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Items: 1 to 20 of 201

1.

Beyond polarization, public preferences suggest policy opportunities to address aging, dying, and family caregiving.

Byock IR, Corbeil YJ, Goodrich ME.

Am J Hosp Palliat Care. 2009 Jun-Jul;26(3):200-8. doi: 10.1177/1049909108328700. Epub 2009 Jan 9.

PMID:
19136642
2.

The desire for support and respite care: preferences of Dutch informal caregivers.

Koopmanschap MA, van Exel NJ, van den Bos GA, van den Berg B, Brouwer WB.

Health Policy. 2004 Jun;68(3):309-20.

PMID:
15113642
3.

Defining distinct caregiver subpopulations by intensity of end-of-life care provided.

Abernethy A, Burns C, Wheeler J, Currow D.

Palliat Med. 2009 Jan;23(1):66-79. doi: 10.1177/0269216308098793. Epub 2008 Nov 7.

PMID:
18996981
4.

Barriers to quality care for dying patients in rural communities.

Van Vorst RF, Crane LA, Barton PL, Kutner JS, Kallail KJ, Westfall JM.

J Rural Health. 2006 Summer;22(3):248-53.

PMID:
16824170
5.

End-of-life care in Italy: personal experience of family caregivers. A content analysis of open questions from the Italian Survey of the Dying of Cancer (ISDOC).

Morasso G, Costantini M, Di Leo S, Roma S, Miccinesi G, Merlo DF, Beccaro M.

Psychooncology. 2008 Nov;17(11):1073-80. doi: 10.1002/pon.1332.

PMID:
18317991
6.

Hispanic American elders: caregiving norms surrounding dying and the use of hospice services.

Talamantes MA, Lawler WR, Espino DV.

Hosp J. 1995;10(2):35-49. Review.

PMID:
7557932
7.

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
8.

A broader view of family caregiving: effects of caregiving and caregiver conditions on depressive symptoms, health, work, and social isolation.

Robison J, Fortinsky R, Kleppinger A, Shugrue N, Porter M.

J Gerontol B Psychol Sci Soc Sci. 2009 Nov;64(6):788-98. doi: 10.1093/geronb/gbp015. Epub 2009 Mar 24.

PMID:
19318470
9.

Terminal care of the dying child. Psychosocial implications of care.

Whittam EH.

Cancer. 1993 May 15;71(10 Suppl):3450-62.

10.

Family response to end-of-life education: differences by ethnicity and stage of caregiving.

Braun KL, Karel H, Zir A.

Am J Hosp Palliat Care. 2006 Aug-Sep;23(4):269-76.

PMID:
17060290
11.

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
12.

'A bed in the middle of nowhere': parents' meanings of place of death for adults with cystic fibrosis.

Lowton K.

Soc Sci Med. 2009 Oct;69(7):1056-62. doi: 10.1016/j.socscimed.2009.07.007. Epub 2009 Aug 18.

PMID:
19692159
13.

Care for the terminally ill: a life-affirming paradigm.

[No authors listed]

Healthc Demand Dis Manag. 1997 Feb;3(2):29-32.

PMID:
10174591
14.

Predictors of well-being in bereaved former hospice caregivers: the role of caregiving stressors, appraisals, and social resources.

Burton AM, Haley WE, Small BJ, Finley MR, Dillinger-Vasille M, Schonwetter R.

Palliat Support Care. 2008 Jun;6(2):149-58. doi: 10.1017/S1478951508000230.

PMID:
18501050
15.
16.

Helping families care for loved ones.

O'Malley S.

Qual Lett Healthc Lead. 1996 Sep;8(7):12-5.

PMID:
10161484
17.
18.

End-of-life care: an agenda for policy improvement.

Shugarman LR, Lorenz K, Lynn J.

Clin Geriatr Med. 2005 Feb;21(1):255-72, xi.

PMID:
15639050
19.

Preferences for location of death of seriously ill hospitalized patients: perspectives from Canadian patients and their family caregivers.

Stajduhar KI, Allan DE, Cohen SR, Heyland DK.

Palliat Med. 2008 Jan;22(1):85-8. doi: 10.1177/0269216307084612.

PMID:
18216081
20.

Experience of dying: concerns of dying patients and of carers.

Terry W, Olson LG, Wilss L, Boulton-Lewis G.

Intern Med J. 2006 Jun;36(6):338-46.

PMID:
16732857

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