Aletaha D, Kerschbaumer A
Klinische Abteilung für Rheumatologie, Medizinische Universität Wien, Währinger Gürtel 18-20, 1090, Wien, Österreich.
Z Rheumatol. 2017 Feb;76(1):8-14. doi: 10.1007/s00393-016-0251-7.
Therapy reduction in rheumatoid arthritis (RA) is still a challenge for physicians as well as for patients. Effective therapy with subsequent achievement of low disease activity or even remission is achievable for numerous patients using currently available treatment options. Therapy discontinuation has therefore become a hot topic and the risk of exacerbation of well-controlled RA must be weighed against the medical and economic benefits of reducing or even discontinuing therapy. This article gives a review of data regarding tapering of therapy in RA, focusing on conventional disease-modifying antirheumatic drug (DMARD) monotherapy, reduction of conventional therapy under continuing therapy with biologics and discontinuation of biologics. Important influencing factors for a safe and successful tapering procedure appear to be disease activity, disease duration and the tapering process itself (i.e. gradual dose reduction vs. abrupt discontinuation). Additionally, the so-called nocebo effect should also be taken into consideration for interpretation of drug tapering studies.
类风湿关节炎(RA)治疗的减量对医生和患者来说仍是一项挑战。使用目前可用的治疗方案,众多患者能够实现有效的治疗并随后达到低疾病活动度甚至缓解。因此,治疗的中断已成为一个热门话题,必须权衡病情得到良好控制的RA病情加重的风险与减少甚至中断治疗的医学和经济效益。本文综述了有关RA治疗减量的数据,重点关注传统改善病情抗风湿药(DMARD)单药治疗、在继续使用生物制剂治疗的情况下减少传统治疗以及停用生物制剂。安全且成功的减量过程的重要影响因素似乎是疾病活动度、病程以及减量过程本身(即逐渐减量与突然停药)。此外,在解释药物减量研究时还应考虑所谓的反安慰剂效应。