472 related articles for article (PubMed ID: 28367679)
1. Initial perceptions of palliative care: An exploratory qualitative study of patients with advanced cancer and their family caregivers.
Collins A; McLachlan SA; Philip J
Palliat Med; 2017 Oct; 31(9):825-832. PubMed ID: 28367679
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Communication about palliative care: A phenomenological study exploring patient views and responses to its discussion.
Collins A; McLachlan SA; Philip J
Palliat Med; 2018 Jan; 32(1):133-142. PubMed ID: 29130425
[TBL] [Abstract][Full Text] [Related]
4. Perceptions of the care received from Australian palliative care services: A caregiver perspective.
Pidgeon TM; Johnson CE; Lester L; Currow D; Yates P; Allingham SF; Bird S; Eagar K
Palliat Support Care; 2018 Apr; 16(2):198-208. PubMed ID: 28357973
[TBL] [Abstract][Full Text] [Related]
5. The experiences of patients with advanced cancer and caregivers presenting to Emergency Departments: A qualitative study.
Philip J; Remedios C; Breen S; Weiland T; Willenberg L; Boughey M; Jelinek G; Lane H; Marck C; Weil J
Palliat Med; 2018 Feb; 32(2):439-446. PubMed ID: 29130378
[TBL] [Abstract][Full Text] [Related]
6. The experience of palliative care service provision for people with non-malignant respiratory disease and their family carers: An all-Ireland qualitative study.
Mc Veigh C; Reid J; Larkin P; Porter S; Hudson P
J Adv Nurs; 2018 Feb; 74(2):383-394. PubMed ID: 28910509
[TBL] [Abstract][Full Text] [Related]
7. Patients', family caregivers', and professionals' perspectives on quality of palliative care: a qualitative study.
Vedel I; Ghadi V; Lapointe L; Routelous C; Aegerter P; Guirimand F
Palliat Med; 2014 Oct; 28(9):1128-38. PubMed ID: 24821709
[TBL] [Abstract][Full Text] [Related]
8. Service user perspectives on palliative care education for health and social care professionals supporting people with learning disabilities.
McLaughlin D; Barr O; McIlfatrick S; McConkey R
BMJ Support Palliat Care; 2015 Dec; 5(5):531-7. PubMed ID: 24644213
[TBL] [Abstract][Full Text] [Related]
9. What is the role of community at the end of life for people dying in advanced age? A qualitative study with bereaved family carers.
Gott M; Wiles J; Moeke-Maxwell T; Black S; Williams L; Kerse N; Trussardi G
Palliat Med; 2018 Jan; 32(1):268-275. PubMed ID: 29130405
[TBL] [Abstract][Full Text] [Related]
10. What's in a name? A qualitative exploration of what is understood by "palliative care" in the emergency department.
Weil J; Weiland TJ; Lane H; Jelinek GA; Boughey M; Marck CH; Philip J
Palliat Med; 2015 Apr; 29(4):293-301. PubMed ID: 25634627
[TBL] [Abstract][Full Text] [Related]
11. The challenges and suffering of caring for people with primary malignant glioma: qualitative perspectives on improving current supportive and palliative care practices.
Collins A; Lethborg C; Brand C; Gold M; Moore G; Sundararajan V; Murphy M; Philip J
BMJ Support Palliat Care; 2014 Mar; 4(1):68-76. PubMed ID: 24644774
[TBL] [Abstract][Full Text] [Related]
12. Resilience for family carers of advanced cancer patients-how can health care providers contribute? A qualitative interview study with carers.
Røen I; Stifoss-Hanssen H; Grande G; Brenne AT; Kaasa S; Sand K; Knudsen AK
Palliat Med; 2018 Sep; 32(8):1410-1418. PubMed ID: 29852808
[TBL] [Abstract][Full Text] [Related]
13. The meaning and experience of bereavement support: A qualitative interview study of bereaved family caregivers.
Kirby E; Kenny K; Broom A; MacArtney J; Good P
Palliat Support Care; 2018 Aug; 16(4):396-405. PubMed ID: 28635585
[TBL] [Abstract][Full Text] [Related]
14. Preparedness for caregiving: A phenomenological study of the experiences of rural Australian family palliative carers.
Mason N; Hodgkin S
Health Soc Care Community; 2019 Jul; 27(4):926-935. PubMed ID: 30810249
[TBL] [Abstract][Full Text] [Related]
15. 'I am part of the community but...' The changing context of rural living for persons with advanced cancer and their families.
Duggleby WD; Penz K; Leipert BD; Wilson DM; Goodridge D; Williams A
Rural Remote Health; 2011; 11(3):1733. PubMed ID: 21787109
[TBL] [Abstract][Full Text] [Related]
16. The 'safe death': An ethnographic study exploring the perspectives of rural palliative care patients and family caregivers.
Rainsford S; Phillips CB; Glasgow NJ; MacLeod RD; Wiles RB
Palliat Med; 2018 Dec; 32(10):1575-1583. PubMed ID: 30229700
[TBL] [Abstract][Full Text] [Related]
17. An ethnography of managing emotions when talking about life-threatening illness.
Ayers NE; Vydelingum V; Arber A
Int Nurs Rev; 2017 Dec; 64(4):486-493. PubMed ID: 28151559
[TBL] [Abstract][Full Text] [Related]
18. Qualitative Study on the Perceptions of Terminally Ill Cancer Patients and Their Family Members Regarding End-of-Life Experiences Focusing on Palliative Sedation.
Eun Y; Hong IW; Bruera E; Kang JH
J Pain Symptom Manage; 2017 Jun; 53(6):1010-1016. PubMed ID: 28192224
[TBL] [Abstract][Full Text] [Related]
19. Experiences of patients and caregivers with early palliative care: A qualitative study.
Hannon B; Swami N; Rodin G; Pope A; Zimmermann C
Palliat Med; 2017 Jan; 31(1):72-81. PubMed ID: 27495814
[TBL] [Abstract][Full Text] [Related]
20. Fluctuating awareness of treatment goals among patients and their caregivers: a longitudinal study of a dynamic process.
Burns CM; Broom DH; Smith WT; Dear K; Craft PS
Support Care Cancer; 2007 Feb; 15(2):187-96. PubMed ID: 16953423
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]