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川崎病中的心血管异常。

Cardiovascular abnormalities in Kawasaki disease.

作者信息

Novelli V M, Galbraith A, Robinson P J, Smallhorn J F, Marshall W C

出版信息

Arch Dis Child. 1984 May;59(5):405-9. doi: 10.1136/adc.59.5.405.

Abstract

Eighteen patients with Kawasaki disease underwent serial, cross sectional echocardiographic examinations to determine the extent and subsequent course of cardiac involvement in this disease. The mean follow up period was 12.3 months. Cardiovascular complications were found in a total of 10 patients (55%). Coronary artery aneurysms were detected in 6 patients (33%), pericardial effusions in two, and one patient had electrocardiographic evidence suggesting inferior myocardial infarction. Coronary artery aneurysms, seen exclusively in infants less than 12 months of age, were found in four to regress over a mean period of 7.5 months (range 1 to 13 months). Electrocardiogram, chest radiographs, and clinical examination were unhelpful in identifying those patients with coronary artery aneurysms. Eight patients (44%) were hypertensive, though only two required treatment. While all patients have survived, serial cross sectional echocardiographs should be performed in children with Kawasaki disease to identify those at risk from potentially fatal complications.

摘要

18名川崎病患者接受了系列横断面超声心动图检查,以确定该疾病中心脏受累的程度及后续病程。平均随访期为12.3个月。总共10名患者(55%)出现心血管并发症。6名患者(33%)检测到冠状动脉瘤,2名患者出现心包积液,1名患者有心电图证据提示下壁心肌梗死。冠状动脉瘤仅见于12个月以下婴儿,4例患者的冠状动脉瘤在平均7.5个月(范围1至13个月)内消退。心电图、胸部X线片和临床检查对识别患有冠状动脉瘤的患者并无帮助。8名患者(44%)患有高血压,不过只有2名患者需要治疗。虽然所有患者均存活,但川崎病患儿应进行系列横断面超声心动图检查,以识别有潜在致命并发症风险的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c230/1628522/c515f760fd44/archdisch00734-0021-a.jpg

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