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Items: 1 to 20 of 113

1.

Dying, death and bereavement: a qualitative study of the views of carers of people with heart failure in the UK.

Small N, Barnes S, Gott M, Payne S, Parker C, Seamark D, Gariballa S.

BMC Palliat Care. 2009 Jun 16;8:6. doi: 10.1186/1472-684X-8-6.

2.

Dying at home: a qualitative study of family carers' views of support provided by GPs community staff.

Seamark D, Blake S, Brearley SG, Milligan C, Thomas C, Turner M, Wang X, Payne S.

Br J Gen Pract. 2014 Dec;64(629):e796-803. doi: 10.3399/bjgp14X682885.

3.

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. Epub 2011 Jul 20.

PMID:
21775409
4.

Experiences of end of life amongst family carers of people with advanced dementia: longitudinal cohort study with mixed methods.

Moore KJ, Davis S, Gola A, Harrington J, Kupeli N, Vickerstaff V, King M, Leavey G, Nazareth I, Jones L, Sampson EL.

BMC Geriatr. 2017 Jul 3;17(1):135. doi: 10.1186/s12877-017-0523-3.

5.

Conducting research interviews with bereaved family carers: when do we ask?

Bentley B, O'Connor M.

J Palliat Med. 2015 Mar;18(3):241-5. doi: 10.1089/jpm.2014.0320. Epub 2014 Dec 17.

6.

Bereaved cancer carers' experience of and preference for palliative care.

Sekelja N, Butow PN, Tattersall MH.

Support Care Cancer. 2010 Sep;18(9):1219-28. doi: 10.1007/s00520-009-0752-x. Epub 2009 Oct 12.

PMID:
19821168
7.

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. Epub 2015 May 5.

PMID:
25944545
8.

Which carers of family members at the end of life need more support from health services and why?

McNamara B, Rosenwax L.

Soc Sci Med. 2010 Apr;70(7):1035-41. doi: 10.1016/j.socscimed.2009.11.029. Epub 2010 Jan 28.

PMID:
20116158
9.

The perspectives of bereaved family carers on dying at home: the study protocol of 'unpacking the home: family carers' reflections on dying at home.

Payne S, Brearley S, Milligan C, Seamark D, Thomas C, Wang X, Blake S, Turner M.

BMC Palliat Care. 2012 Nov 22;11:23. doi: 10.1186/1472-684X-11-23.

10.

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
11.

Experiences of dying, death and bereavement in motor neurone disease: a qualitative study.

Whitehead B, O'Brien MR, Jack BA, Mitchell D.

Palliat Med. 2012 Jun;26(4):368-78. doi: 10.1177/0269216311410900. Epub 2011 Jun 28.

PMID:
21712334
12.

Dying at home of cancer: whose needs are being met? The experience of family carers and healthcare professionals (a multiperspective qualitative study).

Pottle J, Hiscock J, Neal RD, Poolman M.

BMJ Support Palliat Care. 2017 Jan 16. pii: bmjspcare-2016-001145. doi: 10.1136/bmjspcare-2016-001145. [Epub ahead of print]

PMID:
28093387
13.

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.

PMID:
24577211
14.

Communication between family carers and health professionals about end-of-life care for older people in the acute hospital setting: a qualitative study.

Caswell G, Pollock K, Harwood R, Porock D.

BMC Palliat Care. 2015 Aug 1;14:35. doi: 10.1186/s12904-015-0032-0.

15.

A qualitative study of recently bereaved people's beliefs about death: implications for bereavement care.

Draper P, Holloway M, Adamson S.

J Clin Nurs. 2014 May;23(9-10):1300-8. doi: 10.1111/jocn.12326. Epub 2013 Sep 5.

PMID:
24003860
16.

Life after care: psychological adjustment to bereavement in family carers of people with dementia.

Vlachogianni A, Efthymiou A, Potamianou D, Sakka P, Orgeta V.

Int Psychogeriatr. 2016 May;28(5):815-23. doi: 10.1017/S104161021500201X. Epub 2015 Dec 9.

PMID:
26648275
17.

Risk factors for developing prolonged grief during bereavement in family carers of cancer patients in palliative care: a longitudinal study.

Thomas K, Hudson P, Trauer T, Remedios C, Clarke D.

J Pain Symptom Manage. 2014 Mar;47(3):531-41. doi: 10.1016/j.jpainsymman.2013.05.022. Epub 2013 Aug 19.

PMID:
23969327
18.

Carers' health status: is it associated with their evaluation of the quality of palliative care?

Fakhoury WK, McCarthy M, Addington-Hall J.

Scand J Soc Med. 1997 Dec;25(4):296-301.

PMID:
9460144
19.

End-of-life care: A qualitative study comparing the views of people with dementia and family carers.

Poole M, Bamford C, McLellan E, Lee RP, Exley C, Hughes JC, Harrison-Dening K, Robinson L.

Palliat Med. 2017 Oct 1:269216317736033. doi: 10.1177/0269216317736033. [Epub ahead of print]

PMID:
29020864
20.

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

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