Scientific article

A comparison of patient characteristics and outcomes in selected European and U.S. rheumatoid arthritis registries

Published inSeminars in arthritis and rheumatism, vol. 40, no. 1, p. 2-14e11
Publication date2010

PURPOSE: Randomized controlled trials (RCTs) have demonstrated the efficacy of biologic agents in the treatment of rheumatic diseases. However, results from RCTs may not be generalizable to clinical practice because of their strict inclusion and exclusion criteria. Assessment of safety using RCT data also is limited by short duration of follow-up and relatively small sample sizes, which generally preclude analysis of longer term outcomes and rare adverse events. In rheumatology, various observational cohorts and registries have been created to complement information obtained from RCTs, some with the primary purpose of monitoring effectiveness and safety of biologic agents. Most registries are either drug based or disease based. These registries include patients with a variety of rheumatic diseases including RA. METHODS: To provide a qualitative comparison of selected U.S. and European rheumatoid arthritis (RA) biologics registries and cohorts including ARTIS, BIOBADASER, BSRBR, BRASS, CLEAR, CORRONA, NDB, RABBIT, SCQM, and VARA. RESULTS: A careful comparison of these registries, as provided in this article, can provide a basis for understanding the many similarities and differences inherent in their design, as well as societal context and content, all of which can significantly impact their results and comparisons across registers. SUMMARY: The increasing use of biologic agents for treatment of rheumatic diseases has raised important questions about cost, safety, and effectiveness of these agents. The unique and variable features of patient populations and registry designs in Europe and the U.S. provide valuable and complementary data on comparative effectiveness and safety of biologic agents to what can be derived from RCTs.

  • Antirheumatic Agents/*therapeutic use
  • Arthritis, Rheumatoid/*drug therapy/epidemiology/metabolism
  • Europe/epidemiology
  • Humans
  • Morbidity
  • Prognosis
  • Randomized Controlled Trials as Topic
  • *Registries
  • Tumor Necrosis Factor-alpha/*antagonists & inhibitors
  • United States/epidemiology
Citation (ISO format)
CURTIS, Jeffrey R. et al. A comparison of patient characteristics and outcomes in selected European and U.S. rheumatoid arthritis registries. In: Seminars in arthritis and rheumatism, 2010, vol. 40, n° 1, p. 2–14e11. doi: 10.1016/j.semarthrit.2010.03.003
Updates (1)
ISSN of the journal0049-0172

Technical informations

Creation23.05.2012 08:44:58
First validation23.05.2012 08:44:58
Update time14.03.2023 17:32:29
Status update14.03.2023 17:32:29
Last indexation28.08.2023 21:51:59
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