Changes in Use of Disease-Modifying Antirheumatic Drugs for Rheumatoid Arthritis in the United States During 1983-2009

被引:32
作者
Kim, Seoyoung C. [1 ]
Yelin, Ed [2 ]
Tonner, Chris [2 ]
Solomon, Daniel H. [1 ]
机构
[1] Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
FEE-FOR-SERVICE; CARE; TRENDS; RECOMMENDATIONS; OUTCOMES;
D O I
10.1002/acr.21997
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective. Use of nonbiologic disease-modifying antirheumatic drugs (DMARDs) and/or biologic DMARDs is generally recommended to improve the prognosis of patients with rheumatoid arthritis (RA). The objective of this study was to describe the changing trends in DMARD use for RA over the past 2 decades. Methods. We analyzed data from an open longitudinal cohort of RA patients recruited from rheumatologists' practices in northern California. We examined baseline demographic and clinical characteristics of the participants and their long-term DMARD use through annual comprehensive structured telephone interviews. Results. A total of 1,507 established RA patients were recruited through 5 enrollment periods between 1983 and 2009. Between 1983 and 2009, the use of any DMARD increased from 71% of all patients to 83% (P for trend < 0.0001). In 2009, 43% received a biologic DMARD, 34% were on both nonbiologic and biologic DMARDs, and 40% were treated with only nonbiologic DMARDs. The 4 most commonly used nonbiologic DMARDs in 2009 were methotrexate (49%), hydroxychloroquine (30%), leflunomide (13%), and sulfasalazine (7%). Etanercept (20%) was the most commonly used biologic DMARD in 2009, followed by infliximab (10%), adalimumab (9%), and abatacept (6%). Use of oral steroids was common (40-50%) and remained similar throughout the study period. Conclusion. There has been a significant increase in the use of DMARDs for RA over the past 2 decades. However, 15% of the individuals with a clinical diagnosis of RA were not receiving DMARDs in 2009. Future research should focus on sociodemographic and clinical factors associated with DMARD use for RA.
引用
收藏
页码:1529 / 1533
页数:5
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