? Population-based projections of place of death
31. Editorial
32. Strategies used in improving and assessing the level of reporting of implementation fidelity in randomised controlled trials of palliative care complex interventions: A systematic review
33. Seeing is believing – healthcare professionals’ perceptions of a complex intervention to improve care towards the end of life: A qualitative interview study
34. Randomised clinical trial of early specialist palliative care plus standard care versus standard care alone in patients with advanced cancer: The Danish Palliative Care Trial
35. Does the EQ-5D capture the concerns measured by the Palliative care Outcome Scale? Mapping the Palliative care Outcome Scale onto the EQ-5D using statistical methods
36. “Keep All Thee ‘Til the End”: Reclaiming the Lifeworld for Patients in the Hospice Setting
37. Variations in the cost of formal and informal health care for patients with advanced chronic disease and refractory breathlessness: A cross-sectional secondary analysis
38. Breathlessness during daily activity: The psychometric properties of the London Chest Activity of Daily Living Scale in patients with advanced disease and refractory breathlessness
39. Discovering the hidden benefits of cognitive interviewing in two languages: The first phase of a validation study of the Integrated Palliative care Outcome Scale
40. Patients’ experiences of a new integrated breathlessness support service for patients with refractory breathlessness: Results of a postal survey
41. Past trends and projections of hospital deaths to inform the integration of palliative care in one of the most ageing countries in the world
42. EAPC White Paper on outcome measurement in palliative care: Improving practice, attaining outcomes and delivering quality services – Recommendations from the European Association for Palliative Care (EAPC) Task Force on Outcome Measurement
43. Home care by general practitioners for cancer patients in the last 3 months of life: An epidemiological study of quality and associated factors
44. The changing demographics of inpatient hospice death: Population-based cross-sectional study in England, 1993–2012
45. Results of a transparent expert consultation on patient and public involvement in palliative care research
46. Patient and carer experiences of clinical uncertainty and deterioration, in the face of limited reversibility: A comparative observational study of the AMBER care bundle
47. ‘Less ticking the boxes, more providing support’: A qualitative study on health professionals’ concerns towards the Liverpool Care of the Dying Pathway
48. Characteristics of episodic breathlessness as reported by patients with advanced chronic obstructive pulmonary disease and lung cancer: Results of a descriptive cohort study
49. What Next in Refractory Breathlessness? Breathlessness? Research Questions for Palliative Care
50. Patterns of dignity-related distress at the end of life: A cross-sectional study of patients with advanced cancer and care home residents
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