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自身免疫性疾病中的炎症和血栓性瓣膜病。

Inflammatory and thrombotic valvulopathies in autoimmune disease.

机构信息

Medicine, Columbia University Irving Medical Center, New York, New York, USA

Medicine, University of Michigan Michigan Medicine, Ann Arbor, Michigan, USA.

出版信息

Heart. 2023 Mar 27;109(8):583-588. doi: 10.1136/heartjnl-2021-319603.

Abstract

Rheumatologic diseases are characterised by loss of immune tolerance, resulting in systemic inflammation. Inflammation and scarring of the endocardium, which lines the inner surface of the heart chambers and valves, can result in valvular thickening and dysfunction. Estimates of prevalence vary depending on the sensitivity of the screening methodology used and range from 30%-50% in systemic lupus and rheumatoid arthritis to 10%-30% in ankylosing spondylitis. Progression of valve disease is a slow process but can result in haemodynamically significant complications. Thromboembolic complications such as cerebrovascular occlusions pose a serious risk of morbidity. The presence of antiphospholipid antibodies increases the risk of valvular disease and thrombotic complications. Anticoagulation is recommended in the presence of antiphospholipid antibodies, but the guidance on the role of immunosuppressive therapy to treat valvular disease is lacking. Surgical valve therapy may be considered in severe disease, but there is increased risk in patients with an autoimmune disease which includes a higher risk of infection, thromboembolic and bleeding complications, as well as cardiovascular events in the setting of premature atherosclerotic heart disease. Therefore, management should be provided in a multidisciplinary team that includes a rheumatologist, a cardiologist and a cardiothoracic surgeon; medical therapy should be optimised before considering a high-risk valve surgery.

摘要

风湿性疾病的特征是免疫耐受丧失,导致全身炎症。心脏腔室和瓣膜内表面的心内膜发生炎症和瘢痕形成,可导致瓣膜增厚和功能障碍。患病率的估计因所使用的筛查方法的敏感性而异,在系统性红斑狼疮和类风湿关节炎中为 30%-50%,在强直性脊柱炎中为 10%-30%。瓣膜病的进展是一个缓慢的过程,但可导致血流动力学显著并发症。血栓栓塞并发症,如脑血管阻塞,构成严重的发病风险。抗磷脂抗体的存在增加了瓣膜病和血栓并发症的风险。存在抗磷脂抗体时推荐抗凝治疗,但缺乏关于免疫抑制疗法治疗瓣膜病作用的指南。在严重疾病中可能需要考虑手术瓣膜治疗,但在包括感染、血栓栓塞和出血并发症风险增加在内的自身免疫性疾病患者中,以及在早发性动脉粥样硬化性心脏病的情况下,心血管事件的风险更高。因此,管理应由包括风湿病学家、心脏病专家和心胸外科医生在内的多学科团队提供;在考虑高风险瓣膜手术之前,应优化药物治疗。

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