McNeal-Davidson Ariane, Fournier Anne, Scuccimarri Rosie, Dancea Adrian, Houde Christine, Bellavance Marc, Dahdah Nagib
Division of Pediatric Cardiology, CHU Sainte-Justine, Université de Montreal, 3175, Côte Sainte-Catherine, Montreal, QC H3T 1C5, Canada.
Pediatr Cardiol. 2013 Jan;34(1):170-8. doi: 10.1007/s00246-012-0409-2. Epub 2012 Jun 17.
Most population-based series reporting on the coronary artery complications after Kawasaki disease (KD) originate from Japan. This study aimed to describe the complete series of KD patients from the province of Quebec in Canada, a predominantly Caucasian population. This retrospective case series was conducted by the Quebec Kawasaki Disease Registry, a multi-institutional collaboration reviewing 89.8 % of all KD cases identified by the Ministry of Health records of hospitalization for KD from the first recognized case in 1976 until 2008. This report describes the course of 38 patients (95 % Caucasians) with a diagnosis of giant coronary artery aneurysms, which represent 1.9 % of all reviewed cases and 26.2 % of those with a coronary aneurysm 5 mm or larger. The age at diagnosis was 5.52 ± 4.04 years, and the follow-up period was 9.26 ± 6.9 years. The KD diagnosis was retrospective at autopsy in two cases and via echocardiography in four cases. The overall freedom from coronary thrombi, coronary intervention, or death was respectively 63.9, 67.5, and 85.1 %. Five deaths occurred as follows: 21 days after onset of fever (2 cases), 1.8 months after onset of fever (1 case), 1 year after retrospectively presumed but previously undiagnosed KD (1 case), and 5.7 years after a KD diagnosis (1 case of sudden cardiac death). Percutaneous transluminal coronary revascularization was attempted in four cases (1 requiring cardiac transplantation), and two other cases underwent primary bypass graft surgery. Whereas this study investigated cases of KD with severe coronary sequelae in the Province of Quebec, larger collaborative studies should be conducted for further understanding of the disease in predominantly non-Asian populations.
大多数关于川崎病(KD)后冠状动脉并发症的基于人群的系列报道都来自日本。本研究旨在描述加拿大魁北克省的完整KD患者系列,该省主要是白种人群体。本回顾性病例系列由魁北克川崎病登记处开展,这是一项多机构合作研究,对1976年首例确诊病例至2008年期间卫生部KD住院记录中识别出的所有KD病例的89.8%进行了回顾。本报告描述了38例诊断为巨大冠状动脉瘤患者(95%为白种人)的病程,这些患者占所有回顾病例的1.9%,占冠状动脉瘤直径5毫米或更大病例的26.2%。诊断时的年龄为5.52±4.04岁,随访期为9.26±6.9年。两例KD诊断是在尸检时回顾性做出的,四例是通过超声心动图做出的。冠状动脉血栓形成、冠状动脉介入或死亡的总体无事件生存率分别为63.9%、67.5%和85.1%。发生了5例死亡,情况如下:发热开始后21天(2例)、发热开始后1.8个月(1例)、回顾性推测但此前未诊断的KD发病后1年(1例)以及KD诊断后5.7年(1例心源性猝死)。4例尝试了经皮腔内冠状动脉血运重建(1例需要心脏移植),另外2例接受了初次搭桥手术。尽管本研究调查了魁北克省患有严重冠状动脉后遗症的KD病例,但仍应开展更大规模的合作研究,以进一步了解主要为非亚洲人群中的该疾病。