Below are the first 10 and last 10 pages of uncorrected machine-read text (when available) of this chapter, followed by the top 30 algorithmically extracted key phrases from the chapter as a whole.
Intended to provide our own search engines and external engines with highly rich, chapter-representative searchable text on the opening pages of each chapter. Because it is UNCORRECTED material, please consider the following text as a useful but insufficient proxy for the authoritative book pages.
Do not use for reproduction, copying, pasting, or reading; exclusively for search engines.
OCR for page 11
Meeting Psychosocial Needs of Women with Breast Cancer 1 Introduction An estimated 251,200 women were diagnosed with invasive and in situ breast cancer in 2002 (American Cancer Society, 2002). For most of these women, initial feelings of shock, disbelief, and distress were followed by physical recovery and a return to good psychological health. A small group of women, however, had lingering and sometimes disabling psychological problems following their diagnosis. Most of these women lived to join the more than 2 million survivors of breast cancer, but may experience episodic or persistent distress. Nearly 40,000 women died of breast cancer in 2002, some of whom experienced poor coping, with inadequate support at the end of life. Of course, the number of people affected by these psychological problems is much greater than the number diagnosed and includes family, friends, and others in the community. The recognition and study of the psychological consequences of the cancer experience is the subject of the discipline of psycho-oncology, a field that emerged as a distinct discipline in the mid 1970s. For the first time, cancer, once a taboo topic, could be discussed openly, and more patients became willing to share their feelings and experience and participate in studies. Breast cancer has been the most extensively studied cancer from the standpoint of psychosocial sequelae, dating back to the mid-twentieth century, and remains the paradigm for the field (Shapiro et al., 2001). In this report, the National Cancer Policy Board reviews the now-extensive psycho-oncology literature to inform policy decisions regarding the delivery of compassionate breast cancer care. The purpose of this report is to:
OCR for page 12
Meeting Psychosocial Needs of Women with Breast Cancer characterize the psychosocial consequences of a diagnosis of breast cancer, evaluate the effectiveness of services to alleviate psychosocial distress, assess the status of psychosocial interventions in the context of contemporary breast cancer care, assess the status of professional education and training and applied clinical and health services research, and propose policies to improve the quality of care and quality of life for women with breast cancer and their families.1 Individuals with cancer may have cancer-specific concerns, such as fear of cancer recurrence, and generalized symptoms such as worry, trouble sleeping, fatigue, and anxiety about going to the doctor. Underlying mental illness may also be exacerbated by the experience of being diagnosed with cancer or living with the disease. To capture the broad range of concerns of individuals with cancer, the Board, in this report, has relied on the definition of “psychosocial distress” from the National Comprehensive Cancer Network. “We have defined ‘distress’ as it applies to cancer, as follows. Distress is an unpleasant experience of an emotional, psychological, social, or spiritual nature that interferes with the ability to cope with cancer treatment. It extends along a continuum, from common normal feelings of vulnerability, sadness, and fears to problems that are disabling, such as true depression, anxiety, panic, and feeling isolated or in a spiritual crisis” (NCCN, 1999:114). ROLE OF THE NATIONAL CANCER POLICY BOARD The National Cancer Policy Board (the Board) was established in March 1997 at the Institute of Medicine (IOM) and National Research Council with core support from the NCI and CDC to address issues that arise in the prevention, control, diagnosis, treatment, and palliation of cancer. The 20-member board includes health-care consumers, providers, and investigators in several disciplines (see membership roster). This report is one of three reports that comprise a Board initiative to address issues of concern for cancer survivors, with an emphasis on what happens following the primary treatment of cancer. The first report in that series, Childhood Cancer Survi- 1 Excluded from this review are the small number of men with breast cancer and healthy women who are at high-risk for breast cancer because of their genetic makeup or family history. The Board recognizes that each of these groups have unique health and psychosocial needs, but elected not to cover them in this report. The Board hopes in future reports to examine issues related to genetic testing and cancer.
OCR for page 13
Meeting Psychosocial Needs of Women with Breast Cancer vorship: Improving Care and Quality of Life, was published in 2003, and the final report on adult survivorship is expected in 2004. These reports (and others) follow and build on the Board’s 1999 report, Ensuring Quality Cancer Care, which recommended strategies to promote evidenced-based, comprehensive, compassionate, and coordinated care throughout the cancer care trajectory. In that report, the Board recommended that individuals have access to psychosocial support services; the report’s focus, however, was on primary treatment, and it did not extensively address issues related to the psychosocial needs of individuals with cancer (Institute of Medicine and National Research Council, 1999). Like its predecessors, this report speaks to stakeholders and policy makers in cancer care, to women with or concerned about breast cancer, and to the interested general public. This in-depth examination of cancer-related psychosocial issues is based, in part, on a 2-day IOM workshop held October 28–29, 2002, “Meeting Psychosocial Needs of Women with Breast Cancer” (see the workshop agenda in Appendix A). In addition to the Board’s core support, the workshop and this report were made possible by a generous grant from the Longaberger Company through the American Cancer Society. Two papers commissioned for the workshop were essential to this report, one by Dr. Patricia A. Ganz, on the assessment of psychosocial distress in clinical practice, and the other by Dr. Pamela J. Goodwin, a review of literature on the effectiveness of psychosocial intervention for women with breast cancer.2 The Board decided to focus on breast cancer largely because of the robust literature and extensive experience in this area. The Board, however, considers breast cancer a paradigm and suggests that the policy recommendations in this report are applicable to the psychosocial care provided generally to individuals with cancer. FRAMEWORK OF THE REPORT The report consists of several background chapters (Chapters 2–8) that summarize evidence that the Board used in formulating its recommendations, presented and discussed in the Executive Summary and Chapters 4, 7, and 8. Chapter 2 reviews the epidemiology of breast cancer to characterize the group of women at risk for psychosocial distress. Chapter 3 characterizes the psychological and social consequences of a diagnosis of breast cancer, the frequency of psychosocial distress, and the availability of assessments tools to help health-care providers identify women who may benefit from psychosocial interventions. 2 These papers are available at www.IOM.edu/ncpb.
OCR for page 14
Meeting Psychosocial Needs of Women with Breast Cancer Chapter 4 presents a brief description of the range of psychosocial interventions that are available, the sites in which they are offered, the providers who offer them, and psycho-oncology education and training opportunities for health-care providers. Chapter 5 reviews the effectiveness of psychosocial interventions with an emphasis on evidence from randomized clinical trials. The chapter concludes with a discussion of outstanding research issues that need to be addressed. Chapter 6 characterizes the delivery of psychosocial services in the context of contemporary breast cancer care, describes a number of service programs, and presents evidence regarding use of psychosocial services by women with breast cancer. Chapter 7 examines barriers to the receipt of psychosocial services, including issues related to access to care and limitations of systems of care. Chapter 8 surveys ongoing clinical and health services research aimed at improving psychosocial care and outlines research priorities to improve services to women with breast cancer. REFERENCES American Cancer Society. 2002. Cancer Facts & Figures 2002. Atlanta: American Cancer Society. Institute of Medicine and National Research Council. 1999. Ensuring Quality Cancer Care. Washington, DC: National Academy Press. Institute of Medicine and National Research Council. 2003. Childhood Cancer Survivorship: Improving Care and Quality of Life. Washington, DC: The National Academies Press. National Comprehensive Cancer Network. 1999. NCCN practice guidelines for the management of psychosocial distress. National Comprehensive Cancer Network. Oncology (Huntingt) 13(5A):113–147. Shapiro SL, Lopez AM, Schwartz GE, Bootzin R, Figueredo AJ, Braden CJ, Kurker SF. 2001. Quality of life and breast cancer: Relationship to psychosocial variables. J Clin Psychol 57(4):501–519.
Representative terms from entire chapter: