Your browser doesn't support javascript.
loading
Racial and Ethnic Disparities in Health-Related Outcomes in Crohn's Disease: Results From the National Health and Wellness Survey.
Burbage, Sabree C; Krupsky, Kathryn L; Cambron-Mellott, M Janelle; Way, Nate; Patel, Aarti A; Liu, Julia J.
Afiliação
  • Burbage SC; Population Health Research, Janssen Scientific Affairs, LLC, Horsham, PA, USA.
  • Krupsky KL; Real-World Evidence, Cerner Enviza, an Oracle Company, Kansas City, MO, USA.
  • Cambron-Mellott MJ; Real-World Evidence, Cerner Enviza, an Oracle Company, Kansas City, MO, USA.
  • Way N; Real-World Evidence, Cerner Enviza, an Oracle Company, Kansas City, MO, USA.
  • Patel AA; Population Health Research, Janssen Scientific Affairs, LLC, Horsham, PA, USA.
  • Liu JJ; Division of Gastroenterology, Morehouse School of Medicine, Atlanta, GA, USA.
Crohns Colitis 360 ; 6(2): otae021, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38660453
ABSTRACT

Background:

Crohn's disease (CD) is a chronic inflammatory condition affecting the entire gastrointestinal tract that is associated with significant humanistic, clinical, and economic burdens. Few studies have assessed the association between CD severity and patient-reported outcomes (PROs), healthcare resource utilization (HCRU), and medical costs; even fewer have examined differences in disease outcomes among patients of various racial/ethnic groups.

Methods:

In this cross-sectional study, sociodemographic data, PROs, and economic outcomes for participants with self-reported CD were collected from the National Health and Wellness Survey (2018-2020). Multivariable analyses were used to assess the association of CD severity and race/ethnicity with health-related quality of life (HRQoL), work productivity and activity impairment (WPAI), HCRU, and medical costs.

Results:

Analyses included 1077 participants with CD (818 non-Hispanic White, 109 non-Hispanic Black, and 150 Hispanic). Participants with self-reported moderate/severe CD reported significantly worse HRQoL and WPAI, greater HCRU, and higher medical costs than those with self-reported mild CD. Non-Hispanic Black participants reported better HRQoL and fewer healthcare provider visits than non-Hispanic White participants. There were no significant differences in PROs between non-Hispanic White and Hispanic groups. Interactions between race/ethnicity and CD severity emerged for some, but not all groups Specifically, non-Hispanic Black participants with moderate/severe CD reported greater absenteeism and more gastroenterologist visits than non-Hispanic Black participants with mild CD.

Conclusions:

Participants with moderate/severe CD reported worse PROs, greater HCRU, and higher medical costs than those with mild CD. Additionally, racial/ethnic differences were found across several HCRU and economic outcomes. Further research is needed to better understand factors contributing to burden among patients with varying CD severity across racial/ethnic groups.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article