Farman Sumaira, Ahmad Nighat Mir, Saeed Muhammad Ahmed, Asad Kanwal, Shabbir Ghulam
Division of Rheumatology, Fatima Memorial Hospital (FMH), Lahore.
J Coll Physicians Surg Pak. 2015 Feb;25(2):129-33.
To determine the frequency of patients with early Rheumatoid Arthritis (RA) achieving disease remission and/or low disease activity after 6 months of treatment with conventional Disease Modifying Anti-Rheumatic Drugs (DMARDs) by using treat-to-target approach in routine clinical practice.
Descriptive study.
Division of Rheumatology, Fatima Memorial Hospital (FMH), College of Medicine and Dentistry, Lahore, from March 2011 to February 2012.
Patients with early RA defined as disease duration ² 1 year were enrolled by purposive sampling, diagnosed as per American College of Rheumatology (ACR) 1987 criteria. Treat-to-target approach was defined as per European League Against Rheumatism (EULAR) 2010 guidelines for treatment of RA with conventional DMARDs. Outcome measures of remission and low disease activity were defined as per DAS 28 score criteria. Patient response to treatment was also determined by EULAR response criteria.
Out of 67 patients, 50 patients completed the 6 months study period, rest were lost to follow-up. All patients were started on Methotrexate and mean weekly dose at 6 months was 18.9 ± 3.8 mg. Remission was achieved in 17 (34%) and target of low disease activity was achieved in 29 (58%) of patients. EULAR good response was seen in 28 (56%), moderate response in 21 (42%) and no response to treatment in 1 (2%).
By applying treat-to-target approach in early RA, achievement of clinical remission or low disease activity with conventional DMARDs is a realistic goal in routine practice.
通过在常规临床实践中采用达标治疗方法,确定早期类风湿关节炎(RA)患者在使用传统改善病情抗风湿药物(DMARDs)治疗6个月后达到疾病缓解和/或低疾病活动度的频率。
描述性研究。
2011年3月至2012年2月,拉合尔医学院和牙科学院法蒂玛纪念医院(FMH)风湿病科。
通过目的抽样纳入病程≥1年的早期RA患者,根据美国风湿病学会(ACR)1987年标准进行诊断。达标治疗方法按照欧洲抗风湿病联盟(EULAR)2010年传统DMARDs治疗RA的指南进行定义。缓解和低疾病活动度的结局指标根据DAS 28评分标准进行定义。患者对治疗的反应也根据EULAR反应标准进行确定。
67例患者中,50例患者完成了6个月的研究期,其余患者失访。所有患者均开始使用甲氨蝶呤,6个月时的平均每周剂量为18.9±3.8毫克。17例(34%)患者达到缓解,29例(58%)患者达到低疾病活动度目标。28例(56%)患者有EULAR良好反应,21例(42%)患者有中度反应,1例(2%)患者对治疗无反应。
在早期RA中应用达标治疗方法,使用传统DMARDs实现临床缓解或低疾病活动度在常规实践中是一个现实的目标。