EpidemIBD: rationale and design of a large-scale epidemiological study of inflammatory bowel disease in Spain
- PMID: 31205485
- PMCID: PMC6535735
- DOI: 10.1177/1756284819847034
EpidemIBD: rationale and design of a large-scale epidemiological study of inflammatory bowel disease in Spain
Abstract
Background: Inflammatory bowel disease (IBD) is associated with a considerable burden to the patient and society. However, current data on IBD incidence and burden are limited because of the paucity of nationwide epidemiological studies, heterogeneous designs, and a low number of participating centers and sample size. The EpidemIBD study is a large-scale investigation to provide an accurate assessment of the incidence of IBD in Spain, as well as treatment patterns and outcomes.
Methods: This multicenter, population-based incidence cohort study included patients aged >18 years with IBD (Crohn's disease, ulcerative colitis, or unclassified IBD) diagnosed during 2017 in 108 hospitals in Spain, covering 50% of the Spanish population. Each participating patient will attend 10 clinic visits during 5 years of follow up. Demographic data, IBD characteristics and family history, complications, treatments, surgeries, and hospital admissions will be recorded.
Results: The EpidemIBD study is the first large-scale nationwide study to investigate the incidence of IBD in Spain. Enrollment is now completed and 3627 patients are currently being followed up.
Conclusions: The study has been designed to overcome many of the limitations of previous European studies into IBD incidence by prospectively recruiting a large number of patients from all regions of Spain. In addition to epidemiological information about the burden of IBD, the 5-year follow-up period will also provide information on treatment patterns, and the natural history and financial burden of IBD.
Keywords: Crohn’s disease; epidemiology; incidence; inflammatory bowel disease; ulcerative colitis.
Conflict of interest statement
Conflict of interest statement: M. Chaparro has served as a speaker, or has received research or education funding from MSD, Abbvie, Hospira, Pfizer, Takeda, Janssen, Ferring, Shire Pharmaceuticals, Dr. Falk Pharma, and Tillotts Pharma. M.J. Casanova has received education funding from Pfizer, Janssen, MSD, Abbvie, Ferring, Faes Farma, and Shire Pharmaceuticals. F. Gomollón has received honoraria for conference attendance from Janssen, Abbvie, Takeda and MSD, financial support for travel and registration to attend international conferences from Abbvie, Takeda and Janssen, and his research group has received financial grants from MSD, Abbvie and Tillots. J.L. Cabriada has served as consultant for, or received research funding from, MSD, Pfizer, Janssen, Takeda and Otsuka Pharma. M. Barreiro-de Acosta has served as a speaker, a consultant and advisory board member for, or has received research funding from, MSD, Abbvie, Janssen, Pfizer, Kern Pharma, Biogen, Takeda, Ferring, Faes Farma, Shire Pharmaceuticals, Dr. Falk Pharma, Tillotts Pharma, Chiesi, Gebro Pharma, Otsuka Pharma-ceutical and Vifor Pharma. S. Riestra has received honoraria for conference attendance from Janssen, Abbvie, Takeda and MSD, financial support for travel and registration to attend conferences from Abbvie, MSD and Janssen, and his research group has received financial grants from MSD, Abbvie and Takeda. M. Rivero has served as a speaker, a consultant and advisory board member for MSD, Abbvie and Janssen. M. Esteve acts as a consultant, assessor or scientific advisor for Abbott, MSD, Tillotts Pharma, Pfizer and Takeda and received research grants for MSD and Tillotts Pharma. J.P. Gisbert has served as a speaker, a consultant and advisory board member for, or has received research funding from, MSD, Abbvie, Hospira, Pfizer, Kern Pharma, Biogen, Takeda, Janssen, Roche, Celgene, Ferring, Faes Farma, Shire Pharmaceuticals, Dr. Falk Pharma, Tillotts Pharma, Chiesi, Casen Fleet, Gebro Pharma, Otsuka Pharmaceutical, Vifor Pharma.
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