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The fate and observed management of giant coronary artery aneurysms secondary to kawasaki disease in the province of quebec: The complete series since 1976

机译:魁北克省继川崎病继发的巨大冠状动脉瘤的命运和观察到的处理:自1976年以来的完整系列

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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.
机译:关于川崎病(KD)后冠状动脉并发症的大多数基于人群的系列报道均来自日本。这项研究旨在描述来自加拿大魁北克省(主要是白种人)的完整KD患者系列。该回顾性病例系列由魁北克川崎疾病登记处进行,魁北克川崎疾病登记处是一个多机构合作机构,审查了卫生部从1976年首次确认的病例到2008年住院的KD住院记录中所确定的所有KD病例的89.8%。 38例(95%的白种人)患有巨人冠状动脉瘤的病程,占所有回顾性病例的1.9%,占5mm或更大的冠状动脉瘤的26.2%。诊断时年龄为5.52±4.04岁,随访时间为9.26±6.9岁。回顾性分析KD诊断为2例,通过超声心动图检查为4例。患冠状动脉血栓形成,冠状动脉介入治疗或死亡的总体自由度分别为63.9%,67.5%和85.1%。发生了五例死亡,分别为:发热后21天(2例),发热后1.8个月(1例),回顾性推测但先前未确诊的KD 1年(1例)和KD诊断后5.7年( 1例心脏猝死)。尝试了四例经皮腔内冠状动脉血运重建术(1例需要心脏移植),另外两例进行了初次搭桥术。尽管这项研究调查了魁北克省患有严重冠状动脉后遗症的KD病例,但应该进行更大范围的合作研究以进一步了解主要是非亚洲人群中的该病。

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