202 related articles for article (PubMed ID: 28062338)
21. Profiles of family caregivers of patients at the end of life at home: a Q-methodological study into family caregiver' support needs.
Bijnsdorp FM; Pasman HRW; Boot CRL; van Hooft SM; van Staa A; Francke AL
BMC Palliat Care; 2020 Apr; 19(1):51. PubMed ID: 32316948
[TBL] [Abstract][Full Text] [Related]
22. Young caregivers in the end-of-life setting: a population-based profile of an emerging group.
Burns CM; LeBlanc TW; Abernethy A; Currow D
J Palliat Med; 2010 Oct; 13(10):1225-35. PubMed ID: 20858060
[TBL] [Abstract][Full Text] [Related]
23. Place of death and the differences in patient quality of death and dying and caregiver burden.
Kinoshita H; Maeda I; Morita T; Miyashita M; Yamagishi A; Shirahige Y; Takebayashi T; Yamaguchi T; Igarashi A; Eguchi K
J Clin Oncol; 2015 Feb; 33(4):357-63. PubMed ID: 25534381
[TBL] [Abstract][Full Text] [Related]
24. Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregivers.
Holm M; Carlander I; Fürst CJ; Wengström Y; Årestedt K; Öhlen J; Henriksson A
BMC Palliat Care; 2015 Apr; 14():16. PubMed ID: 25903781
[TBL] [Abstract][Full Text] [Related]
25. Barriers to palliative care in people with chronic obstructive pulmonary disease in home care: A qualitative study of the perspective of professional caregivers.
Mousing CA; Timm H; Lomborg K; Kirkevold M
J Clin Nurs; 2018 Feb; 27(3-4):650-660. PubMed ID: 28722811
[TBL] [Abstract][Full Text] [Related]
26. Exploring the Support Needs of Family Caregivers of Patients with Brain Cancer Using the CSNAT: A Comparative Study with Other Cancer Groups.
Aoun SM; Deas K; Howting D; Lee G
PLoS One; 2015; 10(12):e0145106. PubMed ID: 26679505
[TBL] [Abstract][Full Text] [Related]
27. Feasibility of a rural palliative supportive service.
Pesut B; Hooper BP; Robinson CA; Bottorff JL; Sawatzky R; Dalhuisen M
Rural Remote Health; 2015; 15(2):3116. PubMed ID: 25939666
[TBL] [Abstract][Full Text] [Related]
28. The preferences and perspectives of family caregivers towards place of care for their relatives at the end-of-life. A systematic review and thematic synthesis of the qualitative evidence.
Woodman C; Baillie J; Sivell S
BMJ Support Palliat Care; 2016 Dec; 6(4):418-429. PubMed ID: 25991565
[TBL] [Abstract][Full Text] [Related]
29. Inequity in the provision of and access to palliative care for cancer patients. Results from the Italian survey of the dying of cancer (ISDOC).
Beccaro M; Costantini M; Merlo DF;
BMC Public Health; 2007 Apr; 7():66. PubMed ID: 17466064
[TBL] [Abstract][Full Text] [Related]
30. Caring at the end of life: do cancer caregivers differ from other caregivers?
Girgis A; Abernethy AP; Currow DC
BMJ Support Palliat Care; 2015 Dec; 5(5):513-7. PubMed ID: 24644201
[TBL] [Abstract][Full Text] [Related]
31. Gender and family caregiving at the end-of-life in the context of old age: A systematic review.
Morgan T; Ann Williams L; Trussardi G; Gott M
Palliat Med; 2016 Jul; 30(7):616-24. PubMed ID: 26814213
[TBL] [Abstract][Full Text] [Related]
32. Vulnerability and access to care for South Asian Sikh and Muslim patients with life limiting illness in Scotland: prospective longitudinal qualitative study.
Worth A; Irshad T; Bhopal R; Brown D; Lawton J; Grant E; Murray S; Kendall M; Adam J; Gardee R; Sheikh A
BMJ; 2009 Feb; 338():b183. PubMed ID: 19190015
[TBL] [Abstract][Full Text] [Related]
33. The role of the Carer Support Needs Assessment Tool in palliative home care: A qualitative study of practitioners' perspectives of its impact and mechanisms of action.
Ewing G; Austin L; Grande G
Palliat Med; 2016 Apr; 30(4):392-400. PubMed ID: 26199133
[TBL] [Abstract][Full Text] [Related]
34. How should we talk about palliative care, death and dying? A qualitative study exploring perspectives from caregivers of people with advanced cancer.
Collins A; McLachlan SA; Philip J
Palliat Med; 2018 Apr; 32(4):861-869. PubMed ID: 29235421
[TBL] [Abstract][Full Text] [Related]
35. Hospital postdischarge intervention trialled with family caregivers of older people in Western Australia: potential translation into practice.
Aoun SM; Stegmann R; Slatyer S; Hill KD; Parsons R; Moorin R; Bronson M; Walsh D; Toye C
BMJ Open; 2018 Nov; 8(11):e022747. PubMed ID: 30413506
[TBL] [Abstract][Full Text] [Related]
36. Strategies for Enhancing Family Participation in Research in the ICU: Findings From a Qualitative Study.
Dotolo D; Nielsen EL; Curtis JR; Engelberg RA
J Pain Symptom Manage; 2017 Aug; 54(2):226-230.e1. PubMed ID: 28438584
[TBL] [Abstract][Full Text] [Related]
37. 'You only have one chance to get it right': A qualitative study of relatives' experiences of caring at home for a family member with terminal cancer.
Totman J; Pistrang N; Smith S; Hennessey S; Martin J
Palliat Med; 2015 Jun; 29(6):496-507. PubMed ID: 25634637
[TBL] [Abstract][Full Text] [Related]
38. Palliative family caregivers' accounts of health care experiences: the importance of "security".
Funk LM; Allan DE; Stajduhar KI
Palliat Support Care; 2009 Dec; 7(4):435-47. PubMed ID: 19939306
[TBL] [Abstract][Full Text] [Related]
39. Providing Informal Care in Terminal Illness: An Analysis of Preferences for Support Using a Discrete Choice Experiment.
Hall J; Kenny P; Hossain I; Street DJ; Knox SA
Med Decis Making; 2014 Aug; 34(6):731-45. PubMed ID: 23942657
[TBL] [Abstract][Full Text] [Related]
40. 'It all depends!': A qualitative study of preferences for place of care and place of death in terminally ill patients and their family caregivers.
Gerber K; Hayes B; Bryant C
Palliat Med; 2019 Jul; 33(7):802-811. PubMed ID: 31046580
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]