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Items: 1 to 20 of 72

1.

[Barriers and challenges in end-of-life care settings from the formal caregivers' point of view].

Hirakawa Y, Uemura K.

Nihon Ronen Igakkai Zasshi. 2013;50(5):671. Japanese. No abstract available.

2.

End-of-life care in Italian hospitals: quality of and satisfaction with care from the caregivers' point of view--results from the Italian Survey of the Dying of Cancer.

Beccaro M, Caraceni A, Costantini M; ISDOC Study Group.

J Pain Symptom Manage. 2010 Jun;39(6):1003-15. doi: 10.1016/j.jpainsymman.2009.11.317.

PMID:
20538184
3.

Factors influencing family caregivers' ability to cope with providing end-of-life cancer care at home.

Stajduhar KI, Martin WL, Barwich D, Fyles G.

Cancer Nurs. 2008 Jan-Feb;31(1):77-85. doi: 10.1097/01.NCC.0000305686.36637.b5.

PMID:
18176135
4.

Transmural care of terminal cancer patients: effects on the quality of life of direct caregivers.

Smeenk FW, de Witte LP, van Haastregt JC, Schipper RM, Biezemans HP, Crebolder HF.

Nurs Res. 1998 May-Jun;47(3):129-36.

PMID:
9610646
5.

Mediating effects of sense of coherence on family caregivers' depressive distress while caring for terminally ill cancer patients.

Tang ST, Cheng CC, Lee KC, Chen CH, Liu LN.

Cancer Nurs. 2013 Nov-Dec;36(6):E25-33. doi: 10.1097/NCC.0b013e31826fc90d.

PMID:
23095855
6.

End-of-life care for rural-dwelling older adults and their primary family caregivers.

Hansen L, Cartwright JC, Craig CE.

Res Gerontol Nurs. 2012 Jan;5(1):6-15. doi: 10.3928/19404921-20111213-01. Epub 2011 Dec 29.

PMID:
22224904
7.

Psychometric testing of the Caregiver Quality of Life Index-Cancer on a Taiwanese family caregiver sample.

Tang WR, Tang ST, Kao CY.

Cancer Nurs. 2009 May-Jun;32(3):220-9. doi: 10.1097/NCC.0b013e31819b5ae8.

PMID:
19295419
8.

Comparing the experiences of rural and urban family caregivers of the terminally ill.

Brazil K, Kaasalainen S, Williams A, Rodriguez C.

Rural Remote Health. 2013 Jan-Mar;13(1):2250. Epub 2013 Jan 7.

9.
10.

Family-centered care: a resource for social work in end-of-life and palliative care.

Kovacs PJ, Bellin MH, Fauri DP.

J Soc Work End Life Palliat Care. 2006;2(1):13-27.

PMID:
17387080
11.

The caregivers' perspective on the end-of-life phase of glioblastoma patients.

Flechl B, Ackerl M, Sax C, Oberndorfer S, Calabek B, Sizoo E, Reijneveld J, Crevenna R, Keilani M, Gaiger A, Dieckmann K, Preusser M, Taphoorn MJ, Marosi C.

J Neurooncol. 2013 May;112(3):403-11. doi: 10.1007/s11060-013-1069-7. Epub 2013 Feb 15.

PMID:
23412776
12.

End-of-life caregivers' perception of medical and psychological support during the final weeks of glioma patients: a questionnaire-based survey.

Heese O, Vogeler E, Martens T, Schnell O, Tonn JC, Simon M, Schramm J, Krex D, Schackert G, Reithmeier T, Nikkhah G, Sabel M, Steiger HJ, Schlegel U, Löffler M, Weller M, Westphal M; German Glioma Network.

Neuro Oncol. 2013 Sep;15(9):1251-6. doi: 10.1093/neuonc/not089. Epub 2013 Jun 28.

13.

End-of-life caregiver interactions with health care providers: learning from the bad.

Guo G, Phillips LR, Reed PG.

J Nurs Care Qual. 2010 Oct-Dec;25(4):334-43. doi: 10.1097/NCQ.0b013e3181db532d.

PMID:
20375703
14.

The caregivers' point of view.

Jaywant S.

Indian J Med Ethics. 2016 Jan-Mar;1(1):23-5. No abstract available.

PMID:
26826657
15.

Home death--the caregivers' experiences.

Singer Y, Bachner YG, Shvartzman P, Carmel S.

J Pain Symptom Manage. 2005 Jul;30(1):70-4.

PMID:
16043009
16.

Caregiving at the end of life: Perceptions of health care quality and quality of life among patients and caregivers.

Fleming DA, Sheppard VB, Mangan PA, Taylor KL, Tallarico M, Adams I, Ingham J.

J Pain Symptom Manage. 2006 May;31(5):407-20.

PMID:
16716871
17.

The lived experience of family caregivers who provided end-of-life care to persons with advanced dementia.

Peacock S, Duggleby W, Koop P.

Palliat Support Care. 2014 Apr;12(2):117-26. doi: 10.1017/S1478951512001034. Epub 2013 Mar 19.

PMID:
23510738
18.

End-of-life care and the effects of bereavement on family caregivers of persons with dementia.

Schulz R, Mendelsohn AB, Haley WE, Mahoney D, Allen RS, Zhang S, Thompson L, Belle SH; Resources for Enhancing Alzheimer's Caregiver Health Investigators.

N Engl J Med. 2003 Nov 13;349(20):1936-42.

19.

Family caregivers' ideal expectations of Canada's Compassionate Care Benefit.

Crooks VA, Williams A, Stajduhar KI, Cohen SR, Allan D, Brazil K.

Health Soc Care Community. 2012 Mar;20(2):172-80. doi: 10.1111/j.1365-2524.2011.01028.x. Epub 2011 Sep 15.

PMID:
21919990
20.

Into the Abyss of someone else's dying: the voice of the end-of-life caregiver.

Phillips LR, Reed PG.

Clin Nurs Res. 2009 Feb;18(1):80-97. doi: 10.1177/1054773808330538.

PMID:
19208822

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