Pahl E, Ettedgui J, Neches W H, Park S C
Division of Pediatric Cardiology, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pennsylvania 15213.
J Am Coll Cardiol. 1989 Nov 1;14(5):1318-25. doi: 10.1016/0735-1097(89)90435-x.
From September 1976 to August 1988, 205 patients with mucocutaneous lymph node syndrome (Kawasaki disease) were evaluated; 29 were suspected of having coronary artery abnormalities because of either abnormalities on echocardiography (n = 21), congestive heart failure (n = 3), prolonged fever (n = 3) or cardiac arrest (n = 2). All 29 underwent cardiac catheterization and 22 were found to have coronary artery abnormalities. An additional 4 patients were diagnosed solely by autopsy; therefore, 26 patients (12%) in this series had coronary artery abnormalities. The clearance of contrast medium from the coronary arteries after aortography was significantly prolonged in patients with coronary artery aneurysms as compared with that in a control group (p less than 0.001). All patients exhibited delayed clearance of contrast medium on the initial aortogram as compared with that on follow-up studies (p less than 0.01). Of the 22 patients with angiographically documented coronary artery abnormalities, 19 had right and 20 had left coronary artery involvement; the majority had diffuse involvement of both vessels. In 15 patients who underwent follow-up catheterization 6 months to 7 years after initial study, complete resolution was observed in only 37% of affected coronary artery segments. In four patients, three of whom were asymptomatic, severely stenotic or occluded coronary artery segments were found on late catheterization. Coronary artery bypass surgery was performed in two of these patients. Echocardiography did not detect any of these stenoses. Although echocardiography is important for initial diagnosis and serial evaluation, angiography is essential to fully define the nature and extent of coronary artery lesions, particularly if stenosis is present.
1976年9月至1988年8月,对205例黏膜皮肤淋巴结综合征(川崎病)患者进行了评估;其中29例因超声心动图异常(n = 21)、充血性心力衰竭(n = 3)、长期发热(n = 3)或心脏骤停(n = 2)而怀疑有冠状动脉异常。所有29例均接受了心导管检查,其中22例被发现有冠状动脉异常。另有4例仅通过尸检确诊;因此,本系列中有26例(12%)患者有冠状动脉异常。与对照组相比,冠状动脉瘤患者主动脉造影后冠状动脉内造影剂的清除明显延长(p < 0.001)。与随访研究相比,所有患者在初次主动脉造影时造影剂清除均延迟(p < 0.01)。在22例经血管造影证实有冠状动脉异常的患者中,19例右冠状动脉受累,20例左冠状动脉受累;大多数患者双侧血管均有弥漫性受累。在初次研究后6个月至7年接受随访心导管检查的15例患者中,仅37%的受累冠状动脉节段观察到完全恢复。在4例患者中,其中3例无症状,后期心导管检查发现严重狭窄或闭塞的冠状动脉节段。其中2例患者接受了冠状动脉搭桥手术。超声心动图未检测到任何这些狭窄。虽然超声心动图对初始诊断和系列评估很重要,但血管造影对于全面确定冠状动脉病变的性质和范围至关重要,特别是在存在狭窄的情况下。