Harrold Leslie R, Harrington J Timothy, Curtis Jeffrey R, Furst Daniel E, Bentley Mary Jane, Shan Ying, Reed George, Kremer Joel, Greenberg Jeffrey D
University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Arthritis Rheum. 2012 Mar;64(3):630-8. doi: 10.1002/art.33380.
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.
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.
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, 31-47% 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.
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.
在美国风湿病学会(ACR)发布治疗建议之前及之后,研究使用生物和非生物改善病情抗风湿药(DMARDs)治疗类风湿关节炎(RA)患者的处方行为。
从北美风湿病研究人员联盟登记处识别出在美国风湿病专家照料下的初治生物制剂的RA患者。如果患者的就诊时间在ACR治疗建议发布之前和/或之后至少6个月(2002年2月至2008年6月与2008年12月至2009年12月这两个时间段),则纳入研究。将研究人群分为两个相互排斥的队列:1)甲氨蝶呤(MTX)单药治疗使用者,以及2)多种非生物DMARD使用者。与ACR建议相比,对因疾病活动而启动或增加生物和非生物DMARD剂量的情况进行横断面和纵向评估。使用逻辑回归评估ACR建议的发布对治疗实践的影响,按疾病活动度分层,并对医生聚类和地理区域进行调整。
就诊1次后,接受MTX单药治疗且疾病活动度中等、预后较差或疾病活动度高的患者中,24% - 37%接受了符合ACR建议的治疗;就诊2次后,MTX单药治疗组中34% - 56%的患者接受了符合建议的治疗。在接受多种非生物DMARDs治疗的患者中,疾病活动度中等或高的患者中,就诊1次后31% - 47%接受了符合建议的治疗,就诊2次后43% - 51%接受了此类治疗。建议的发布并未显著改变疾病活动患者的治疗模式。
大量患有活动性疾病的RA患者未接受符合当前ACR治疗建议的治疗。需要创新方法来改善治疗。