4.4 Review

Preventing disability in inflammatory bowel disease

Journal

THERAPEUTIC ADVANCES IN GASTROENTEROLOGY
Volume 10, Issue 11, Pages 865-876

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1756283X17732720

Keywords

Crohn's disease; disability; functioning; inflammatory bowel disease; multiple sclerosis; rheumatoid arthritis; ulcerative colitis

Funding

  1. Merck
  2. Abbvie
  3. Janssen
  4. Ferring
  5. Tillots
  6. Celgene
  7. Takeda
  8. Norgine
  9. GSK
  10. Allergan
  11. Takeda France
  12. MSD France
  13. Ferring France
  14. Genentech
  15. Mitsubishi
  16. Vifor
  17. Therakos
  18. Pharmacosmos
  19. Pilege
  20. BMS
  21. UCB-pharma
  22. Hospira
  23. Celltrion
  24. Biogaran
  25. Boerhinger-Ingelheim
  26. Lilly
  27. Pfizer
  28. HAC-Pharma
  29. Index Pharmaceuticals
  30. Amgen
  31. Sandoz
  32. Forward Pharma GmbH
  33. Biogen
  34. Lycera
  35. Samsung Bioepis

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Disability is a common worldwide health challenge and it has been increasing over the past 3 decades. The treatment paradigm has changed dramatically in inflammatory bowel diseases (IBDs) from control of symptoms towards full control of disease (clinical and endoscopic remission) with the goal of preventing organ damage and disability. These aims are broadly similar to rheumatoid arthritis and multiple sclerosis. Since the 1990s, our attention has focused on quality of life in IBD, which is a subjective measure. However, as an objective end-point in clinical trials and population studies, measures of disability in IBD have been proposed. Disability is defined as ... any restriction or lack (resulting from an impairment) of ability to perform an activity in the manner or within the range considered normal for a human being.' Recently, after 10 years of an international collaborative effort with the World Health Organization (WHO), a disability index was developed and validated. This index ideally would assist with the assessment of disease progression in IBD. In this review, we will provide the evidence to support the use of disability in IBD patients, including experience from rheumatoid arthritis and multiple sclerosis. New treatment strategies, and validation studies that have underpinned the interest and quantification of disability in IBD, will be discussed.

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