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成人川崎病的管理

Management of Kawasaki disease in adults.

作者信息

Denby Kara J, Clark Daniel E, Markham Larry W

机构信息

Departments of Internal Medicine and Pediatrics, Vanderbilt University Medical Center, Nashville, USA.

Divisions of Cardiovascular Medicine and Pediatric Cardiology, Vanderbilt University Medical Center, Nashville, USA.

出版信息

Heart. 2017 Nov;103(22):1760-1769. doi: 10.1136/heartjnl-2017-311774. Epub 2017 Jul 27.

Abstract

Kawasaki disease is the most common childhood vasculitis in the USA and the most common cause of acquired cardiac disease in children in developed countries. Since the vast majority of Kawasaki disease initially presents at <5 years of age, many adult cardiologists are unfamiliar with the pathophysiology of this disease. This vasculitis has a predilection for coronary arteries with a high complication rate across the lifespan for those with medium to large coronary artery aneurysms. An inflammatory cascade produces endothelial dysfunction and damage to the vascular wall, leading to aneurysmal dilatation. Later, pseudonormalisation of the vascular lumen occurs through vascular remodelling and layering thrombus, but this does not necessarily indicate resolution of disease or reduction of risk for future complications. There is a growing prevalence of Kawasaki disease, making it increasingly relevant for adult cardiologists as this population transitions into adulthood. As the 2017 American Heart Association (AHA) and 2014 Japanese Circulation Society (JCS) guidelines emphasise, Kawasaki disease requires rigorous follow-up with cardiac stress testing and non-invasive imaging to detect progressive stenosis, thrombosis and luminal occlusion that may lead to myocardial ischaemia and infarction. Due to differences in disease mechanisms, coronary disease due to Kawasaki disease should be managed with different pharmacological and non-pharmacological treatment algorithms than atherosclerotic coronary disease. This review addresses gaps in the current knowledge of the disease and its optimal treatment, differences in the AHA and JCS guidelines, targets for future research and obstacles to transition of care from adolescence into adulthood.

摘要

川崎病是美国最常见的儿童血管炎,也是发达国家儿童后天性心脏病的最常见病因。由于绝大多数川崎病最初在5岁以下发病,许多成人心脏病专家并不熟悉这种疾病的病理生理学。这种血管炎易累及冠状动脉,对于患有中至大型冠状动脉瘤的患者,其在整个生命周期中的并发症发生率都很高。炎症级联反应会导致内皮功能障碍和血管壁损伤,进而引起动脉瘤样扩张。之后,血管腔会通过血管重塑和血栓分层实现假性正常化,但这并不一定表明疾病得到缓解或未来并发症风险降低。川崎病的患病率在不断上升,随着这一人群步入成年期,这使得它与成人心脏病专家的相关性越来越高。正如2017年美国心脏协会(AHA)和2014年日本循环学会(JCS)指南所强调的,川崎病需要通过心脏负荷试验和无创成像进行严格随访,以检测可能导致心肌缺血和梗死的进行性狭窄、血栓形成和管腔闭塞。由于疾病机制不同,川崎病所致的冠状动脉疾病应采用与动脉粥样硬化性冠状动脉疾病不同的药物和非药物治疗方案。本综述阐述了目前对该疾病及其最佳治疗方法认识上的差距、AHA和JCS指南的差异、未来研究的目标以及从青少年到成年期护理过渡的障碍。

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