Background: The Ulcerative Colitis (UC) Narrative global survey assessed aspects of living with UC. This analysis aimed to identify health care disparities, social determinants of health, and emotional impacts related to UC disease management, patient experience, and quality of life. Methods: The survey was conducted by The Harris Poll from August 2017 to February 2018 among adults with UC. Responses from 1000 patients in the United States, Canada, Japan, France, and Finland were analyzed based on patient income, employment status, educational level, age, sex, and psychological comorbidities. Odds ratios (ORs) with significant P values (P
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Odufalu, F. D., Dubinsky, M. C., Peyrin-Biroulet, L., Ylänne, K., Sipes, A., Cappelleri, J. C., … Panaccione, R. (2023). Health Care Disparities, Social Determinants of Health, and Emotional Impacts in Patients with Ulcerative Colitis: Results from a Global Ulcerative Colitis Narrative Patient Survey. Inflammatory Bowel Diseases, 29(11), 1681–1692. https://doi.org/10.1093/ibd/izad102
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