| Unmet care needs of advanced cancer patients and their informal caregivers: a systematic review |
36 |
| Advance care planning in dementia: recommendations for healthcare professionals |
18 |
| Exploring the meaning and practice of self-care among palliative care nurses and doctors: a qualitative study |
15 |
| Just too busy living in the moment and surviving: barriers to accessing health care for structurally vulnerable populations at end-of-life |
13 |
| Whose job? The staffing of advance care planning support in twelve international healthcare organizations: a qualitative interview study |
11 |
| Experiences and challenges of home care nurses and general practitioners in home-based palliative care - a qualitative study |
11 |
| Patient's and health care provider's perspectives on music therapy in palliative care - an integrative review |
9 |
| Symptom management, nutrition and hydration at end-of-life: a qualitative exploration of patients', carers' and health professionals' experiences and further research questions |
9 |
| Paediatric palliative care improves patient outcomes and reduces healthcare costs: evaluation of a home-based program |
8 |
| Exploring the vagueness of Religion & Spirituality in complex pediatric decisionmaking: a qualitative study |
8 |
| Telehealth in palliative care is being described but not evaluated: a systematic review |
8 |
| Never at ease - family carers within integrated palliative care: a multinational, mixed method study |
8 |
| Palliative care specialists' perceptions concerning referral of haematology patients to their services: findings from a qualitative study |
8 |
| Integrating palliative care in long-term care facilities across Europe (PACE): protocol of a cluster randomized controlled trial of the 'PACE Steps to Success' intervention in seven countries |
8 |
| A painful experience of limited understanding: healthcare professionals' experiences with palliative care of people with severe dementia in Norwegian nursing homes |
8 |
| The contribution of a MOOC to community discussions around death and dying |
8 |
| Using co-design to develop an intervention to improve communication about the heart failure trajectory and end-of-life care |
7 |
| Systematic development and adjustment of the German version of the Supportive and Palliative Care Indicators Tool (SPICT-DE) |
7 |
| Key features of palliative care service delivery to Indigenous peoples in Australia, New Zealand, Canada and the United States: a comprehensive review |
7 |
| Barriers and facilitators to the implementation of a paediatric palliative care team |
7 |
| Health-related quality of life and its socio-economic and cultural predictors among advanced cancer patients: evidence from the APPROACH cross-sectional survey in Hyderabad-India |
7 |
| Differences in do-not-resuscitate orders, hospice care utilization, and late referral to hospice care between cancer and non-cancer decedents in a tertiary Hospital in Taiwan between 2010 and 2015: a hospital-based observational study |
7 |
| Chemotherapy and palliative care near end-of life: examining the appropriateness at a cancer institute for colorectal cancer patients |
6 |
| Implementation of knowledge-based palliative care in nursing homes and pre-post post evaluation by cross-over design: a study protocol |
6 |
| Challenges in a six-phase process of questionnaire adaptation: findings from the French translation of the Integrated Palliative care Outcome Scale |
6 |
| The second patient? Family members of cancer patients and their role in end-of-life decision making |
6 |
| Voices that matter: end-of-life care in two acute hospitals from the perspective of bereaved relatives |
6 |
| Comparing unplanned and potentially planned home deaths: a population-based cross-sectional study |
6 |
| The 'lived experience' of palliative care patients in one acute hospital setting - a qualitative study |
6 |
| Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
6 |
| Study protocol for a multi-methods study: SAVOIR - evaluation of specialized outpatient palliative care (SAPV) in Germany: outcomes, interactions, regional differences |
6 |
| Use of hospital palliative care according to the place of death and disease one year before death in 2013: a French national observational study |
6 |
| Palliative radiotherapy near the end of life |
6 |
| Professionals' perceptions and current practices of integrated palliative care in chronic heart failure and chronic obstructive pulmonary disease: a qualitative study in Belgium |
6 |
| Assigned nurses and a professional relationship: a qualitative study of COPD patients' perspective on a new palliative outpatient structure named CAPTAIN |
6 |
| Palliative care for people with schizophrenia: a qualitative study of an under-serviced group in need |
6 |
| Are care staff equipped for end-of-life communication? A cross-sectional study in long-term care facilities to identify determinants of self-efficacy |
6 |
| Timing of palliative care referral and aggressive cancer care toward the end-of-life in pancreatic cancer: a retrospective, single-center observational study |
5 |
| Advance care planning with patients on hemodialysis: an implementation study |
5 |
| Perceptions of trained laypersons in end-of-life or advance care planning conversations: a qualitative meta-synthesis |
5 |
| Advance care planning after hospital discharge: qualitative analysis of facilitators and barriers from patient interviews |
5 |
| It doesn't exist.: negotiating palliative care from a culturally and linguistically diverse patient and caregiver perspective |
5 |
| Residential aged care residents and components of end of life care in an Australian hospital |
5 |
| Palliative care for homeless people: a systematic review of the concerns, care needs and preferences, and the barriers and facilitators for providing palliative care |
5 |
| The availability and effectiveness of tools supporting shared decision making in metastatic breast cancer care: a review |
5 |
| A qualitative study of health care professionals' views and experiences of paediatric advance care planning |
5 |
| Psychological burden in family caregivers of patients with advanced cancer at initiation of specialist inpatient palliative care |
5 |
| Self-competence in death work among health and social care workers: a region-wide survey in Hong Kong |
5 |
| The experience of caring for patients at the end-of-life stage in non-palliative care settings: a qualitative study |
5 |
| Facilitating successful implementation of a person-centred intervention to support family carers within palliative care: a qualitative study of the CarerSupport Needs Assessment Tool (CSNAT) intervention |
5 |
