Biological and Immunomodulator Use in Crohn's Disease in a Medicaid Population

Mark H Flasar1, Jingdong Chao, A Burak Ozbay

  • 1*Division of Gastroenterology and Hepatology, University of Maryland School of Medicine, Baltimore, Maryland; †AbbVie Inc., North Chicago, Illinois; and ‡Analysis Group Inc., Boston, Massachusetts.

Inflammatory Bowel Diseases
|February 26, 2016
PubMed

Insights

Treatment disparities in Crohn's disease (CD) may affect Hispanic (H) patients with severe disease. African Americans (AA) and Whites (W) showed similar use of immunomodulators and biologics for CD. Further research is needed for H patients.

Area of Science:

  • Gastroenterology and Hepatology
  • Health Services Research
  • Pharmacoeconomics

Background:

  • Previous reports suggest lower use of immunomodulators and biologics in African Americans (AA) with Crohn's disease (CD) compared to Whites (W).
  • Limited data exist regarding treatment disparities for Hispanic (H) populations with CD.
  • Understanding racial and ethnic differences in biologic and immunomodulator use is crucial for equitable CD management.

Purpose of the Study:

  • To investigate potential racial and ethnic disparities in the initiation of immunomodulators and biologics among patients with Crohn's disease (CD).
  • To compare the utilization of biologic therapies for CD across White (W), African American (AA), and Hispanic (H) patient groups.
  • To assess the impact of disease severity on treatment access for different racial and ethnic groups with CD.

Main Methods:

  • Analysis of Medicaid databases from three states (August 1998-July 2009) for patients diagnosed with Crohn's disease (CD).
  • Assessment of CD-related treatments, comorbidities, healthcare utilization, and time to first biologic claim.
  • Application of Cox proportional hazard regression models to evaluate the effect of race and ethnicity on biologic initiation, adjusting for covariates and disease severity.

Main Results:

  • No significant differences in immunomodulator initiation were observed between White (W), African American (AA), and Hispanic (H) patients (18%, 17%, 17% respectively).
  • Overall biologic initiation rates were similar across W, AA, and H patients (7%, 9%, 5% respectively); adjusted models showed no significant disparities between AA and W, or H and W.
  • However, after adjusting for disease severity (hospitalization post-diagnosis), Hispanic (H) patients were significantly less likely to initiate biologics compared to White (W) patients (hazard ratio 0.40).

Conclusions:

  • Disparities in immunomodulator or biologic use between African Americans (AA) and Whites (W) with Crohn's disease (CD) may not be significant.
  • Hispanic (H) patients with more severe CD may face significant barriers to accessing biologic therapies compared to White (W) patients.
  • Further research is warranted to confirm these findings and explore the underlying reasons for treatment disparities in specific populations with severe CD.
Abstract

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