(类风湿性关节炎)。

Deutsche medizinische Wochenschrift (1946) Pub Date : 2025-04-01 Epub Date: 2025-04-08 DOI:10.1055/a-2286-6620
Jutta Bauhammer, Christoph Fiehn
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引用次数: 0

摘要

类风湿性关节炎(RA)是一种炎症性全身性疾病,主要但不完全影响关节和其他肌肉骨骼系统结构。它最典型的表现是由高度炎症性自身免疫性滑膜炎引起的多发性关节炎。关节外表现也可表现为肺间质性疾病或血管炎,主要影响小血管。早期、有针对性的治疗可对疾病的进展产生重大影响;然而,如果不进行治疗,患者很可能经历不可逆转的功能丧失和死亡率增加。建议在确诊后立即服用DMARD。在没有禁忌症的情况下,首选甲氨蝶呤。在大多数情况下,暂时添加糖皮质激素,3-6个月后完全停止给药。治疗遵循以缓解为目标的治疗原则。疾病活动性和缓解是通过结合临床表现、患者陈述和炎症活动性实验室测试的分数来计算的。治疗被认为是有效的,达到至少50%的分数降低。12周后评估评分反应,24周后评估治疗目标。如果不满足2项中的1项,并且没有出现疾病严重进展的危险因素,那么在甲氨蝶呤之后,将首先使用另一种常规系统性DMARD策略;否则,可以给予生物(b)DMARD或其他靶向合成DMARD。如上所述进行重新评价,如果没有达到目标,将使用其他b-或ts-DMARDs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Rheumatoid Arthritis].

Rheumatoid arthritis (RA) is an inflammatory systemic disease that mainly, but not exclusively, affects the joints and other structures of the musculoskeletal system. It most typically manifests in polyarthritis due to a highly inflammatory autoimmune synovitis. Extra-articular manifestations might also show in the shape of an interstitial lung disease or vasculitis, mainly affecting the small vessels. Early, well-targeted treatment can have a major impact on the progression of the disease; without treatment, however, patients are most likely to experience an irreversible loss of functionality and increased mortality. The administration of a DMARD starting as soon as being diagnosed is recommended. The first choice in medication should be methotrexate whenever there are no contraindications. In most cases, glucocorticoids are added temporarily with administration coming to a complete stop after 3-6 months. Therapy follows the treat-to-target principle aiming at remission. Disease activity and remission are calculated in scores combining clinical findings, patients' statements and laboratory tests for inflammatory activity. Treatment is considered responsive with achieving a minimum of a 50% reduction of the score. Score responses are evaluated after 12 weeks, therapeutic targets after 24. If 1 of the 2 is not met and there are no risk factors present for a severe progression of the disease, then another strategy with conventional systemic (cs)DMARD will first be used after methotrexate; otherwise biological (b)DMARD or other targeted synthetic (ts)DMARD can be given. Re-evaluation is carried out as described above, and if the target is not met, other b- or ts-DMARDs will be used.

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