KirbyEBroomAGoodPWoottonJAdamsJ. Families and the transition to specialist palliative care. Mortality. 2014;19(4):323–341.
2.
CsikaiELMartinSS. Bereaved hospice caregivers’ views of the transition to hospice. Soc Work Health Care. 2010;49(5):387–400.
3.
TownsendALIshlerKJShapiroBMFord-PitorakEMatthewsCR. Levels, types, and predictors of family caregiver strain during hospice home care for an older adult. J Soc Work End Life Palliat Care. 2010;6(1-2):51–72.
4.
KehlKA. How hospice staff members prepare family caregivers for the patient’s final days of life: an exploratory study. Palliat Med. 2015;29(2):128–137.
5.
Le SageMR. Linguistic competence/language access services (LAS) in end-of-life and palliative care. J Soc Work End Life Palliat Care. 2007;2(4):3–31.
6.
DunneKSullivanK. Family experiences of palliative care in the acute hospital setting. Int J Palliat Nurs. 2000;6(4):170–178.
7.
SearleCKellyM. A comparison of hospice and hospital care for people who die: views of the surviving spouse. Palliat Med. 1997;11(2):93–100.
8.
Menzies-LythI. Containing Anxiety in Institutions: Selected Essays. London: Free Association Books; 1988.
9.
KouvacsPBellinMFauriD. Family-centred care: a resource for social work in end-of-life and palliative care. J Soc Work End Life Palliat Care. 2006;2(1):13–27.
10.
RobinsonJGottMIngletonC. Patient and family experiences of palliative care in hospital: what do we know?An integrative review. Palliat Med. 2014;28(1):18–33.
11.
RousseauP.Reflections from the bedside. Deathbed memories. J Palliat Care. 2014;30(2):125–126.