Department of Pharmacology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Rheumatol Int. 2012 Mar;32(3):743-8. doi: 10.1007/s00296-010-1646-4. Epub 2010 Dec 16.
The present study was conducted in Indian rheumatoid arthritis (RA) patients prescribed disease-modifying anti-rheumatic drugs (DMARDs) to determine the incidence and type of adverse drug reactions (ADRs) leading to their withdrawal in the initial 6 months of therapy. This was considered important as pharmacogenetic variations in the pattern of RA in different populations and genetic differences in efficacy and safety to drugs demand separate studies to be conducted in different populations. Hospital records were used to identify 1,000 consecutive patients with RA fulfilling the American College of Rheumatology criteria and having at least 6-month follow-up. Age, gender, duration of arthritis, drug usage and ADR-related drug withdrawal were recorded from the charts. Most of the patients were put on single DMARD. Combined use of DMARD was less frequent and non-use of DMARD was common; however, disease control was good. The commonest DMARD used in our hospital was hydroxychloroquine 444 (44%) and the commonest combination used was methotrexate with hydroxychloroquine by 55 (6%). Sulphasalazine use showed preference to young and males. Supportive drugs used were NSAIDs by 883 (88%), corticosteroids by 646 (65%), paracetamol by 594 (59%) and amitriptyline by 88 (9%). Incidence of ADR-related DMARD withdrawal was maximum with leflunomide 2/15 (13.33%) followed by methotrexate 9/116 (7.76%), sulphasalazine 6/185 (3.24%), chloroquine 3/131 (2.29%) and hydroxychloroquine 8/444 (1.8%). Severity and symptomatology of disease, genetic pattern of patients, financial status, previous experience of the clinicians and patients, availability of drugs, patient expectations and compliance were the main factors that lead to a difference in pattern of therapy in our patients compared to other population.
本研究在印度类风湿关节炎(RA)患者中进行,这些患者接受了疾病修饰抗风湿药物(DMARDs)治疗,以确定在治疗的最初 6 个月内导致其停药的不良药物反应(ADR)的发生率和类型。这一点很重要,因为不同人群中 RA 的遗传模式和药物疗效及安全性的遗传差异需要在不同人群中进行单独的研究。从病历中确定了 1000 名符合美国风湿病学会标准且至少有 6 个月随访的连续 RA 患者。从图表中记录了年龄、性别、关节炎持续时间、药物使用情况和与 ADR 相关的停药情况。大多数患者接受了单一 DMARD 治疗。联合使用 DMARD 的情况较少,不使用 DMARD 的情况较常见,但疾病控制良好。我们医院最常用的 DMARD 是羟氯喹 444(44%),最常用的联合用药是甲氨蝶呤联合羟氯喹,共 55(6%)例。柳氮磺胺吡啶在年轻人和男性中更受欢迎。使用的辅助药物包括 883 例非甾体抗炎药(88%)、646 例皮质类固醇(65%)、594 例扑热息痛(59%)和 88 例阿米替林(9%)。与 DMARD 相关的停药 ADR 发生率最高的是来氟米特 2/15(13.33%),其次是甲氨蝶呤 9/116(7.76%)、柳氮磺胺吡啶 6/185(3.24%)、氯喹 3/131(2.29%)和羟氯喹 8/444(1.8%)。疾病的严重程度和症状、患者的遗传模式、经济状况、临床医生和患者的既往经验、药物的可获得性、患者的期望和依从性是导致我们的患者与其他人群治疗模式存在差异的主要因素。