Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.

Journal Article (Journal Article)

CONTEXT: Perceived discriminatory experiences in society have been associated with a higher burden of pain among some minority patient populations. OBJECTIVES: To describe the extent to which patients with sickle cell disease (SCD) perceive discrimination from health care providers and to examine the association of these experiences with the burden of chronic SCD pain. METHODS: Cross-sectional analysis of data collected at baseline of a prospective cohort study of SCD patient experiences of care (n = 291). Perceived race-based and disease-based discrimination from health care providers were measured using subscales adapted from the Interpersonal Processes of Care Survey. Discrimination scores were examined for their association with patient characteristics and measures of pain burden using descriptive, bivariate, and multivariate analytic techniques. RESULTS: Respondents reported a greater burden of race-based discrimination from health care providers than has been previously reported by African Americans, and they reported a greater amount of disease-based vs. race-based discrimination. Age and having difficulty persuading providers about pain were the only patient characteristics independently associated with race-based discrimination, whereas older age, greater emergency room utilization, having difficulty persuading providers about pain, daily chronic pain, fewer good days during a week, and a higher severity of pain on their good days were independently associated with greater disease-based discrimination. CONCLUSION: Perceived disease-based, but not race-based, discrimination was found to be associated with a greater range of self-reported pain among patients with SCD. If causal, this finding could signal an important new approach to mitigating the burden of pain experienced by persons with SCD.

Full Text

Duke Authors

Cited Authors

  • Haywood, C; Diener-West, M; Strouse, J; Carroll, CP; Bediako, S; Lanzkron, S; Haythornthwaite, J; Onojobi, G; Beach, MC; IMPORT Investigators,

Published Date

  • November 2014

Published In

Volume / Issue

  • 48 / 5

Start / End Page

  • 934 - 943

PubMed ID

  • 24742787

Pubmed Central ID

  • PMC4198520

Electronic International Standard Serial Number (EISSN)

  • 1873-6513

Digital Object Identifier (DOI)

  • 10.1016/j.jpainsymman.2014.02.002


  • eng

Conference Location

  • United States