Harrold Leslie R, Reed George W, Kremer Joel M, Curtis Jeffrey R, Solomon Daniel H, Hochberg Marc C, Kavanaugh Arthur, Saunders Katherine C, Shan Ying, Spruill Tanya M, Pappas Dimitrios A, Greenberg Jeffrey D
Department of Medicine, University of Massachusetts Medical School, AC7-201, 55 Lake Avenue North, Worcester, MA, 01655, USA.
Corrona, LLC, Southborough, MA, USA.
Arthritis Res Ther. 2016 Apr 26;18:94. doi: 10.1186/s13075-016-0992-3.
Factors associated with care concordant with the American College of Rheumatology (ACR) recommendations for the use of disease-modifying antirheumatic drugs (DMARDs) in rheumatoid arthritis (RA) are unknown.
We identified a national cohort of biologic-naive patients with RA with visits between December 2008 and February 2013. Treatment acceleration (initiation or dose escalation of biologic and nonbiologic DMARDs) in response to moderate to high disease activity (using the Clinical Disease Activity Index) was assessed. The population was divided into two subcohorts: (1) methotrexate (MTX)-only users and (2) multiple nonbiologic DMARD users. In both subcohorts, we compared the characteristics of patients who received care consistent with the ACR recommendations (e.g., prescriptions for treatment acceleration) and their providers with the characteristics of those who did not at the conclusion of one visit and over two visits, using logistic regression and adjusting for clustering of patients by rheumatologist.
Our study included 741 MTX monotherapy and 995 multiple nonbiologic DMARD users cared for by 139 providers. Only 36.2 % of MTX monotherapy users and 39.6 % of multiple nonbiologic DMARD users received care consistent with the recommendations after one visit, which increased over two visits to 78.3 % and 76.2 %, respectively (25-30 % achieved low disease activity by the second visit without DMARD acceleration). Increasing time since the ACR publication on RA treatment recommendations was not associated with improved adherence.
Allowing two encounters for treatment acceleration was associated with an increase in care concordant with the recommendations; however, time since publication was not.
与美国风湿病学会(ACR)关于类风湿关节炎(RA)使用改善病情抗风湿药物(DMARDs)的建议相一致的治疗相关因素尚不清楚。
我们确定了一个全国性队列,该队列中的RA患者在2008年12月至2013年2月期间就诊,且之前未使用过生物制剂。评估了针对中度至高度疾病活动(使用临床疾病活动指数)的治疗加速情况(生物和非生物DMARDs的起始或剂量增加)。将人群分为两个亚组:(1)仅使用甲氨蝶呤(MTX)的患者和(2)使用多种非生物DMARDs的患者。在两个亚组中,我们使用逻辑回归并针对风湿病学家对患者的聚类情况进行调整,比较了在一次就诊结束时和两次就诊时接受符合ACR建议的治疗(例如,治疗加速处方)的患者及其医疗服务提供者的特征与未接受符合建议治疗的患者及其医疗服务提供者的特征。
我们的研究纳入了由139名医疗服务提供者诊治的741名单用MTX治疗的患者和995名使用多种非生物DMARDs的患者。一次就诊后,仅36.2%的MTX单药治疗患者和39.6%的使用多种非生物DMARDs的患者接受了符合建议的治疗,两次就诊后这一比例分别增至78.3%和76.2%(25 - 30%的患者在第二次就诊时未加速使用DMARDs的情况下达到了低疾病活动度)。自ACR发布RA治疗建议以来时间的增加与依从性的改善无关。
允许进行两次治疗加速就诊与符合建议的治疗增加相关;然而,自发布以来的时间长短并非如此。