Burden of Crohn’s disease in the United States: long-term healthcare and work-loss related costs

42Citations
Citations of this article
69Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Aims: To quantify the long-term direct and indirect costs among patients with Crohn’s disease (CD) and specific subgroups of these patients in the United States from the private payer’s perspective. Materials and methods: This retrospective study used the OptumHealth Care Solutions, Inc database (01 January 1999–31 March 2017) to match (1:5) adult patients with ≥2 claims for CD to patients without inflammatory bowel disease (IBD). Patterns observed during follow-up (i.e. biologics, opioids, or steroids; CD-related surgery; moderate-to-severe disease; and comorbidities) were used to identify CD subgroups. Comparisons of healthcare resource utilization, work loss days, and direct and indirect work loss-related costs were made between matched cohorts. Descriptive analyses of costs were conducted within each CD subgroup. Results: There were 6,715 and 33,575 patients in the CD and non-IBD cohorts, respectively. The direct burden was significantly higher in the CD cohort compared to the non-IBD cohort, with 0.34 inpatient admissions per patient per year (PPPY) versus 0.12 (217% increase; p

Cite

CITATION STYLE

APA

Manceur, A. M., Ding, Z., Muser, E., Obando, C., Voelker, J., Pilon, D., … Lefebvre, P. (2020). Burden of Crohn’s disease in the United States: long-term healthcare and work-loss related costs. Journal of Medical Economics, 1092–1101. https://doi.org/10.1080/13696998.2020.1789649

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free