Palliative Care for Families: Remembering the Hidden Patients

Families of patients receiving palliative care are profoundly affected by the challenges of the illness. They observe care that the patient receives, provide care for the patient, and receive support from health professionals in the form of information, counselling, or practical assistance. As they witness and participate in the patient's care, they judge the quality of care that the patient receives. They often see themselves as the patient's care advocates and may harbour regret and guilt if they believe that the patient did not have the best possible care. The illness experience profoundly affects family members' psychological and physical health; recognition of this has coined the term “hidden patients.” This article briefly synthesizes empirical work that suggests how to best support families in a palliative care context. We discuss how to define the family, emphasizing a systems approach to family care. We describe the impact of the illness on the family in terms of family members' health, family communication issues, psychological issues, needs for information, physical care demands, and family costs of caring.

[1]  I. Higginson,et al.  What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness , 2003, Palliative medicine.

[2]  P. Northouse,et al.  Communication and Cancer: Issues Confronting Patients, Health Professionals, and Family Members , 1987 .

[3]  L. Northouse The Impact of Cancer on the Family: An Overview , 1985 .

[4]  J. Sloan,et al.  Family Members’ Perceptions of Palliative Cancer Care: Predictors of Family Functioning and Family Members’ Health , 1996, Journal of palliative care.

[5]  B. Given,et al.  Family and out-of-pocket costs for women with breast cancer. , 1994, Cancer practice.

[6]  S. Nikoletti,et al.  Congruence between Patients’ and Family Caregivers’ Perceptions of Symptom Distress in Patients with Terminal Cancer , 1998, Journal of palliative care.

[7]  Peter Hudson,et al.  Positive aspects and challenges associated with caring for a dying relative at home. , 2004, International journal of palliative nursing.

[8]  M. Fallon,et al.  ABC of Palliative Care , 1997 .

[9]  H. Schofield,et al.  A profile of Australian family caregivers: diversity of roles and circumstances , 1977, Australian and New Zealand journal of public health.

[10]  S. Morris,et al.  The carer's place in the cancer situation: where does the carer stand in the medical setting? , 2001, European journal of cancer care.

[11]  A. Stedeford Couples facing death. II--Unsatisfactory communication. , 1981, British medical journal.

[12]  L. Kristjanson,et al.  The impact of cancer on the family , 2004 .

[13]  Walker Cl Siblings of children with cancer. , 1990 .

[14]  B. Ferrell,et al.  Managing cancer pain at home: the decisions and ethical conflicts of patients, family caregivers, and homecare nurses. , 1993, Oncology nursing forum.

[15]  C Levine,et al.  The economic value of informal caregiving. , 1999, Health affairs.

[16]  C. Mclauchlan ABC of major trauma. Handling distressed relatives and breaking bad news. , 1990, BMJ.

[17]  V Mor,et al.  The changing needs of patients with cancer at home. A longitudinal view , 1992, Cancer.

[18]  J. Addington-hall,et al.  ABC of palliative care: The carers , 1998, BMJ.

[19]  S. C. Galloway Young adults' reactions to the death of a parent. , 1990, Oncology nursing forum.

[20]  J. Bottorff,et al.  Comforting: exploring the work of cancer nurses. , 2006, Journal of advanced nursing.

[21]  I. Byock The meaning and value of death. , 2002, Journal of palliative medicine.

[22]  L. Kristjanson,et al.  Information and support needs of adolescent children of women with breast cancer. , 2004, Oncology nursing forum.

[23]  S. Aranda,et al.  Home Caregivers of the Person With Advanced Cancer: AN AUSTRALIAN PERSPECTIVE , 2001, Cancer nursing.

[24]  R. McCorkle,et al.  Enhancing caregiver outcomes in palliative care. , 2001, Cancer control : journal of the Moffitt Cancer Center.

[25]  S. Zisook,et al.  Depression through the first year after the death of a spouse. , 1991, The American journal of psychiatry.

[26]  D. Dudgeon,et al.  Perceptions of the role of the school in providing information and support to adolescent children of women with breast cancer. , 2000, Journal of advanced nursing.

[27]  Lackey Nr,et al.  Identifying the needs of home caregivers of patients with cancer. , 1992 .

[28]  Sumon YusufPhotoshare Care , 1890, The Hospital.

[29]  S. Barclay,et al.  Does hospital at home for palliative care facilitate death at home? Randomised controlled trial , 1999, BMJ.

[30]  T. Madan Dying with dignity. , 1992, Social science & medicine.

[31]  L. Northouse,et al.  Cancer and the family: strategies to assist spouses. , 1993, Seminars in oncology nursing.

[32]  S. D'haese Palliative Care Nursing: A guide to Practice , 2004 .

[33]  Galloway Sc Young adults' reactions to the death of a parent. , 1990 .

[34]  N. Lackey,et al.  Identifying the needs of home caregivers of patients with cancer. , 1992, Oncology nursing forum.

[35]  T. Quill,et al.  Working with families in palliative care: one size does not fit all. , 2006, Journal of palliative medicine.

[36]  C. Kemp Terminal Illness: A Guide to Nursing Care , 1995 .

[37]  D. Fairclough,et al.  Understanding Economic and Other Burdens of Terminal Illness: The Experience of Patients and Their Caregivers , 2000, Annals of Internal Medicine.

[38]  H. Chochinov,et al.  Dying to Pay: The Cost of End-of-Life Care , 1998, Journal of palliative care.

[39]  S. Bloch,et al.  Family grief. , 1994, The British journal of psychiatry : the journal of mental science.

[40]  L. Kristjanson,et al.  The family's cancer journey: A literature review , 1994, Cancer nursing.