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Items: 1 to 20 of 185

1.
2.

Motor Neurone Disease family carers' experiences of caring, palliative care and bereavement: an exploratory qualitative study.

Aoun SM, Connors SL, Priddis L, Breen LJ, Colyer S.

Palliat Med. 2012 Sep;26(6):842-50. doi: 10.1177/0269216311416036.

PMID:
21775409
3.

Hospice at home service: the carer's perspective.

McLaughlin D, Sullivan K, Hasson F.

Support Care Cancer. 2007 Feb;15(2):163-70.

PMID:
16944220
4.

Experiences and needs of bereaved carers during palliative and end-of-life care for people with chronic obstructive pulmonary disease.

Hasson F, Spence A, Waldron M, Kernohan G, McLaughlin D, Watson B, Cochrane B.

J Palliat Care. 2009 Autumn;25(3):157-63.

PMID:
19824276
5.

Bereaved informal cancer carers making sense of their palliative care experiences at home.

Wong WK, Ussher J.

Health Soc Care Community. 2009 May;17(3):274-82. doi: 10.1111/j.1365-2524.2008.00828.x.

PMID:
19207604
6.

Valued aspects of primary palliative care: content analysis of bereaved carers' descriptions.

Grande GE, Farquhar MC, Barclay SI, Todd CJ.

Br J Gen Pract. 2004 Oct;54(507):772-8.

7.

Strength through adversity: bereaved cancer carers' accounts of rewards and personal growth from caring.

Wong WK, Ussher J, Perz J.

Palliat Support Care. 2009 Jun;7(2):187-96. doi: 10.1017/S1478951509000248.

PMID:
19538801
8.

Bereaved carers' views of a hospice at home service.

Exley C, Tyrer F.

Int J Palliat Nurs. 2005 May;11(5):242-6.

PMID:
15944499
9.

The perceptions and experiences of nurses and bereaved families towards bereavement care in an oncology unit.

Chan HY, Lee LH, Chan CW.

Support Care Cancer. 2013 Jun;21(6):1551-6. doi: 10.1007/s00520-012-1692-4.

PMID:
23262810
10.

Supporting family carers providing end-of-life home care: a qualitative study on the impact of a hospice at home service.

Jack BA, O'Brien MR, Scrutton J, Baldry CR, Groves KE.

J Clin Nurs. 2015 Jan;24(1-2):131-40. doi: 10.1111/jocn.12695.

PMID:
25236658
11.

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. doi: 10.1177/0269216315584865.

PMID:
25944545
12.

Can short hospice enrollment be long enough? Comparing the perspectives of hospice professionals and family caregivers.

Waldrop DP, Rinfrette ES.

Palliat Support Care. 2009 Mar;7(1):37-47. doi: 10.1017/S1478951509000066.

PMID:
19619373
13.

Support needs of informal hospice caregivers: a qualitative study.

Kutner J, Kilbourn KM, Costenaro A, Lee CA, Nowels C, Vancura JL, Anderson D, Keech TE.

J Palliat Med. 2009 Dec;12(12):1101-4. doi: 10.1089/jpm.2009.0178.

15.
16.

Between worlds: the experiences and needs of former family carers.

Cronin P, Hynes G, Breen M, McCarron M, McCallion P, O'Sullivan L.

Health Soc Care Community. 2015 Jan;23(1):88-96. doi: 10.1111/hsc.12149.

PMID:
25307354
18.

Communication behaviors and patient and caregiver emotional concerns: a description of home hospice communication.

Clayton MF, Reblin M, Carlisle M, Ellington L.

Oncol Nurs Forum. 2014 May;41(3):311-21. doi: 10.1188/14.ONF.311-321.

PMID:
24769595
19.
20.

Exploring barriers to assessment of bereavement risk in palliative care: perspectives of key stakeholders.

Sealey M, O'Connor M, Aoun SM, Breen LJ.

BMC Palliat Care. 2015 Oct 14;14:49. doi: 10.1186/s12904-015-0046-7.

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