Newburger Jane W, Takahashi Masato, Gerber Michael A, Gewitz Michael H, Tani Lloyd Y, Burns Jane C, Shulman Stanford T, Bolger Ann F, Ferrieri Patricia, Baltimore Robert S, Wilson Walter R, Baddour Larry M, Levison Matthew E, Pallasch Thomas J, Falace Donald A, Taubert Kathryn A
Pediatrics. 2004 Dec;114(6):1708-33. doi: 10.1542/peds.2004-2182.
Kawasaki disease is an acute self-limited vasculitis of childhood that is characterized by fever, bilateral nonexudative conjunctivitis, erythema of the lips and oral mucosa, changes in the extremities, rash, and cervical lymphadenopathy. Coronary artery aneurysms or ectasia develop in approximately 15% to 25% of untreated children and may lead to ischemic heart disease or sudden death.
A multidisciplinary committee of experts was convened to revise the American Heart Association recommendations for diagnosis, treatment, and long-term management of Kawasaki disease. The writing group proposes a new algorithm to aid clinicians in deciding which children with fever for > or =5 days and < or =4 classic criteria should undergo echocardiography [correction], receive intravenous gamma globulin (IVIG) treatment, or both for Kawasaki disease. The writing group reviews the available data regarding the initial treatment for children with acute Kawasaki disease, as well for those who have persistent or recrudescent fever despite initial therapy with IVIG, including IVIG retreatment and treatment with corticosteroids, tumor necrosis factor-alpha antagonists, and abciximab. Long-term management of patients with Kawasaki disease is tailored to the degree of coronary involvement; recommendations regarding antiplatelet and anticoagulant therapy, physical activity, follow-up assessment, and the appropriate diagnostic procedures to evaluate cardiac disease are classified according to risk strata.
Recommendations for the initial evaluation, treatment in the acute phase, and long-term management of patients with Kawasaki disease are intended to assist physicians in understanding the range of acceptable approaches for caring for patients with Kawasaki disease. The ultimate decisions for case management must be made by physicians in light of the particular conditions presented by individual patients.
川崎病是一种儿童期急性自限性血管炎,其特征为发热、双侧非渗出性结膜炎、唇及口腔黏膜红斑、四肢变化、皮疹和颈部淋巴结肿大。未经治疗的儿童中约15%至25%会发生冠状动脉瘤或扩张,可能导致缺血性心脏病或猝死。
召集了一个多学科专家委员会来修订美国心脏协会关于川崎病诊断、治疗和长期管理的建议。写作小组提出了一种新的算法,以帮助临床医生决定哪些发热≥5天且具备≤4条典型标准的儿童应接受超声心动图检查[校正]、接受静脉注射丙种球蛋白(IVIG)治疗或两者皆用,以诊断川崎病。写作小组回顾了有关急性川崎病患儿初始治疗的数据,以及那些尽管初始接受IVIG治疗仍持续发热或复发发热的患儿的数据,包括IVIG再次治疗以及使用皮质类固醇、肿瘤坏死因子-α拮抗剂和阿昔单抗治疗的数据。川崎病患者的长期管理根据冠状动脉受累程度进行调整;关于抗血小板和抗凝治疗、体力活动、随访评估以及评估心脏病的适当诊断程序的建议根据风险分层进行分类。
川崎病患者初始评估、急性期治疗和长期管理的建议旨在帮助医生了解照顾川崎病患者的可接受方法范围。病例管理的最终决策必须由医生根据个体患者呈现的具体情况做出。