Wang Nan-Koong, Hsieh Li-Yin, Shen Ching-Tsuen, Lin Yung-Ming
Department of Pediatrics, Cathay General Hospital, 280 Jen-Ai Road, Section 4, Taipei, Taiwan.
J Formos Med Assoc. 2002 Mar;101(3):177-82.
Coronary arteriovenous fistula (CAVF) is a rare congenital anomaly in pediatric patients. Its clinical manifestations vary considerably and its long-term outcome is not fully understood. This study sought to determine the natural history and long-term outcome in CAVF patients treated over a 17-year period at Cathay General Hospital in Taipei.
The medical records of all 10 pediatric patients (five boys and five girls aged between 15 days and 15 years) with CAVF treated from 1983 through 2000 at our hospital were reviewed. Data collected included symptoms and signs, the findings of electrocardiography, echocardiography, catheterization, and angiography, and surgical results.
CAVF was diagnosed on the basis of color Doppler echocardiography in eight patients and by cardiac catheterization and angiography in two. Congestive heart failure was found in four patients and both myocardial ischemia and infarction were found in two patients. Most of the affected coronary arteries were tortuous and dilated with a mean diameter of 12.6 mm (range 5-40 mm). Under cardiopulmonary bypass, fistulous terminations were sutured in seven patients, three of whom were found to have multiple fistulous openings. Postoperative follow-up examinations revealed that all of the affected coronary arteries and fistulas remained dilated and tortuous, except in one patient. Two patients who had distal CAVF developed coronary thrombus, calcification, and ventricular aneurysm at 2 and 10 years after operation, respectively. Another patient developed fistulous recanalization 7 years after operation, but this abnormal channel had disappeared again 3 years after recanalization. One patient developed an iatrogenic CAVF 8 years after surgical repair of tetralogy of Fallot.
Unlike adults, pediatric patients with CAVF tend to be symptomatic. Ligation of the fistulous termination alone does not reduce the size of the fistula. Our findings indicate that long-term follow-up is essential due to the possibility of postoperative recanalization, persistent dilation of the coronary artery and ostium, thrombus formation, calcification, and myocardial infarction. In addition, postoperative antiplatelet therapy is recommended, especially in patients with distal CAVF and abnormally dilated coronary arteries.
冠状动脉瘘(CAVF)在儿科患者中是一种罕见的先天性异常。其临床表现差异很大,长期预后尚未完全明确。本研究旨在确定在台北国泰综合医院接受治疗17年的CAVF患者的自然病史和长期预后。
回顾了1983年至2000年在我院接受治疗的10例儿科CAVF患者(5例男孩和5例女孩,年龄在15天至15岁之间)的病历。收集的数据包括症状和体征、心电图、超声心动图、心导管检查和血管造影的结果以及手术结果。
8例患者通过彩色多普勒超声心动图诊断为CAVF,2例通过心导管检查和血管造影诊断。4例患者出现充血性心力衰竭,2例患者同时出现心肌缺血和梗死。大多数受累冠状动脉迂曲扩张,平均直径为12.6毫米(范围5 - 40毫米)。在体外循环下,7例患者的瘘口被缝合,其中3例发现有多个瘘口。术后随访检查显示,除1例患者外,所有受累冠状动脉和瘘管仍呈扩张和迂曲状态。2例远端CAVF患者分别在术后2年和10年出现冠状动脉血栓形成、钙化和室壁瘤。另1例患者在术后7年出现瘘管再通,但再通3年后该异常通道又消失了。1例患者在法洛四联症手术修复8年后出现医源性CAVF。
与成人不同,儿科CAVF患者往往有症状。仅结扎瘘口并不能减小瘘管大小。我们的研究结果表明,由于术后可能出现再通、冠状动脉和瘘口持续扩张、血栓形成、钙化和心肌梗死,长期随访至关重要。此外,建议术后进行抗血小板治疗,尤其是对于远端CAVF和冠状动脉异常扩张的患者。