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首页> 外文期刊>Current treatment options in neurology >Prevention of Stroke in Rheumatoid Arthritis
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Prevention of Stroke in Rheumatoid Arthritis

机译:类风湿关节炎中风的预防

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摘要

Recognizing that systemic inflammation is a major contributor to the increased risk of cardiovascular disease (CVD), including stroke, in rheumatoid arthritis (RA) serves as the basis for prevention strategies for cerebrovascular disease in RA. In addition to traditional cardiovascular risk factors, recognize that RA may be an independent risk factor for cerebrovascular accident (CVA). The risk of CVD should be assessed in each patient with RA, utilizing modified risk score calculators. Careful monitoring and control of systemic inflammation should be undertaken in conjunction with assessing each patient's CVD risk, acknowledging the benefits and risks of specific RA-directed therapies. Emphasis should be given to early and aggressive control of inflammation in RA patients, particularly those with seropositivity, increased inflammatory markers, long disease duration (>10 years), and/or extra-articular manifestations. In RA patients requiring glucocorticoid therapy, attempts should be made to use or wean to the minimal effective dose (preferably less than 7.5 mg/day). It should be recognized that both disease-modifying antirheumatic drugs (DMARDs), particularly methotrexate, and tumor necrosis factor (TNF)-alpha inhibitors partially mitigate the risk of CVD. In patients with inadequate control of inflammation with DMARDs, consideration should be given to switch to anti-TNF agents earlier in the disease process. Modifiable risk factors should be addressed as per guidelines for the general population. Active RA may be considered as a risk equivalent to diabetes mellitus when applying these guidelines. With regard to lipid management and use of statin therapy, further studies are required given the apparent "lipid paradox" in RA. Use of aspirin for primary prevention in RA has not been well studied; however, when aspirin is used for secondary prevention, one should recognize that concomitant use of nonsteroidal anti-inflammatory drugs (NSAIDs) may decrease the antiplatelet effect. Given the cardiovascular risk associated with NSAIDs, the lowest possible dose for the shortest time should be used.
机译:认识到系统性炎症是类风湿性关节炎(RA)中包括中风的心血管疾病(CVD)风险增加的主要原因,这是RA预防脑血管疾病策略的基础。除了传统的心血管危险因素,认识到RA可能是脑血管意外(CVA)的独立危险因素。应使用改良的风险评分计算器评估每位RA患者的CVD风险。在评估每个患者的CVD风险的同时,应仔细监测和控制全身性炎症,并确认特定RA定向疗法的益处和风险。应重点注意RA患者的炎症的早期和积极控制,特别是那些血清反应阳性,炎症标志物增加,疾病持续时间长(> 10年)和/或关节外表现的患者。在需要糖皮质激素治疗的RA患者中,应尝试使用或戒断至最小有效剂量(最好小于7.5 mg /天)。应当认识到,疾病缓解型抗风湿药(DMARD),尤其是甲氨蝶呤和肿瘤坏死因子(TNF)-α抑制剂均能部分缓解CVD的风险。对于用DMARD无法充分控制炎症的患者,应考虑在疾病过程的早期改用抗TNF药物。可改变的危险因素应按照一般人群的指南处理。应用这些指南时,活动性RA可能被视为与糖尿病等效的风险。关于脂质管理和他汀类药物治疗的使用,鉴于RA中明显的“脂质悖论”,需要进一步的研究。阿司匹林在RA一级预防中的应用尚未得到充分研究。但是,当使用阿司匹林进行二级预防时,应该认识到,同时使用非甾体类抗炎药(NSAIDs)可能会降低抗血小板作用。考虑到与非甾体抗炎药有关的心血管风险,应在最短时间内使用尽可能低的剂量。

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