4181.0: Tuesday, November 14, 2000 - 3:30 PM

Abstract #10569

Developing innovative community plans for reducing racial disparities in access to end-of-life care

Walter J. Jones, PhD1, Susan I. DesHarnais, PhD1, and Jerome Kurent, MD2. (1) Department of Health Administration and Policy, Medical University of South Carolina, 171 Ashley Avenue, Charleston, SC 29425, 843-792-8464, jonesw@musc.edu, (2) Center for the Study of Aging, Medical University of South Carolina, 171 Ashley Avenue, Charleston, SC 29425

A growing amount of research has documented disparities between African-American and white populations with respect to access to end-of-life care. Decisions regarding end-of-life care are complex, and require substantial and effective patient-provider communication. Unfortunately, there is considerable evidence that white health providers' communication with African-American patients is often seriously flawed. Language patterns and social mores often differ between the two groups. In addition, many African-Americans (who are disproportionately likely to be medically uninsured and to reside in medically underserved areas) are often suspicious of end-of-life care options that are offered to them by the largely white medical establishment, feeling that they are often simply a covert effort to save money by reducing medical services. This leads to unsatisfactory decisionmaking on care options for terminally ill African-American patients, particularly for those patients who are low income and from medically underserved areas. To overcome these racial disparities, providers must better understand the reasons for patient-provider communication problems, and develop innovative community programs that can overcome them. The developing research of the authors analyzes the reasons for provider communication problems with terminally ill African-American cancer and congestive heart failure (CHF) patients. Using specific examples obtained from existing end-of-life care programs, the authors also show how these problems can be overcome through the development of community-based structures that entail innovative provider training programs (including the use of on-line curricula for physician training), more effectively targeted resources, more community-friendly caregiving structures, and greater family and community involvement with medical providers.

Learning Objectives: At the conclusion of this presentation, the participant should be able to: 1. Understand the racial disparities that currently exist in access to end-of-life care. 2. Recognize the problems that often exist in provider - patient communication with respect to African-American patients. 3. List the reasons for such communication problems, as shown by research findings. 4. Assess alternative methods for overcoming communication problems with end-of-life African-American patients, as illustrated by specific community-based programs

Keywords: End-of-Life Care, Patient Perspective

Presenting author's disclosure statement:
Organization/institution whose products or services will be discussed: None
I do not have any significant financial interest/arrangement or affiliation with any organization/institution whose products or services are being discussed in this session.

The 128th Annual Meeting of APHA