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Items: 1 to 20 of 128

2.

Risk Factors for Anticipatory Grief in Family Members of Terminally Ill Veterans Receiving Palliative Care Services.

Burke LA, Clark KA, Ali KS, Gibson BW, Smigelsky MA, Neimeyer RA.

J Soc Work End Life Palliat Care. 2015;11(3-4):244-66. doi: 10.1080/15524256.2015.1110071.

PMID:
26654060
3.

Service preferences among family caregivers of the terminally ill.

Brazil K, Bedard M, Krueger P, Abernathy T, Lohfeld L, Willison K.

J Palliat Med. 2005 Feb;8(1):69-78.

PMID:
15662175
4.

Post-mortal bereavement of family caregivers in Germany: a prospective interview-based investigation.

Wiese CH, Morgenthal HC, Bartels UE, Vossen-Wellmann A, Graf BM, Hanekop GG.

Wien Klin Wochenschr. 2010 Jul;122(13-14):384-9. doi: 10.1007/s00508-010-1396-z. Epub 2010 Jul 8.

PMID:
20602281
5.

Place of death and the differences in patient quality of death and dying and caregiver burden.

Kinoshita H, Maeda I, Morita T, Miyashita M, Yamagishi A, Shirahige Y, Takebayashi T, Yamaguchi T, Igarashi A, Eguchi K.

J Clin Oncol. 2015 Feb 1;33(4):357-63. doi: 10.1200/JCO.2014.55.7355. Epub 2014 Dec 22.

PMID:
25534381
6.

Cancer family caregivers during the palliative, hospice, and bereavement phases: a review of the descriptive psychosocial literature.

Williams AL, McCorkle R.

Palliat Support Care. 2011 Sep;9(3):315-25. doi: 10.1017/S1478951511000265. Review.

PMID:
21838952
7.

Sadness, anxiety, and experiences with emotional support among veteran and nonveteran patients and their families at the end of life.

Holland JM, Currier JM, Kirkendall A, Keene JR, Luna N.

J Palliat Med. 2014 Jun;17(6):708-11. doi: 10.1089/jpm.2013.0485. Epub 2014 Mar 7.

PMID:
24605892
8.

Do we need to change our understanding of anticipatory grief in caregivers? A systematic review of caregiver studies during end-of-life caregiving and bereavement.

Nielsen MK, Neergaard MA, Jensen AB, Bro F, Guldin MB.

Clin Psychol Rev. 2016 Mar;44:75-93. doi: 10.1016/j.cpr.2016.01.002. Epub 2016 Jan 8. Review.

PMID:
26796738
10.

Advanced cancer at home: caregiving and bereavement.

Rossi Ferrario S, Cardillo V, Vicario F, Balzarini E, Zotti AM.

Palliat Med. 2004 Mar;18(2):129-36.

PMID:
15046409
11.

Preparing family caregivers for death and bereavement. Insights from caregivers of terminally ill patients.

Hebert RS, Schulz R, Copeland VC, Arnold RM.

J Pain Symptom Manage. 2009 Jan;37(1):3-12. doi: 10.1016/j.jpainsymman.2007.12.010. Epub 2008 Jun 6.

PMID:
18538977
12.

The meaning of the music: the role of music in palliative care music therapy as perceived by bereaved caregivers of advanced cancer patients.

Magill L.

Am J Hosp Palliat Care. 2009 Feb-Mar;26(1):33-9. doi: 10.1177/1049909108327024. Epub 2008 Dec 1.

PMID:
19047488
13.

The impact of additional support services on caregivers of hospice patients and hospice social workers.

Empeño J, Raming NT, Irwin SA, Nelesen RA, Lloyd LS.

Omega (Westport). 2013;67(1-2):53-61.

14.

[Individual neonatal end-of-life care and family-centred bereavement support].

Garten L, von der Hude K, Rösner B, Klapp C, Bührer C.

Z Geburtshilfe Neonatol. 2013 Jun;217(3):95-102. doi: 10.1055/s-0033-1347207. Epub 2013 Jun 28. German.

PMID:
23812919
15.

Experience of meaning in life in bereaved informal caregivers of palliative care patients.

Brandstätter M, Kögler M, Baumann U, Fensterer V, Küchenhoff H, Borasio GD, Fegg MJ.

Support Care Cancer. 2014 May;22(5):1391-9. doi: 10.1007/s00520-013-2099-6. Epub 2014 Jan 3.

PMID:
24382677
16.

Hospice at home service: the carer's perspective.

McLaughlin D, Sullivan K, Hasson F.

Support Care Cancer. 2007 Feb;15(2):163-70. Epub 2006 Aug 30.

PMID:
16944220
17.

Palliative family caregivers' accounts of health care experiences: the importance of "security".

Funk LM, Allan DE, Stajduhar KI.

Palliat Support Care. 2009 Dec;7(4):435-47. doi: 10.1017/S1478951509990447.

PMID:
19939306
18.

End of life considerations in the head and neck cancer patient.

Sciubba JJ.

Oral Oncol. 2009 Apr-May;45(4-5):431-4. doi: 10.1016/j.oraloncology.2008.06.001. Epub 2008 Sep 18. Review.

PMID:
18804409
19.

Caregiver outcomes of partners in dementia care: effect of a care coordination program for veterans with dementia and their family members and friends.

Bass DM, Judge KS, Snow AL, Wilson NL, Morgan R, Looman WJ, McCarthy CA, Maslow K, Moye JA, Randazzo R, Garcia-Maldonado M, Elbein R, Odenheimer G, Kunik ME.

J Am Geriatr Soc. 2013 Aug;61(8):1377-86. doi: 10.1111/jgs.12362. Epub 2013 Jul 19.

PMID:
23869899
20.

Enabling a family caregiver-led assessment of support needs in home-based palliative care: Potential translation into practice.

Aoun S, Toye C, Deas K, Howting D, Ewing G, Grande G, Stajduhar K.

Palliat Med. 2015 Dec;29(10):929-38. doi: 10.1177/0269216315583436. Epub 2015 Apr 20.

PMID:
25895538

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