124 related articles for article (PubMed ID: 22067680)
1. Challenges in home-based palliative care in Norway: a qualitative study of spouses' experiences.
Hunstad I; Foelsvik Svindseth M
Int J Palliat Nurs; 2011 Aug; 17(8):398-404. PubMed ID: 22067680
[TBL] [Abstract][Full Text] [Related]
2. "I didn't want to be in charge and yet I was": Bereaved caregivers' accounts of providing home care for family members with advanced cancer.
Mohammed S; Swami N; Pope A; Rodin G; Hannon B; Nissim R; Hales S; Zimmermann C
Psychooncology; 2018 Apr; 27(4):1229-1236. PubMed ID: 29388714
[TBL] [Abstract][Full Text] [Related]
3. 'My wife is my doctor at home': A qualitative study exploring the challenges of home-based palliative care in a resource-poor setting.
Salifu Y; Almack K; Caswell G
Palliat Med; 2021 Jan; 35(1):97-108. PubMed ID: 32945248
[TBL] [Abstract][Full Text] [Related]
4. Palliative care for Parkinson's disease: Patient and carer's perspectives explored through qualitative interview.
Fox S; Cashell A; Kernohan WG; Lynch M; McGlade C; O'Brien T; O'Sullivan SS; Foley MJ; Timmons S
Palliat Med; 2017 Jul; 31(7):634-641. PubMed ID: 27683476
[TBL] [Abstract][Full Text] [Related]
5. A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer.
Barlund AS; André B; Sand K; Brenne AT
BMC Palliat Care; 2021 Jan; 20(1):7. PubMed ID: 33419428
[TBL] [Abstract][Full Text] [Related]
6. Hospice at home service: the carer's perspective.
McLaughlin D; Sullivan K; Hasson F
Support Care Cancer; 2007 Feb; 15(2):163-70. PubMed ID: 16944220
[TBL] [Abstract][Full Text] [Related]
7. The responsibility to quench thirst by providing drinks when a relative is dying spouses' experience in specialist palliative home care.
Friedrichsen M; Waldréus N; Milovanovic M; Schaller AS; Jaarsma P; Jaarsma T
BMC Palliat Care; 2023 Nov; 22(1):184. PubMed ID: 37981710
[TBL] [Abstract][Full Text] [Related]
8. Doing what it takes: a qualitative study of New Zealand carers' experiences of giving home-based palliative care to loved ones.
McKinlay E; Vaipuna K; O'Toole T; Golds H; Adams A
N Z Med J; 2021 Apr; 134(1533):21-32. PubMed ID: 33927421
[TBL] [Abstract][Full Text] [Related]
9. Bereaved carers' accounts of the end of life and the role of care providers in a 'good death': A qualitative study.
Holdsworth LM
Palliat Med; 2015 Oct; 29(9):834-41. PubMed ID: 25944545
[TBL] [Abstract][Full Text] [Related]
10. Carers' needs in advanced heart failure: A systematic narrative review.
Doherty LC; Fitzsimons D; McIlfatrick SJ
Eur J Cardiovasc Nurs; 2016 Jun; 15(4):203-12. PubMed ID: 25922473
[TBL] [Abstract][Full Text] [Related]
11. Rural palliative care transitions from home to hospital: carers' experiences.
Hatcher I; Harms L; Walker B; Stokes S; Lowe A; Foran K; Tarrant J
Aust J Rural Health; 2014 Aug; 22(4):160-4. PubMed ID: 25123619
[TBL] [Abstract][Full Text] [Related]
12. Home-based palliative care in Sydney, Australia: the carer's perspective on the provision of informal care.
Zapart S; Kenny P; Hall J; Servis B; Wiley S
Health Soc Care Community; 2007 Mar; 15(2):97-107. PubMed ID: 17286671
[TBL] [Abstract][Full Text] [Related]
13. From neighbour to carer: An exploratory study on the role of non-kin-carers in end-of-life care at home for older people living alone.
Pleschberger S; Wosko P
Palliat Med; 2017 Jun; 31(6):559-565. PubMed ID: 27609606
[TBL] [Abstract][Full Text] [Related]
14. Quality of end-of-life care for those who die at home: views and experiences of bereaved relatives and carers.
Lees C; Mayland C; West A; Germaine A
Int J Palliat Nurs; 2014 Feb; 20(2):63-7. PubMed ID: 24577211
[TBL] [Abstract][Full Text] [Related]
15. Care arrangements for community-dwelling people with dementia in Germany as perceived by informal carers - a cross-sectional pilot survey in a provincial-rural setting.
von Kutzleben M; Reuther S; Dortmann O; Holle B
Health Soc Care Community; 2016 May; 24(3):283-96. PubMed ID: 25727732
[TBL] [Abstract][Full Text] [Related]
16. Dying at "home" - a qualitative study of end-of-life care in rural Northern Norway from the perspective of health care professionals.
Ervik B; Dønnem T; Johansen ML
BMC Health Serv Res; 2023 Dec; 23(1):1359. PubMed ID: 38053081
[TBL] [Abstract][Full Text] [Related]
17. The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study.
O'Brien MR; Whitehead B; Jack BA; Mitchell JD
Disabil Rehabil; 2012; 34(3):247-56. PubMed ID: 22087569
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Palliative care at home: carers and medication management.
Anderson BA; Kralik D
Palliat Support Care; 2008 Dec; 6(4):349-56. PubMed ID: 19006589
[TBL] [Abstract][Full Text] [Related]
20. Exploring comprehensibility and manageability in palliative home care: an interview study of dying cancer patients' informal carers.
Milberg A; Strang P
Psychooncology; 2004 Sep; 13(9):605-18. PubMed ID: 15334529
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
