Approximately 1.5 million new cases of cancer were expected to be diagnosed in the United States in 2009, and that number is expected to rise in 2010. Many patients diagnosed with cancer will eventually require support from a family caregiver. In fact, family caregivers form the foundation of the health care system in the United States, supporting advances in treatment such as multimodality treatment protocols given in outpatient and home settings.
Note: Some citations in the text of this section are followed by a level of evidence. The PDQ editorial boards use a formal ranking system to help the reader judge the strength of evidence linked to the reported results of a therapeutic strategy. (Refer to the PDQ summary on Levels of Evidence for more information.)
Incidence and Mortality
Note: Estimated new cases and deaths from testicular cancer in the United States in 2011:
New cases: 8,290.
Also referred to as informal caregivers, family caregivers provide a complex array of support tasks that extend across physical, psychological, spiritual, and emotional domains. Generally speaking, more women than men become caregivers, most caregivers are related to the person who has cancer, and most caregivers are aged 55 years or older.[5,6]
Family caregivers play an important role in the management of cancer; enlisting their cooperation and including them as the unit of care from the outset are considered critical ingredients to effective cancer management. Most oncology teams recognize this and try to include family caregivers in treatment planning, decision making, and implementation. However, for interventions to be feasible, they must be appropriate within the constraints of busy oncology practices and service delivery environments. Short-term hospital admissions may also restrict the time available to implement supportive strategies for caregivers.
Information about the following is included in this summary:
An overview of the caregiver's perspective across the illness trajectory in cancer.
Typical caregiver roles and concerns.
In this summary, unless otherwise stated, evidence and practice issues as they relate to adults are discussed. The evidence and application to practice related to children may differ significantly from information related to adults. When specific information about the care of children is available, it is summarized under its own heading.
American Cancer Society.: Cancer Statistics 2009: A Presentation from the American Cancer Society. Atlanta, Ga: American Cancer Society, 2009. Available online. Last accessed June 16, 2011.
American Cancer Society.: Cancer Facts and Figures 2010. Atlanta, Ga: American Cancer Society, 2010. Also available online. Last accessed June 16, 2011.
Schumacher KL, Stewart BJ, Archbold PG, et al.: Effects of caregiving demand, mutuality, and preparedness on family caregiver outcomes during cancer treatment. Oncol Nurs Forum 35 (1): 49-56, 2008.
Honea NJ, Brintnall R, Given B, et al.: Putting Evidence into Practice: nursing assessment and interventions to reduce family caregiver strain and burden. Clin J Oncol Nurs 12 (3): 507-16, 2008.
Alecxih LMB, Zeruld S, Olearczyk B: Characteristics of Caregivers Based on the Survey of Income and Program Participation. National Family Caregiver Support Program: Selected Issue Briefs. Washington, DC: U.S. Department of Health and Human Services, Administration on Aging, 2001. Also available online. Last accessed June 16, 2011.
Sherwood PR, Given BA, Given CW, et al.: Predictors of distress in caregivers of persons with a primary malignant brain tumor. Res Nurs Health 29 (2): 105-20, 2006.
Glajchen M: The emerging role and needs of family caregivers in cancer care. J Support Oncol 2 (2): 145-55, 2004 Mar-Apr.
Hudson PL, Aranda S, Kristjanson LJ: Meeting the supportive needs of family caregivers in palliative care: challenges for health professionals. J Palliat Med 7 (1): 19-25, 2004.