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Prescribing practices in a US cohort of rheumatoid arthritis patients before and after publication of the American College of Rheumatology treatment recommendations

期刊

ARTHRITIS AND RHEUMATISM
卷 64, 期 3, 页码 630-638

出版社

WILEY-BLACKWELL
DOI: 10.1002/art.33380

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资金

  1. NIH [AR-053856, AR-053351, AR-054412]
  2. Arthritis Foundation
  3. Abbott
  4. Amgen
  5. Bristol-Myers Squibb
  6. Centocor
  7. Genentech
  8. Lilly
  9. Roche
  10. Innovations Consulting
  11. CME Outfitters
  12. Health Interactions
  13. Elsevier
  14. CORRONA registry
  15. Pfizer
  16. Crescedro
  17. UCB
  18. Actelion
  19. Biogen Idec
  20. Gilead
  21. GlaxoSmithKline
  22. Merck
  23. Nitec
  24. Novartis
  25. Wyeth
  26. Xoma
  27. AstraZeneca

向作者/读者索取更多资源

Objective To examine prescribing practices in the use of biologic and nonbiologic disease-modifying antirheumatic drugs (DMARDs) to treat patients with rheumatoid arthritis (RA), before and after publication of the American College of Rheumatology (ACR) treatment recommendations. Methods. Biologics-naive RA patients under the care of a rheumatologist in the US were identified from the Consortium of Rheumatology Researchers of North America registry. Patients were included if their visits occurred prior to and/ or at least 6 months after publication of the ACR treatment recommendations (time periods of February 2002-June 2008 versus December 2008-December 2009). The population was divided into 2 mutually exclusive cohorts: 1) methotrexate (MTX) monotherapy users, and 2) multiple nonbiologic DMARD users. Initiation or dose escalation of biologic and nonbiologic DMARDs in response to active disease was assessed cross-sectionally and longitudinally in comparison to the ACR recommendations. The impact of the publication of the ACR recommendations on treatment practices was assessed using logistic regression, stratified by disease activity and adjusted for clustering of physicians and geographic region. Results. After 1 visit, 24-37% of patients receiving MTX monotherapy who had moderate disease activity and a poor prognosis or high disease activity received care consistent with the ACR recommendations; after 2 visits, 34-56% of the MTX monotherapy group received care consistent with the recommendations. In the patients receiving multiple nonbiologic DMARDs, 3147% of those with moderate or high disease activity received care consistent with the recommendations after 1 visit, and 43-51% received such care after 2 visits. Publication of the recommendations did not significantly change treatment patterns for those with active disease. Conclusion. Substantial numbers of RA patients with active disease did not receive care consistent with the current ACR treatment recommendations. Innovative approaches to improve care are necessary.

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