4.4 Review

Disparities in lupus care and outcomes

Journal

CURRENT OPINION IN RHEUMATOLOGY
Volume 21, Issue 2, Pages 102-109

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/BOR.0b013e328323daad

Keywords

health disparities; heath care access; socioeconomic status; systemic lupus erythematosus

Categories

Funding

  1. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [K12HD051959] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [P60AR047782] Funding Source: NIH RePORTER
  3. NIAMS NIH HHS [P60 AR047782, P60 AR047782-08] Funding Source: Medline
  4. NICHD NIH HHS [K12 HD051959, K12 HD051959-03] Funding Source: Medline

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Purpose of review Systemic lupus erythematosus (SLE), an inflammatory rheumatic disease characterized by autoantibody production and diverse clinical manifestations, disproportionately affects vulnerable groups: women, racial and ethnic minorities, the poor and those lacking medical insurance and education. We summarize the current knowledge of the disparities observed in SLE and highlight recent research that aims to dissect the causes of these disparities and identify the potentially modifiable factors contributing to them. Recent findings Several remediable causes, including lack of education, self-efficacy and access to quality, experienced healthcare have been found to contribute to observed disparities in SLE prevalence and outcomes. Summary SLE is associated with alarming disparities in incidence, severity and outcomes. The causes of these disparities are under study by several research groups. Identifying potentially correctable contributory factors should allow the development of effective strategies to improve the healthcare delivery and outcomes in all SLE patients.

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