Deng, Jie Fu, Mei R. Armer, Jane M. Cormier, Janice N. Radina, M. Elise Thiadens, Saskia R.J. Weiss, Jan Tuppo, Catherine M. Dietrich, Mary S. and Ridner, Sheila H. 2017. Factors Associated with Reported Infection and Lymphedema Symptoms among Individuals with Extremity Lymphedema. Rehabilitation Nursing, Vol. 40, Issue. 5, p. 310.
Willis, Karen Lewis, Sophie Ng, Fiona and Wilson, Leigh 2017. The Experience of Living With Metastatic Breast Cancer—A Review of the Literature. Health Care for Women International, Vol. 36, Issue. 5, p. 514.
Heiney, Sue P. Underwood, Sandra Millon Tavakoli, Abbas Adams, Swann Arp Wells, Linda M. and Bryant, Lisa H. 2017. Randomized trial of therapeutic group by teleconference. Cancer, Vol. 118, Issue. 15, p. 3822.
Lewis, Joanne M. DiGiacomo, Michelle Currow, David C. and Davidson, Patricia M. 2017. Dying in the Margins: Understanding Palliative Care and Socioeconomic Deprivation in the Developed World. Journal of Pain and Symptom Management, Vol. 42, Issue. 1, p. 105.
Lu, Hsueh-Yi Shaw, Bret R. and Gustafson, David H. 2017. Online health consultation: Examining uses of an interactive cancer communication tool by low-income women with breast cancer. International Journal of Medical Informatics, Vol. 80, Issue. 7, p. 518.
Kaiser, Natalie C. Hartoonian, Narineh and Owen, Jason E. 2017. Toward a cancer-specific model of psychological distress: population data from the 2003–2005 National Health Interview Surveys. Journal of Cancer Survivorship, Vol. 4, Issue. 4, p. 291.
Disparities in breast cancer survival and treatment for African American and low income women are well documented, yet poorly understood. As care for women with metastatic breast cancer (MBC) evolves to a chronic care model, any inequities in optimal treatment and management of symptoms must also be identified and eliminated. The purpose of this study was to explore how race and income status influence women's experiences with MBC, particularly the management of symptoms, by describing the perceived challenges and barriers to achieving optimal symptom management among women with MBC and exploring whether the perceived challenges and barriers differed according to race or income.
Quantitative techniques were used to assess demographics, clinical characteristics, symptom distress, and quality of life and to classify women into groups according to race and income. Qualitative techniques were used to explore the perceived challenges, barriers, and potential influences of race and income on management of symptoms in a prospective sample of 48 women with MBC.
Commonalities of themes across all groups were faith, hope, and progressive loss. Low-income African American women uniquely experienced greater physical and social distress and more uncertainty about treatment and treatment goals than the other delineated racial and economic groups.
There are many commonalities to the challenges of illness presented to women with MBC. There are also interesting, emerging thematic racial and economic differences, most compelling among the low income African American women with resultant practice and research implications.
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