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2. A review of paper-based advance care planning aids.

3. A cross-sectional study on advance care planning documentation attitudes during national advance care planning week in a South-East Asian country.

4. The elements of end-of-life care provision in paediatric intensive care units: a systematic integrative review.

5. Defining and quantifying population-level need for children's palliative care: findings from a rapid scoping review.

6. Paediatric oncologists' perspectives on Strategic solutions to develop Integrated Cancer Palliative Care: feedback intervention theory as an explanatory Framework.

7. Healthcare practitioners' perspectives of providing palliative care to patients from culturally diverse backgrounds: a qualitative systematic review.

8. How does ethnicity affect presence of advance care planning in care records for individuals with advanced disease? A mixed-methods systematic review.

9. Community-based palliative care needs and barriers to access among cancer patients in rural north India: a Participatory action research.

10. Non-invasive technology to assess hydration status in advanced cancer to explore relationships between fluid status and symptoms: an observational study using bioelectrical impedance analysis.

11. Palliative and end-of-life care research in Scotland 2006-2015: a systematic scoping review.

12. Factors related to advance directives completion among cancer patients: a systematic review.

13. Eye donation in hospice and hospital palliative care settings: perceptions, practice, and service development needs – findings from a national survey.

14. Dignity of patients with palliative needs in the Middle East: an integrative review.

15. Palliative care and new technologies. The use of smart sensor technologies and its impact on the Total Care principle.

16. A nationwide neurosurgical inter-disciplinary service for cancer-related refractory pain.

17. Children with palliative care needs – the landscape of the nordic countries.

18. Does ethnicity affect pain management for people with advanced disease? A mixed methods cross-national systematic review of ‘very high’ Human Development Index English-speaking countries.

19. Rural healthcare professionals' participation in Medical Assistance in Dying (MAiD): beyond a binary decision.

20. Distinct experiences and care needs of advanced cancer patients with good ECOG performance status: a qualitative phenomenological study.

21. Assisted dying: principles, possibilities, and practicalities. An English physician's perspective.

22. What helps or hinders effective end-of-life care in adult intensive care units in Middle Eastern countries? A systematic review.

23. A Dutch paediatric palliative care guideline: a systematic review and evidence-based recommendations for symptom treatment.

24. "Tie your camel first, then rely on God": reconceptualizing Javanese Islamic values to support palliative care at home.

25. Experiential training course on spirituality for multidisciplinary palliative care teams in a hospital setting: a feasibility study.

26. How blogs support the transfer of knowledge into practice in the field of dementia palliative care: a survey of facilitators and barriers.

27. What should we report? Lessons learnt from the development and implementation of serious adverse event reporting procedures in non-pharmacological trials in palliative care.

28. A scoping review of the evidence for community-based dementia palliative care services and their related service activities.

29. Simulation-based learning in palliative care in postgraduate nursing education: a scoping review.

30. Telehealth in palliative care is being described but not evaluated: a systematic review.

31. Non-invasive ventilation in the care of patients with chronic obstructive pulmonary disease with palliative care needs: a scoping review.

32. Measuring palliative care integration in Malawi through service provision, access, and training indicators: the Waterloo Coalition Initiative.

33. Taiwanese family members' bereavement experience following an expected death: a systematic review and narrative synthesis.

34. Parents' hope in perinatal and neonatal palliative care: a scoping review.

35. Palliative care for children: methodology for the development of a national clinical practice guideline.

36. Experiences and access of palliative and end of life care for older people from minority ethnic groups: a scoping review.

39. Physicians' attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence.

40. A new scale assessing the stressors and rewards of children's hospice work.

41. Preferences and end of life care for residents of aged care facilities: a mixed methods study.

43. Exploration of the acceptability and usability of advance care planning tools in long term care homes.

44. Equity and the financial costs of informal caregiving in palliative care: a critical debate.

45. An exploration of the experiences of professionals supporting patients approaching the end of life in medicines management at home. A qualitative study.

46. The needs, models of care, interventions and outcomes of palliative care in the Caribbean: a systematic review of the evidence.

47. Public perceptions of advance care planning (ACP) from an international perspective: a scoping review.

48. Could palliative sedation be seen as unnamed euthanasia?: a survey among healthcare professionals in oncology.

49. Impact of information and communication software on multiprofessional team collaboration in outpatient palliative care – a qualitative study on providers' perspectives.

50. Context and mechanisms that enable implementation of specialist palliative care Needs Rounds in care homes: results from a qualitative interview study.