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Date: Oct. 23, 2007
Contacts: Christine Stencel, Media Relations Officer
Kimberly Berryman, Media Relations Assistant
Office of News and Public Information
202-334-2138; e-mail <firstname.lastname@example.org>
FOR IMMEDIATE RELEASE
Eradicating Tumors Is Not Enough; Cancer Care Providers Need to Proactively Address Patients' Psychological and Social Needs As Well
The report proposes a new standard of care under which all oncology care providers would systematically screen patients for distress and other problems; connect patients with health care or service providers who have resources to tackle these issues and coordinate care with these professionals; and periodically re-evaluate patients to determine if any changes in care are needed.
To achieve this standard, the report recommends an evidence-based model for ensuring that psychosocial health services are an integral part of cancer care and provides strategies for implementing this model in settings with varying levels of resources. The vision laid out in the report could apply to the care of other serious chronic illnesses as well, noted the authoring committee.
"Killing cancer cells is important, but it's not enough to ensure that the adverse effects of patients' therapies don't undermine their gains," said committee chair Nancy E. Adler, vice chair, department of psychiatry, and director, Center for Health and Community, University of California, San Francisco. "This report provides an action plan for overcoming the barriers to psychosocial health services that patients need to be as healthy and whole as possible during and after cancer treatment."
Many of the services and resources already exist, often at no cost to patients, but oncology providers are not proactively identifying patients' needs and helping them find and use these resources, the committee noted. Because many of these services are free or are reimbursable through health insurance providers and programs, the creation of new benefits or payment mechanisms would not be necessary for the most part, the report says.
Cancer patients' psychosocial needs range from information about their therapies and the potential physical side effects, to treatment for depression, stress, or other mental and emotional conditions; assistance with daily activities that they can no longer perform independently; and assistance with transportation, prosthetics, medications, and other supplies they cannot afford or to which they do not have ready access. The report lists multiple resources of free services and information available to cancer patients and their families.
The committee acknowledged that currently there are not enough psychosocial services and resources to meet the needs of all patients and that cancer care providers can only partially resolve some problems, such as lack of health insurance or poverty. However, this should not preclude attempts to remedy as many psychosocial problems as possible.
Because individual clinical practices vary by their setting and patient population as well as by available resources, they will also vary in how they implement the proposed standard of care. The report offers examples of how some large and small practices deliver this care successfully and suggests ways that even providers with limited resources could do so.
"Many cancer care providers may be surprised at the array of psychosocial health services available nationwide at no cost to patients," said committee member Patricia Ganz, director, cancer prevention and control research, Jonsson Comprehensive Cancer Center, University of California, Los Angeles. "Our report also provides practical guidance to providers about how they can design their practices to better address their patients' needs."
The policies and practices of many health insurance purchasers and payers support the delivery of psychosocial health care, but they are not delivering this care uniformly, the committee concluded. Not all insurance plans fully use available mechanisms to compensate providers for assessments and interventions to develop tailored care plans, help patients manage their illnesses, and coordinate their care with other providers.
Group purchasers -- Medicare, Medicaid, and employers -- and health insurance plans should assess how psychosocial care is addressed in their agreements with each other and with health care providers and determine the adequacy of payment rates, the report says. They may find, for example, that interventions are currently covered in their payment and reimbursement mechanisms. However, mechanisms may need to be developed for reimbursing higher-than-average levels of care coordination.
Multiple organizations could significantly influence cancer care providers' adherence to the proposed standard of care. The National Cancer Institute, as the nation's leader in developing better approaches to cancer care, could include requirements for addressing psychosocial health needs in its protocols, standards, and programs. Standard-setting organizations such as the National Comprehensive Cancer Network -- an alliance of 20 leading cancer centers in the
The study was sponsored by the National Institutes of Health. Established in 1970 under the charter of the National Academy of Sciences, the
Copies of Cancer Care for the Whole Patient: Meeting Psychosocial Health Needs are available from the National Academies Press; tel. 202-334-3313 or 1-800-624-6242 or on the Internet at http://www.nap.edu. Reporters may obtain a copy from the Office of News and Public Information (contacts listed above).
[ This news release and report are available at http://national-academies.org ]
Board on Health Care Services
Committee on Psychosocial Services to Cancer Patients/Families in a Community Setting
Nancy E. Adler, Ph.D. (Chair)
Professor of Medical Psychology, and
Department of Psychiatry
Rhonda J. Robinson Beale, M.D.
Chief Medical Officer
United Behavioral Health
Diane Blum, M.S.W.
Patricia A. Ganz, M.D.
UCLA Schools of Medicine and Public Health and
Sherry Glied, Ph.D.
Professor and Chair
Department of Health Policy and Management
Jessie Gruman, Ph.D.
Center for the Advancement of Health
Michael Hoge, Ph.D.
Professor of Psychology
Jimmie C. Holland, M.D.
Wayne E. Chapman Chair in Psychiatric Oncology
Melissa M. Hudson, M.D.
After Completion of Therapy Clinic
St. Jude Children’s
Sherrie H. Kaplan, Ph.D.
Associate Dean for Clinical Policy and Health Services Research
Alicia Matthews, Ph.D.
Ruth Mccorkle, Ph.D.
Center for Excellence in Chronic Illness Care
Harold Alan Pincus, M.D.
Department of Psychiatry
Director of Quality and Outcomes Research
New York-Presbyterian Hospital
Lee Schwartzberg, M.D., F.A.C.P.
Senior Partner and Medical Director
The West Clinic
Edward H. Wagner, M.D., M.P.H., F.A.C.P.
MacColl Institute for Healthcare Innovation
Center for Health Studies
Group Health Cooperative
Terrie Wetle, Ph.D.
Associate Dean of Medicine
Public Health and Public Policy
Ann E.K. Page