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Items: 1 to 20 of 280

1.

Canada's Compassionate Care Benefit: is it an adequate public health response to addressing the issue of caregiver burden in end-of-life care?

Williams AM, Eby JA, Crooks VA, Stajduhar K, Giesbrecht M, Vuksan M, Cohen SR, Brazil K, Allan D.

BMC Public Health. 2011 May 18;11:335. doi: 10.1186/1471-2458-11-335.

2.

Critically examining diversity in end-of-life family caregiving: implications for equitable caregiver support and Canada's Compassionate Care Benefit.

Giesbrecht M, Crooks VA, Williams A, Hankivsky O.

Int J Equity Health. 2012 Nov 1;11:65. doi: 10.1186/1475-9276-11-65.

3.

Differential impacts of care-giving across three caregiver groups in Canada: end-of-life care, long-term care and short-term care.

Williams AM, Wang L, Kitchen P.

Health Soc Care Community. 2014 Mar;22(2):187-96. doi: 10.1111/hsc.12075. Epub 2013 Oct 31.

4.

Impacts of care-giving and sources of support: a comparison of end-of-life and non-end-of-life caregivers in Canada.

Williams AM, Wang L, Kitchen P.

Health Soc Care Community. 2016 Mar;24(2):214-24. doi: 10.1111/hsc.12205. Epub 2015 Mar 2.

PMID:
25727849
5.

The information transfer and knowledge acquisition geographies of family caregivers: an analysis of Canada's Compassionate Care Benefit.

Crooks VA, Williams A, Stajduhar KI, Allan DE, Cohen SR.

Can J Nurs Res. 2007 Sep;39(3):36-54.

PMID:
17970459
6.

Perspectives from the frontlines: palliative care providers' expectations of Canada's compassionate care benefit programme.

Giesbrecht M, Crooks VA, Williams A.

Health Soc Care Community. 2010 Nov;18(6):643-52. doi: 10.1111/j.1365-2524.2010.00937.x.

PMID:
20584086
7.

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.

8.

Issues in end-of-life care: patient, caregiver, and clinician perceptions.

Farber SJ, Egnew TR, Herman-Bertsch JL, Taylor TR, Guldin GE.

J Palliat Med. 2003 Feb;6(1):19-31.

PMID:
12710572
9.

The importance of place and time in translating knowledge about Canada's Compassionate Care Benefit to informal caregivers.

Dykeman S, Williams A.

J Soc Work End Life Palliat Care. 2013;9(4):289-307. doi: 10.1080/15524256.2013.846888.

10.

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
11.

Caregiver- and patient-directed interventions for dementia: an evidence-based analysis.

Health Quality Ontario.

Ont Health Technol Assess Ser. 2008;8(4):1-98. Epub 2008 Oct 1.

12.

Modeling costs and burden of informal caregiving for persons with bipolar disorder.

Wolff N, Perlick DA, Kaczynski R, Calabrese J, Nierenberg A, Miklowitz DJ.

J Ment Health Policy Econ. 2006 Jun;9(2):99-110.

PMID:
17007487
13.

The uncompassionate elements of the Compassionate Care Benefits Program: a critical analysis.

Flagler J, Dong W.

Glob Health Promot. 2010 Mar;17(1):50-9. doi: 10.1177/1757975909356636.

PMID:
20357352
14.

Canada's Compassionate Care Benefit: views of family caregivers in chronic illness.

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

Int J Palliat Nurs. 2006 Sep;12(9):438-45.

PMID:
17077803
15.

The health and well-being of caregivers of children with cerebral palsy.

Raina P, O'Donnell M, Rosenbaum P, Brehaut J, Walter SD, Russell D, Swinton M, Zhu B, Wood E.

Pediatrics. 2005 Jun;115(6):e626-36.

PMID:
15930188
16.

Addressing the burden of stroke caregivers: a literature review.

Camak DJ.

J Clin Nurs. 2015 Sep;24(17-18):2376-82. doi: 10.1111/jocn.12884. Epub 2015 Jun 10. Review.

PMID:
26095074
18.

Caregiver profiles and determinants of caregiving burden in Ghana.

Sanuade OA, Boatemaa S.

Public Health. 2015 Jul;129(7):941-7. doi: 10.1016/j.puhe.2015.05.016. Epub 2015 Jun 23.

PMID:
26115592
19.

An evaluation of Canada's Compassionate Care Benefit from a family caregiver's perspective at end of life.

Crooks VA, Williams A.

BMC Palliat Care. 2008 Aug 28;7:14. doi: 10.1186/1472-684X-7-14.

20.

Psychosocial factors of caregiver burden in child caregivers: results from the new national study of caregiving.

Cohen SA, Cook S, Kelley L, Sando T, Bell AE.

Health Qual Life Outcomes. 2015 Aug 7;13:120. doi: 10.1186/s12955-015-0317-2.

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