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Choosing to End African American Health Disparities in Patients With Systemic Lupus Erythematosus.
Liang, Matthew H; Lew, Edward R; Fraser, Patricia A; Flower, Cindy; Hennis, Edward H; Bae, Sang-Cheol; Hennis, Anselm; Tikly, Mohammed; Roberts, W Neal.
Afiliación
  • Liang MH; Veterans Affairs Boston Healthcare System, Brigham and Women's Hospital, and Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
  • Lew ER; University of Massachusetts Amherst.
  • Fraser PA; Brigham and Women's Hospital, Boston, Massachusetts.
  • Flower C; University of the West Indies, Cave Hill campus, Barbados.
  • Hennis EH; Allegheny General Hospital, Pittsburgh, Pennsylvania.
  • Bae SC; Hanyang University Hospital for Rheumatic Diseases, Hanyang University Institute for Rheumatology Research, and Hanyang Institute of Bioscience and Biotechnology, Seoul, Korea.
  • Hennis A; University of the West Indies, Cave Hill campus, Barbados.
  • Tikly M; The Chris Hani Baragwanath Academic Hospital, Johannesburg, South Africa, and Life Roseacres Hospital, Primrose, Germiston, South Africa.
  • Roberts WN; University of Kentucky Medical Center, Lexington.
Arthritis Rheumatol ; 76(6): 823-835, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38229482
ABSTRACT
Systemic lupus erythematosus (SLE) is three times more common and its manifestations are more severe in African American women compared to women of other races. It is not clear whether this is due to genetic differences or factors related to the physical or social environments, differences in health care, or a combination of these factors. Health disparities in patients with SLE between African American patients and persons of other races have been reported since the 1960s and are correlated with measures of lower socioeconomic status. Risk factors for these disparities have been demonstrated, but whether their mitigation improves outcomes for African American patients has not been tested except in self-efficacy. In 2002, the first true US population-based study of patients with SLE with death certificate records was conducted, which demonstrated a wide disparity between the number of African American women and White women dying from SLE. Five years ago, another study showed that SLE mortality rates in the United States had improved but that the African American patient mortality disparity persisted. Between 2014 and 2021, one study demonstrated racism's deleterious effects in patients with SLE. Racism may have been the unmeasured confounder, the proverbial "elephant in the room"-unnamed and unstudied. The etymology of "risk factor" has evolved from environmental risk factors to social determinants to now include structural injustice/structural racism. Racism in the United States has a centuries-long existence and is deeply ingrained in US society, making its detection and resolution difficult. However, racism being man made means Man can choose to change the it. Health disparities in patients with SLE should be addressed by viewing health care as a basic human right. We offer a conceptual framework and goals for both individual and national actions.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Negro o Afroamericano / Disparidades en Atención de Salud / Lupus Eritematoso Sistémico Tipo de estudio: Risk_factors_studies Aspecto: Determinantes_sociais_saude / Equity_inequality Límite: Female / Humans País/Región como asunto: America do norte Idioma: En Revista: Arthritis Rheumatol Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Negro o Afroamericano / Disparidades en Atención de Salud / Lupus Eritematoso Sistémico Tipo de estudio: Risk_factors_studies Aspecto: Determinantes_sociais_saude / Equity_inequality Límite: Female / Humans País/Región como asunto: America do norte Idioma: En Revista: Arthritis Rheumatol Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos