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Items: 1 to 20 of 1037

1.

Talking with terminally ill patients and their caregivers about death, dying, and bereavement: is it stressful? Is it helpful?

Emanuel EJ, Fairclough DL, Wolfe P, Emanuel LL.

Arch Intern Med. 2004 Oct 11;164(18):1999-2004.

PMID:
15477434
2.

Talking about death, dying, and bereavement with terminally ill patients and their caregivers.

Schachter L.

Arch Intern Med. 2005 Jun 27;165(12):1437; author reply 1437. No abstract available.

PMID:
15983296
3.

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.

PMID:
18538977
4.

Understanding economic and other burdens of terminal illness: the experience of patients and their caregivers.

Emanuel EJ, Fairclough DL, Slutsman J, Emanuel LL.

Ann Intern Med. 2000 Mar 21;132(6):451-9.

PMID:
10733444
5.

What is a good death? Terminally ill patients dealing with normative expectations around death and dying.

Goldsteen M, Houtepen R, Proot IM, Abu-Saad HH, Spreeuwenberg C, Widdershoven G.

Patient Educ Couns. 2006 Dec;64(1-3):378-86.

PMID:
16872786
6.

Determinants of death in an inpatient hospice for terminally ill cancer patients.

Tang ST, McCorkle R, Bradley EH.

Palliat Support Care. 2004 Dec;2(4):361-70.

PMID:
16594398
7.

Preferences for place of care and place of death among informal caregivers of the terminally ill.

Brazil K, Howell D, Bedard M, Krueger P, Heidebrecht C.

Palliat Med. 2005 Sep;19(6):492-9.

PMID:
16218162
8.

Discussing end-of-life issues with terminally ill cancer patients and their carers: a qualitative study.

Clayton JM, Butow PN, Arnold RM, Tattersall MH.

Support Care Cancer. 2005 Aug;13(8):589-99.

PMID:
15645187
9.

Meaninglessness in terminally ill cancer patients: a validation study and nurse education intervention trial.

Morita T, Murata H, Hirai K, Tamura K, Kataoka J, Ohnishi H, Akizuki N, Kurihara Y, Akechi T, Uchitomi Y; Japanese Spiritual Care Task Force..

J Pain Symptom Manage. 2007 Aug;34(2):160-70.

PMID:
17544250
10.
11.

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
12.
14.

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
15.

Assistance from family members, friends, paid care givers, and volunteers in the care of terminally ill patients.

Emanuel EJ, Fairclough DL, Slutsman J, Alpert H, Baldwin D, Emanuel LL.

N Engl J Med. 1999 Sep 23;341(13):956-63.

16.
17.

Randomized controlled trial of a prompt list to help advanced cancer patients and their caregivers to ask questions about prognosis and end-of-life care.

Clayton JM, Butow PN, Tattersall MH, Devine RJ, Simpson JM, Aggarwal G, Clark KJ, Currow DC, Elliott LM, Lacey J, Lee PG, Noel MA.

J Clin Oncol. 2007 Feb 20;25(6):715-23.

PMID:
17308275
18.

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.

PMID:
20116158
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